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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by year, source, volume, issue, page.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2201 | 0 | 0 | 2201 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):162-162 Jin P; Ceman S; Zarnescu DC; Nakamoto M; Mowrey J; Jongens TA; Nelson DL; Moses K; Warren ST Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. | 0 | 0 |
| 2202 | 0 | 0 | 2202 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 |
| 2203 | 0 | 0 | 2203 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; Brunberg JA; Zhang L; Jardini T; Harris SW; Herman K; Berry-Kravis E; Tassone F; Hagerman PJ 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 |
| 2204 | 0 | 0 | 2204 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Jiang Y; Wakui K; Liu Q; Kashork CD; Lehoczky J; Shaffer LG; Beaudet AL A fragile X mental retardation protein interacting protein maps to the proximal breakpoint of the Prader-Willi syndrome common deletion region. | 0 | 0 |
| 2205 | 0 | 0 | 2205 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):266-266 Hagerman RJ; Jacquemont S; Tassone F; Greco C; Brunberg J; Hessl D; Harris S; Zhang L; Jardini T; Ruiz L; Gane L; Hagerman PJ Fragile X-associated tremor/ataxia syndrome (FXTAS) involvement in females | 0 | 0 |
| 2206 | 0 | 0 | 2206 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 |
| 2207 | 0 | 0 | 2207 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):314-314 Medne L; Russell K; Ming J; Krantz ID; Souders M; Levy S; Gupta A; Spinner NB; Zackai EH; Morrissette JJD Subtelomeric FISH analysis in 108 autistic patients as adjunct to chromosome analysis and fragile X testing | 0 | 0 |
| 2208 | 0 | 0 | 2208 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):330-330 Herman K; Nowicki S; Tassone F; Koldewyn K; Bacalman S; Jacquemont S; Barboto I; Levine R; Hagerman P; Hagerman R Correlations between DNA, FMRP, and mRNA levels and ADOS-G and ADI-R scores in patients with Fragile X Syndrome. | 0 | 0 |
| 2209 | 0 | 0 | 2209 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 |
| 2210 | 0 | 0 | 2210 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 |
| 2211 | 0 | 0 | 2211 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 |
| 2212 | 0 | 0 | 2212 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):372-372 Reddy K Autism: Incidence of cytogenetic abnormality and fragile-X syndrome. | 0 | 0 |
| 2213 | 0 | 0 | 2213 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 |
| 2214 | 0 | 0 | 2214 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):383-383 Rigby AS; Turk J; Mills AC; James N; Hollis C; Cornish K; Dalton A; Manly T Social functioning in male premutation carriers of Fragile X (FRAX) syndrome | 0 | 0 |
| 2215 | 0 | 0 | 2215 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 |
| 2216 | 0 | 0 | 2216 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):555-555 Di Maria E; Grasso M; Pigullo S; Faravelli F; Abbruzzese G; Barone P; Martinelli P; Ratto S; Sciolla R; Bellone E; Dagna-Bricarelli F; Ajmar F; Mandich P Further evidence that a tremor/ataxia syndrome may occur in Fragile X premutation carriers: findings from two clinical series. | 0 | 0 |
| 2217 | 0 | 0 | 2217 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):557-557 Gantois I; Vandesompele J; Speleman F; D'Hooge R; Severijnen LA; Willemsen R; Tassone F; Kooy RF Expression profiling reveals involvement of the GABA(A) receptor subunit delta in the fragile X syndrome. | 0 | 0 |
| 2218 | 0 | 0 | 2218 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 |
| 2219 | 0 | 0 | 2219 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):586-586 Greco CM; Tassone F; Jaquemont S; Hagerman RJ; Sahota PK; Delacourte A; Maurage CA; Hagerman PJ Intranuclear neuronal inclusions in two female carriers of the fragile X premutation | 0 | 0 |
