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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by year, source, volume, issue, page.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2101 | 0 | 0 | 2101 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):430-430 Jakupciak JP; O'Connell CD; Atha DA; Richie KL Standardization of PCR amplification for fragile X trinucleotide repeat measurements. | 0 | 0 |
| 2102 | 0 | 0 | 2102 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):431-431 Jenkins EC; Li SY; Yao XL; Lanter S; Sudhalter V; et al. Detecting mosaic FMR-1 (fragile X) mutations: Southern blotting versus monoclonal antibody analysis. | 0 | 0 |
| 2103 | 0 | 0 | 2103 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):436-436 Patel ZM; Menon SR; D'souza AK; Adhia RA; Sanghavi DA; et al. Validity of the analysis of FMRP expression in blood smears as a screening method for the fragile X syndrome in Indian population. | 0 | 0 |
| 2104 | 0 | 0 | 2104 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):438-438 Zhou Y; Chong SS Simplified molecular diagnostic testing for fragile X syndrome using methylation-specific PCR (ms-PCR). | 0 | 0 |
| 2105 | 0 | 0 | 2105 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):554-554 Heine-Sur D; Pico G; Torres-Juan L; Bernues M; Iglesias J; et al. A female with Fragile-X shows an affected male-like phenotype and skewed inactivation of the functional chromosome. | 0 | 0 |
| 2106 | 0 | 0 | 2106 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):585-585 Essop FB; Greenberg J; Basel D; Krause A Molecular analysis of a fragile X family with two females homozygous for a premutation. | 0 | 0 |
| 2107 | 0 | 0 | 2107 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):586-586 Nolin SL; Houck GE; Gargano AD; Brown WT Large fragile X premutatin alleles may often contain two AGG Interruptions. | 0 | 0 |
| 2108 | 0 | 0 | 2108 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):635-635 Dobkin CS; Ding X; Brown WT; El Idrissi A Reduced hippocampal GABAa receptors and increased kainic acid seizure susceptibility in the fragile X mouse. | 0 | 0 |
| 2109 | 0 | 0 | 2109 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):667-667 Brown WT; Nolin S; Houck GE; Ding XH; Glicksman A; et al. The Fragile X Syndrome: Screening and prenatal diagnosis. | 0 | 0 |
| 2110 | 0 | 0 | 2110 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):669-669 Mallolas J; Badenas C; Rite M; Soler A; Borrell A; et al. Prospective study of molecular fragile X syndrome prenatal diagnosis. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2111 | 6 | 26 | 2111 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(1):37-45 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping | 2 | 3 |
| 2112 | 14 | 42 | 2112 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(2):161-167 Irwin SA; Patel B; Idupulapati M; Harris JB; Crisostomo RA; et al. Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: A quantitative examination | 48 | 75 |
| 2113 | 7 | 18 | 2113 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):110-115 Stoll C Problems in the diagnosis of fragile X syndrome in young children are still present | 3 | 4 |
| 2114 | 4 | 7 | 2114 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):156-161 Kjaer I; Hjalgrim H; Russell BG Cranial and hand skeleton in fragile X syndrome | 0 | 1 |
| 2115 | 20 | 55 | 2115 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(1):81-90 Sun HT; Cohen S; Kaufmann WE Annexin-1 is abnormally expressed in fragile X syndrome: Two-dimensional electrophoresis study in lymphocytes | 4 | 9 |
| 2116 | 15 | 32 | 2116 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(3):226-230 Schultz-Pedersen S; Hasle H; Olsen JH; Friedrich U Evidence of decreased risk of cancer in individuals with fragile X | 0 | 2 |
| 2117 | 27 | 39 | 2117 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(4):314-319 Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; et al. Neurobehavioral phenotype in carriers of the fragile X premutation | 8 | 9 |
| 2118 | 0 | 0 | 2118 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Daly E; Moore CJ; Schmitz N; Jacobs PA; Davis KE; et al. Premutation expansion of CGG triplet repeats affects brain; A study of male carriers of Fragile X syndrome | 0 | 0 |
| 2119 | 1 | 1 | 2119 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Moore CJ; Daly E; Tassone F; Jacobs PA; Davies KE; et al. Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 2120 | 17 | 54 | 2120 2001 AMERICAN JOURNAL OF PSYCHIATRY 158(7):1040-1051 Kwon H; Menon V; Eliez S; Warsofsky IS; White CD; et al. Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavioral and molecular measures | 11 | 24 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2121 | 17 | 37 | 2121 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):16-27 Bailey DB; Hatton DD; Tassone F; Skinner M; Taylor AK Variability in FMRP and early development in males with fragile X syndrome | 16 | 15 |
| 2122 | 13 | 43 | 2122 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):28-38 Belser RC; Sudhalter V Conversational characteristics of children with fragile X syndrome: Repetitive speech | 9 | 12 |
| 2123 | 23 | 55 | 2123 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(3):216-230 Roberts JE; Mirrett P; Burchinal M Receptive and expressive communication development of young males with fragile X syndrome | 6 | 10 |
| 2124 | 16 | 58 | 2124 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(5):389-400 Sudhalter V; Belser RC Conversational characteristics of children with fragile x syndrome: Tangential language | 5 | 8 |
| 2125 | 27 | 32 | 2125 2001 ANNALS OF CLINICAL BIOCHEMISTRY 38:264-271 Saha S; Karmakar P; Chatterjee C; Banerjee D; Das S; et al. Fragile X syndrome in Calcutta, India | 2 | 4 |
| 2126 | 0 | 0 | 2126 2001 ANNALS OF NEUROLOGY 50(3):S108-S108 Berry-Kravis E Characterization of epilepsy in fragile X syndrome | 0 | 0 |
| 2127 | 15 | 30 | 2127 2001 ARQUIVOS DE NEURO-PSIQUIATRIA 59(1):83-88 Boy R; Correia PS; Llerena JC; Machado-Ferreira MD; Pimentel MMG Fragile X syndrome confirmed by molecular analysis: a case-control study with pre and post-puberal patients | 0 | 0 |
| 2128 | 0 | 0 | 2128 2001 AUSTRALIAN JOURNAL OF PSYCHOLOGY 53(1):58-58 Gould E Melatonin profiles and sleep characteristics in boys with fragile X Syndrome: A preliminary study | 0 | 0 |
| 2129 | 0 | 28 | 2129 2001 BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY 65(7):1568-1574 Tani S; Itoh T; Kato M; Kobayashi T; Tsukagoshi N In vivo and in vitro analyses of the AmyR binding site of the Aspergillus nidulans agdA promoter; Requirement of the CGG direct repeat for induction and high affinity binding of AmyR | 0 | 4 |
| 2130 | 34 | 53 | 2130 2001 BRAIN 124:1610-1618 Eliez S; Blasey CM; Freund LS; Hastie T; Reiss AL Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome | 9 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2131 | 34 | 88 | 2131 2001 BRAIN RESEARCH BULLETIN 56(3-4):367-373 Grabczyk E; Kumari D; Usdin K Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency | 0 | 4 |
| 2132 | 45 | 85 | 2132 2001 BRAIN RESEARCH BULLETIN 56(3-4):375-382 Bardoni B; Schenck A; Mandel JL The Fragile X mental retardation protein | 6 | 9 |
| 2133 | 35 | 62 | 2133 2001 BRAIN RESEARCH BULLETIN 56(3-4):383-387 Chiurazzi P; Neri G Pharmacological reactivation of inactive genes: The fragile X experience | 0 | 1 |
| 2134 | 25 | 47 | 2134 2001 CELL 107(4):477-487 Brown V; Jin P; Ceman S; Darnell JC; O'Donnell WT; et al. Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome | 80 | 162 |
| 2135 | 17 | 85 | 2135 2001 CELL 107(4):489-499 Darnell JC; Jensen KB; Jin P; Brown V; Warren ST; et al. Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function | 74 | 149 |
| 2136 | 16 | 17 | 2136 2001 CELL 107(5):555-557 Kaytor MD; Orr HT RNA targets of the fragile X protein | 6 | 15 |
| 2137 | 20 | 37 | 2137 2001 CELL 107(5):591-603 Zhang YQ; Bailey AM; Matthies HJG; Renden RB; Smith MA; et al. Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function | 57 | 98 |
