HistCite - index: Fragile X (expanded)

Mon Apr 4 11:09:33 2005

Papers with one of the following phrases in the title:
fragile x or FMRP or trinucleotitde expansion or nucleotide expansion or cgg

Nodes: 2647, Authors: 5321, Journals: 428, Outer References: 16458, Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by year, source, volume, issue, page.
Page 9: 1 2 3 4 5 6 7 8 9

# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2401 0 0 2401 2003 BIOLOGICAL PSYCHIATRY 53(8):49S-49S
Daly EM; Moore CJ; Schmitz N; Morris R; Murphy KC; et al.
Expansion of CGG trinucleotide repeats: Effect on neuropsychology of male premutation carriers of Fragile X syndrome
0 0
2402 0 0 2402 2003 BIOLOGICAL PSYCHIATRY 53(8):152S-152S
Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al.
The effect of premutation CGG trinucleotide repeat expansion, and %FMRP(+) lymphocytes reduction, on brain anatomy
0 0
2403 38 53 2403 2003 BIOLOGY OF THE CELL 95(3-4):221-228
Schaeffer C; Beaulande M; Ehresmann C; Ehresmann B; Moine H
The RNA binding protein FMRP: new connections and missing links
3 8
2404 23 62 2404 2003 BMC MOLECULAR BIOLOGY 4
Chandler SP; Kansagra P; Hirst MC
Fragile X (CGG)(n) repeats induce a transcriptional repression in cis upon a linked promoter: Evidence for a chromatin mediated effect
0 3
2405 13 41 2405 2003 BRAIN RESEARCH 971(1):83-89
Galvez R; Gopal AR; Greenough WT
Somatosensory cortical barrel dendritic abnormalities in a mouse model of the fragile X mental retardation syndrome
4 6
2406 26 36 2406 2003 BRAIN RESEARCH 972(1-2):9-15
Segal M; Kreher U; Greenberger V; Braun K
Is fragile X mental retardation protein involved in activity-induced plasticity of dendritic spines?
0 1
2407 20 38 2407 2003 BRAIN TOPOGRAPHY 15(3):165-171
Castren M; Paakkonen A; Tarkka IM; Ryynanen M; Partanen J
Augmentation of auditory N1 in children with fragile X syndrome
2 2
2408 36 62 2408 2003 CELL 112(3):317-327
Zalfa F; Giorgi M; Primerano B; Moro A; Di Penta A; et al.
The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at Synapses
37 69
2409 4 6 2409 2003 CLINICAL GENETICS 64(1):54-56
Rogers C; Partington MW; Turner GM
Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome
3 4
2410 0 1 2410 2003 CLINICAL GENETICS 64(2):106-108
Leavitt BR
Something lost in the translation: 'premutations' in the FMR1 gene cause Fragile X tremor/ataxia syndrome (FXTAS)
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2411 69 87 2411 2003 CURRENT OPINION IN PEDIATRICS 15(6):559-566
Chiurazzi P; Neri G; Oostra BA
Understanding the biological underpinnings of fragile X syndrome
2 5
2412 43 136 2412 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):65-76
Greene E; Handa V; Kumari D; Usdin K
Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia
0 0
2413 97 168 2413 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):111-123
Bakker CE; Oostra BA
Understanding fragile X syndrome: insights from animal models
4 5
2414 11 59 2414 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):140-146
Fleming K; Riser DK; Kumari D; Usdin K
Instability of the fragile X syndrome repeat in mice: the effect of age, diet and mutations in genes that affect DNA replication, recombination and repair proficiency
0 0
2415 19 33 2415 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):206-212
Hagerman PJ; Greco CM; Hagerman RJ
A cerebellar tremor/ataxia syndrome among fragile X premutation carriers
4 7
2416 24 62 2416 2003 DEVELOPMENT 130(22):5543-5552
Lee A; Li WJ; Xu KY; Bogert BA; Su K; et al.
Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1
10 15
2417 152 233 2417 2003 DEVELOPMENT AND PSYCHOPATHOLOGY 15(4):927-968
Reiss AL; Dant CC
The behavioral neurogenetics of fragile X syndrome: Analyzing gene-brain-behavior relationships in child developmental psychopathologies
0 0
2418 0 0 2418 2003 DEVELOPMENTAL BIOLOGY 259(2):528-529
Qin M; Kang J; Smith CB
Increased local rates of cerebral protein synthesis in fragile X knockout mice.
0 0
2419 14 24 2419 2003 EUROPEAN CHILD & ADOLESCENT PSYCHIATRY 12(4):172-177
Sabaratnam M; Murthy NV; Wijeratne A; Buckingham A; Payne S
Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome - A prospective ten-year follow-up study
0 1
2420 28 61 2420 2003 EXPERIMENTAL CELL RESEARCH 289(1):95-107
Bardoni B; Willemsen R; Weiler IJ; Schenck A; Severijnen LA; et al.
NUFIP 1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosome
6 7
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2421 28 34 2421 2003 GENETIC TESTING 7(4):303-308
Gasteiger M; Grasbon-Frod E; Neitzel B; Kooy F; Holinski-Feder E
FMR1 gene deletion/reversion: A pitfall of fragile X carrier testing
0 0
2422 20 29 2422 2003 GENETIC TESTING 7(4):339-343
Rife M; Badenas C; Mallolas J; Jimenez L; Cervera R; et al.
Incidence of Fragile X in 5,000 consecutive newborn males
0 2
2423 3 7 2423 2003 GENETIC TESTING 7(4):345-346
Adir V; Shahak E; Dar H; Borochowitz ZU
Detection of X chromosome aneuploidy using Southern blot analysis during routine population-based screening for Fragile X syndrome
0 0
2424 15 55 2424 2003 GENETICS IN MEDICINE 5(5):378-384
Skinner D; Sparkman KL; Bailey DB
Screening for fragile X syndrome: Parent attitudes and perspectives
1 1
2425 28 41 2425 2003 HEREDITY 90(3):206-211
Arrieta I; Penagarikano O; Tele M; Ortega B; Flores P; et al.
The FMR1 CGG repeat and linked microsatellite markers in two Basque valleys
0 0
2426 1 4 2426 2003 HUMAN GENETICS 112(5-6):619-620
Macpherson J; Waghorn A; Hammans S; Jacobs P
Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia
9 18
2427 34 43 2427 2003 HUMAN GENETICS 113(5):371-376
Arocena DG; Breece KE; Hagerman PJ
Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population
1 2
2428 20 56 2428 2003 HUMAN MOLECULAR GENETICS 12(9):949-959
Willemsen R; Hoogeveen-Westerveld M; Reis S; Holstege J; Severijnen LAWFM; et al.
The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome
11 19
2429 39 53 2429 2003 HUMAN MOLECULAR GENETICS 12(14):1689-1698
Bardoni B; Castets M; Huot ME; Schenck A; Adinolfi S; et al.
82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization
8 8
2430 23 44 2430 2003 HUMAN MOLECULAR GENETICS 12(23):3067-3074
Chen LS; Tassone F; Sahota P; Hagerman PJ
The (CGG)(n) repeat element within the 5 ' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter
3 3
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2431 40 52 2431 2003 HUMAN MOLECULAR GENETICS 12(23):3087-3096
Mazroui R; Huot ME; Tremblay S; Boilard N; Labelle Y; et al.
Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs
4 4
2432 21 53 2432 2003 HUMAN MOLECULAR GENETICS 12(24):3295-3305
Ceman S; O'Donnell WT; Reed M; Patton S; Pohl J; et al.
Phosphorylation influences the translation state of FMRP-associated polyribosomes
12 15
2433 21 29 2433 2003 HUMAN REPRODUCTION 18(8):1637-1640
Gersak K; Meden-Vrtovec H; Peterlin B
Fragile X premutation in women with sporadic premature ovarian failure in Slovenia
0 0
2434 0 34 2434 2003 INTERNAL MEDICINE 42(1):110-116
Momoi A; Komura Y; Kumon L; Tamai M; Tarumi Y; et al.
Mesenteric venous thrombosis in hereditary protein c deficiency with the mutation at Arg169 (CGG -> TGG)
0 1
2435 45 118 2435 2003 INTERNATIONAL REVIEW OF RESEARCH IN MENTAL RETARDATION, VOL 27 27:83-119
Murphy MM; Abbeduto L
Language and communication in fragile X syndrome
0 0
2436 20 54 2436 2003 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 33(1):55-67
Lesniak-Karpiak K; Mazzocco MMM; Ross JL
Behavioral assessment of social anxiety in females with Turner or fragile X syndrome
0 6
2437 30 56 2437 2003 JOURNAL OF BIOLOGICAL CHEMISTRY 278(18):15669-15678
Sung YJ; Dolzhanskaya N; Nolin SL; Brown T; Currie JR; et al.
The fragile X mental retardation protein FMRP binds elongation factor 1A mRNA and negatively regulates its translation in vivo
8 13
2438 10 57 2438 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(4):267-275
Johnston C; Hessl D; Blasey C; Eliez S; Erba H; et al.
Factors associated with parenting stress in mothers of children with fragile X syndrome
0 1
2439 0 0 2439 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(5):393-393
Hansen R; Goodlin-Jones B; Nowicki S; Heeren M; Herman K; et al.
Behavioral phenotypes in older children with autistic spectrum disorders and fragile X: Similarities and differences
0 0
2440 0 0 2440 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1200-1200
Cotton RW; Word CJ
Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54.
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2441 0 0 2441 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1201-1201
Clarke GW
Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54.
0 0
2442 0 0 2442 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1202-1202
Thompson WC; Taroni F; Aitken CGG
Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54. Author's response
0 0
2443 7 32 2443 2003 JOURNAL OF INTELLECTUAL & DEVELOPMENTAL DISABILITY 28(2):135-144
Richdale AL
A descriptive analysis of sleep behaviour in children with Fragile X
1 1
2444 0 0 2444 2003 JOURNAL OF MEDICAL GENETICS 40:S15-S15
Ennis S; Collins A; Morton NE
SNP-based haplotypes and LD blocks in the fragile X region
0 0
2445 0 0 2445 2003 JOURNAL OF MEDICAL GENETICS 40:S49-S49
Dalton A; Mills AC; Rigby A; Manly T; Hollis C; et al.
The neuropsychological phenotype of fragile X premutation males
0 0
2446 0 0 2446 2003 JOURNAL OF MEDICAL GENETICS 40:S80-S80
Payne S; Powell CM
Fragile-X intermediate alleles - instability and inconclusion
0 0
2447 18 22 2447 2003 JOURNAL OF MEDICAL GENETICS 40(5):377-379
Willemsen R; Smits A; Severijnen LA; Jansen M; Jacobs A; et al.
Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis
3 3
2448 28 41 2448 2003 JOURNAL OF MEDICAL GENETICS 40(7):535-539
de Vries BBA; Severijnen LA; Jacobs A; Olmer R; Halley DJJ; et al.
FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics
1 1
2449 0 0 2449 2003 JOURNAL OF NEUROCHEMISTRY 85:1-1
Huber KM
Recent progress in understanding the neural mechanisms of Fragile X Syndrome
0 0
2450 19 35 2450 2003 JOURNAL OF NEUROGENETICS 17(2-3):223-230
Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; et al.
Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2451 0 0 2451 2003 JOURNAL OF PSYCHOSOMATIC RESEARCH 55(2):156-156
Mirzaei M; Karam GA; Mahmoudi M
Evaluation of prevalence the fragile X syndrome in 52 patients with moderate mental retardation with cytogenetic methods.
0 0
2452 8 10 2452 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(3):372-375
Lombroso PJ
Genetics of childhood disorders: XLVIII. Learning and memory, part 1: Fragile X syndrome update
0 0
2453 2 5 2453 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(5):516-517
Lung FW; Chen PJ
Fragile X syndrome in adolescent prostitutes in southern Taiwan
0 1
2454 21 28 2454 2003 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 102(1):12-16
Chi J; Chen DJ; Lin CN; Chiu CY; Huang CB; et al.
Feasibility of blood spot PCR in large-scale screening of fragile X syndrome in southern Taiwan
0 0
2455 23 69 2455 2003 LANGUAGE SPEECH AND HEARING SERVICES IN SCHOOLS 34(4):320-331
Mirrett PL; Roberts JE
Early intervention practices and communication intervention strategies for young males with fragile X syndrome
0 0
2456 27 61 2456 2003 MOLECULAR BRAIN RESEARCH 110(2):267-278
Todd PK; Malter JS; Mack KJ
Whisker stimulation-dependent translation of FMRP in the barrel cortex requires activation of type I metabotropic glutamate receptors
4 3
2457 0 0 2457 2003 MOVEMENT DISORDERS 18(9):1091-1091
Kraft S; Parboosingh J; Suchowersky O
Absence of fragile X premutation alleles in patients referred with spinocerebellar ataxia
0 0
2458 1 1 2458 2003 NATURE REVIEWS GENETICS 4(10):758-758
Casci T
Fragile X: a class of its own
0 0
2459 1 3 2459 2003 NATURE REVIEWS NEUROSCIENCE 4(4):245-245
Jones R
Cell biology or the neuron - FMRP and its many partners
0 0
2460 1 1 2460 2003 NATURE REVIEWS NEUROSCIENCE 4(10):776-777
Casci T
Neurological disorders - Fragile X: a class of its own
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2461 13 26 2461 2003 NEURON 37(4):555-558
Antar LN; Bassell GJ
Sunrise at the synapse: The FMRP mRNP shaping the synaptic interface
11 25
2462 7 10 2462 2003 NEURON 38(6):843-845
Billuart P; Chelly J
From fragile X mental retardation protein to Rac1 GTPase: New insights from fly CYFIP
1 2
2463 22 64 2463 2003 NEURON 38(6):887-898
Schenck A; Bardoni B; Langmann C; Harden N; Mandel JL; et al.
CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein
11 23
2464 7 35 2464 2003 NEURON 39(5):739-747
Jin P; Zarnescu DC; Zhang FP; Pearson CE; Lucchesi JC; et al.
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila
10 23
2465 41 101 2465 2003 NEUROPSYCHOLOGY 17(4):646-657
Loesch DZ; Bui QM; Grigsby J; Butler E; Epstein J; et al.
Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X
1 1
2466 14 26 2466 2003 NEUROSCIENCE 119(1):9-13
D'Antuono M; Merlo D; Avoli M
Involvement of cholinergic and GABAergic systems in the fragile X knockout mice
0 2
2467 22 39 2467 2003 NEUROSCIENCE 120(4):1005-1017
Chen L; Yun SW; Seto J; Liu W; Toth M
The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences
10 11
2468 21 50 2468 2003 NUCLEIC ACIDS RESEARCH 31(14):3963-3970
Weisman-Shomer P; Cohen E; Hershco I; Khateb S; Wolfovitz-Barchad O; et al.
The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)(n)
3 5
2469 10 23 2469 2003 NUCLEIC ACIDS RESEARCH 31(21):6243-6248
Handa V; Saha T; Usdin K
The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer
3 7
2470 8 36 2470 2003 PEDIATRICS 111(2):407-416
Bailey DB; Skinner D; Sparkman KL
Discovering fragile X syndrome: Family experiences and perceptions
5 6
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2471 24 41 2471 2003 PRENATAL DIAGNOSIS 23(4):345-351
Wald NJ; Morris JK
A new approach to antenatal screening for Fragile X syndrome
1 3
2472 1 1 2472 2003 PRENATAL DIAGNOSIS 23(9):771-771
Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; et al.
Pilot study for the neonatal screening of fragile X syndrome (vol 22, pg 459, 2002)
0 0
2473 22 45 2473 2003 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 100(24):14374-14378
Todd PK; Mack KJ; Malter JS
The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95
8 13
2474 0 21 2474 2003 PROTEIN EXPRESSION AND PURIFICATION 27(2):365-374
McNulty DE; Claffee BA; Huddleston MJ; Kane JF
Mistranslational errors associated with the rare arginine codon CGG in Escherichia coli
1 6
2475 18 33 2475 2003 RNA-A PUBLICATION OF THE RNA SOCIETY 9(10):1198-1207
Ramos A; Hollingworth D; Pastore A
G-quartet-dependent recognition between the FMRP RGG box and RNA
7 12
2476 37 55 2476 2003 TRENDS IN BIOCHEMICAL SCIENCES 28(3):152-158
Jin P; Warren ST
New insights into fragile X syndrome: from molecules to neurobehaviors
18 34
2477 36 60 2477 2003 TRENDS IN GENETICS 19(3):148-154
Kooy RF
Of mice and the fragile X syndrome
10 13
2478 12 40 2478 2003 YONSEI MEDICAL JOURNAL 44(4):583-592
Demirhan O; Tastemir D; Diler RS; Firat S; Avei A
A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome
1 1
2479 5 10 2479 2004 ACTA PHARMACOLOGICA SINICA 25(7):973-976
Sun YJ; Han X
Dynamic behavior of fragile X full mutations in cultured female fetal fibroblasts
0 0
2480 41 80 2480 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):805-816
Hagerman PJ; Hagerman RJ
The fragile-X premutation: A maturing perspective
8 14
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2481 15 26 2481 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):1051-1056
Hagerman RJ; Leavitt BR; Farzin F; Jacquemont S; Greco CM; et al.
Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation
3 7
2482 1 1 2482 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(2):352-352
Hagerman; Hagerman
The fragile-X premutation: A maturing perspective (vol 74, pg 805, 2003)
0 0
2483 2 10 2483 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):730-731
Mandel JL
Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation
1 1
2484 1 5 2484 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):731-732
Salomons GS; Ropers HH
Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation - Reply
0 0
2485 19 29 2485 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):129-132
Rife M; Nadal A; Mila M; Willemsen R
Immunohistochemical FMRP studies in a full mutated female fetus
0 0
2486 9 16 2486 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):213-215
Marshall I; Betensky BP; Goseco A; Vogiatzi MV; Flieder D
Fragile x and mosaic 45,X/46,XY mixed gonadal dysgenesis in a girl with ambiguous genitalia
0 0
2487 3 5 2487 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 125A(3):320-320
Milunsky JM; Maher TA
Fragile X carrier screening and spinocerebellar ataxia in older males
0 3
2488 21 48 2488 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 126A(1):9-17
Kau ASM; Tierney E; Bukelis I; Stump MH; Kates WR; et al.
Social behavior profile in young males with fragile X syndrome: Characteristics and specificity
0 2
2489 31 38 2489 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 128A(3):250-255
Penagarikano O; Gil A; Telez M; Ortega B; Flores P; et al.
A new insight into fragile X syndrome among Basque population
0 0
2490 25 40 2490 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(2):184-189
Zeesman S; Zwaigenbaum L; Whelan DT; Hagerman RJ; Tassone F; et al.
Paternal transmission of fragile X syndrome
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2491 20 26 2491 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):218-224
Biancalana V; Beldjord C; Taillandier A; Szpiro-Tapia S; Cusin V; et al.
Five years of molecular diagnosis of Fragile X syndrome(1997-2001): A collaborative study reporting 95% of the activity in France
0 1
2492 24 59 2492 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):225-234
Kaufmann WE; Cortell R; Kau CSM; Bukelis I; Tierney E; et al.
Autism spectrum disorder in fragile X syndrome: Communication, social interaction, and specific behaviors
0 0
2493 11 16 2493 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):326-328
Clarke NF; Mowat D; Kooy RF; Reyniers E; Willemsen R
Fragile X syndrome phenotype with normal FMR1 gene studies
0 0
2494 0 42 2494 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 126B(1):46-50
Devlin B; Bennett P; Dawson G; Figlewicz DA; Grigorenko EL; et al.
Alleles of a Reelin CGG repeat do not convey liability to autism in a sample from the CPEA network
0 3
2495 17 51 2495 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):208-218
Philofsky A; Hepburn SL; Hayes A; Hagerman R; Rogers SJ
Linguistic and cognitive functioning and autism symptoms in young children with fragile X syndrome
0 1
2496 14 79 2496 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):237-254
Abbeduto L; Seltzer MM; Shattuck P; Krauss MW; Orsmond G; et al.
Psychological well-being and coping in mothers of youths with autism, Down syndrome, or fragile X syndrome
0 1
2497 0 0 2497 2004 ANNALS OF NEUROLOGY 56:S104-S104
Cortell R; Bukelis I; Gray RM; Cox C; Tierney E; et al.
Autism spectrum disorder in boys with Fragile X: Serial evaluation
0 0
2498 14 50 2498 2004 ARCHIVES OF GENERAL PSYCHIATRY 61(3):281-288
Garrett AS; Menon V; MacKenzie K; Reiss AL
Here's looking at you, kid - Neural systems underlying face and gaze processing in fragile X syndrome
0 1
2499 0 0 2499 2004 BEHAVIOR GENETICS 34(6):638-638
Fisch GS; Simensen RJ; Schroer RJ
Longitudinal assessment of cognitive-behavioral features of children and adolescents with either autism or the fragile X mutation
0 0
2500 0 0 2500 2004 BIOLOGICAL PSYCHIATRY 55:159S-159S
Daly EM; Moore CJ; Simmons A; Tassone F; Tysoe C; et al.
A H-1 magnetic resonance spectroscopy study of males with premutation expansion of CGG trinucleoticle repeats
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2501 28 62 2501 2004 BRAIN 127:591-601
Kogan CS; Boutet I; Cornish K; Zangenehpour S; Mullen KT; et al.
Differential impact of the FMR1 gene on visual processing in fragile X syndrome
2 2
2502 23 40 2502 2004 BRAIN 127:2672-2681
Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al.
The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy
0 0
2503 12 21 2503 2004 BRAIN & DEVELOPMENT 26(6):380-383
Suwa K; Momoi MY
Non-invasive screening of fragile X syndrome A using urine and hair roots
0 0
2504 3 6 2504 2004 BRAIN AND COGNITION 54(3):235-239
Cornish K; Swainson R; Cunnington R; Wilding J; Morris P; et al.
Do women with fragile X syndrome have problems in switching attention: Preliminary findings from ERP and fMRI
0 0
2505 0 0 2505 2004 BRAIN AND COGNITION 56(1):121-121
Kogan C; Boutet I; Cornish K; Andermann E; DerKaloustian V; et al.
Evidence for a transient channel visual deficit in Fragile X Syndrome
0 0
2506 60 135 2506 2004 CELLULAR AND MOLECULAR LIFE SCIENCES 61(14):1714-1728
Denman RB; Dolzhanskaya N; Sung YJ
Regulating a translational regulator: mechanisms cells use to control the activity of the fragile X mental retardation protein
1 2
2507 51 120 2507 2004 CNS DRUGS 18(11):687-703
Tsiouris JA; Brown WT
Neuropsychiatric symptoms of fragile X syndrome - Pathophysiology and pharmacotherapy
0 0
2508 24 47 2508 2004 COGNITIVE NEUROPSYCHOLOGY 21(6):579-596
Keenan JM; Simon JA
Inference deficits in women with Fragile X Syndrome: A problem in working memory
0 0
2509 16 47 2509 2004 CURRENT BIOLOGY 14(12):1025-1034
Xu KY; Bogert BA; Li WJ; Su K; Lee A; et al.
The fragile X-related gene affects the crawling behavior of Drosophila larvae by regulating the mRNA level of the DEG/ENaC protein pickpocket1
2 3
2510 20 37 2510 2004 CURRENT BIOLOGY 14(20):1863-1870
Pan LY; Zhang YQ; Woodruff E; Broadie K
The Drosophila fragile X gene negatively regulates neuronal elaboration and synaptic differentiation
2 2
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2511 16 38 2511 2004 CYTOGENETIC AND GENOME RESEARCH 105(2-4):448-454
Errijgers V; Kooy RF
Genetic modifiers in mice: the example of the fragile X mouse model
0 0
2512 18 58 2512 2004 DEVELOPMENTAL BIOLOGY 270(2):290-307
Zhang YQ; Matthies HJG; Mancuso J; Andrews HK; Woodruff E; et al.
The Drosophila fragile X-related gene regulates axoneme differentiation during spermatogenesis
3 3
2513 5 41 2513 2004 DEVELOPMENTAL SCIENCE 7(1):116-130
Scerif G; Cornish K; Wilding J; Driver J; Karmiloff-Smith A
Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome
1 1
2514 17 55 2514 2004 EMBO JOURNAL 23(16):3346-3355
Rackham O; Brown CM
Visualization of RNA-protein interactions in living cells: FMRP and IMP1 interact on mRNAs
3 4
2515 11 19 2515 2004 EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY 112(2):189-191
Bussani C; Papi L; Sestini R; Baldinotti F; Bucciantini S; et al.
Premature ovarian failure and fragile X premutation: a study on 45 women
0 0
2516 35 49 2516 2004 EXPERIMENTAL NEUROLOGY 189(2):343-353
Schrier M; Severijnen LA; Reis S; Rife M; van't Padje S; et al.
Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cells
0 0
2517 0 0 2517 2004 FERTILITY AND STERILITY 82:S246-S247
Malcov M; Carmon A; Mey-Raz N; Ben Yosef D; Lessing JB; et al.
Preimplantation genetic diagnosis for fragile X syndrome in Israel
0 0
2518 21 34 2518 2004 GENE 343(2):231-238
Guduric-Fuchs J; Mohrlen F; Frohme M; Frank U
A fragile X mental retardation-like gene in a cnidarian
0 0
2519 41 114 2519 2004 GENES BRAIN AND BEHAVIOR 3(6):337-359
Yan QJ; Asafo-Adjei PK; Arnold HM; Brown RE; Bauchwitz RP
A phenotypic and molecular characterization of the fmr1-tm1Cgr Fragile X mouse
1 1
2520 0 0 2520 2004 GENETIC COUNSELING 15(2):239-286
[Anon]
Abstracts of the 11(th) International Workshop on Fragile X and X-Linked Mental Retardation - 27-30 August 2003, Pafos, Cyprus
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2521 27 42 2521 2004 GENETIC EPIDEMIOLOGY 26(4):294-304
Huggins RM; Loesch DZ; Qian GQ; Bui QM; Mitchell RJ; et al.
Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-X
0 0
2522 0 0 2522 2004 GENETICS IN MEDICINE 6(4):300-300
MacKenzie JJ; Sumargo IV; Taylor SA
A cryptic full mutation in a male with a classical fragile X phenotype.
0 0
2523 0 0 2523 2004 GENETICS IN MEDICINE 6(4):352-352
Han X; Chehab F; Powell B; Phalin-Rague J
A high mental functioning fragile X male with a de novo 103bp deletion including entire CGG repeat region in > 50% of his peripheral leukocytes.
