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Nodes: 1364,
Authors: 3358,
Journals: 307,
Outer References: 11901,
Words: 2507
Collection span: 1995 - 2005
View: Overview. Sorted by journal name.
Page 1: 1 2 3 4 5
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1 | 0 | 1 | 296 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):191-192 Fombonne E The fragile X syndrome | 0 | 0 |
| 2 | 5 | 25 | 297 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):195-201 Mandel JL The fragile X mental retardation syndrome: the FMR1 gene and its mutations | 0 | 0 |
| 3 | 7 | 24 | 298 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):202-208 Hagerman RJ Fragile X syndrome: meeting the challenges of diagnosis and care | 0 | 0 |
| 4 | 6 | 16 | 299 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):209-212 Fombonne E Epidemiological studies of fragile X syndrome | 0 | 0 |
| 5 | 4 | 9 | 300 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):221-223 Ponsot G Fragile X syndrome. Early recognition. | 0 | 0 |
| 6 | 3 | 9 | 301 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):224-226 Gerard CL; Guillotte E; Servel F; Barbeau M Assessment and remediation of communication disorders in children with fragile X syndrome | 0 | 0 |
| 7 | 1 | 10 | 302 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):227-231 Roge B Fragile X syndrome. Special education: the French context | 0 | 0 |
| 8 | 0 | 27 | 303 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):232-238 Turk J Treatments and services for individuals with fragile X syndrome and their families | 0 | 0 |
| 9 | 0 | 0 | 810 2001 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 221:U3-U3 Rodesittisuk P; Romero RM; Haworth IS Conformation of fragile X-associated triplet repeat DNA containing C-C mismatch pairs. | 0 | 0 |
| 10 | 1 | 19 | 157 1996 ACTA BIOCHIMICA POLONICA 43(2):383-388 Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; et al. Analysis of unstable DNA sequence in FRM1 gene in Polish families with fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 11 | 8 | 28 | 933 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 |
| 12 | 2 | 10 | 1196 2004 ACTA PHARMACOLOGICA SINICA 25(7):973-976 Sun YJ; Han X Dynamic behavior of fragile X full mutations in cultured female fetal fibroblasts | 0 | 0 |
| 13 | 0 | 0 | 1 1995 AMERICAN JOURNAL OF EPIDEMIOLOGY 141(11):S50-S50 DAWSON DV; LACHIEWICZ AM BEHAVIORAL EPIDEMIOLOGY OF FRAGILE-X SYNDROME IN FEMALE PEDIATRIC POPULATIONS | 0 | 0 |
| 14 | 0 | 37 | 2 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1042-1051 QUAN F; ZONANA J; GUNTER K; PETERSON KL; MAGENIS RE; et al. AN ATYPICAL CASE OF FRAGILE-X SYNDROME CAUSED BY A DELETION THAT INCLUDES THE FMRI GENE | 19 | 30 |
| 15 | 0 | 65 | 3 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1147-1155 FISCH GS; SNOW K; THIBODEAU SN; CHALIFAUX M; HOLDEN JJA; et al. THE FRAGILE-X PREMUTATION IN CARRIERS AND ITS EFFECT ON MUTATION SIZE IN OFFSPRING | 28 | 35 |
| 16 | 0 | 51 | 4 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(2):351-361 ZHONG N; YANG WH; DOBKIN C; BROWN WT FRAGILE-X GENE INSTABILITY - ANCHORING AGGS AND LINKED MICROSATELLITES | 54 | 82 |
| 17 | 1 | 54 | 5 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(3):609-618 DEGRAAFF E; WILLEMSEN R; ZHONG N; DEDIESMULDERS CEM; BROWN WT; et al. INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF THE FMR1 PROTEIN IN A MALE FRAGILE-X PATIENT WITH A LUNG-TUMOR | 26 | 32 |