| 2138 | 23 | 34 | 2138 2001 CELLULAR AND MOLECULAR NEUROBIOLOGY 21(1):29-38 Castren M; Haapasalo A; Oostra BA; Castren E Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons | 3 | 3 |
| 2139 | 66 | 100 | 2139 2001 CLINICAL GENETICS 60(6):399-408 Oostra BA; Chiurazzi P The fragile X gene and its function | 5 | 11 |
| 2140 | 37 | 73 | 2140 2001 COGNITIVE NEUROPSYCHOLOGY 18(1):1-18 Simon JA; Keenan JM; Pennington BF; Taylor AK; Hagerman RJ Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence | 8 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2141 | 9 | 25 | 2141 2001 COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING 4(3):265-272 Murray J; Cuckle H Cystic fibrosis and fragile X syndrome: The arguments for antenatal screening | 1 | 2 |
| 2142 | 65 | 94 | 2142 2001 CURRENT OPINION IN PSYCHIATRY 14(5):443-449 Eliez S; Feinstein C The fragile X syndrome: bridging the gap from gene to behavior | 0 | 1 |
| 2143 | 0 | 1 | 2143 2001 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 43(2):142-142 [Anon] Monozygotic boys with fragile X syndrome (vol 42, pg 768, 2000) | 0 | 0 |
| 2144 | 16 | 86 | 2144 2001 DEVELOPMENTAL PSYCHOBIOLOGY 39(2):107-123 Roberts JE; Boccia ML; Bailey DB; Hatton DD; Skinner M Cardiovascular indices of physiological arousal in boys with fragile X syndrome | 7 | 7 |
| 2145 | 12 | 27 | 2145 2001 DIAGNOSTIC MOLECULAR PATHOLOGY 10(1):34-40 Tzeng CC; Lin SJ; Chen YJ; Kuo PL; Jong YJ; et al. An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome | 1 | 3 |
| 2146 | 3 | 21 | 2146 2001 ELECTROPHORESIS 22(6):1188-1193 Sung WC; Lee GB; Tzeng CC; Chen SH Plastic microchip electrophoresis for genetic screening: The analysis of polymerase chain reactions products of fragile X (CGG)n alleles | 0 | 12 |
| 2147 | 22 | 62 | 2147 2001 EMBO JOURNAL 20(17):4803-4813 Schaeffer C; Bardoni B; Mandel JL; Ehresmann B; Ehresmann C; et al. The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif | 66 | 97 |
| 2148 | 13 | 17 | 2148 2001 EUROPEAN JOURNAL OF HUMAN GENETICS 9(9):724-727 Larsen LA; Vuust J; Nystad M; Evseeva I; Van Ghelue M; et al. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia | 1 | 3 |
| 2149 | 0 | 0 | 2149 2001 FASEB JOURNAL 15(4):A710-A710 Lenert P; Stunz LL; Krieg AM; Ashman RF Down-regulation of CgG-induced B cell NF-kappa B, AP-1 and NF-IL-6 inhibitory oligonucleotides (ODN) | 0 | 0 |
| 2150 | 25 | 49 | 2150 2001 GENETIC EPIDEMIOLOGY 20(1):129-144 Sharma D; Gupta M; Thelma BK Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population | 4 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2151 | 4 | 6 | 2151 2001 GENETIC TESTING 5(2):139-140 Gilbert F Comment: How many are too many when discussing triplet repeats in the FMR1 gene and the fragile X syndrome? | 0 | 1 |
| 2152 | 1 | 42 | 2152 2001 GENETICS 157(2):717-725 Su MA; Wisotzkey RG; Newfeld SJ A screen for modifiers of decapentaplegic mutant phenotypes identifies lilliputian, the only member of the Fragile-X/Burkitt's lymphoma family of transcription factors in Drosophila melanogaster | 0 | 6 |
| 2153 | 108 | 154 | 2153 2001 GENETICS IN MEDICINE 3(5):359-371 Crawford DC; Acuna JM; Sherman SL FMR1 and the fragile X syndrome: Human genome epidemiology review | 17 | 25 |
| 2154 | 6 | 48 | 2154 2001 GENOME RESEARCH 11(8):1382-1391 Mathews DJ; Kashuk C; Brightwell G; Eichler EE; Chakravarti A Sequence variation within the fragile x locus | 0 | 3 |
| 2155 | 35 | 47 | 2155 2001 HUMAN GENETICS 108(6):450-458 Weinhausel A; Haas OA Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR | 2 | 6 |
| 2156 | 22 | 31 | 2156 2001 HUMAN MOLECULAR GENETICS 10(4):329-338 Laggerbauer B; Ostareck D; Keidel EM; Ostareck-Lederer A; Fischer U Evidence that fragile X mental retardation protein is a negative regulator of translation | 84 | 106 |
| 2157 | 37 | 47 | 2157 2001 HUMAN MOLECULAR GENETICS 10(14):1449-1454 Kenneson A; Zhang FP; Hagedorn CH; Warren ST Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers | 36 | 46 |
| 2158 | 29 | 45 | 2158 2001 HUMAN MOLECULAR GENETICS 10(16):1693-1699 Bontekoe CJM; Bakker CE; Nieuwenhuizen IM; van der Linde H; Lans H; et al. Instability of a (CGG)(98) repeat in the Fmr1 promoter | 12 | 15 |
| 2159 | 23 | 64 | 2159 2001 HUMAN MOLECULAR GENETICS 10(24):2803-2811 Huot ME; Mazroui R; Leclerc P; Khandjian EW Developmental expression of the fragile X-related 1 proteins in mouse testis: association with microtubule elements | 5 | 7 |
| 2160 | 7 | 25 | 2160 2001 HUMAN REPRODUCTION 16(3):457-462 Hundscheid RDL; Braat DDM; Kiemeney LALM; Smits APT; Thomas CMG Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives | 8 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2161 | 0 | 22 | 2161 2001 IN VIVO 15(1):105-108 Kotsinas A; Gorgoulis VG; Zacharatos P; Liloglou T; Leonardou P; et al. A new rare allele at the CGG repeat polymorphism in the first intron of human c-H-ras gene | 0 | 0 |
| 2162 | 19 | 31 | 2162 2001 INFANTS AND YOUNG CHILDREN 14(1):24-33 Bailey DB; Roberts JE; Mirrett P; Hatton DD Identifying infants and toddlers with fragile X syndrome: Issues and recommendations | 6 | 6 |
| 2163 | 16 | 33 | 2163 2001 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 31(2):165-174 Bailey DB; Hatton DD; Skinner M; Mesibov G Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome | 16 | 22 |
| 2164 | 10 | 28 | 2164 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(6):4357-4364 Kumari D; Usdin K Interaction of the transcription factors USF1, USF2, and alpha-Pal/Nrf-1 with the FMR1 promoter - Implications for Fragile X mental retardation syndrome | 15 | 23 |
| 2165 | 15 | 58 | 2165 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(19):16439-16446 Kamath-Loeb AS; Loeb LA; Johansson E; Burgers PMJ; Fry M Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)(n) trinucleotide repeat sequence | 4 | 44 |
| 2166 | 8 | 71 | 2166 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(21):18605-18613 Bacolla A; Pradhan S; Larson JE; Roberts RJ; Wells RD Recombinant human DNA (cytosine-5) methyltransferase - III. Allosteric control, reaction order, and influence of plasmid topology and triplet repeat length on methylation of the fragile X CGG center dot CCG sequence | 0 | 15 |
| 2167 | 0 | 14 | 2167 2001 JOURNAL OF CRYSTAL GROWTH 226(1):101-106 Jung IH; Yoshikawa A; Lebbou K; Fukuda T; Auh KH Crystal growth by micro-pulling-down of Ca3Ga2Ge4O14 (CGG) type-Sr3Nb1-xGa3 (+) (5/3)xSi2O14 compounds | 0 | 8 |
| 2168 | 0 | 0 | 2168 2001 JOURNAL OF DENTAL RESEARCH 80(4):1133-1133 Sabbagh A Clinical and panoramic radiographic considerations of oral conditions in Fragile X Syndrome (Martin-Bell Syndrome) | 0 | 0 |
| 2169 | 0 | 1 | 2169 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(5):337-337 Floet AW Children with fragile X syndrome: A parents' guide | 0 | 0 |
| 2170 | 13 | 31 | 2170 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):353-359 Myers GF; Mazzocco MMM; Maddalena A; Reiss AL No widespread psychological effect of the fragile X premutation in childhood: Evidence from a preliminary controlled study | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2171 | 18 | 34 | 2171 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):409-417 Rogers SJ; Wehner EA; Hagerman R The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders | 13 | 24 |
| 2172 | 18 | 24 | 2172 2001 JOURNAL OF KOREAN MEDICAL SCIENCE 16(3):271-275 Kwon SH; Lee KS; Hyun MC; Song KE; Kim JK Molecular screening for Fragile X syndrome in mentally handicapped children in Korea | 0 | 0 |
| 2173 | 11 | 91 | 2173 2001 JOURNAL OF LEARNING DISABILITIES 34(6):520-533 Mazzocco MMM Math learning disability and math LD subtypes: Evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1 | 2 | 8 |
| 2174 | 0 | 0 | 2174 2001 JOURNAL OF MEDICAL GENETICS 38:S39-S39 Moore C; Daly EM; Tassone F; Schmitz N; Hagerman P; et al. Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 2175 | 0 | 0 | 2175 2001 JOURNAL OF MEDICAL GENETICS 38:S40-S40 Daly E; Moore CJ; Schmitz N; Jacobs P; Davies K; et al. Premutation expansion of CGG triplet repeats affects brain; a study of Male Carriers of Fragile X Syndrome | 0 | 0 |