0 0
2524 15 49 2524 2004 GENOMICS 83(1):106-118
Naumann F; Remus R; Schmitz B; Doerfler W
Gene structure and expression of the 5 '-(CGG)(n)-3 '-binding protein (CGGBP1)
0 1
2525 3 40 2525 2004 GENOMICS 84(1):69-81
Sarafidou T; Kahl C; Martinez-Garay I; Mangelsdorf M; Gesk S; et al.
Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein
0 0
2526 32 55 2526 2004 GROWTH HORMONE & IGF RESEARCH 14:S158-S165
Mandel JL; Biancalana V
Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues
0 0
2527 0 9 2527 2004 HEMOGLOBIN 28(3):173-176
Regtuijt ME; Harteveld CL; Van Delft P; Akkermans N; Giordano PC
Hb Suan-Dok [alpha 109(G16)Leu -> Arg; CTG--> CGG (alpha 2)] - Described in a patient of African ancestry
0 0
2528 21 42 2528 2004 HUMAN MOLECULAR GENETICS 13(1):79-89
Wang HP; Ku L; Osterhout DJ; Li W; Ahmadian A; et al.
Developmentally-programmed FMRP expression in oligodendrocytes: a potential role of FMRP in regulating translation in oligodendroglia progenitors
1 3
2529 13 32 2529 2004 HUMAN MOLECULAR GENETICS 13(5):543-549
Beilina A; Tassone F; Schwartz PH; Sahota P; Hagerman PJ
Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element
4 6
2530 1 5 2530 2004 ISRAEL JOURNAL OF PSYCHIATRY AND RELATED SCIENCES 41(1):70-70
Kandil ST; Bilici M; Aksu HB; Celep F; Karaguzel A
Early infantile autism and fragile X anomaly
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2531 22 55 2531 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(4):460-469
Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; et al.
Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population
6 15
2532 1 1 2532 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2945
Barrett SK; Drazin T; Rosa D; Kupchik GS
Genetic counseling for families of patients with fragile X syndrome
0 0
2533 2 6 2533 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2946
Hagerman PJ; Hagerman RJ; Gane LW
Genetic counseling for families of patients with fragile X syndrome - In reply
1 1
2534 1 1 2534 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 292(17):2086-2086
Hagerman P
Genetic counseling for families of patients with fragile X syndrome (vol 291, pg 2945, 2004)
0 0
2535 5 50 2535 2004 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 34(1):41-48
Seltzer MM; Abbeduto L; Krauss MW; Greenberg J; Swe A
Comparison groups in autism family research: Down syndrome, fragile X syndrome, and schizophrenia
0 2
2536 60 103 2536 2004 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY 45(6):1042-1053
Cornish KM; Turk J; Wilding J; Sudhalter V; Munir F; et al.
Annotation: Deconstructing the attention deficit in fragile X syndrome: a developmental neuropsychological approach
0 0
2537 22 57 2537 2004 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 89(9):4569-4574
Welt CK; Smith PC; Taylor AE
Evidence of early ovarian aging in fragile X premutation carriers
0 0
2538 0 30 2538 2004 JOURNAL OF CLINICAL MICROBIOLOGY 42(8):3538-3548
Otsuka Y; Parniewski P; Zwolska Z; Kai M; Fujino T; et al.
Characterization of a trinucleotide repeat sequence (CGG)(5) and potential use in restriction fragment length polymorphism typing of Mycobacterium tuberculosis
0 1
2539 6 36 2539 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(1):21-27
Mirrett PL; Bailey DB; Roberts JE; Hatton DD
Developmental screening and detection of developmental delays in infants and toddlers with fragile X syndrome
0 0
2540 30 54 2540 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(6):392-398
Goodlin-Jones BL; Tassone F; Gane LW
Autistic spectrum disorder and the fragile X premutation
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2541 0 1 2541 2004 JOURNAL OF FORENSIC SCIENCES 49(1):192-193
Brenner CH; Inman K
Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54.
0 0
2542 0 3 2542 2004 JOURNAL OF FORENSIC SCIENCES 49(1):194-195
Thompson WC; Taroni PF; Aitken CGG
'Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54. - Response
0 0
2543 1 13 2543 2004 JOURNAL OF HUMAN GENETICS 49(2):97-101
Nagao K; Fujii K; Yamada M; Miyashita T
Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes
0 0
2544 0 0 2544 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:287-287
Brown W; Nolin S; Dobkin C; Houck G; Glicksman A; et al.
Frequency of fragile X in multiplex autism: Testing the AGRE families
0 0
2545 0 0 2545 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:288-288
Brown WT; Nolin S; Houck G; Ding X; Glicksman A; et al.
The fragile X syndrome (FXS): Screening and prenatal diagnosis
0 0
2546 0 0 2546 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294
Turk J; Das D; Howlin P; Barber N; Mottaleb M; et al.
A follow-up of intellectual, social, communicatory & adaptive functioning in boys & young men with fragile X syndrome
0 0
2547 0 0 2547 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294
Einfeld SL; Tonge BJ; Turner G; Smith E
Longitudinal course of behavioural and emotional problems in Prader-Willi, Fragile X, Williams and Down syndromes
0 0
2548 0 0 2548 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:324-324
Abbeduto L; Murphy MM
Language, communication, and the behavioural phenotype of Down syndrome (DS): Insights from fragile X syndrome (FXS) and typical development
0 0
2549 0 0 2549 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:325-325
Abbeduto L; Murphy MM; Giles N; Bruno L; Richmond EK; et al.
Understanding language in context: Comparisons of Down syndrome (DS) with fragile X syndrome and typical development
0 0
2550 0 0 2550 2004 JOURNAL OF INVESTIGATIVE MEDICINE 52(1):S101-S101
Nowicki ST; Jacquemont S; Li L; Nguyen DV; Gregg JP; et al.
An approach to identify epistatic genes involved in the development of autism spectrum disorder in patients with fragile X syndrome
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2551 0 0 2551 2004 JOURNAL OF MEDICAL GENETICS 41:S64-S64
Turner A; Myring J; Stephens M; Antoniadi T; Butler R
The Problem with Premutations: Assessment of new methods for fragile-X screening.
0 0
2552 0 0 2552 2004 JOURNAL OF MEDICAL GENETICS 41:S82-S82
McConachie M; Conlin L; McKay F; Gillespie K; Berg J
A false negative PCR result in a boy with Fragile X syndrome
0 0
2553 10 16 2553 2004 JOURNAL OF MEDICAL GENETICS 41(4)
Zhou Y; Law HY; Boehm CD; Yoon CS; Cutting GR; et al.
Robust fragile X (CGG)(n) genotype classification using a methylation specific triple PCR assay
0 0
2554 12 15 2554 2004 JOURNAL OF MEDICAL GENETICS 41(4)
Tassone F; Hagerman RJ; Garcia-Arocena D; Khandjian EW; Greco CM; et al.
Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome
0 2
2555 41 65 2555 2004 JOURNAL OF MOLECULAR BIOLOGY 343(1):43-53
Menon RP; Gibson TJ; Pastore A
The C terminus of fragile X mental retardation protein interacts with the multi-domain ran-binding protein in the microtubule-organising centre
0 0
2556 0 0 2556 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409
Lee JY; Zhang YT; Hopcus-Niccum D; Mulvihill JJ; Li SB
A mosaicism of 45,X/46,XX/47,XXX uncovered by molecular fragile X testing
0 0
2557 0 0 2557 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409
Williams J; Lyon E; Miller C; Mao R
Chromosome aneuploidy detected by fragile X southern blot and PCR analysis
0 0
2558 19 34 2558 2004 JOURNAL OF MOLECULAR HISTOLOGY 35(4):389-395
Reis SA; Willemsen R; van Unen L; Hoogeveen AT; Oostra BA
Prospects of TAT-mediated protein therapy for fragile X syndrome
0 0
2559 12 37 2559 2004 JOURNAL OF NEUROSCIENCE 24(11):2648-2655
Antar LN; Afroz R; Dictenberg JB; Carroll RC; Bassell GJ
Metabotropic glutamate receptor activation regulates Fragile X mental retardation protein and Fmr1 mRNA localization differentially in dendrites and at synapses
10 15
2560 40 97 2560 2004 JOURNAL OF NEUROSCIENCE 24(25):5798-5809
Michel CI; Kraft R; Restifo LL
Defective neuronal development in the mushroom bodies of Drosophila Fragile X Mental Retardation 1 Mutants
6 7
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2561 23 34 2561 2004 JOURNAL OF NEUROSCIENCE 24(33):7272-7276
Stefani G; Fraser CE; Darnell JC; Darnell RB
Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells
2 3
2562 16 25 2562 2004 JOURNAL OF NEUROSCIENCE 24(47):10579-10583
Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al.
Visual experience regulates transient expression and dendritic localization of Fragile X mental retardation protein
1 1
2563 1 1 2563 2004 JOURNAL OF NEUROSCIENCE 24(50):CP3-CP4
Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al.
Visual experience regulates transient expression and dendritic localization of fragile X mental retardation protein (vol 24, pg 10579, 2004)
0 0
2564 7 21 2564 2004 JOURNAL OF THE NEUROLOGICAL SCIENCES 227(1):115-118
Garland EM; Vnencak-Jones CL; Biaggioni I; Davis TL; Montine TJ; et al.
Fragile X gene premutation in multiple system atrophy
0 0
2565 0 0 2565 2004 LANCET NEUROLOGY 3(12):701-701
Nelson R
Drosophila model increases understanding of fragile-X syndrome
0 0
2566 0 0 2566 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):1-2
Crnic LS; Hagerman R
Preface: Fragile X syndrome: Frontiers of understanding gene-brain-behavior relationships
0 0
2567 16 48 2567 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):3-10
Bailey DB
Newborn screening for fragile X syndrome
0 1
2568 34 67 2568 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):11-16
Cornish K; Sudhalter V; Turk J
Attention and language in fragile X
1 1
2569 39 74 2569 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):17-24
Hessl D; Rivera SM; Reiss AL
The neuroanatomy and neuroendocrinotogy of fragile X syndrome
1 2
2570 29 55 2570 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):25-30
Hagerman PJ; Hagerman RJ
Fragile X-associated tremor/ataxia syndrome (FXTAS)
0 1
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2571 39 66 2571 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):31-41
Loesch DZ; Huggins RM; Hagerman RJ
Phenotypic variation and FMRP levels in fragile X
1 1
2572 15 45 2572 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):42-48
Berry-Kravis E; Potanos K
Psychopharmacology in fragile X syndrome - Present and future
0 0
2573 19 32 2573 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):49-52
Darnell JC; Warren ST; Darnell RB
The fragile X mental retardation protein, FMRP, recognizes G-quartets
0 1
2574 24 54 2574 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):53-59
Beckel-Mitchener A; Greenough WT
Correlates across the structural, functional, and molecular phenotypes of fragile X syndrome
0 2
2575 42 102 2575 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):60-67
Willemsen R; Oostra BA; Bassell GJ; Dictenberg J
The fragile X syndrome: From molecular genetics to neurobiology
2 5
2576 21 82 2576 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):68-74
Siomi H; Ishizuka A; Siomi MC
RNA interference: A new mechanism by which FMRP acts in the normal brain? What can drosophila teach us?
1 4
2577 7 66 2577 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):75-81
Rattazzi MC; LaFauci G; Brown WT
Prospects for gene therapy in the fragile X syndrome
0 0
2578 15 36 2578 2004 MOLECULAR BRAIN RESEARCH 131(1-2):101-109
Lauterborn JC
Stress induced changes in cortical and hypothalamic c-fos expression are altered in fragile X mutant mice
0 0
2579 11 11 2579 2004 MOLECULAR HUMAN REPRODUCTION 10(10):773-776
Rife M; Badenas C; Quinto L; Puigoriol E; Tazon B; et al.
Analysis of CGG variation through 642 meioses in Fragile X families
1 1
2580 1 50 2580 2004 MOLECULAR MICROBIOLOGY 54(3):742-754
Blaha B; Semsey S; Ferenczi S; Csiszovszki Z; Papp PP; et al.
A proline tRNA(CGG) gene encompassing the attachment site of temperate phage 16-3 is functional and convertible to suppressor tRNA
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2581 11 41 2581 2004 MOLECULAR PSYCHIATRY 9(4):417-425
Frankland PW; Wang Y; Rosner B; Shimizu T; Balleine BW; et al.
Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice
0 1
2582 0 0 2582 2004 MOVEMENT DISORDERS 19:S20-S20
Zhao Y; Puong K; Law H; Wong M; Ng I; et al.
Fragile X premutation alleles in patients with sporadic cerebellar ataxia
0 0
2583 0 0 2583 2004 MOVEMENT DISORDERS 19:S21-S21
Hall DA; Pelak VS; Hagerman RJ; Hagerman PJ; Leehey MA
Ocular motility in Fragile X premutation carriers and Fragile X associated tremor/ataxia syndrome (FXTAS)
0 0
2584 0 0 2584 2004 MOVEMENT DISORDERS 19:S338-S338
Leehey MA; Berry-Kravis E; Jacquemont S; Zhang L; Hagerman R; et al.
Misdiagnosis of fragile X associated tremor/ataxia syndrome (FXTAS)
0 0
2585 0 0 2585 2004 MOVEMENT DISORDERS 19:S339-S339
Leehey MA; Zhang L; Wheelock V; Tassone F; Hagerman R; et al.