| 2220 | 0 | 0 | 2220 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):587-587 Tassone F; Hagerman RJ; Garcia D; Sahota PK; Khandjian EW; Greco CM; Hagerman PJ Intranuclear inclusions in fragile X-associated tremor/ataxia syndrome neuronal cells from five premutation carriers. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2221 | 30 | 44 | 2221 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 | 2 |
| 2222 | 6 | 8 | 2222 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 |
| 2223 | 11 | 18 | 2223 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 |
| 2224 | 5 | 14 | 2224 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 |
| 2225 | 15 | 28 | 2225 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 117A(1):21-29 Glaser B; Hessl D; Dyer-Friedman J; Johnston C; Wisbeck J; Taylor A; Reiss A Biological and environmental contributions to adaptive behavior in fragile X syndrome | 0 | 4 |
| 2226 | 17 | 43 | 2226 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 | 0 |
| 2227 | 20 | 41 | 2227 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 | 3 |
| 2228 | 35 | 62 | 2228 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 122A(1):13-23 Loesch DZ; Huggins RM; Bui QM; Taylor AK; Pratt C; Epstein J; Hagerman RJ Effect of fragile x status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis | 0 | 1 |
| 2229 | 11 | 22 | 2229 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 122A(2):108-114 Heine-Suner D; Torres-Juan L; Morla M; Busquets X; Barcelo F; Pico G; Bonilla L; Govea N; Bernues M; Rosell J Fragile-X syndrome and skewed X-chromosome inactivation within a family: A female member with complete inactivation of the functional X chromosome | 0 | 0 |
| 2230 | 28 | 58 | 2230 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; Moseley M; Reiss AL White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2231 | 19 | 46 | 2231 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 121B(1):119-127 Aziz M; Stathopulu E; Callias M; Taylor C; Turk J; Oostra B; Willemsen R; Patton M Clinical features of boys with fragile X premutations and intermediate alleles | 0 | 4 |
| 2232 | 0 | 0 | 2232 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 |
| 2233 | 15 | 39 | 2233 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160 Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; Karadottir S; O'Brien A Receptive language skills of adolescents and young adults with Down or fragile X syndrome | 2 | 3 |
| 2234 | 29 | 60 | 2234 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(5):314-326 Demark JL; Feldman MA; Holden JJA Behavioral relationship between autism and fragile X syndrome | 0 | 0 |
| 2235 | 22 | 50 | 2235 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(6):373-390 Hatton DD; Wheeler AC; Skinner ML; Bailey DB; Sullivan KM; Roberts JE; Mirrett P; Clark RD Adaptive behavior in children with fragile X syndrome | 0 | 0 |
| 2236 | 9 | 21 | 2236 2003 ANNALES DE GENETIQUE 46(1):53-55 Santos CB; Hjalgrim H; Carneiro FRG; Ribeiro M; Boy RT; Pimentel MMG Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunction | 0 | 0 |
| 2237 | 15 | 31 | 2237 2003 ANNALS OF NEUROLOGY 53(5):616-623 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; Hagerman P; Goetz CG Tremor and ataxia in fragile X premutation carriers: Blinded videotape study | 8 | 12 |
| 2238 | 0 | 0 | 2238 2003 ANNALS OF NEUROLOGY 54:S105-S106 Kaufmann WE; Danko CG; Kau ASM; Thevarajah S; Bukelis I; Tierney E; Neuberger I Increased protein acetylation in lymphocytes predicts autistic behavior in Fragile X syndrome | 0 | 0 |
| 2239 | 0 | 0 | 2239 2003 ANNALS OF NEUROLOGY 54:S144-S144 Berry-Kravis E; Potanos K Clinical response to psychopharmacology for behavior in Fragile X syndrome | 0 | 0 |
| 2240 | 0 | 0 | 2240 2003 ANNALS OF NEUROLOGY 54:S150-S150 Berry-Kravis E; Potanos K Stimulant therapy in fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2241 | 11 | 15 | 2241 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 |
| 2242 | 13 | 30 | 2242 2003 ARCHIVES OF NEUROLOGY 60(1):117-121 Leehey MA; Munhoz RP; Lang AE; Brunberg JA; Grigsby J; Greco C; Jacquemont S; Tassone F; Lozano AM; Hagerman PJ; Hagerman RJ The fragile X premutation presenting as essential tremor | 6 | 13 |