| 2176 | 0 | 0 | 2176 2001 JOURNAL OF MEDICAL GENETICS 38:S63-S63 Warburton S; Waters J; Davison V Targeted diagnostic testing for fragile X syndrome | 0 | 0 |
| 2177 | 0 | 0 | 2177 2001 JOURNAL OF MEDICAL GENETICS 38:S64-S64 Wakeling W; King W; Taylor R Chemiluminescence detection offers a safe, effective and convenient alternative to radioisotopic labelling of probes for detection of Fragile X syndrome and other single gene disorders | 0 | 0 |
| 2178 | 14 | 19 | 2178 2001 JOURNAL OF MEDICAL GENETICS 38(7):453-456 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA | 16 | 22 |
| 2179 | 15 | 47 | 2179 2001 JOURNAL OF SPECIAL EDUCATION 34(4):194-202 Symons FJ; Clark RD; Roberts JP; Bailey DB Classroom behavior of elementary school-age boys with fragile X syndrome | 2 | 3 |
| 2180 | 0 | 10 | 2180 2001 MATERIALS LETTERS 51(2):129-134 Jung IH; Kang YH; Joo K; Yoshikawa A; Fukuda T; et al. Ca3Ga2Ge4O14 (CGG)-type Sr3Nb0.95Ga3.083Si2O14 single crystal grown by the Czochralski method for piezoelectric applications | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2181 | 11 | 17 | 2181 2001 MEDICAL PRINCIPLES AND PRACTICE 10(2):73-78 Alkhalaf M; Verghese L; Mushtaq SK Cytogenetic and immunohistochemical characterization of fragile X syndrome in a Kuwaiti family: Rapid antibody test for the diagnosis of mental retardation patients | 0 | 0 |
| 2182 | 2 | 13 | 2182 2001 MOLECULAR AND CELLULAR ENDOCRINOLOGY 183:S77-S85 Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; et al. PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome | 0 | 10 |
| 2183 | 65 | 108 | 2183 2001 MOLECULAR GENETICS AND METABOLISM 74(1-2):89-97 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behavior relationships | 1 | 2 |
| 2184 | 0 | 2 | 2184 2001 MONATSSCHRIFT KINDERHEILKUNDE 149(3):264-264 Gladtke E Trimethoprim in the fragile X syndrome? | 0 | 0 |
| 2185 | 0 | 0 | 2185 2001 NEUROIMAGE 13(6):S1076-S1076 Moore CJ; Daly EM; Schmitz N; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of male carriers of Fragile X syndrome | 0 | 0 |
| 2186 | 3 | 10 | 2186 2001 NEUROLOGY 57(1):127-130 Hagerman RJ; Leehey M; Heinrichs W; Tassone F; Wilson R; et al. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 45 | 74 |
| 2187 | 26 | 47 | 2187 2001 NEUROPSYCHOLOGY 15(2):290-299 Bennetto L; Pennington BF; Porter D; Taylor AK; Hagerman RJ Profile of cognitive functioning in women with the fragile X mutation | 10 | 13 |
| 2188 | 8 | 20 | 2188 2001 NEUROREPORT 12(11):2573-2576 Rojas DC; Benkers TL; Rogers SJ; Teale PD; Reite ML; et al. Auditory evoked magnetic fields in adults with fragile X syndrome | 3 | 4 |
| 2189 | 15 | 43 | 2189 2001 NEUROSCIENCE 103(4):1043-1050 Chen L; Toth M Fragile X mice develop sensory hyperreactivity to auditory stimuli | 21 | 34 |
| 2190 | 20 | 36 | 2190 2001 NUCLEIC ACIDS RESEARCH 29(11):2276-2283 Li ZZ; Zhang YY; Ku L; Wilkinson KD; Warren ST; et al. The fragile X mental retardation protein inhibits translation via interacting with mRNA | 72 | 93 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2191 | 6 | 47 | 2191 2001 NUCLEIC ACIDS RESEARCH 29(22):4684-4690 Fojtik P; Vorlickova M The fragile X chromosome (GCC) repeat folds into a DNA tetraplex at neutral pH | 0 | 1 |
| 2192 | 25 | 40 | 2192 2001 PEDIATRICS 108(5):art. no.-e88 Hessl D; Dyer-Friedman J; Glaser B; Wisbeck J; Barajas RG; et al. The influence of environmental and genetic factors on behavior problems and autistic symptoms in boys and girls with fragile X syndrome | 0 | 8 |
| 2193 | 13 | 31 | 2193 2001 PRENATAL DIAGNOSIS 21(6):504-511 Apessos A; Abou-Sleiman PM; Harper JC; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 1 | 16 |
| 2194 | 10 | 36 | 2194 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98(13):7101-7106 Greenough WT; Klintsova AY; Irwin SA; Galvez R; Bates KE; et al. Synaptic regulation of protein synthesis and the fragile X protein | 42 | 63 |
| 2195 | 19 | 36 | 2195 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98(15):8844-8849 Schenck A; Bardoni B; Moro A; Bagni C; Mandel JL A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P | 27 | 51 |
| 2196 | 5 | 18 | 2196 2001 REVISTA DE NEUROLOGIA 33:S6-S9 Glover G; Bernabe MJ; Carbonell P Gnosis of fragile X syndrome | 0 | 0 |
| 2197 | 19 | 22 | 2197 2001 REVISTA DE NEUROLOGIA 33:S9-S13 Ramos-Fuentes FJ New methods for the diagnosis of fragile X syndrome: A study of the FMRP in blood and hair | 0 | 0 |
| 2198 | 21 | 30 | 2198 2001 REVISTA DE NEUROLOGIA 33:S14-S19 Tejada MI Prevention of fragile X syndrome by prenatal genetic diagnosis: Advantages and controversial aspects | 0 | 0 |
| 2199 | 8 | 25 | 2199 2001 REVISTA DE NEUROLOGIA 33:S20-S23 Mila M; Mallolas J Fragile X syndrome: Premature ovarian failure. Preimplantation and preconception genetic diagnosis | 0 | 0 |
| 2200 | 13 | 30 | 2200 2001 REVISTA DE NEUROLOGIA 33:S24-S29 Cornish K; Munir F; Wilding J A neuropsychological and behavioural profile of a attention deficits in fragile X syndrome | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2201 | 9 | 15 | 2201 2001 REVISTA DE NEUROLOGIA 33:S29-S32 Brun-Gasca C; Artigas-Pallares J Psycholinguistic aspects of fragile X chromosome syndrome | 0 | 1 |
| 2202 | 3 | 19 | 2202 2001 REVISTA DE NEUROLOGIA 33:S32-S36 Goldson E Sensory integration and fragile X syndrome | 0 | 0 |
| 2203 | 2 | 12 | 2203 2001 REVISTA DE NEUROLOGIA 33:S37-S41 Carrasco M Informing members of families affected by fragile X syndrome of this diagnosis | 0 | 0 |
| 2204 | 15 | 42 | 2204 2001 REVISTA DE NEUROLOGIA 33:S41-S50 Artigas-Pallares J; Brun-Gasca C Medical treatment of fragile X syndrome | 0 | 0 |
| 2205 | 63 | 105 | 2205 2001 REVISTA DE NEUROLOGIA 33:S51-S57 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behaviour relationships | 0 | 0 |
| 2206 | 14 | 29 | 2206 2001 REVISTA DE NEUROLOGIA 33:S62-S65 Chiurazzi P; Neri G Experimental therapy: Reactivation of the FMR1 gene involved in fragile X syndrome | 0 | 0 |
| 2207 | 3 | 52 | 2207 2001 REVISTA DE NEUROLOGIA 33:S65-S70 Calvani M; D'Iddio S; de Gaetano A; Mariotti P; Mosconi L; et al. L-acetylcarnityne treatment on fragile X patients hyperactive behaviour | 0 | 0 |
| 2208 | 9 | 40 | 2208 2001 REVISTA DE NEUROLOGIA 33:S70-S76 de Diego-Otero Y Experimental therapeutic models for fragile X syndrome | 0 | 0 |
| 2209 | 0 | 7 | 2209 2001 REVISTA DE NEUROLOGIA 33:S77-S81 Safont-Tria NB Psychomotricity and fragile X syndrome | 0 | 0 |
| 2210 | 0 | 7 | 2210 2001 REVISTA DE NEUROLOGIA 33:S82-S87 Furgang R Language therapy in fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2211 | 0 | 0 | 2211 2001 REVISTA DE NEUROLOGIA 33:S88-S90 [Anon] Interdisciplinary conference on the fragile X syndrome - Barcelona, October 27-28, 2001 - Abstracts | 0 | 0 |
| 2212 | 0 | 0 | 2212 2001 SCIENCE 294(5548):1809-1809 Sohn E Genetics - Fragile X's missing partners identified | 0 | 1 |
| 2213 | 10 | 13 | 2213 2001 SCIENCE 294(5551):2487-2488 Moine H; Mandel JL Biomedicine - Do G quartets orchestrate fragile X pathology? | 4 | 9 |
| 2214 | 13 | 27 | 2214 2001 SEIZURE-EUROPEAN JOURNAL OF EPILEPSY 10(1):60-63 Sabaratnam M; Vroegop PG; Gangadharan SK Epilepsy and EEG findings in 18 males with fragile X syndrome | 4 | 6 |
| 2215 | 70 | 102 | 2215 2001 SEMINARS IN REPRODUCTIVE MEDICINE 19(2):159-165 Kenneson A; Warren ST The female and the fragile X reviewed | 1 | 3 |
| 2216 | 16 | 28 | 2216 2002 ACTA PAEDIATRICA 91(5):535-539 Hecimovic S; Tarnik IP; Baric I; Cakarun Z; Pavelic K Screening for fragile X syndrome: results from a school for mentally retarded children | 1 | 1 |
| 2217 | 0 | 0 | 2217 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):175-175 Jin P; Zhang F; Zarnescu DC; Moses K; Lucchesi JC; et al. A Drosophila model of fragile X premutation: CGG repeat instability and dominant-negative effects of premutation riboCGG repeat. | 0 | 0 |