A preliminary observation: Increased frequency of fragile X expanded alleles in patients that meet diagnostic criteria for MSA
0 0
2586 0 0 2586 2004 MOVEMENT DISORDERS 19:S359-S360
Di Maria E; Grasso M; Abbruzzese G; Mandich P; Ratto S; et al.
The role for Fragile X premutation in essential tremor and spinocerebellar ataxia: Findings from two cohorts of Italian patients
0 0
2587 0 0 2587 2004 MOVEMENT DISORDERS 19:S444-S444
Puong K; Zhao Y; Law H; Wong M; Ng I; et al.
Screening for Fragile X premutation alleles in patients with essential tremor
0 0
2588 0 0 2588 2004 MOVEMENT DISORDERS 19(9):1122-1122
Leehey MA; Hall D; Rice C; Jacquemont S; Zhang L; et al.
The clinical course of fragile X-associated tremor/ataxia syndrome (FXTAS).
0 0
2589 0 0 2589 2004 MOVEMENT DISORDERS 19(9):1127-1127
Hall DA; Rice CD; Hagerman RR; Hagerman PR; Berry-Kravis E; et al.
Medical treatment for the fragile x-associated tremor/ataxia syndrome.
0 0
2590 47 73 2590 2004 NATURE CELL BIOLOGY 6(11):1048-1053
Jin P; Alisch RS; Warren ST
RNA and microRNAs in fragile X mental retardation
2 3
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2591 22 39 2591 2004 NATURE NEUROSCIENCE 7(2):113-117
Jin P; Zarnescu DC; Ceman S; Nakamoto M; Mowrey J; et al.
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway
16 38
2592 1 2 2592 2004 NATURE REVIEWS NEUROSCIENCE 5(1):4-4
Jones R
Neurological disorders: Fragile X functions
0 0
2593 0 0 2593 2004 NEUROBIOLOGY OF AGING 25:S434-S434
Westmark CJ; Malter JS
FMRP mediates mGluR1-activated translation of APP
0 0
2594 0 0 2594 2004 NEUROLOGY 62(7):A48-A48
Hagerman PJ; Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; et al.
Penetrance of the Fragile X-associated Tremor/Ataxia Syndrome (FXTAS) in a premutation carrier population: Initial results from a California family-based study
0 0
2595 7 10 2595 2004 NEUROLOGY 63(2):362-363
Tan EK; Zhao Y; Puong KY; Law HY; Chan LL; et al.
Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort
0 4
2596 8 37 2596 2004 NEUROLOGY 63(9):1634-1639
Kogan CS; Bertone A; Cornish K; Boutet I; Kaloustian VMD; et al.
Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome
0 0
2597 5 7 2597 2004 NEUROLOGY 63(11):2188-2189
Pugliese P; Annesi G; Cutuli N; Arabia G; Nicoletti G; et al.
The fragile X premutation presenting as postprandial hypotension
0 0
2598 51 75 2598 2004 NEUROLOGY INDIA 52(1):36-42
Pandey UB; Phadke SR; Mittal B
Molecular diagnosis and genetic counseling for fragile X mental retardation
0 0
2599 52 101 2599 2004 NEUROPSYCHOLOGIA 42(14):1934-1947
Moore CJ; Daly EM; Schmitz N; Tassone F; Tysoe C; et al.
A neuropsychological investigation of male premutation carriers of fragile X syndrome
0 0
2600 6 23 2600 2004 NEUROREPORT 15(10):1579-1583
Greicius MD; Boyett-Anderson JM; Menon V; Reiss AL
Reduced basal forebrain and hippocampal activation during memory encoding in girls with fragile X syndrome
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2601 24 42 2601 2004 NEUROREPORT 15(16):2447-2450
Veneri M; Zalfa F; Bagni C
FMRP and its target RNAs: fishing for the specificity
0 0
2602 17 41 2602 2004 NUCLEIC ACIDS RESEARCH 32(1):298-306
Fojtik P; Kejnovska I; Vorlickova M
The guanine-rich fragile X chromosome repeats are reluctant to form tetraplexes
0 2
2603 24 40 2603 2004 NUCLEIC ACIDS RESEARCH 32(7):2129-2137
Gabus C; Mazroui R; Tremblay S; Khandjian EW; Darlix JL
The fragile X mental retardation protein has nucleic acid chaperone properties
2 5
2604 18 44 2604 2004 NUCLEIC ACIDS RESEARCH 32(14):4145-4154
Khateb S; Weisman-Shomer P; Hershco I; Loeb LA; Fry M
Destabilization of tetraplex structures of the fragile X repeat sequence (CGG)(n) is mediated by homolog-conserved domains in three members of the hnRNP family
0 0
2605 0 1 2605 2004 PRAXIS DER KINDERPSYCHOLOGIE UND KINDERPSYCHIATRIE 53(8):593-594
Irblich D
The fragile X syndrome - A guide for parents
0 0
2606 6 8 2606 2004 PRENATAL DIAGNOSIS 24(1):67-68
Delatycki MB; Sheffield LJ; Wake S; Cohen J
Screening approach for Fragile X syndrome
0 0
2607 0 1 2607 2004 PRENATAL DIAGNOSIS 24(1):68-69
Wald NJ; Morris JK
Reply: Prenatal screen for Fragile X syndrome
0 0
2608 6 12 2608 2004 PRIMARY CARE 31(3):621-+
Wiesner GL; Cassidy SB; Grimes SJ; Matthews AL; Acheson LS
Clinical consult: developmental delay/fragile X syndrome
0 0
2609 14 57 2609 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(10):3615-3620
Menon V; Leroux J; White CD; Reiss AL
Frontostriatal deficits in fragile X syndrome: Relation to FMR1 gene expression
0 0
2610 26 61 2610 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(36):13357-13362
Khandjian EW; Huot ME; Tremblay S; Davidovic L; Mazroui R; et al.
Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles
6 7
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2611 25 53 2611 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(42):15201-15206
Lu R; Wang HP; Liang Z; Ku L; O'Donnell WT; et al.
The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development
3 3
2612 15 21 2612 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17329-17330
Miyashiro K; Eberwine J
Fragile X syndrome: (What's) lost in translation?
0 0
2613 18 61 2613 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17428-17433
Ling SC; Fahrner PS; Greenough WT; Gelfand VI
Transport of Drosophila fragile X rental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein
0 1
2614 28 50 2614 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17504-17509
Weiler IJ; Spangler CC; Klintsova AY; Grossman AW; Kim SH; et al.
Fragile X mental retardation protein is necessary for neurotransmitter-activated protein translation at synapses
0 0
2615 1 1 2615 2004 PROTEIN EXPRESSION AND PURIFICATION 37(1):264-264
McNulty DE; Claffee BA; Huddleston MJ; Kane JF
Mistranslational errors associated with the rare arginine codon CGG in Escherichia coli (vol 27, pg 365, 2003)
0 0
2616 3 53 2616 2004 QUALITATIVE HEALTH RESEARCH 14(6):741-759
Medved MI; Brockmeier J
Making sense of traumatic experiences: Telling your life with fragile X syndrome
0 0
2617 0 1 2617 2004 REPRODUCTIVE BIOMEDICINE ONLINE 8(3):337-337
[Anon]
Late onset fragile X syndrome
0 0
2618 2 7 2618 2004 REVISTA DE NEUROLOGIA 38(1):7-11
Artigas-Pallares J; Brun-Gasca C
Can the behavioural phenotype of Fragile X syndrome be attributed to mental retardation and to attention deficit hyperactivity disorder?
0 0
2619 33 95 2619 2004 TRENDS IN NEUROSCIENCES 27(7):370-377
Bear MF; Huber KM; Warren ST
The mGIuR theory of fragile X mental retardation
8 10
2620 18 41 2620 2005 AMERICAN JOURNAL OF HUMAN GENETICS 76(2):302-311
Edamura KN; Leonard MR; Pearson CE
Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2621 28 50 2621 2005 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 132A(1):25-32
Skinner M; Hooper S; Hatton DD; Robert J; Mirrett P; et al.
Mapping nonverbal IQ in young boys with fragile X syndrome
0 0
2622 12 18 2622 2005 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 132A(2):210-214
Angeli CB; Capelli LP; Auricchio MTBM; Vianna-Morgante AM; Mingroni-Netto RC; et al.
AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations
0 0
2623 16 20 2623 2005 ANNALS OF NEUROLOGY 57(1):144-147
Berry-Kravis E; Potanos K; Weinberg D; Zhou LL; Goetz CG
Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation
0 1
2624 10 98 2624 2005 APPLIED PSYCHOLINGUISTICS 26(1):7-27
Rice ML; Warren SF; Betz SK
Language symptoms of developmental language disorders: An overview of autism, Down syndrome, fragile X, specific language impairment, and Williams syndrome
0 1
2625 5 13 2625 2005 ARCHIVES DE PEDIATRIE 12(2):176-179
Vantalon V; Briard-Luginbuhl V; Mouren MC
Fragile X syndrome and very early onset schizophrenia: a female case study
0 0
2626 10 47 2626 2005 BIOCHEMICAL JOURNAL 386:297-303
Kumari D; Gabrielian A; Wheeler D; Usdin K
The roles of Sp1, Sp3, USF1/USF2 and NRF-1 in the regulation and three-dimensional structure of the Fragile X mental retardation gene promoter
0 0
2627 29 49 2627 2005 BRAIN AND COGNITION 57(1):53-60
Cornish K; Kogan C; Turk J; Manly T; James N; et al.
The emerging fragile X premutation phenotype: Evidence from the domain of social cognition
0 0
2628 17 20 2628 2005 CELLULAR AND MOLECULAR LIFE SCIENCES 62(2):251-252
Zalfa F; Bagni C
Another view of the role of FMRP in translational regulation
0 0
2629 16 52 2629 2005 DEVELOPMENTAL CELL 8(1):43-52
Zarnescu DC; Jin P; Betschinger J; Nakamoto M; Wang Y; et al.
Fragile X protein functions with Lgl and the PAR complex in flies and mice
0 0
2630 9 43 2630 2005 DEVELOPMENTAL CELL 8(3):331-342
Costa A; Wang Y; Dockendorff TC; Erdjument-Bromage H; Tempst P; et al.
The Drosophila fragile X protein functions as a negative regulator in the orb autoregulatory pathway
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2631 1 33 2631 2005 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 47(2):94-104
Weiskop S; Richdale A; Matthews J
Behavioural treatment to reduce sleep problems in children with autism or fragile X syndrome
0 0
2632 0 1 2632 2005 EDUCATIONAL REVIEW 57(2):258-260
Reid G
Educating children with Fragile X syndrome
0 0
2633 19 26 2633 2005 FEBS JOURNAL 272(3):872-878
Pozdnyakova I; Regan L
New insights into Fragile X syndrome - Relating genotype to phenotype at the molecular level
0 0
2634 23 68 2634 2005 HUMAN MOLECULAR GENETICS 14(6):835-844
Castets M; Schaeffer C; Bechara E; Schenck A; Khandjian EW; et al.
FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts
0 0
2635 2 4 2635 2005 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 293(3):296-296
Toft M; Farrer M
Premutation alleles and fragile X-associated tremor/ataxia syndrome
0 0
2636 1 3 2636 2005 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 293(3):296-297
Deng H; Le WD; Jankovic J
Premutation alleles and fragile X-associated tremor/ataxia syndrome - Reply
0 0
2637 21 46 2637 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(6):4498-4503
Mulvihill DJ; Edamura KN; Hagerman KA; Pearson CE; Wang YH
Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome
0 0
2638 23 47 2638 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(7):5750-5763
Garnon J; Lachance C; Di Marco S; Hel Z; Marion D; et al.
Fragile X-related protein FXR1P regulates proinflammatory cytokine tumor necrosis factor expression at the post-transcriptional level
0 0
2639 3 8 2639 2005 JOURNAL OF CLINICAL NEUROSCIENCE 12(1):42-43
Storey E; Billimoria P
Increased T-2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndrome
0 0
2640 0 0 2640 2005 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 76(1):151-151
Ealing J; Mavrogiannis LA; Kingston H; Cockburn DJ; Taylor GR; et al.
An atypical tetra nucleotide expansion in DM2 (PROMM)
0 0
# LCR NCR Nodes / Date / Journal / Authors LCS GCS
2641 25 61 2641 2005 MOLECULAR & CELLULAR PROTEOMICS 4(3):278-290
Zhang YQ; Friedman DB; Wang Z; Woodruff E; Pan LY; et al.
Protein expression profiling of the Drosophila fragile X mutant brain reveals up-regulation of monoamine synthesis
0 0
2642 4 10 2642 2005 NEURON 45(5):642-644
Dolen G; Bear MF
Courting a cure for Fragile X
0 0
2643 11 56 2643 2005 NEURON 45(5):753-764
McBride SMJ; Choi CH; Wang Y; Liebelt D; Braunstein E; et al.
Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome
1 1
2644 19 34 2644 2005 NEUROSCIENCE LETTERS 377(3):141-146
El Idrissi A; Ding XH; Scalia J; Trenkner E; Brown WT; et al.