| 2243 | 2 | 12 | 2243 2003 ARCHIVES OF NEUROLOGY 60(9):1197-1200 Kalidas S; Smith DP Functional genomics, fragile X syndrome, and RNA interference | 0 | 0 |
| 2244 | 1 | 26 | 2244 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 |
| 2245 | 9 | 26 | 2245 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 | 2 | 3 |
| 2246 | 26 | 40 | 2246 2003 BIOCHEMISTRY 42(35):10437-10444 Adinolfi S; Ramos A; Martin SR; Dal Piaz F; Pucci P; Bardoni B; Mandel JL; Pastore A The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding | 2 | 3 |
| 2247 | 4 | 6 | 2247 2003 BIOFUTUR (229):36-37 Nourrit F Fragile X and interference. | 0 | 0 |
| 2248 | 0 | 0 | 2248 2003 BIOLOGICAL PSYCHIATRY 53(8):49S-49S Daly EM; Moore CJ; Schmitz N; Morris R; Murphy KC; Murphy DG Expansion of CGG trinucleotide repeats: Effect on neuropsychology of male premutation carriers of Fragile X syndrome | 0 | 0 |
| 2249 | 18 | 62 | 2249 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 | 2 |
| 2250 | 12 | 41 | 2250 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 | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2251 | 25 | 36 | 2251 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 |
| 2252 | 20 | 38 | 2252 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 | 1 | 1 |
| 2253 | 34 | 62 | 2253 2003 CELL 112(3):317-327 Zalfa F; Giorgi M; Primerano B; Moro A; Di Penta A; Reis S; Oostra B; Bagni C The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at Synapses | 16 | 38 |
| 2254 | 4 | 6 | 2254 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 | 3 |
| 2255 | 0 | 1 | 2255 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 |
| 2256 | 65 | 87 | 2256 2003 CURRENT OPINION IN PEDIATRICS 15(6):559-566 Chiurazzi P; Neri G; Oostra BA Understanding the biological underpinnings of fragile X syndrome | 0 | 0 |
| 2257 | 37 | 136 | 2257 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 |
| 2258 | 88 | 168 | 2258 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):111-123 Bakker CE; Oostra BA Understanding fragile X syndrome: insights from animal models | 0 | 0 |
| 2259 | 7 | 59 | 2259 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 |
| 2260 | 18 | 33 | 2260 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 | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2261 | 22 | 62 | 2261 2003 DEVELOPMENT 130(22):5543-5552 Lee A; Li WJ; Xu KY; Bogert BA; Su K; Gao FB Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1 | 2 | 3 |
| 2262 | 150 | 233 | 2262 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 |
| 2263 | 0 | 0 | 2263 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 |
| 2264 | 14 | 24 | 2264 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 | 0 |
| 2265 | 26 | 34 | 2265 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 |
| 2266 | 19 | 29 | 2266 2003 GENETIC TESTING 7(4):339-343 Rife M; Badenas C; Mallolas J; Jimenez L; Cervera R; Maya A; Glover G; Rivera F; Mila M Incidence of Fragile X in 5,000 consecutive newborn males | 0 | 0 |
| 2267 | 3 | 7 | 2267 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 |
| 2268 | 15 | 55 | 2268 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 |
| 2269 | 1 | 4 | 2269 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 | 5 | 6 |
| 2270 | 26 | 43 | 2270 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 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2271 | 36 | 53 | 2271 2003 HUMAN MOLECULAR GENETICS 12(14):1689-1698 Bardoni B; Castets M; Huot ME; Schenck A; Adinolfi S; Corbin F; Pastore A; Khandjian EW; Mandel JL 82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization | 3 | 3 |
| 2272 | 38 | 52 | 2272 2003 HUMAN MOLECULAR GENETICS 12(23):3087-3096 Mazroui R; Huot ME; Tremblay S; Boilard N; Labelle Y; Khandjian EW Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs | 2 | 2 |
| 2273 | 20 | 29 | 2273 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 |
| 2274 | 45 | 118 | 2274 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 |
| 2275 | 20 | 54 | 2275 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 | 1 |