| 2218 | 0 | 0 | 2218 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):185-185 Jacquemont S; Hagerman RJ; Leehey M; Greco C; Brunberg J; et al. Characterization of a progressive neurological condition in older adult male carriers of the fragile X premutation. | 2 | 2 |
| 2219 | 0 | 0 | 2219 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):259-259 Hagerman PJ; Greco CM; Hagerman RJ; Tassone F; Chudley AE; et al. Neuronal intranuclear inclusions in a tremor/ataxia syndrome among fragile X premutation carriers. | 0 | 0 |
| 2220 | 0 | 0 | 2220 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):270-270 Griffin KJ; Bei T; Meck J; Wong LJ; Bondy C; et al. Gender ambiguity and fragile X: a new syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2221 | 0 | 0 | 2221 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):287-287 Hagerman R; Goodlin-Jones BL; Spence S; Albrect L; Bacalman S; et al. The fragile X premutation and autistic spectrum disorders. | 0 | 0 |
| 2222 | 0 | 0 | 2222 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):288-288 Harris SW; Goodlin-Jones BL; Bacalman S; Jardini T; Rao S; et al. Fragile X and autism diagnosis by two standard methodologies. | 0 | 0 |
| 2223 | 0 | 0 | 2223 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):331-331 Tassone F; Sahota P; Pleasant N; Laird C; Hagerman P Methylation analysis of the promoter region in fragile X males with hypermethylated, full mutation alleles | 0 | 0 |
| 2224 | 0 | 0 | 2224 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):338-338 Naumann F; Schmitz B; Doerfler W Expression of the human and murine 5 '-(CGG)(n)-3 '-binding proteins CGGBP1. | 0 | 0 |
| 2225 | 0 | 0 | 2225 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):347-347 Brown WT; Nolin SL; Dobkin CS; Houck GS; Glicksman A; et al. Frequency of fragile X in multiplex autism: Testing the AGRE families. | 0 | 0 |
| 2226 | 0 | 0 | 2226 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):373-373 Ennis S; Brightwell G; Collins A; Jacobs P; Morton NE Phylogeny of fragile X haplotypes from an English population. | 0 | 0 |
| 2227 | 0 | 0 | 2227 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):377-377 Zabala WM; Nava N; Gonzalez S; Delgado W; Borjas L; et al. Clinical and molecular analysis of the fragile X syndrome in mentally retarded males from the Venezuelan northwestern region. | 0 | 0 |
| 2228 | 0 | 0 | 2228 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):384-384 Chen S; Schoof JM; Lemoine CJ; Gordon CL; Scott CR Prevalence survey of the Fragile X E syndrome referred for Fragile X syndrome testing in boys with mental retardation. | 0 | 0 |
| 2229 | 0 | 0 | 2229 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):505-505 Dobkin CS; Ding XH; Houck GE; Mitchell E; Brown WT; et al. A rare Eag I polymorphism that may confound fragile X diagnosis. | 0 | 0 |
| 2230 | 0 | 0 | 2230 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):507-507 Neri G; Tabolacci E; Pietrobono R; Pomponi MG; Chiurazzi P Histone hyperacetylation and reactivation of the fragile X syndrome gene. | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2231 | 0 | 0 | 2231 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):518-518 Maranduba CMC; Vianna-Morgante AM; Passos-Bueno MR P172H mutation in the TM4SF2 gene accounts for 1% of non-fragile X mental retardation in Brazilian patients. | 0 | 0 |
| 2232 | 0 | 0 | 2232 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):523-523 Bastaki LA; Al-Awadi SA; Hegazi FA; Turky NA; Mustafa MA; et al. PCR technique and significance in fragile X syndrome. | 0 | 0 |
| 2233 | 10 | 37 | 2233 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):923-932 Coffee B; Zhang FP; Ceman S; Warren ST; Reines D Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile X syndrome | 3 | 14 |
| 2234 | 9 | 18 | 2234 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 107(2):136-142 Loesch DZ; Huggins RM; Taylor AK Application of robust pedigree analysis in studies of complex genotype-phenotype relationships in fragile X syndrome | 5 | 7 |
| 2235 | 6 | 7 | 2235 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 107(4):344-345 Vink GR; Froster UG Comparison of FMR1-protein expression in lymphocytes, methylation pattern in Southern blot analysis, and IQ values in three sisters with the fragile X syndrome | 1 | 1 |
| 2236 | 18 | 62 | 2236 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 108(2):105-116 Hatton DD; Hooper SR; Bailey DB; Skinner ML; Sullivan KM; et al. Problem behavior in boys with fragile X syndrome | 6 | 7 |
| 2237 | 12 | 32 | 2237 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 110(1):36-44 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Carrier testing in fragile X syndrome: When to tell and test | 0 | 0 |
| 2238 | 27 | 43 | 2238 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 110(3):226-233 Crawford DC; Meadows KL; Newman JL; Taft LF; Scott E; et al. Prevalence of the fragile x syndrome in African-Americans | 3 | 4 |
| 2239 | 13 | 28 | 2239 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(2):140-146 Irwin SA; Idupulapati M; Gilbert ME; Harris JB; Chakravarti AB; et al. Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice | 11 | 14 |
| 2240 | 30 | 43 | 2240 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(3):243-252 Mingroni-Netto RC; Angeli CB; Auricchio MTBM; Leal-Mesquita ER; Ribeiro-dos-Santos AKC; et al. Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2241 | 3 | 36 | 2241 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(4):381-387 Steinhausen HC; von Gontard A; Spohr HL; Hauffa BP; Eiholzer U; et al. Behavioral phenotypes in four mental retardation syndromes: Fetal alcohol syndrome, Prader-Willi syndrome, fragile X syndrome, and tuberosis sclerosis | 0 | 2 |
| 2242 | 0 | 0 | 2242 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 114(7):832-832 Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al. The effect of premutation CGG trinucleotide repeat expansion, and expression of FMR-1 protein, on brain anatomy | 0 | 0 |
| 2243 | 0 | 0 | 2243 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 114(7):833-833 Steyaert J; Borghgraef M; Fryns JP A distinct neurocognitive phenotype in female fragile X premutation carriers | 0 | 0 |
| 2244 | 14 | 47 | 2244 2002 AMERICAN JOURNAL OF NEURORADIOLOGY 23(10):1757-1766 Brunberg JA; Jacquemont S; Hagerman RJ; Berry-Kravis EM; Grigsby J; et al. Fragile X premutation carriers: Characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction | 17 | 27 |
| 2245 | 8 | 44 | 2245 2002 AMERICAN JOURNAL OF OCCUPATIONAL THERAPY 56(5):538-546 Baranek GT; Chin YKH; Hess LMG; Yankee JG; Hatton DD; et al. Sensory processing correlates of occupational performance in children with fragile X syndrome: Preliminary findings | 1 | 1 |
| 2246 | 17 | 42 | 2246 2002 AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY 11(4):295-304 Roberts JE; Mirrett P; Anderson K; Burchinal M; Neebe E Early communication, symbolic behavior, and social profiles of young males with fragile X syndrome | 0 | 0 |
| 2247 | 0 | 0 | 2247 2002 ANNALS OF NEUROLOGY 52(3):S86-S86 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; et al. Tremor and ataxia in adult fragile X premutation carriers: Blinded videotape evaluation | 0 | 0 |
| 2248 | 99 | 179 | 2248 2002 ANNUAL REVIEW OF NEUROSCIENCE 25:315-338 O'Donnell WT; Warren ST A decade of molecular studies of fragile X syndrome | 0 | 63 |
| 2249 | 13 | 35 | 2249 2002 ARCHIVES OF MEDICAL RESEARCH 33(2):128-135 Wang TS; Hsieh LJ; Hsu TY; Chung CH; Li SY DNA damage and repair in lymphoblastoid cell lines from normal donors and fragile X syndrome patients | 0 | 1 |
| 2250 | 17 | 30 | 2250 2002 ARQUIVOS DE NEURO-PSIQUIATRIA 60(4):981-985 Yonamine SM; da Silva AA Characteristics of the communication in individuals with fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2251 | 12 | 24 | 2251 2002 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 292(4):1063-1069 Denman RB; Sung YJ Species-specific and isoform-specific RNA binding of human and mouse fragile X mental retardation proteins | 6 | 6 |