Decreased GABA(A) receptor expression in the seizure-prone fragile X mouse
0 0
2645 24 45 2645 2005 NUCLEIC ACIDS RESEARCH 33(2):451-463
Napierala M; Michalowski D; de Mezer M; Krzyzosiak WJ
Facile FMR1 mRNA structure regulation by interruptions in CGG repeats
0 0
2646 29 46 2646 2005 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 102(6):2180-2185
Aschrafi A; Cunningham BA; Edelman GM; Vanderklish PW
The fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain
0 0
2647 59 77 2647 2005 TRENDS IN GENETICS 21(1):37-45
Zhang YQ; Broadie K
Fathoming fragile X in fruit flies
1 1

#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
2401	0	0	2401 2003 BIOLOGICAL PSYCHIATRY 53(8):49S-49S Daly EM; Moore CJ; Schmitz N; Morris R; Murphy KC; et al. Expansion of CGG trinucleotide repeats: Effect on neuropsychology of male premutation carriers of Fragile X syndrome	0	0
2402	0	0	2402 2003 BIOLOGICAL PSYCHIATRY 53(8):152S-152S Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al. The effect of premutation CGG trinucleotide repeat expansion, and %FMRP(+) lymphocytes reduction, on brain anatomy	0	0
2403	38	53	2403 2003 BIOLOGY OF THE CELL 95(3-4):221-228 Schaeffer C; Beaulande M; Ehresmann C; Ehresmann B; Moine H The RNA binding protein FMRP: new connections and missing links	3	8
2404	23	62	2404 2003 BMC MOLECULAR BIOLOGY 4 Chandler SP; Kansagra P; Hirst MC Fragile X (CGG)(n) repeats induce a transcriptional repression in cis upon a linked promoter: Evidence for a chromatin mediated effect	0	3
2405	13	41	2405 2003 BRAIN RESEARCH 971(1):83-89 Galvez R; Gopal AR; Greenough WT Somatosensory cortical barrel dendritic abnormalities in a mouse model of the fragile X mental retardation syndrome	4	6
2406	26	36	2406 2003 BRAIN RESEARCH 972(1-2):9-15 Segal M; Kreher U; Greenberger V; Braun K Is fragile X mental retardation protein involved in activity-induced plasticity of dendritic spines?	0	1
2407	20	38	2407 2003 BRAIN TOPOGRAPHY 15(3):165-171 Castren M; Paakkonen A; Tarkka IM; Ryynanen M; Partanen J Augmentation of auditory N1 in children with fragile X syndrome	2	2
2408	36	62	2408 2003 CELL 112(3):317-327 Zalfa F; Giorgi M; Primerano B; Moro A; Di Penta A; et al. The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at Synapses	37	69
2409	4	6	2409 2003 CLINICAL GENETICS 64(1):54-56 Rogers C; Partington MW; Turner GM Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome	3	4
2410	0	1	2410 2003 CLINICAL GENETICS 64(2):106-108 Leavitt BR Something lost in the translation: 'premutations' in the FMR1 gene cause Fragile X tremor/ataxia syndrome (FXTAS)	0	0
#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
2411	69	87	2411 2003 CURRENT OPINION IN PEDIATRICS 15(6):559-566 Chiurazzi P; Neri G; Oostra BA Understanding the biological underpinnings of fragile X syndrome	2	5
2412	43	136	2412 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):65-76 Greene E; Handa V; Kumari D; Usdin K Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia	0	0
2413	97	168	2413 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):111-123 Bakker CE; Oostra BA Understanding fragile X syndrome: insights from animal models	4	5
2414	11	59	2414 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):140-146 Fleming K; Riser DK; Kumari D; Usdin K Instability of the fragile X syndrome repeat in mice: the effect of age, diet and mutations in genes that affect DNA replication, recombination and repair proficiency	0	0
2415	19	33	2415 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):206-212 Hagerman PJ; Greco CM; Hagerman RJ A cerebellar tremor/ataxia syndrome among fragile X premutation carriers	4	7
2416	24	62	2416 2003 DEVELOPMENT 130(22):5543-5552 Lee A; Li WJ; Xu KY; Bogert BA; Su K; et al. Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1	10	15
2417	152	233	2417 2003 DEVELOPMENT AND PSYCHOPATHOLOGY 15(4):927-968 Reiss AL; Dant CC The behavioral neurogenetics of fragile X syndrome: Analyzing gene-brain-behavior relationships in child developmental psychopathologies	0	0
2418	0	0	2418 2003 DEVELOPMENTAL BIOLOGY 259(2):528-529 Qin M; Kang J; Smith CB Increased local rates of cerebral protein synthesis in fragile X knockout mice.	0	0
2419	14	24	2419 2003 EUROPEAN CHILD & ADOLESCENT PSYCHIATRY 12(4):172-177 Sabaratnam M; Murthy NV; Wijeratne A; Buckingham A; Payne S Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome - A prospective ten-year follow-up study	0	1
2420	28	61	2420 2003 EXPERIMENTAL CELL RESEARCH 289(1):95-107 Bardoni B; Willemsen R; Weiler IJ; Schenck A; Severijnen LA; et al. NUFIP 1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosome	6	7
#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
2421	28	34	2421 2003 GENETIC TESTING 7(4):303-308 Gasteiger M; Grasbon-Frod E; Neitzel B; Kooy F; Holinski-Feder E FMR1 gene deletion/reversion: A pitfall of fragile X carrier testing	0	0
2422	20	29	2422 2003 GENETIC TESTING 7(4):339-343 Rife M; Badenas C; Mallolas J; Jimenez L; Cervera R; et al. Incidence of Fragile X in 5,000 consecutive newborn males	0	2
2423	3	7	2423 2003 GENETIC TESTING 7(4):345-346 Adir V; Shahak E; Dar H; Borochowitz ZU Detection of X chromosome aneuploidy using Southern blot analysis during routine population-based screening for Fragile X syndrome	0	0
2424	15	55	2424 2003 GENETICS IN MEDICINE 5(5):378-384 Skinner D; Sparkman KL; Bailey DB Screening for fragile X syndrome: Parent attitudes and perspectives	1	1
2425	28	41	2425 2003 HEREDITY 90(3):206-211 Arrieta I; Penagarikano O; Tele M; Ortega B; Flores P; et al. The FMR1 CGG repeat and linked microsatellite markers in two Basque valleys	0	0
2426	1	4	2426 2003 HUMAN GENETICS 112(5-6):619-620 Macpherson J; Waghorn A; Hammans S; Jacobs P Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia	9	18
2427	34	43	2427 2003 HUMAN GENETICS 113(5):371-376 Arocena DG; Breece KE; Hagerman PJ Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population	1	2
2428	20	56	2428 2003 HUMAN MOLECULAR GENETICS 12(9):949-959 Willemsen R; Hoogeveen-Westerveld M; Reis S; Holstege J; Severijnen LAWFM; et al. The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome	11	19
2429	39	53	2429 2003 HUMAN MOLECULAR GENETICS 12(14):1689-1698 Bardoni B; Castets M; Huot ME; Schenck A; Adinolfi S; et al. 82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization	8	8
2430	23	44	2430 2003 HUMAN MOLECULAR GENETICS 12(23):3067-3074 Chen LS; Tassone F; Sahota P; Hagerman PJ The (CGG)(n) repeat element within the 5 ' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter	3	3
#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
2431	40	52	2431 2003 HUMAN MOLECULAR GENETICS 12(23):3087-3096 Mazroui R; Huot ME; Tremblay S; Boilard N; Labelle Y; et al. Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs	4	4
2432	21	53	2432 2003 HUMAN MOLECULAR GENETICS 12(24):3295-3305 Ceman S; O'Donnell WT; Reed M; Patton S; Pohl J; et al. Phosphorylation influences the translation state of FMRP-associated polyribosomes	12	15
2433	21	29	2433 2003 HUMAN REPRODUCTION 18(8):1637-1640 Gersak K; Meden-Vrtovec H; Peterlin B Fragile X premutation in women with sporadic premature ovarian failure in Slovenia	0	0
2434	0	34	2434 2003 INTERNAL MEDICINE 42(1):110-116 Momoi A; Komura Y; Kumon L; Tamai M; Tarumi Y; et al. Mesenteric venous thrombosis in hereditary protein c deficiency with the mutation at Arg169 (CGG -> TGG)	0	1
2435	45	118	2435 2003 INTERNATIONAL REVIEW OF RESEARCH IN MENTAL RETARDATION, VOL 27 27:83-119 Murphy MM; Abbeduto L Language and communication in fragile X syndrome	0	0
2436	20	54	2436 2003 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 33(1):55-67 Lesniak-Karpiak K; Mazzocco MMM; Ross JL Behavioral assessment of social anxiety in females with Turner or fragile X syndrome	0	6
2437	30	56	2437 2003 JOURNAL OF BIOLOGICAL CHEMISTRY 278(18):15669-15678 Sung YJ; Dolzhanskaya N; Nolin SL; Brown T; Currie JR; et al. The fragile X mental retardation protein FMRP binds elongation factor 1A mRNA and negatively regulates its translation in vivo	8	13
2438	10	57	2438 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(4):267-275 Johnston C; Hessl D; Blasey C; Eliez S; Erba H; et al. Factors associated with parenting stress in mothers of children with fragile X syndrome	0	1
2439	0	0	2439 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(5):393-393 Hansen R; Goodlin-Jones B; Nowicki S; Heeren M; Herman K; et al. Behavioral phenotypes in older children with autistic spectrum disorders and fragile X: Similarities and differences	0	0
2440	0	0	2440 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1200-1200 Cotton RW; Word CJ Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54.	0	0
#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
2441	0	0	2441 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1201-1201 Clarke GW Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54.	0	0
2442	0	0	2442 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1202-1202 Thompson WC; Taroni F; Aitken CGG Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54. Author's response	0	0
2443	7	32	2443 2003 JOURNAL OF INTELLECTUAL & DEVELOPMENTAL DISABILITY 28(2):135-144 Richdale AL A descriptive analysis of sleep behaviour in children with Fragile X	1	1
2444	0	0	2444 2003 JOURNAL OF MEDICAL GENETICS 40:S15-S15 Ennis S; Collins A; Morton NE SNP-based haplotypes and LD blocks in the fragile X region	0	0
2445	0	0	2445 2003 JOURNAL OF MEDICAL GENETICS 40:S49-S49 Dalton A; Mills AC; Rigby A; Manly T; Hollis C; et al. The neuropsychological phenotype of fragile X premutation males	0	0
2446	0	0	2446 2003 JOURNAL OF MEDICAL GENETICS 40:S80-S80 Payne S; Powell CM Fragile-X intermediate alleles - instability and inconclusion	0	0
2447	18	22	2447 2003 JOURNAL OF MEDICAL GENETICS 40(5):377-379 Willemsen R; Smits A; Severijnen LA; Jansen M; Jacobs A; et al. Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis	3	3
2448	28	41	2448 2003 JOURNAL OF MEDICAL GENETICS 40(7):535-539 de Vries BBA; Severijnen LA; Jacobs A; Olmer R; Halley DJJ; et al. FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics	1	1
2449	0	0	2449 2003 JOURNAL OF NEUROCHEMISTRY 85:1-1 Huber KM Recent progress in understanding the neural mechanisms of Fragile X Syndrome	0	0
2450	19	35	2450 2003 JOURNAL OF NEUROGENETICS 17(2-3):223-230 Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; et al. Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation	0	0
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2451	0	0	2451 2003 JOURNAL OF PSYCHOSOMATIC RESEARCH 55(2):156-156 Mirzaei M; Karam GA; Mahmoudi M Evaluation of prevalence the fragile X syndrome in 52 patients with moderate mental retardation with cytogenetic methods.	0	0
2452	8	10	2452 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(3):372-375 Lombroso PJ Genetics of childhood disorders: XLVIII. Learning and memory, part 1: Fragile X syndrome update	0	0
2453	2	5	2453 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(5):516-517 Lung FW; Chen PJ Fragile X syndrome in adolescent prostitutes in southern Taiwan	0	1
2454	21	28	2454 2003 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 102(1):12-16 Chi J; Chen DJ; Lin CN; Chiu CY; Huang CB; et al. Feasibility of blood spot PCR in large-scale screening of fragile X syndrome in southern Taiwan	0	0
2455	23	69	2455 2003 LANGUAGE SPEECH AND HEARING SERVICES IN SCHOOLS 34(4):320-331 Mirrett PL; Roberts JE Early intervention practices and communication intervention strategies for young males with fragile X syndrome	0	0
2456	27	61	2456 2003 MOLECULAR BRAIN RESEARCH 110(2):267-278 Todd PK; Malter JS; Mack KJ Whisker stimulation-dependent translation of FMRP in the barrel cortex requires activation of type I metabotropic glutamate receptors	4	3
2457	0	0	2457 2003 MOVEMENT DISORDERS 18(9):1091-1091 Kraft S; Parboosingh J; Suchowersky O Absence of fragile X premutation alleles in patients referred with spinocerebellar ataxia	0	0
2458	1	1	2458 2003 NATURE REVIEWS GENETICS 4(10):758-758 Casci T Fragile X: a class of its own	0	0
2459	1	3	2459 2003 NATURE REVIEWS NEUROSCIENCE 4(4):245-245 Jones R Cell biology or the neuron - FMRP and its many partners	0	0
2460	1	1	2460 2003 NATURE REVIEWS NEUROSCIENCE 4(10):776-777 Casci T Neurological disorders - Fragile X: a class of its own	0	0