| 2276 | 28 | 56 | 2276 2003 JOURNAL OF BIOLOGICAL CHEMISTRY 278(18):15669-15678 Sung YJ; Dolzhanskaya N; Nolin SL; Brown T; Currie JR; Denman RB The fragile X mental retardation protein FMRP binds elongation factor 1A mRNA and negatively regulates its translation in vivo | 5 | 9 |
| 2277 | 10 | 57 | 2277 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(4):267-275 Johnston C; Hessl D; Blasey C; Eliez S; Erba H; Dyer-Friedman J; Glaser B; Reiss AL Factors associated with parenting stress in mothers of children with fragile X syndrome | 0 | 0 |
| 2278 | 0 | 0 | 2278 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(5):393-393 Hansen R; Goodlin-Jones B; Nowicki S; Heeren M; Herman K; Harris S; Bacalman S; Hagerman R Behavioral phenotypes in older children with autistic spectrum disorders and fragile X: Similarities and differences | 0 | 0 |
| 2279 | 7 | 32 | 2279 2003 JOURNAL OF INTELLECTUAL & DEVELOPMENTAL DISABILITY 28(2):135-144 Richdale AL A descriptive analysis of sleep behaviour in children with Fragile X | 0 | 0 |
| 2280 | 0 | 0 | 2280 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2281 | 0 | 0 | 2281 2003 JOURNAL OF MEDICAL GENETICS 40:S49-S49 Dalton A; Mills AC; Rigby A; Manly T; Hollis C; Turk J; Cornish K The neuropsychological phenotype of fragile X premutation males | 0 | 0 |
| 2282 | 0 | 0 | 2282 2003 JOURNAL OF MEDICAL GENETICS 40:S80-S80 Payne S; Powell CM Fragile-X intermediate alleles - instability and inconclusion | 0 | 0 |
| 2283 | 18 | 22 | 2283 2003 JOURNAL OF MEDICAL GENETICS 40(5):377-379 Willemsen R; Smits A; Severijnen LA; Jansen M; Jacobs A; De Bruyn E; Oostra B Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis | 3 | 3 |
| 2284 | 28 | 41 | 2284 2003 JOURNAL OF MEDICAL GENETICS 40(7):535-539 de Vries BBA; Severijnen LA; Jacobs A; Olmer R; Halley DJJ; Oostra BA; Willemsen R FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics | 1 | 1 |
| 2285 | 0 | 0 | 2285 2003 JOURNAL OF NEUROCHEMISTRY 85:1-1 Huber KM Recent progress in understanding the neural mechanisms of Fragile X Syndrome | 0 | 0 |
| 2286 | 19 | 35 | 2286 2003 JOURNAL OF NEUROGENETICS 17(2-3):223-230 Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; Romac S Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation | 0 | 0 |
| 2287 | 0 | 0 | 2287 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 |
| 2288 | 8 | 10 | 2288 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 |
| 2289 | 2 | 5 | 2289 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 |
| 2290 | 20 | 28 | 2290 2003 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 102(1):12-16 Chi J; Chen DJ; Lin CN; Chiu CY; Huang CB; Chiu PC; Lin CH; Lin SJ; Tzeng CC Feasibility of blood spot PCR in large-scale screening of fragile X syndrome in southern Taiwan | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2291 | 23 | 69 | 2291 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 |
| 2292 | 0 | 0 | 2292 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 |
| 2293 | 1 | 1 | 2293 2003 NATURE REVIEWS GENETICS 4(10):758-758 Casci T Fragile X: a class of its own | 0 | 0 |
| 2294 | 1 | 1 | 2294 2003 NATURE REVIEWS NEUROSCIENCE 4(10):776-777 Casci T Neurological disorders - Fragile X: a class of its own | 0 | 0 |
| 2295 | 7 | 10 | 2295 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 | 1 |
| 2296 | 21 | 64 | 2296 2003 NEURON 38(6):887-898 Schenck A; Bardoni B; Langmann C; Harden N; Mandel JL; Giangrande A CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein | 5 | 9 |
| 2297 | 5 | 35 | 2297 2003 NEURON 39(5):739-747 Jin P; Zarnescu DC; Zhang FP; Pearson CE; Lucchesi JC; Moses K; Warren ST RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila | 4 | 9 |
| 2298 | 41 | 101 | 2298 2003 NEUROPSYCHOLOGY 17(4):646-657 Loesch DZ; Bui QM; Grigsby J; Butler E; Epstein J; Huggins RM; Taylor AK; Hagerman RJ 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 |
| 2299 | 14 | 26 | 2299 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 | 1 |
| 2300 | 21 | 39 | 2300 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 | 3 | 3 |
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