| 2252 | 5 | 9 | 2252 2002 BRAIN & DEVELOPMENT 24(8):766-769 Incorpora G; Sorge G; Sorge A; Pavone L Epilepsy in fragile X syndrome | 2 | 3 |
| 2253 | 14 | 46 | 2253 2002 BRAIN RESEARCH 927(1):8-17 Nielsen DM; Derber WJ; McClellan DA; Crnic LS Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndrome | 11 | 15 |
| 2254 | 7 | 21 | 2254 2002 CELLULAR & MOLECULAR BIOLOGY LETTERS 7(3):877-883 Denman RB Methylation of the arginine-glycine-rich region in the fragile X mental retardation protein FMRP differentially affects RNA binding | 2 | 6 |
| 2255 | 9 | 18 | 2255 2002 CLINICAL GENETICS 61(1):13-20 O'Connell CD; Atha DH; Jakupciak JP; Richie KI Standardization of PCR amplification for fragile X trinucleotide repeat measurements | 0 | 3 |
| 2256 | 5 | 37 | 2256 2002 CURRENT BIOLOGY 12(15):1331-1335 Inoue SB; Shimoda M; Nishinokubi I; Siomi MC; Okamura M; et al. A role for the Drosophila fragile X-related gene in circadian output | 13 | 17 |
| 2257 | 11 | 20 | 2257 2002 CURRENT BIOLOGY 12(24):R852-R854 Carthew RW RNA interference: The fragile X syndrome connection | 3 | 10 |
| 2258 | 38 | 51 | 2258 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):278-283 Hagerman RJ; Hagerman PJ The fragile X premutation: into the phenotypic fold | 15 | 25 |
| 2259 | 60 | 93 | 2259 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):284-293 Bardoni B; Mandel JL Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes | 31 | 39 |
| 2260 | 66 | 84 | 2260 2002 CYTOGENETIC AND GENOME RESEARCH 99(1-4):257-264 Oostra BA; Willemsen R The X chromosome and fragile X mental retardation | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2261 | 17 | 25 | 2261 2002 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 44(11):724-728 Berry-Kravis E Epilepsy in fragile X syndrome | 5 | 6 |
| 2262 | 42 | 139 | 2262 2002 DEVELOPMENTAL PSYCHOBIOLOGY 40(3):323-338 Churchill JD; Grossman AW; Irwin SA; Galvez R; Klintsova AY; et al. A converging-methods approach to fragile X syndrome | 2 | 8 |
| 2263 | 14 | 57 | 2263 2002 DEVELOPMENTAL PSYCHOBIOLOGY 41(2):133-146 Keysor CS; Mazzocco MMM; McLeod DR; Hoehn-Saric R Physiological arousal in females with fragile X or Turner syndrome | 1 | 2 |
| 2264 | 0 | 0 | 2264 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:55-56 Carmichael B Fragile X Syndrome - its impact on families | 0 | 0 |
| 2265 | 0 | 0 | 2265 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:63-63 Hagerman PJ; Greco CM; Tassone F; Chudley A; Del Bigio MR; et al. Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers | 0 | 0 |
| 2266 | 0 | 0 | 2266 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Afifi HH; Abdel-Aleem AK; Shaheen OO Fragile X syndrome: clinical and behavioral study. | 0 | 0 |
| 2267 | 0 | 0 | 2267 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Loesch DZ Effect of prennutation in the FMR1 gene on cognitive and physical phenotype in fragile X assessed by pedigree analysis. | 0 | 0 |
| 2268 | 0 | 0 | 2268 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:227-227 Steinbach P; Jakubiczka S; Bettecken T X inactivation and fragile X methylation in human placentas | 0 | 0 |
| 2269 | 0 | 0 | 2269 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-228 Tzeng C; Chen W; Huang K Prevalence of fragile-X female carrier in Taiwan is lower than expected | 0 | 0 |
| 2270 | 0 | 0 | 2270 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-229 Biancalana V; Beldjord C; de Martinville B; Bieth E; Blayau M; et al. 5 years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study of 22 laboratories in France. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2271 | 0 | 0 | 2271 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Deelen WH; Jansen C; Ramlakhan SR; Labrijn-Marks I; Olmer R; et al. Five years experience with DIG labeled probes on Southern blots applied in Fragile X diagnostics | 0 | 0 |
| 2272 | 0 | 0 | 2272 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Hasanzad M; Amini SH; Taghizadeh F; Teimourian S; Karimi-Nejad R; et al. Analysis of FMR 1 methylation in Fragile X syndrome in Iranian population | 0 | 0 |
| 2273 | 0 | 0 | 2273 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Gryschenko NV; Malarchuk SG; Livshits LA CGG-repeat expansion and metilation status of the promotor region of FMR1 gene analysis in the Fragile-X sindrome patients from Ukraine | 0 | 0 |
| 2274 | 0 | 0 | 2274 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Zalfa F; Primerano B; Lauro C; Giorgi M; Moro A; et al. Towards an understanding of the Fragile X syndrome: FMRP is translated at the synapses where it acts as a translational regulator | 0 | 0 |
| 2275 | 0 | 0 | 2275 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Gantois I; Reyniers E; Kooy F Differential gene expression in the fragile X mouse model | 0 | 0 |
| 2276 | 2 | 2 | 2276 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Bardoni B; Schenck A; van de Bor V; Giangrande A; Mandel J Drosophila as a model to study the physiological pathway in which FMRP (Fragile X Mental Retardation Protein) is involved | 0 | 0 |
| 2277 | 0 | 0 | 2277 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-232 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; et al. Quantitative analysis of DNA demethylation and trascriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 0 | 0 |
| 2278 | 0 | 0 | 2278 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:232-232 McKelvie KB; Reynolds A; Tassone F; Taylor AK; Hagerman RJ Evidence for skewed X chromosome inactivation in females with the fragile X full mutation | 0 | 0 |
| 2279 | 0 | 0 | 2279 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:323-323 Wilson R; Epstein JH; McKelvie K; Grisgby J; Nagamoto H; et al. Psychological and neuropsychological findings in adults with the premutation and full mutation for Fragile X Syndrome | 0 | 0 |
| 2280 | 0 | 0 | 2280 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:323-323 O'Connor R; Riley K; Epstein J; Wilson R; McKelvie K; et al. Analysis of ADHD subtypes in Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2281 | 10 | 43 | 2281 2002 GENES & DEVELOPMENT 16(19):2491-2496 Caudy AA; Myers M; Hannon GJ; Hammond SM Fragile X-related protein and VIG associate with the RNA interference machinery | 26 | 109 |
| 2282 | 15 | 79 | 2282 2002 GENES & DEVELOPMENT 16(19):2497-2508 Ishizuka A; Siomi MC; Siomi H A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins | 27 | 91 |
| 2283 | 0 | 0 | 2283 2002 GENETIC COUNSELING 13(2):207-261 [Anon] Abstracts of the 10th International Workshop on Fragile X and X-Linked Mental Retardation - 19-22 September 2001, Frascati, Italy | 0 | 0 |
| 2284 | 31 | 49 | 2284 2002 GENETICS AND MOLECULAR BIOLOGY 25(1):1-6 de Diego Y; Hmadcha A; Moron F; Lucas M; Carrasco M; et al. Fragile X founder effect and distribution of CGG repeats among the mentally retarded population of Andalusia, South Spain | 0 | 0 |
| 2285 | 19 | 33 | 2285 2002 GENOMICS 80(2):151-157 Baskaran S; Datta S; Mandal A; Gulati N; Totey SM; et al. Instability of CGG repeats in transgenic mice | 0 | 0 |
| 2286 | 22 | 46 | 2286 2002 GENOMICS 80(4):423-432 Peier AM; Nelson DL Instability of a premutation-sized CGG repeat in FMR1 YAC transgenic mice | 2 | 3 |
| 2287 | 15 | 44 | 2287 2002 HUMAN BRAIN MAPPING 16(4):206-218 Rivera SM; Menon V; White CD; Glaser B; Reiss AL Functional brain activation during arithmetic processing in females with fragile X Syndrome is related to FMRI protein expression | 7 | 14 |
| 2288 | 31 | 40 | 2288 2002 HUMAN MOLECULAR GENETICS 11(4):371-378 Dombrowski C; Levesque S; Morel ML; Rouillard P; Morgan K; et al. Premutation and intermediate-size FMR1 alleles in 10,572 males from the general population: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles | 22 | 34 |
| 2289 | 28 | 57 | 2289 2002 HUMAN MOLECULAR GENETICS 11(24):3007-3017 Mazroui R; Huot ME; Tremblay S; Filion C; Labelle Y; et al. Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression | 24 | 31 |