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2461	13	26	2461 2003 NEURON 37(4):555-558 Antar LN; Bassell GJ Sunrise at the synapse: The FMRP mRNP shaping the synaptic interface	11	25
2462	7	10	2462 2003 NEURON 38(6):843-845 Billuart P; Chelly J From fragile X mental retardation protein to Rac1 GTPase: New insights from fly CYFIP	1	2
2463	22	64	2463 2003 NEURON 38(6):887-898 Schenck A; Bardoni B; Langmann C; Harden N; Mandel JL; et al. CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein	11	23
2464	7	35	2464 2003 NEURON 39(5):739-747 Jin P; Zarnescu DC; Zhang FP; Pearson CE; Lucchesi JC; et al. RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila	10	23
2465	41	101	2465 2003 NEUROPSYCHOLOGY 17(4):646-657 Loesch DZ; Bui QM; Grigsby J; Butler E; Epstein J; et al. Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X	1	1
2466	14	26	2466 2003 NEUROSCIENCE 119(1):9-13 D'Antuono M; Merlo D; Avoli M Involvement of cholinergic and GABAergic systems in the fragile X knockout mice	0	2
2467	22	39	2467 2003 NEUROSCIENCE 120(4):1005-1017 Chen L; Yun SW; Seto J; Liu W; Toth M The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences	10	11
2468	21	50	2468 2003 NUCLEIC ACIDS RESEARCH 31(14):3963-3970 Weisman-Shomer P; Cohen E; Hershco I; Khateb S; Wolfovitz-Barchad O; et al. The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)(n)	3	5
2469	10	23	2469 2003 NUCLEIC ACIDS RESEARCH 31(21):6243-6248 Handa V; Saha T; Usdin K The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer	3	7
2470	8	36	2470 2003 PEDIATRICS 111(2):407-416 Bailey DB; Skinner D; Sparkman KL Discovering fragile X syndrome: Family experiences and perceptions	5	6
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2471	24	41	2471 2003 PRENATAL DIAGNOSIS 23(4):345-351 Wald NJ; Morris JK A new approach to antenatal screening for Fragile X syndrome	1	3
2472	1	1	2472 2003 PRENATAL DIAGNOSIS 23(9):771-771 Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; et al. Pilot study for the neonatal screening of fragile X syndrome (vol 22, pg 459, 2002)	0	0
2473	22	45	2473 2003 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 100(24):14374-14378 Todd PK; Mack KJ; Malter JS The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95	8	13
2474	0	21	2474 2003 PROTEIN EXPRESSION AND PURIFICATION 27(2):365-374 McNulty DE; Claffee BA; Huddleston MJ; Kane JF Mistranslational errors associated with the rare arginine codon CGG in Escherichia coli	1	6
2475	18	33	2475 2003 RNA-A PUBLICATION OF THE RNA SOCIETY 9(10):1198-1207 Ramos A; Hollingworth D; Pastore A G-quartet-dependent recognition between the FMRP RGG box and RNA	7	12
2476	37	55	2476 2003 TRENDS IN BIOCHEMICAL SCIENCES 28(3):152-158 Jin P; Warren ST New insights into fragile X syndrome: from molecules to neurobehaviors	18	34
2477	36	60	2477 2003 TRENDS IN GENETICS 19(3):148-154 Kooy RF Of mice and the fragile X syndrome	10	13
2478	12	40	2478 2003 YONSEI MEDICAL JOURNAL 44(4):583-592 Demirhan O; Tastemir D; Diler RS; Firat S; Avei A A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome	1	1
2479	5	10	2479 2004 ACTA PHARMACOLOGICA SINICA 25(7):973-976 Sun YJ; Han X Dynamic behavior of fragile X full mutations in cultured female fetal fibroblasts	0	0
2480	41	80	2480 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):805-816 Hagerman PJ; Hagerman RJ The fragile-X premutation: A maturing perspective	8	14
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2481	15	26	2481 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):1051-1056 Hagerman RJ; Leavitt BR; Farzin F; Jacquemont S; Greco CM; et al. Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation	3	7
2482	1	1	2482 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(2):352-352 Hagerman; Hagerman The fragile-X premutation: A maturing perspective (vol 74, pg 805, 2003)	0	0
2483	2	10	2483 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):730-731 Mandel JL Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation	1	1
2484	1	5	2484 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):731-732 Salomons GS; Ropers HH Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation - Reply	0	0
2485	19	29	2485 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):129-132 Rife M; Nadal A; Mila M; Willemsen R Immunohistochemical FMRP studies in a full mutated female fetus	0	0
2486	9	16	2486 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):213-215 Marshall I; Betensky BP; Goseco A; Vogiatzi MV; Flieder D Fragile x and mosaic 45,X/46,XY mixed gonadal dysgenesis in a girl with ambiguous genitalia	0	0
2487	3	5	2487 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 125A(3):320-320 Milunsky JM; Maher TA Fragile X carrier screening and spinocerebellar ataxia in older males	0	3
2488	21	48	2488 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 126A(1):9-17 Kau ASM; Tierney E; Bukelis I; Stump MH; Kates WR; et al. Social behavior profile in young males with fragile X syndrome: Characteristics and specificity	0	2
2489	31	38	2489 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 128A(3):250-255 Penagarikano O; Gil A; Telez M; Ortega B; Flores P; et al. A new insight into fragile X syndrome among Basque population	0	0
2490	25	40	2490 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(2):184-189 Zeesman S; Zwaigenbaum L; Whelan DT; Hagerman RJ; Tassone F; et al. Paternal transmission of fragile X syndrome	0	0
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2491	20	26	2491 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):218-224 Biancalana V; Beldjord C; Taillandier A; Szpiro-Tapia S; Cusin V; et al. Five years of molecular diagnosis of Fragile X syndrome(1997-2001): A collaborative study reporting 95% of the activity in France	0	1
2492	24	59	2492 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):225-234 Kaufmann WE; Cortell R; Kau CSM; Bukelis I; Tierney E; et al. Autism spectrum disorder in fragile X syndrome: Communication, social interaction, and specific behaviors	0	0
2493	11	16	2493 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):326-328 Clarke NF; Mowat D; Kooy RF; Reyniers E; Willemsen R Fragile X syndrome phenotype with normal FMR1 gene studies	0	0
2494	0	42	2494 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 126B(1):46-50 Devlin B; Bennett P; Dawson G; Figlewicz DA; Grigorenko EL; et al. Alleles of a Reelin CGG repeat do not convey liability to autism in a sample from the CPEA network	0	3
2495	17	51	2495 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):208-218 Philofsky A; Hepburn SL; Hayes A; Hagerman R; Rogers SJ Linguistic and cognitive functioning and autism symptoms in young children with fragile X syndrome	0	1
2496	14	79	2496 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):237-254 Abbeduto L; Seltzer MM; Shattuck P; Krauss MW; Orsmond G; et al. Psychological well-being and coping in mothers of youths with autism, Down syndrome, or fragile X syndrome	0	1
2497	0	0	2497 2004 ANNALS OF NEUROLOGY 56:S104-S104 Cortell R; Bukelis I; Gray RM; Cox C; Tierney E; et al. Autism spectrum disorder in boys with Fragile X: Serial evaluation	0	0
2498	14	50	2498 2004 ARCHIVES OF GENERAL PSYCHIATRY 61(3):281-288 Garrett AS; Menon V; MacKenzie K; Reiss AL Here's looking at you, kid - Neural systems underlying face and gaze processing in fragile X syndrome	0	1
2499	0	0	2499 2004 BEHAVIOR GENETICS 34(6):638-638 Fisch GS; Simensen RJ; Schroer RJ Longitudinal assessment of cognitive-behavioral features of children and adolescents with either autism or the fragile X mutation	0	0
2500	0	0	2500 2004 BIOLOGICAL PSYCHIATRY 55:159S-159S Daly EM; Moore CJ; Simmons A; Tassone F; Tysoe C; et al. A H-1 magnetic resonance spectroscopy study of males with premutation expansion of CGG trinucleoticle repeats	0	0
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2501	28	62	2501 2004 BRAIN 127:591-601 Kogan CS; Boutet I; Cornish K; Zangenehpour S; Mullen KT; et al. Differential impact of the FMR1 gene on visual processing in fragile X syndrome	2	2
2502	23	40	2502 2004 BRAIN 127:2672-2681 Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy	0	0
2503	12	21	2503 2004 BRAIN & DEVELOPMENT 26(6):380-383 Suwa K; Momoi MY Non-invasive screening of fragile X syndrome A using urine and hair roots	0	0
2504	3	6	2504 2004 BRAIN AND COGNITION 54(3):235-239 Cornish K; Swainson R; Cunnington R; Wilding J; Morris P; et al. Do women with fragile X syndrome have problems in switching attention: Preliminary findings from ERP and fMRI	0	0
2505	0	0	2505 2004 BRAIN AND COGNITION 56(1):121-121 Kogan C; Boutet I; Cornish K; Andermann E; DerKaloustian V; et al. Evidence for a transient channel visual deficit in Fragile X Syndrome	0	0
2506	60	135	2506 2004 CELLULAR AND MOLECULAR LIFE SCIENCES 61(14):1714-1728 Denman RB; Dolzhanskaya N; Sung YJ Regulating a translational regulator: mechanisms cells use to control the activity of the fragile X mental retardation protein	1	2
2507	51	120	2507 2004 CNS DRUGS 18(11):687-703 Tsiouris JA; Brown WT Neuropsychiatric symptoms of fragile X syndrome - Pathophysiology and pharmacotherapy	0	0
2508	24	47	2508 2004 COGNITIVE NEUROPSYCHOLOGY 21(6):579-596 Keenan JM; Simon JA Inference deficits in women with Fragile X Syndrome: A problem in working memory	0	0
2509	16	47	2509 2004 CURRENT BIOLOGY 14(12):1025-1034 Xu KY; Bogert BA; Li WJ; Su K; Lee A; et al. The fragile X-related gene affects the crawling behavior of Drosophila larvae by regulating the mRNA level of the DEG/ENaC protein pickpocket1	2	3
2510	20	37	2510 2004 CURRENT BIOLOGY 14(20):1863-1870 Pan LY; Zhang YQ; Woodruff E; Broadie K The Drosophila fragile X gene negatively regulates neuronal elaboration and synaptic differentiation	2	2
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2511	16	38	2511 2004 CYTOGENETIC AND GENOME RESEARCH 105(2-4):448-454 Errijgers V; Kooy RF Genetic modifiers in mice: the example of the fragile X mouse model	0	0
2512	18	58	2512 2004 DEVELOPMENTAL BIOLOGY 270(2):290-307 Zhang YQ; Matthies HJG; Mancuso J; Andrews HK; Woodruff E; et al. The Drosophila fragile X-related gene regulates axoneme differentiation during spermatogenesis	3	3
2513	5	41	2513 2004 DEVELOPMENTAL SCIENCE 7(1):116-130 Scerif G; Cornish K; Wilding J; Driver J; Karmiloff-Smith A Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome	1	1
2514	17	55	2514 2004 EMBO JOURNAL 23(16):3346-3355 Rackham O; Brown CM Visualization of RNA-protein interactions in living cells: FMRP and IMP1 interact on mRNAs	3	4
2515	11	19	2515 2004 EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY 112(2):189-191 Bussani C; Papi L; Sestini R; Baldinotti F; Bucciantini S; et al. Premature ovarian failure and fragile X premutation: a study on 45 women	0	0
2516	35	49	2516 2004 EXPERIMENTAL NEUROLOGY 189(2):343-353 Schrier M; Severijnen LA; Reis S; Rife M; van't Padje S; et al. Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cells	0	0
2517	0	0	2517 2004 FERTILITY AND STERILITY 82:S246-S247 Malcov M; Carmon A; Mey-Raz N; Ben Yosef D; Lessing JB; et al. Preimplantation genetic diagnosis for fragile X syndrome in Israel	0	0
2518	21	34	2518 2004 GENE 343(2):231-238 Guduric-Fuchs J; Mohrlen F; Frohme M; Frank U A fragile X mental retardation-like gene in a cnidarian	0	0
2519	41	114	2519 2004 GENES BRAIN AND BEHAVIOR 3(6):337-359 Yan QJ; Asafo-Adjei PK; Arnold HM; Brown RE; Bauchwitz RP A phenotypic and molecular characterization of the fmr1-tm1Cgr Fragile X mouse	1	1
2520	0	0	2520 2004 GENETIC COUNSELING 15(2):239-286 [Anon] Abstracts of the 11(th) International Workshop on Fragile X and X-Linked Mental Retardation - 27-30 August 2003, Pafos, Cyprus	0	0
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2521	27	42	2521 2004 GENETIC EPIDEMIOLOGY 26(4):294-304 Huggins RM; Loesch DZ; Qian GQ; Bui QM; Mitchell RJ; et al. Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-X	0	0
2522	0	0	2522 2004 GENETICS IN MEDICINE 6(4):300-300 MacKenzie JJ; Sumargo IV; Taylor SA A cryptic full mutation in a male with a classical fragile X phenotype.	0	0
2523	0	0	2523 2004 GENETICS IN MEDICINE 6(4):352-352 Han X; Chehab F; Powell B; Phalin-Rague J A high mental functioning fragile X male with a de novo 103bp deletion including entire CGG repeat region in > 50% of his peripheral leukocytes.	0	0
2524	15	49	2524 2004 GENOMICS 83(1):106-118 Naumann F; Remus R; Schmitz B; Doerfler W Gene structure and expression of the 5 '-(CGG)(n)-3 '-binding protein (CGGBP1)	0	1