| 2290 | 2 | 3 | 2290 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(1):60-61 Rapin I Legitimacy of comparing fragile X with autism questioned | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2291 | 17 | 39 | 2291 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(2):107-114 Fisch GS; Simensen RJ; Schroer RJ Longitudinal changes in cognitive and adaptive Behavior scores in children and adolescents with the fragile X mutation or autism | 2 | 3 |
| 2292 | 0 | 53 | 2292 2002 JOURNAL OF BACTERIOLOGY 184(1):177-182 Semsey S; Blaha B; Koles K; Orosz L; Papp PP Site-specific integrative elements of rhizobiophage 16-3 can integrate into proline tRNA (CGG) genes in different bacterial genera | 1 | 6 |
| 2293 | 0 | 44 | 2293 2002 JOURNAL OF BIOLOGICAL CHEMISTRY 277(23):21041-21049 Vargason JM; Ho PS The effect of cytosine methylation on the structure and geometry of the Holliday junction - The structure of d(CCGGTACm(5)CGG) at 1.5 angstrom resolution | 0 | 9 |
| 2294 | 14 | 54 | 2294 2002 JOURNAL OF BIOLOGICAL CHEMISTRY 277(40):37804-37810 Ohashi S; Koike K; Omori A; Ichinose S; Ohara S; et al. Identification of mRNA/protein (mRNP) complexes containing Pur alpha, mStaufen, Fragile X Protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor | 18 | 48 |
| 2295 | 4 | 53 | 2295 2002 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 43(7):949-957 von Gontard A; Backes M; Laufersweiler-Plass C; Wendland C; Lehmkuhl G; et al. Psychopathology and familial stress - comparison of boys with Fragile X syndrome and Spinal Muscular Atrophy | 0 | 1 |
| 2296 | 0 | 0 | 2296 2002 JOURNAL OF COGNITIVE NEUROSCIENCE :50-51 Scerif G; Wilding J; Cornish K; Driver J; Humphreys K; et al. Executive control in visual search for multiple targets in toddlers with Fragile X Syndrome | 0 | 0 |
| 2297 | 8 | 61 | 2297 2002 JOURNAL OF COGNITIVE NEUROSCIENCE 14(2):160-171 Tamm L; Menon V; Johnston CK; Hessl DR; Reiss AL fMRI study of cognitive interference processing in females with fragile X syndrome | 6 | 10 |
| 2298 | 32 | 51 | 2298 2002 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 23(6):416-423 Loesch DZ; Huggins RM; Bui QM; Epstein JL; Taylor AK; et al. Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile X males and females assessed by robust pedigree analysis | 6 | 6 |
| 2299 | 6 | 29 | 2299 2002 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 46:328-339 Kuo AY; Reiss AL; Freund LS; Huffman LC Family environment and cognitive abilities in girls with fragile-X syndrome | 2 | 3 |
| 2300 | 0 | 0 | 2300 2002 JOURNAL OF MEDICAL GENETICS 39:S73-S73 Bilgen T; Keser I; Mihci E; Tacoy S; Haspolat S; et al. Screening of the FMR1 gene (CCG)n expansion by expand long PCR in families with fragile X syndrome in antalya province. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2301 | 0 | 0 | 2301 2002 JOURNAL OF MEDICAL GENETICS 39:S76-S76 Jani A; Hodsdon P; Churchley K; Crocker M; Stefanou E; et al. An atypical week for the Oxford Fragile X service: Two interesting cases | 0 | 0 |
| 2302 | 18 | 20 | 2302 2002 JOURNAL OF MEDICAL GENETICS 39(3):196-200 Tarleton J; Kenneson A; Taylor AK; Crandall K; Fletcher R; et al. A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype | 0 | 0 |
| 2303 | 0 | 0 | 2303 2002 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 61(5):450-450 Greco CM; Hagerman RJ; Tassone F; Chudley AE; Del Bigio MR; et al. Neuronal and astrocytic intranuclear inclusions in Fragile X carriers with cerebellar tremor/ataxia and cognitive changes. | 0 | 0 |
| 2304 | 67 | 98 | 2304 2002 JOURNAL OF NEUROSCIENCE RESEARCH 70(5):623-630 Todd PK; Malter JS Fragile X mental retardation protein in plasticity and disease | 1 | 4 |
| 2305 | 13 | 25 | 2305 2002 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 41(3):237-244 Dyer-Friedman J; Glaser B; Hessl D; Johnston C; Huffman LC; et al. Genetic and environmental influences on the cognitive outcomes of children with fragile X syndrome | 6 | 6 |
| 2306 | 0 | 0 | 2306 2002 JOURNAL OF THE AMERICAN GERIATRICS SOCIETY 50(4):S48-S48 Grigsby J; Leehey M; Hagerman RJ; Epstein J; Wilson R; et al. Dementia and a tremor-ataxia disorder among older male carriers of the fragile X premutation. | 0 | 1 |
| 2307 | 0 | 0 | 2307 2002 LANCET NEUROLOGY 1(3):141-141 May TS Evidence of altered synaptic plasticity found in fragile X syndrome | 0 | 0 |
| 2308 | 10 | 13 | 2308 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):131-134 Kaufmann WE Neurobiology of fragile X syndrome: From molecular genetics to neurobehavioral phenotype | 0 | 2 |
| 2309 | 55 | 82 | 2309 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):135-144 Kaufmann WE; Cohen S; Sun HT; Ho G Molecular phenotype of fragile X syndrome: FMRP, FXRPs, and protein targets | 1 | 1 |
| 2310 | 15 | 20 | 2310 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):145-147 Feng Y Fragile X mental retardation: Misregulation of protein synthesis in the developing brain? | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2311 | 43 | 64 | 2311 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):148-155 Hoogeveen AT; Willemsen R; Oostra BA Fragile X syndrome, the fragile X related proteins, and animal models | 1 | 4 |
| 2312 | 10 | 14 | 2312 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):156-158 Churchill JD; Beckel-Mitchener A; Weiler IJ; Greenough WT Effects of fragile X syndrome and an FMR1 knockout mouse model on forebrain neuronal cell biology | 0 | 0 |
| 2313 | 20 | 42 | 2313 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):159-167 Kates WR; Folley BS; Lanham DC; Capone GT; Kaufmann WE Cerebral growth in fragile X syndrome: Review and comparison with Down syndrome | 2 | 6 |
| 2314 | 16 | 35 | 2314 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):168-173 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; et al. Influence of stimulants on electrodermal studies in fragile X syndrome | 3 | 3 |
| 2315 | 25 | 35 | 2315 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):174-178 Kau ASM; Meyer WA; Kaufmann WE Early development in males with fragile X syndrome: A review of the literature | 2 | 3 |
| 2316 | 33 | 52 | 2316 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):179-186 Keysor CS; Mazzocco MMM A developmental approach to understanding fragile X syndrome in females | 8 | 9 |
| 2317 | 17 | 43 | 2317 2002 MOLECULAR AND CELLULAR BIOLOGY 22(23):8332-8341 Otero YD; Severijnen LA; van Cappellen G; Schrier M; Oostra B; et al. Transport of fragile X mental retardation protein via granules in neurites of PC12 cells | 17 | 24 |
| 2318 | 23 | 53 | 2318 2002 MOLECULAR AND CELLULAR BIOLOGY 22(24):8438-8447 Siomi MC; Higashijima K; Ishizuka A; Siomi H Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties | 14 | 16 |
| 2319 | 23 | 75 | 2319 2002 MOLECULAR AND CELLULAR NEUROSCIENCE 19(2):138-151 Li JX; Pelletier MR; Velazquez JLP; Carlen PL Reduced cortical synaptic plasticity and GluR1 expression associated with fragile X mental retardation protein deficiency | 18 | 20 |
| 2320 | 35 | 66 | 2320 2002 MONATSSCHRIFT KINDERHEILKUNDE 150(12):1486-+ Backes M; von Gontard A Behavioural phenotype of fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2321 | 0 | 0 | 2321 2002 MOVEMENT DISORDERS 17:S351-S351 Leehey MA; Grigsby J; Rubinstein D; Jacquemont S; Greco C; et al. Parkinsonism, tremor and ataxia in a female fragile X carrier | 1 | 1 |
| 2322 | 8 | 16 | 2322 2002 NATURE MEDICINE 8(11):1204-1205 Hansen RS; Laird CD A new regulatory pathway for fragile X syndrome? | 0 | 0 |
| 2323 | 2 | 3 | 2323 2002 NATURE REVIEWS GENETICS 3(1):4-5 Patterson M Twin-track approach to fragile X | 0 | 0 |
| 2324 | 8 | 27 | 2324 2002 NEUROBIOLOGY OF DISEASE 10(3):211-218 D'Agata V; Warren ST; Zhao WQ; Torre ER; Alkon DL; et al. Gene expression profiles in a transgenic animal model of fragile X syndrome | 0 | 14 |
| 2325 | 18 | 39 | 2325 2002 NEUROBIOLOGY OF DISEASE 11(1):53-63 Schenck A; Van de Bor V; Bardoni B; Giangrande A Novel features of dFMR1, the Drosophila orthologue of the fragile X mental retardation protein | 4 | 5 |