2525	3	40	2525 2004 GENOMICS 84(1):69-81 Sarafidou T; Kahl C; Martinez-Garay I; Mangelsdorf M; Gesk S; et al. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein	0	0
2526	32	55	2526 2004 GROWTH HORMONE & IGF RESEARCH 14:S158-S165 Mandel JL; Biancalana V Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues	0	0
2527	0	9	2527 2004 HEMOGLOBIN 28(3):173-176 Regtuijt ME; Harteveld CL; Van Delft P; Akkermans N; Giordano PC Hb Suan-Dok [alpha 109(G16)Leu -> Arg; CTG--> CGG (alpha 2)] - Described in a patient of African ancestry	0	0
2528	21	42	2528 2004 HUMAN MOLECULAR GENETICS 13(1):79-89 Wang HP; Ku L; Osterhout DJ; Li W; Ahmadian A; et al. Developmentally-programmed FMRP expression in oligodendrocytes: a potential role of FMRP in regulating translation in oligodendroglia progenitors	1	3
2529	13	32	2529 2004 HUMAN MOLECULAR GENETICS 13(5):543-549 Beilina A; Tassone F; Schwartz PH; Sahota P; Hagerman PJ Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element	4	6
2530	1	5	2530 2004 ISRAEL JOURNAL OF PSYCHIATRY AND RELATED SCIENCES 41(1):70-70 Kandil ST; Bilici M; Aksu HB; Celep F; Karaguzel A Early infantile autism and fragile X anomaly	0	0
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2531	22	55	2531 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(4):460-469 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; et al. Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population	6	15
2532	1	1	2532 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2945 Barrett SK; Drazin T; Rosa D; Kupchik GS Genetic counseling for families of patients with fragile X syndrome	0	0
2533	2	6	2533 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2946 Hagerman PJ; Hagerman RJ; Gane LW Genetic counseling for families of patients with fragile X syndrome - In reply	1	1
2534	1	1	2534 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 292(17):2086-2086 Hagerman P Genetic counseling for families of patients with fragile X syndrome (vol 291, pg 2945, 2004)	0	0
2535	5	50	2535 2004 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 34(1):41-48 Seltzer MM; Abbeduto L; Krauss MW; Greenberg J; Swe A Comparison groups in autism family research: Down syndrome, fragile X syndrome, and schizophrenia	0	2
2536	60	103	2536 2004 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY 45(6):1042-1053 Cornish KM; Turk J; Wilding J; Sudhalter V; Munir F; et al. Annotation: Deconstructing the attention deficit in fragile X syndrome: a developmental neuropsychological approach	0	0
2537	22	57	2537 2004 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 89(9):4569-4574 Welt CK; Smith PC; Taylor AE Evidence of early ovarian aging in fragile X premutation carriers	0	0
2538	0	30	2538 2004 JOURNAL OF CLINICAL MICROBIOLOGY 42(8):3538-3548 Otsuka Y; Parniewski P; Zwolska Z; Kai M; Fujino T; et al. Characterization of a trinucleotide repeat sequence (CGG)(5) and potential use in restriction fragment length polymorphism typing of Mycobacterium tuberculosis	0	1
2539	6	36	2539 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(1):21-27 Mirrett PL; Bailey DB; Roberts JE; Hatton DD Developmental screening and detection of developmental delays in infants and toddlers with fragile X syndrome	0	0
2540	30	54	2540 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(6):392-398 Goodlin-Jones BL; Tassone F; Gane LW Autistic spectrum disorder and the fragile X premutation	0	0
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2541	0	1	2541 2004 JOURNAL OF FORENSIC SCIENCES 49(1):192-193 Brenner CH; Inman K Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54.	0	0
2542	0	3	2542 2004 JOURNAL OF FORENSIC SCIENCES 49(1):194-195 Thompson WC; Taroni PF; Aitken CGG 'Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54. - Response	0	0
2543	1	13	2543 2004 JOURNAL OF HUMAN GENETICS 49(2):97-101 Nagao K; Fujii K; Yamada M; Miyashita T Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes	0	0
2544	0	0	2544 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:287-287 Brown W; Nolin S; Dobkin C; Houck G; Glicksman A; et al. Frequency of fragile X in multiplex autism: Testing the AGRE families	0	0
2545	0	0	2545 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:288-288 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; et al. The fragile X syndrome (FXS): Screening and prenatal diagnosis	0	0
2546	0	0	2546 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294 Turk J; Das D; Howlin P; Barber N; Mottaleb M; et al. A follow-up of intellectual, social, communicatory & adaptive functioning in boys & young men with fragile X syndrome	0	0
2547	0	0	2547 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294 Einfeld SL; Tonge BJ; Turner G; Smith E Longitudinal course of behavioural and emotional problems in Prader-Willi, Fragile X, Williams and Down syndromes	0	0
2548	0	0	2548 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:324-324 Abbeduto L; Murphy MM Language, communication, and the behavioural phenotype of Down syndrome (DS): Insights from fragile X syndrome (FXS) and typical development	0	0
2549	0	0	2549 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:325-325 Abbeduto L; Murphy MM; Giles N; Bruno L; Richmond EK; et al. Understanding language in context: Comparisons of Down syndrome (DS) with fragile X syndrome and typical development	0	0
2550	0	0	2550 2004 JOURNAL OF INVESTIGATIVE MEDICINE 52(1):S101-S101 Nowicki ST; Jacquemont S; Li L; Nguyen DV; Gregg JP; et al. An approach to identify epistatic genes involved in the development of autism spectrum disorder in patients with fragile X syndrome	0	0
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2551	0	0	2551 2004 JOURNAL OF MEDICAL GENETICS 41:S64-S64 Turner A; Myring J; Stephens M; Antoniadi T; Butler R The Problem with Premutations: Assessment of new methods for fragile-X screening.	0	0
2552	0	0	2552 2004 JOURNAL OF MEDICAL GENETICS 41:S82-S82 McConachie M; Conlin L; McKay F; Gillespie K; Berg J A false negative PCR result in a boy with Fragile X syndrome	0	0
2553	10	16	2553 2004 JOURNAL OF MEDICAL GENETICS 41(4) Zhou Y; Law HY; Boehm CD; Yoon CS; Cutting GR; et al. Robust fragile X (CGG)(n) genotype classification using a methylation specific triple PCR assay	0	0
2554	12	15	2554 2004 JOURNAL OF MEDICAL GENETICS 41(4) Tassone F; Hagerman RJ; Garcia-Arocena D; Khandjian EW; Greco CM; et al. Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome	0	2
2555	41	65	2555 2004 JOURNAL OF MOLECULAR BIOLOGY 343(1):43-53 Menon RP; Gibson TJ; Pastore A The C terminus of fragile X mental retardation protein interacts with the multi-domain ran-binding protein in the microtubule-organising centre	0	0
2556	0	0	2556 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409 Lee JY; Zhang YT; Hopcus-Niccum D; Mulvihill JJ; Li SB A mosaicism of 45,X/46,XX/47,XXX uncovered by molecular fragile X testing	0	0
2557	0	0	2557 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409 Williams J; Lyon E; Miller C; Mao R Chromosome aneuploidy detected by fragile X southern blot and PCR analysis	0	0
2558	19	34	2558 2004 JOURNAL OF MOLECULAR HISTOLOGY 35(4):389-395 Reis SA; Willemsen R; van Unen L; Hoogeveen AT; Oostra BA Prospects of TAT-mediated protein therapy for fragile X syndrome	0	0
2559	12	37	2559 2004 JOURNAL OF NEUROSCIENCE 24(11):2648-2655 Antar LN; Afroz R; Dictenberg JB; Carroll RC; Bassell GJ Metabotropic glutamate receptor activation regulates Fragile X mental retardation protein and Fmr1 mRNA localization differentially in dendrites and at synapses	10	15
2560	40	97	2560 2004 JOURNAL OF NEUROSCIENCE 24(25):5798-5809 Michel CI; Kraft R; Restifo LL Defective neuronal development in the mushroom bodies of Drosophila Fragile X Mental Retardation 1 Mutants	6	7
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2561	23	34	2561 2004 JOURNAL OF NEUROSCIENCE 24(33):7272-7276 Stefani G; Fraser CE; Darnell JC; Darnell RB Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells	2	3
2562	16	25	2562 2004 JOURNAL OF NEUROSCIENCE 24(47):10579-10583 Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al. Visual experience regulates transient expression and dendritic localization of Fragile X mental retardation protein	1	1
2563	1	1	2563 2004 JOURNAL OF NEUROSCIENCE 24(50):CP3-CP4 Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al. Visual experience regulates transient expression and dendritic localization of fragile X mental retardation protein (vol 24, pg 10579, 2004)	0	0
2564	7	21	2564 2004 JOURNAL OF THE NEUROLOGICAL SCIENCES 227(1):115-118 Garland EM; Vnencak-Jones CL; Biaggioni I; Davis TL; Montine TJ; et al. Fragile X gene premutation in multiple system atrophy	0	0
2565	0	0	2565 2004 LANCET NEUROLOGY 3(12):701-701 Nelson R Drosophila model increases understanding of fragile-X syndrome	0	0
2566	0	0	2566 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):1-2 Crnic LS; Hagerman R Preface: Fragile X syndrome: Frontiers of understanding gene-brain-behavior relationships	0	0
2567	16	48	2567 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):3-10 Bailey DB Newborn screening for fragile X syndrome	0	1
2568	34	67	2568 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):11-16 Cornish K; Sudhalter V; Turk J Attention and language in fragile X	1	1
2569	39	74	2569 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):17-24 Hessl D; Rivera SM; Reiss AL The neuroanatomy and neuroendocrinotogy of fragile X syndrome	1	2
2570	29	55	2570 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):25-30 Hagerman PJ; Hagerman RJ Fragile X-associated tremor/ataxia syndrome (FXTAS)	0	1
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2571	39	66	2571 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):31-41 Loesch DZ; Huggins RM; Hagerman RJ Phenotypic variation and FMRP levels in fragile X	1	1
2572	15	45	2572 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):42-48 Berry-Kravis E; Potanos K Psychopharmacology in fragile X syndrome - Present and future	0	0
2573	19	32	2573 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):49-52 Darnell JC; Warren ST; Darnell RB The fragile X mental retardation protein, FMRP, recognizes G-quartets	0	1
2574	24	54	2574 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):53-59 Beckel-Mitchener A; Greenough WT Correlates across the structural, functional, and molecular phenotypes of fragile X syndrome	0	2
2575	42	102	2575 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):60-67 Willemsen R; Oostra BA; Bassell GJ; Dictenberg J The fragile X syndrome: From molecular genetics to neurobiology	2	5
2576	21	82	2576 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):68-74 Siomi H; Ishizuka A; Siomi MC RNA interference: A new mechanism by which FMRP acts in the normal brain? What can drosophila teach us?	1	4
2577	7	66	2577 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):75-81 Rattazzi MC; LaFauci G; Brown WT Prospects for gene therapy in the fragile X syndrome	0	0
2578	15	36	2578 2004 MOLECULAR BRAIN RESEARCH 131(1-2):101-109 Lauterborn JC Stress induced changes in cortical and hypothalamic c-fos expression are altered in fragile X mutant mice	0	0
2579	11	11	2579 2004 MOLECULAR HUMAN REPRODUCTION 10(10):773-776 Rife M; Badenas C; Quinto L; Puigoriol E; Tazon B; et al. Analysis of CGG variation through 642 meioses in Fragile X families	1	1
2580	1	50	2580 2004 MOLECULAR MICROBIOLOGY 54(3):742-754 Blaha B; Semsey S; Ferenczi S; Csiszovszki Z; Papp PP; et al. A proline tRNA(CGG) gene encompassing the attachment site of temperate phage 16-3 is functional and convertible to suppressor tRNA	0	0
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2581	11	41	2581 2004 MOLECULAR PSYCHIATRY 9(4):417-425 Frankland PW; Wang Y; Rosner B; Shimizu T; Balleine BW; et al. Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice	0	1
2582	0	0	2582 2004 MOVEMENT DISORDERS 19:S20-S20 Zhao Y; Puong K; Law H; Wong M; Ng I; et al. Fragile X premutation alleles in patients with sporadic cerebellar ataxia	0	0
2583	0	0	2583 2004 MOVEMENT DISORDERS 19:S21-S21 Hall DA; Pelak VS; Hagerman RJ; Hagerman PJ; Leehey MA Ocular motility in Fragile X premutation carriers and Fragile X associated tremor/ataxia syndrome (FXTAS)	0	0