| 2326 | 24 | 59 | 2326 2002 NEUROBIOLOGY OF DISEASE 11(1):221-229 Castren M; Lampinen KE; Miettinen R; Koponen E; Sipola I; et al. BDNF regulates the expression of fragile X mental retardation protein mRNA in the hippocampus | 2 | 4 |
| 2327 | 0 | 0 | 2327 2002 NEUROLOGY 58(6):987-987 Munoz DG Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 0 | 0 |
| 2328 | 0 | 0 | 2328 2002 NEUROLOGY 58(6):987-988 Hagerman RJ; Greco C; Jacquemont S; Leehy M; Hagerman P Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X - Reply | 0 | 0 |
| 2329 | 0 | 0 | 2329 2002 NEUROLOGY 58(7):A481-A482 Leehey MA; Brunberg JA; Lang AE; Jacquemont S; Rubinstein D; et al. MRI increased T2 signal intensity in the cerebellar peduncles: Specific for the fragile X premutation tremor/ataxia syndrome? | 0 | 0 |
| 2330 | 0 | 0 | 2330 2002 NEUROLOGY 58(7):A482-A482 Munhoz RP; Lozano AM; Lang AE Fragile X syndrome premutation mistaken as essential tremor: An unrecognized source of diagnostic confusion | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2331 | 9 | 20 | 2331 2002 NEURON 34(6):859-862 Gao FB Understanding fragile X syndrome: Insights from retarded flies | 6 | 8 |
| 2332 | 20 | 52 | 2332 2002 NEURON 34(6):961-972 Morales J; Hiesinger PR; Schroeder AJ; Kume K; Verstreken P; et al. Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain | 28 | 37 |
| 2333 | 15 | 32 | 2333 2002 NEUROPSYCHOLOGIA 40(8):1343-1349 Wilding J; Cornish K; Munir F Further delineation of the executive deficit in males with fragile-X syndrome | 7 | 8 |
| 2334 | 19 | 36 | 2334 2002 NUCLEIC ACIDS RESEARCH 30(14):3278-3285 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; et al. Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 3 | 9 |
| 2335 | 8 | 58 | 2335 2002 NUCLEIC ACIDS RESEARCH 30(17):3672-3681 Weisman-Shomer P; Cohen E; Fry M Distinct domains in the CArG-box binding factor A destabilize tetraplex forms of the fragile X expanded sequence d(CGG)(n) | 2 | 3 |
| 2336 | 27 | 80 | 2336 2002 OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA 29(2):367-+ Wenstrom KD Fragile X and other trinucleotide repeat diseases | 1 | 3 |
| 2337 | 0 | 0 | 2337 2002 ONKOLOGIE 25(5):482-483 Diel I; Chatsiproios D Concept of integrated gyneco-oncological care: Centrum fur ganzheitliche gynakologie (CGG Klinik GmbH) | 0 | 0 |
| 2338 | 0 | 10 | 2338 2002 PANMINERVA MEDICA 44(1):7-10 Bargagna S; Canepa G; Tinelli F Social adjustment in children with Down mental retardation (MRD) and Fragile-X mental retardation (MRX) | 0 | 1 |
| 2339 | 13 | 27 | 2339 2002 PEDIATRICS 109(1) Flynn BJ; Myers SM; Cera PJ; Mowad JJ Testicular torsion in an adolescent with fragile X syndrome | 0 | 0 |
| 2340 | 18 | 22 | 2340 2002 PRENATAL DIAGNOSIS 22(6):459-462 Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; et al. Pilot study for the neonatal screening of fragile X syndrome | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2341 | 13 | 40 | 2341 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99(11):7746-7750 Huber KM; Gallagher SM; Warren ST; Bear MF Altered synaptic plasticity in a mouse model of fragile X mental retardation | 35 | 61 |
| 2342 | 23 | 52 | 2342 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99(24):15758-15763 Qin M; Kang J; Smith CB Increased rates of cerebral glucose metabolism in a mouse model of fragile X mental retardation | 5 | 6 |
| 2343 | 19 | 43 | 2343 2002 PSYCHONEUROENDOCRINOLOGY 27(7):855-872 Hessl D; Glaser B; Dyer-Friedman J; Blasey C; Hastie T; et al. Cortisol and behavior in fragile X syndrome | 6 | 9 |
| 2344 | 28 | 41 | 2344 2002 RNA-A PUBLICATION OF THE RNA SOCIETY 8(12):1482-1488 Primerano B; Tassone F; Hagerman RJ; Hagerman P; Amaldi F; et al. Reduced FMR1 mRNA translation efficiency in Fragile X patients with premutations | 11 | 14 |
| 2345 | 0 | 22 | 2345 2002 SCHIZOPHRENIA RESEARCH 58(1):37-41 Akahane A; Kunugi H; Tanaka H; Nanko S Association analysis of polymorphic CGG repeat in 5 ' UTR of the reelin and VLDLR genes with schizophrenia | 0 | 4 |
| 2346 | 0 | 0 | 2346 2002 SCIENTIST 16(20):8-8 Johnston N Fragile X, an RNAi connection? | 0 | 0 |
| 2347 | 13 | 15 | 2347 2002 TRENDS IN MOLECULAR MEDICINE 8(3):102-103 Oostra BA Functions of the fragile X protein | 6 | 8 |
| 2348 | 32 | 39 | 2348 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(2):454-464 Nolin SL; Brown WT; Glicksman A; Houck GE; Gargano AD; et al. Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles | 13 | 21 |
| 2349 | 19 | 36 | 2349 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(4):869-878 Jacquemont S; Hagerman RJ; Leehey M; Grigsby J; Zhang L; et al. Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates | 26 | 44 |
| 2350 | 0 | 0 | 2350 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):162-162 Jin P; Ceman S; Zarnescu DC; Nakamoto M; Mowrey J; et al. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2351 | 0 | 0 | 2351 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Allen E; Letz R; Sherman S Association of FMR1 CGG repeat size, X-inactivation ratio and transcript level with cognitive performance among women. | 0 | 0 |
| 2352 | 0 | 0 | 2352 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Cronister A; Teicher J; Custer T; Rohlfs EM Prevalence of premutation and intermediate alleles among patients referred for fragile X carrier testing. | 0 | 0 |
| 2353 | 0 | 0 | 2353 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Jiang Y; Wakui K; Liu Q; Kashork CD; Lehoczky J; et al. A fragile X mental retardation protein interacting protein maps to the proximal breakpoint of the Prader-Willi syndrome common deletion region. | 0 | 0 |
| 2354 | 0 | 0 | 2354 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; 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 |
| 2355 | 0 | 0 | 2355 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):266-266 Hagerman RJ; Jacquemont S; Tassone F; Greco C; Brunberg J; et al. Fragile X-associated tremor/ataxia syndrome (FXTAS) involvement in females | 0 | 0 |
| 2356 | 0 | 0 | 2356 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):296-296 Harris SW; Tassone F; Barbato I; Hagerman RJ FMRP, FMR1-mRNA, and psychopathology correlations in women with the fragile X premutation. | 0 | 0 |
| 2357 | 0 | 0 | 2357 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):314-314 Medne L; Russell K; Ming J; Krantz ID; Souders M; et al. Subtelomeric FISH analysis in 108 autistic patients as adjunct to chromosome analysis and fragile X testing | 0 | 0 |
| 2358 | 0 | 0 | 2358 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):330-330 Herman K; Nowicki S; Tassone F; Koldewyn K; Bacalman S; et al. Correlations between DNA, FMRP, and mRNA levels and ADOS-G and ADI-R scores in patients with Fragile X Syndrome. | 0 | 0 |
| 2359 | 0 | 0 | 2359 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):337-337 Nolin SL; Houck GE; Glicksman A; Gargano AD; Brown WT Large fragile X premutation alleles may often contain two AGG interruptions. | 0 | 0 |
| 2360 | 0 | 0 | 2360 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):348-348 Tabolacci E; Pietrobono R; Chiurazzi P; Neri G Variation of histone acetylation/methylation in the FMR1 gene of the fragile X syndrome following pharmacological reactivation. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2361 | 0 | 0 | 2361 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):348-348 O'Donnell WT; Ceman S; Warren ST Phosphorylation of the fragile X mental retardation protein regulates translation of its mRNA ligands. | 0 | 0 |
| 2362 | 0 | 0 | 2362 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):372-372 Reddy K Autism: Incidence of cytogenetic abnormality and fragile-X syndrome. | 0 | 0 |
| 2363 | 0 | 0 | 2363 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):377-377 Ennis S; Collins A; Morton NE The use of SNP-based haplotypes and LD blocks to positionally clone modifying determinants of expansion of the Fragile X triplet repeat | 0 | 0 |
| 2364 | 0 | 0 | 2364 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):383-383 Rigby AS; Turk J; Mills AC; James N; Hollis C; et al. Social functioning in male premutation carriers of Fragile X (FRAX) syndrome | 0 | 0 |