2584	0	0	2584 2004 MOVEMENT DISORDERS 19:S338-S338 Leehey MA; Berry-Kravis E; Jacquemont S; Zhang L; Hagerman R; et al. Misdiagnosis of fragile X associated tremor/ataxia syndrome (FXTAS)	0	0
2585	0	0	2585 2004 MOVEMENT DISORDERS 19:S339-S339 Leehey MA; Zhang L; Wheelock V; Tassone F; Hagerman R; et al. A preliminary observation: Increased frequency of fragile X expanded alleles in patients that meet diagnostic criteria for MSA	0	0
2586	0	0	2586 2004 MOVEMENT DISORDERS 19:S359-S360 Di Maria E; Grasso M; Abbruzzese G; Mandich P; Ratto S; et al. The role for Fragile X premutation in essential tremor and spinocerebellar ataxia: Findings from two cohorts of Italian patients	0	0
2587	0	0	2587 2004 MOVEMENT DISORDERS 19:S444-S444 Puong K; Zhao Y; Law H; Wong M; Ng I; et al. Screening for Fragile X premutation alleles in patients with essential tremor	0	0
2588	0	0	2588 2004 MOVEMENT DISORDERS 19(9):1122-1122 Leehey MA; Hall D; Rice C; Jacquemont S; Zhang L; et al. The clinical course of fragile X-associated tremor/ataxia syndrome (FXTAS).	0	0
2589	0	0	2589 2004 MOVEMENT DISORDERS 19(9):1127-1127 Hall DA; Rice CD; Hagerman RR; Hagerman PR; Berry-Kravis E; et al. Medical treatment for the fragile x-associated tremor/ataxia syndrome.	0	0
2590	47	73	2590 2004 NATURE CELL BIOLOGY 6(11):1048-1053 Jin P; Alisch RS; Warren ST RNA and microRNAs in fragile X mental retardation	2	3
#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
2591	22	39	2591 2004 NATURE NEUROSCIENCE 7(2):113-117 Jin P; Zarnescu DC; Ceman S; Nakamoto M; Mowrey J; et al. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway	16	38
2592	1	2	2592 2004 NATURE REVIEWS NEUROSCIENCE 5(1):4-4 Jones R Neurological disorders: Fragile X functions	0	0
2593	0	0	2593 2004 NEUROBIOLOGY OF AGING 25:S434-S434 Westmark CJ; Malter JS FMRP mediates mGluR1-activated translation of APP	0	0
2594	0	0	2594 2004 NEUROLOGY 62(7):A48-A48 Hagerman PJ; Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; et al. Penetrance of the Fragile X-associated Tremor/Ataxia Syndrome (FXTAS) in a premutation carrier population: Initial results from a California family-based study	0	0
2595	7	10	2595 2004 NEUROLOGY 63(2):362-363 Tan EK; Zhao Y; Puong KY; Law HY; Chan LL; et al. Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort	0	4
2596	8	37	2596 2004 NEUROLOGY 63(9):1634-1639 Kogan CS; Bertone A; Cornish K; Boutet I; Kaloustian VMD; et al. Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome	0	0
2597	5	7	2597 2004 NEUROLOGY 63(11):2188-2189 Pugliese P; Annesi G; Cutuli N; Arabia G; Nicoletti G; et al. The fragile X premutation presenting as postprandial hypotension	0	0
2598	51	75	2598 2004 NEUROLOGY INDIA 52(1):36-42 Pandey UB; Phadke SR; Mittal B Molecular diagnosis and genetic counseling for fragile X mental retardation	0	0
2599	52	101	2599 2004 NEUROPSYCHOLOGIA 42(14):1934-1947 Moore CJ; Daly EM; Schmitz N; Tassone F; Tysoe C; et al. A neuropsychological investigation of male premutation carriers of fragile X syndrome	0	0
2600	6	23	2600 2004 NEUROREPORT 15(10):1579-1583 Greicius MD; Boyett-Anderson JM; Menon V; Reiss AL Reduced basal forebrain and hippocampal activation during memory encoding in girls with fragile X syndrome	0	0
#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
2601	24	42	2601 2004 NEUROREPORT 15(16):2447-2450 Veneri M; Zalfa F; Bagni C FMRP and its target RNAs: fishing for the specificity	0	0
2602	17	41	2602 2004 NUCLEIC ACIDS RESEARCH 32(1):298-306 Fojtik P; Kejnovska I; Vorlickova M The guanine-rich fragile X chromosome repeats are reluctant to form tetraplexes	0	2
2603	24	40	2603 2004 NUCLEIC ACIDS RESEARCH 32(7):2129-2137 Gabus C; Mazroui R; Tremblay S; Khandjian EW; Darlix JL The fragile X mental retardation protein has nucleic acid chaperone properties	2	5
2604	18	44	2604 2004 NUCLEIC ACIDS RESEARCH 32(14):4145-4154 Khateb S; Weisman-Shomer P; Hershco I; Loeb LA; Fry M Destabilization of tetraplex structures of the fragile X repeat sequence (CGG)(n) is mediated by homolog-conserved domains in three members of the hnRNP family	0	0
2605	0	1	2605 2004 PRAXIS DER KINDERPSYCHOLOGIE UND KINDERPSYCHIATRIE 53(8):593-594 Irblich D The fragile X syndrome - A guide for parents	0	0
2606	6	8	2606 2004 PRENATAL DIAGNOSIS 24(1):67-68 Delatycki MB; Sheffield LJ; Wake S; Cohen J Screening approach for Fragile X syndrome	0	0
2607	0	1	2607 2004 PRENATAL DIAGNOSIS 24(1):68-69 Wald NJ; Morris JK Reply: Prenatal screen for Fragile X syndrome	0	0
2608	6	12	2608 2004 PRIMARY CARE 31(3):621-+ Wiesner GL; Cassidy SB; Grimes SJ; Matthews AL; Acheson LS Clinical consult: developmental delay/fragile X syndrome	0	0
2609	14	57	2609 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(10):3615-3620 Menon V; Leroux J; White CD; Reiss AL Frontostriatal deficits in fragile X syndrome: Relation to FMR1 gene expression	0	0
2610	26	61	2610 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(36):13357-13362 Khandjian EW; Huot ME; Tremblay S; Davidovic L; Mazroui R; et al. Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles	6	7
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2611	25	53	2611 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(42):15201-15206 Lu R; Wang HP; Liang Z; Ku L; O'Donnell WT; et al. The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development	3	3
2612	15	21	2612 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17329-17330 Miyashiro K; Eberwine J Fragile X syndrome: (What's) lost in translation?	0	0
2613	18	61	2613 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17428-17433 Ling SC; Fahrner PS; Greenough WT; Gelfand VI Transport of Drosophila fragile X rental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein	0	1
2614	28	50	2614 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17504-17509 Weiler IJ; Spangler CC; Klintsova AY; Grossman AW; Kim SH; et al. Fragile X mental retardation protein is necessary for neurotransmitter-activated protein translation at synapses	0	0
2615	1	1	2615 2004 PROTEIN EXPRESSION AND PURIFICATION 37(1):264-264 McNulty DE; Claffee BA; Huddleston MJ; Kane JF Mistranslational errors associated with the rare arginine codon CGG in Escherichia coli (vol 27, pg 365, 2003)	0	0
2616	3	53	2616 2004 QUALITATIVE HEALTH RESEARCH 14(6):741-759 Medved MI; Brockmeier J Making sense of traumatic experiences: Telling your life with fragile X syndrome	0	0
2617	0	1	2617 2004 REPRODUCTIVE BIOMEDICINE ONLINE 8(3):337-337 [Anon] Late onset fragile X syndrome	0	0
2618	2	7	2618 2004 REVISTA DE NEUROLOGIA 38(1):7-11 Artigas-Pallares J; Brun-Gasca C Can the behavioural phenotype of Fragile X syndrome be attributed to mental retardation and to attention deficit hyperactivity disorder?	0	0
2619	33	95	2619 2004 TRENDS IN NEUROSCIENCES 27(7):370-377 Bear MF; Huber KM; Warren ST The mGIuR theory of fragile X mental retardation	8	10
2620	18	41	2620 2005 AMERICAN JOURNAL OF HUMAN GENETICS 76(2):302-311 Edamura KN; Leonard MR; Pearson CE Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells	0	0
#	LCR	NCR	Nodes / Date / Journal / Authors	LCS	GCS
2621	28	50	2621 2005 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 132A(1):25-32 Skinner M; Hooper S; Hatton DD; Robert J; Mirrett P; et al. Mapping nonverbal IQ in young boys with fragile X syndrome	0	0
2622	12	18	2622 2005 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 132A(2):210-214 Angeli CB; Capelli LP; Auricchio MTBM; Vianna-Morgante AM; Mingroni-Netto RC; et al. AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations	0	0
2623	16	20	2623 2005 ANNALS OF NEUROLOGY 57(1):144-147 Berry-Kravis E; Potanos K; Weinberg D; Zhou LL; Goetz CG Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation	0	1
2624	10	98	2624 2005 APPLIED PSYCHOLINGUISTICS 26(1):7-27 Rice ML; Warren SF; Betz SK Language symptoms of developmental language disorders: An overview of autism, Down syndrome, fragile X, specific language impairment, and Williams syndrome	0	1
2625	5	13	2625 2005 ARCHIVES DE PEDIATRIE 12(2):176-179 Vantalon V; Briard-Luginbuhl V; Mouren MC Fragile X syndrome and very early onset schizophrenia: a female case study	0	0
2626	10	47	2626 2005 BIOCHEMICAL JOURNAL 386:297-303 Kumari D; Gabrielian A; Wheeler D; Usdin K The roles of Sp1, Sp3, USF1/USF2 and NRF-1 in the regulation and three-dimensional structure of the Fragile X mental retardation gene promoter	0	0
2627	29	49	2627 2005 BRAIN AND COGNITION 57(1):53-60 Cornish K; Kogan C; Turk J; Manly T; James N; et al. The emerging fragile X premutation phenotype: Evidence from the domain of social cognition	0	0
2628	17	20	2628 2005 CELLULAR AND MOLECULAR LIFE SCIENCES 62(2):251-252 Zalfa F; Bagni C Another view of the role of FMRP in translational regulation	0	0
2629	16	52	2629 2005 DEVELOPMENTAL CELL 8(1):43-52 Zarnescu DC; Jin P; Betschinger J; Nakamoto M; Wang Y; et al. Fragile X protein functions with Lgl and the PAR complex in flies and mice	0	0
2630	9	43	2630 2005 DEVELOPMENTAL CELL 8(3):331-342 Costa A; Wang Y; Dockendorff TC; Erdjument-Bromage H; Tempst P; et al. The Drosophila fragile X protein functions as a negative regulator in the orb autoregulatory pathway	0	0
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2631	1	33	2631 2005 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 47(2):94-104 Weiskop S; Richdale A; Matthews J Behavioural treatment to reduce sleep problems in children with autism or fragile X syndrome	0	0
2632	0	1	2632 2005 EDUCATIONAL REVIEW 57(2):258-260 Reid G Educating children with Fragile X syndrome	0	0
2633	19	26	2633 2005 FEBS JOURNAL 272(3):872-878 Pozdnyakova I; Regan L New insights into Fragile X syndrome - Relating genotype to phenotype at the molecular level	0	0
2634	23	68	2634 2005 HUMAN MOLECULAR GENETICS 14(6):835-844 Castets M; Schaeffer C; Bechara E; Schenck A; Khandjian EW; et al. FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts	0	0
2635	2	4	2635 2005 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 293(3):296-296 Toft M; Farrer M Premutation alleles and fragile X-associated tremor/ataxia syndrome	0	0
2636	1	3	2636 2005 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 293(3):296-297 Deng H; Le WD; Jankovic J Premutation alleles and fragile X-associated tremor/ataxia syndrome - Reply	0	0
2637	21	46	2637 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(6):4498-4503 Mulvihill DJ; Edamura KN; Hagerman KA; Pearson CE; Wang YH Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome	0	0
2638	23	47	2638 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(7):5750-5763 Garnon J; Lachance C; Di Marco S; Hel Z; Marion D; et al. Fragile X-related protein FXR1P regulates proinflammatory cytokine tumor necrosis factor expression at the post-transcriptional level	0	0
2639	3	8	2639 2005 JOURNAL OF CLINICAL NEUROSCIENCE 12(1):42-43 Storey E; Billimoria P Increased T-2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndrome	0	0
2640	0	0	2640 2005 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 76(1):151-151 Ealing J; Mavrogiannis LA; Kingston H; Cockburn DJ; Taylor GR; et al. An atypical tetra nucleotide expansion in DM2 (PROMM)	0	0
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2641	25	61	2641 2005 MOLECULAR & CELLULAR PROTEOMICS 4(3):278-290 Zhang YQ; Friedman DB; Wang Z; Woodruff E; Pan LY; et al. Protein expression profiling of the Drosophila fragile X mutant brain reveals up-regulation of monoamine synthesis	0	0
2642	4	10	2642 2005 NEURON 45(5):642-644 Dolen G; Bear MF Courting a cure for Fragile X	0	0
2643	11	56	2643 2005 NEURON 45(5):753-764 McBride SMJ; Choi CH; Wang Y; Liebelt D; Braunstein E; et al. Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome	1	1
2644	19	34	2644 2005 NEUROSCIENCE LETTERS 377(3):141-146 El Idrissi A; Ding XH; Scalia J; Trenkner E; Brown WT; et al. Decreased GABA(A) receptor expression in the seizure-prone fragile X mouse	0	0
2645	24	45	2645 2005 NUCLEIC ACIDS RESEARCH 33(2):451-463 Napierala M; Michalowski D; de Mezer M; Krzyzosiak WJ Facile FMR1 mRNA structure regulation by interruptions in CGG repeats	0	0
2646	29	46	2646 2005 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 102(6):2180-2185 Aschrafi A; Cunningham BA; Edelman GM; Vanderklish PW The fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain	0	0
2647	59	77	2647 2005 TRENDS IN GENETICS 21(1):37-45 Zhang YQ; Broadie K Fathoming fragile X in fruit flies	1	1

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