| 2365 | 0 | 0 | 2365 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):457-457 Mirakhory M; Aleyassin A Study of folic acid pathway genes alteration in fragile X syndrome. | 0 | 0 |
| 2366 | 0 | 0 | 2366 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):555-555 Di Maria E; Grasso M; Pigullo S; Faravelli F; Abbruzzese G; et al. Further evidence that a tremor/ataxia syndrome may occur in Fragile X premutation carriers: findings from two clinical series. | 0 | 0 |
| 2367 | 0 | 0 | 2367 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):557-557 Gantois I; Vandesompele J; Speleman F; D'Hooge R; Severijnen LA; et al. Expression profiling reveals involvement of the GABA(A) receptor subunit delta in the fragile X syndrome. | 0 | 0 |
| 2368 | 0 | 0 | 2368 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):573-573 Wronska A; Ju W; Brown WT; Zhong N Studies of FMRP-binding RNAs with a yeast tri-hybrid system. | 0 | 0 |
| 2369 | 0 | 0 | 2369 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):585-585 Fan H; Booker JK; McCandless SE; Shashi V; Farber RA Mosaicism for FMR1 gene full mutation and deletion in a fragile X female. | 0 | 0 |
| 2370 | 0 | 0 | 2370 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):586-586 Greco CM; Tassone F; Jaquemont S; Hagerman RJ; Sahota PK; et al. Intranuclear neuronal inclusions in two female carriers of the fragile X premutation | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2371 | 0 | 0 | 2371 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):587-587 Tassone F; Hagerman RJ; Garcia D; Sahota PK; Khandjian EW; et al. Intranuclear inclusions in fragile X-associated tremor/ataxia syndrome neuronal cells from five premutation carriers. | 0 | 0 |
| 2372 | 0 | 0 | 2372 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):589-589 Chen LS; Tassone F; Sahota P; Hagerman PJ The (CGG)(n) repeat elements within the 5 ' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter. | 0 | 0 |
| 2373 | 31 | 44 | 2373 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(1):44-51 Steyaert J; Legius E; Borghgraef M; Fryns JP A distinct neurocognitive phenotype in female fragile-X premutation carriers assessed with visual attention tasks | 0 | 4 |
| 2374 | 6 | 8 | 2374 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(1):99-100 Banes SL; Begleiter ML; Butler MG 45,X/46,XY mosaicism and fragile X syndrome | 0 | 0 |
| 2375 | 11 | 18 | 2375 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(2):176-178 Stalker HJ; Keller KL; Gray BA; Zori RT Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader-Willi-Like phenotype | 0 | 0 |
| 2376 | 5 | 14 | 2376 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 117A(1):6-9 Hundscheid RDL; Smits APT; Thomas CMG; Kiemeney LALM; Braat DDM Female carriers of fragile X premutations have no increased risk for additional diseases other than premature ovarian failure | 0 | 3 |
| 2377 | 15 | 28 | 2377 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 117A(1):21-29 Glaser B; Hessl D; Dyer-Friedman J; Johnston C; Wisbeck J; et al. Biological and environmental contributions to adaptive behavior in fragile X syndrome | 0 | 6 |
| 2378 | 17 | 43 | 2378 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 118A(2):115-121 Symons FJ; Clark RD; Hatton DD; Skinner M; Bailey DB Self-injurious behavior in young boys with fragile X syndrome | 0 | 3 |
| 2379 | 20 | 41 | 2379 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 118A(2):127-134 Loesch DZ; Huggins RM; Bui QM; Taylor AK; Hagerman RJ Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: A new perspective | 0 | 5 |
| 2380 | 35 | 62 | 2380 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 122A(1):13-23 Loesch DZ; Huggins RM; Bui QM; Taylor AK; Pratt C; et al. Effect of fragile x status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis | 0 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2381 | 12 | 22 | 2381 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 122A(2):108-114 Heine-Suner D; Torres-Juan L; Morla M; Busquets X; Barcelo F; et al. Fragile-X syndrome and skewed X-chromosome inactivation within a family: A female member with complete inactivation of the functional X chromosome | 0 | 1 |
| 2382 | 29 | 58 | 2382 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 118B(1):81-88 Barnea-Goraly N; Eliez S; Hedeus M; Menon V; White CD; et al. White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging | 0 | 6 |
| 2383 | 20 | 46 | 2383 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 121B(1):119-127 Aziz M; Stathopulu E; Callias M; Taylor C; Turk J; et al. Clinical features of boys with fragile X premutations and intermediate alleles | 0 | 8 |
| 2384 | 0 | 0 | 2384 2003 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 189(6):S117-S117 Musci TJ; Caughey AB Cost-effectiveness analysis of prenatal population-based fragile X carrier screening | 0 | 0 |
| 2385 | 15 | 39 | 2385 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160 Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; et al. Receptive language skills of adolescents and young adults with Down or fragile X syndrome | 2 | 5 |
| 2386 | 29 | 60 | 2386 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(5):314-326 Demark JL; Feldman MA; Holden JJA Behavioral relationship between autism and fragile X syndrome | 1 | 2 |
| 2387 | 22 | 50 | 2387 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(6):373-390 Hatton DD; Wheeler AC; Skinner ML; Bailey DB; Sullivan KM; et al. Adaptive behavior in children with fragile X syndrome | 0 | 1 |
| 2388 | 10 | 21 | 2388 2003 ANNALES DE GENETIQUE 46(1):53-55 Santos CB; Hjalgrim H; Carneiro FRG; Ribeiro M; Boy RT; et al. Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunction | 0 | 0 |
| 2389 | 15 | 31 | 2389 2003 ANNALS OF NEUROLOGY 53(5):616-623 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; et al. Tremor and ataxia in fragile X premutation carriers: Blinded videotape study | 11 | 14 |
| 2390 | 0 | 0 | 2390 2003 ANNALS OF NEUROLOGY 54:S105-S106 Kaufmann WE; Danko CG; Kau ASM; Thevarajah S; Bukelis I; et al. Increased protein acetylation in lymphocytes predicts autistic behavior in Fragile X syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2391 | 0 | 0 | 2391 2003 ANNALS OF NEUROLOGY 54:S144-S144 Berry-Kravis E; Potanos K Clinical response to psychopharmacology for behavior in Fragile X syndrome | 0 | 0 |
| 2392 | 0 | 0 | 2392 2003 ANNALS OF NEUROLOGY 54:S150-S150 Berry-Kravis E; Potanos K Stimulant therapy in fragile X syndrome | 0 | 0 |
| 2393 | 11 | 15 | 2393 2003 ARCHIVES DE PEDIATRIE 10(5):401-402 Ramos FJ; Willemsen R Diagnosis of the Fragile X Syndrome by the analysis of FMRP expression in blood and hair roots | 0 | 0 |
| 2394 | 13 | 30 | 2394 2003 ARCHIVES OF NEUROLOGY 60(1):117-121 Leehey MA; Munhoz RP; Lang AE; Brunberg JA; Grigsby J; et al. The fragile X premutation presenting as essential tremor | 12 | 23 |
| 2395 | 2 | 12 | 2395 2003 ARCHIVES OF NEUROLOGY 60(9):1197-1200 Kalidas S; Smith DP Functional genomics, fragile X syndrome, and RNA interference | 0 | 0 |
| 2396 | 1 | 26 | 2396 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 303(1):81-90 Monleon D; Esteve V; Celda B NMR study of hexanucleotide d(CCGCGG)(2) containing two triplet repeats of fragile X syndrome | 0 | 0 |
| 2397 | 9 | 26 | 2397 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 305(2):434-441 Dolzhanskaya N; Sung YJ; Conti J; Currie JR; Denman RB The fragile X mental retardation protein interacts with U-rich RNAs in a yeast three-hybrid system | 5 | 7 |
| 2398 | 14 | 43 | 2398 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 310(1):1-7 Denman RB Deja vu all over again: FMRP binds U-rich target mRNAs | 2 | 4 |
| 2399 | 27 | 40 | 2399 2003 BIOCHEMISTRY 42(35):10437-10444 Adinolfi S; Ramos A; Martin SR; Dal Piaz F; Pucci P; et al. The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding | 6 | 7 |
| 2400 | 4 | 6 | 2400 2003 BIOFUTUR (229):36-37 Nourrit F Fragile X and interference. | 0 | 0 |