| 18 | 0 | 0 | 6 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):40-40 FENG Y; EBERHART DE; WARREN ST THE PROTEIN ABSENT IN FRAGILE-X SYNDROME (FMRP) IS A RIBOSOME-ASSOCIATED PROTEIN | 0 | 0 |
| 19 | 0 | 0 | 7 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):135-135 STALEYGANE L; FLYNN L; CRONISTERSILVERMAN A; HAGERMAN RJ EXPANDING THE ROLE OF THE GENETIC COUNSELOR WORKING WITH FRAGILE-X FAMILIES | 0 | 0 |
| 20 | 0 | 0 | 8 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):152-152 HUGHES MR; HADDAD BR; SUBRAMANIAN S; NASONKIN I; COTA J; et al. SINGLE-CELL DETECTION OF THE FMR1, HD, AND SCA1 TRINUCLEOTIDE REPEATS - APPLICATION TO PREIMPLANTATION DIAGNOSIS AND INSTABILITY ANALYSIS OF FRAGILE-X SYNDROME, HUNTINGTON DISEASE, AND SPINO-CEREBELLAR ATAXIA TYPE-1 | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 21 | 0 | 0 | 9 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):153-153 BLACK SH; LEVINSON G; HARTON GL; PALMER FT; SISSON ME; et al. PREIMPLANTATION GENETIC TESTING (PGT) FOR FRAGILE-X (FRAX) | 2 | 3 |
| 22 | 0 | 0 | 10 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):196-196 EBERHART DE; FENG Y; WARREN ST IDENTIFICATION OF A CYTOPLASMIC ANCHOR DOMAIN RESPONSIBLE FOR THE SUBCELLULAR-LOCALIZATION OF THE FRAGILE-X MENTAL-RETARDATION PROTEIN, FMRP | 0 | 0 |
| 23 | 0 | 0 | 11 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):211-211 NELSON DL; KUNST CB; LUGENBEEL KA; RYDER OA; WARREN ST; et al. EVOLUTION OF THE CRYPTIC FMR1 CGG REPEAT | 0 | 0 |
| 24 | 0 | 0 | 12 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):494-494 GIANGRECO CA; STEELE MW; ASTON CE; CUMMINS JH; WENGER SL CLINICAL-CRITERIA FOR FRAGILE-X SOUTHERN BLOT DNA DIAGNOSTIC TESTING | 0 | 0 |
| 25 | 0 | 0 | 13 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):585-585 WRIGHTTALAMANTE C; CHEEMA A; RIDDLE JE; LUCKEY D; TAYLOR A; et al. A CONTROLLED-STUDY OF LONGITUDINAL IQ CHANGES IN FEMALES AND MALES WITH FRAGILE-X SYNDROME | 0 | 0 |
| 26 | 0 | 0 | 14 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):655-655 JENKINS EC; DOBKIN CS; DING X; LI SY; HOUCK GE; et al. THRESHOLD CGG REPEAT SIZE FOR FRAGILE SITE EXPRESSION WITHOUT METHYLATION IDENTIFIED IN LYMPHOCYTE, LYMPHOBLASTOID AND CLONAL LYMPHOBLASTOID CULTURES FROM AN FMR1 UNMETHYLATED MOSAIC FULL MUTATION INDIVIDUAL | 0 | 0 |
| 27 | 0 | 0 | 15 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):671-671 MARINI T; PFLUEGER S; NABER S; KARPELLS S; NAEEM R A 5-YEAR EXPERIENCE WITH FRAGILE-X TESTING | 0 | 0 |
| 28 | 0 | 0 | 16 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):692-692 RANCHINO B; TARAVATH A; KALICHMAN M; BURTON BB; MCCORQUODALE MM; et al. SELECTION AGAINST A MARKER CHROMOSOME IN FRAGILE-X-STRESSED CULTURES | 0 | 0 |
| 29 | 0 | 0 | 17 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):869-869 WINKELER KA; WARREN ST VARIATIONS IN THE LENGTH OF THE CGG-REPEAT OF FMR-1 AFFECT GENE-EXPRESSION | 0 | 0 |
| 30 | 0 | 1 | 18 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):906-906 ASHLEY AE; MEADOWS KL; SHERMAN SL TRANSMISSION CHARACTERISTICS OF THE FMR-1 MUTATION IN THE COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 31 | 0 | 0 | 19 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):913-913 BROWN WT; ZHONG N; KAJANOJA E; SMITS B; CURLEY D; et al. FRAGILE-X FOUNDER CHROMOSOME EFFECTS AND NEW MUTATIONS | 0 | 0 |
| 32 | 0 | 0 | 20 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):919-919 CHIURAZZI P; KOZAK L; GENUARDI M; GIOVANNUCCIUZIELLI ML; BUSSANI C; et al. FRAGILE-X SYNDROME - ROUNDER CHROMOSOMES IN ITALY | 0 | 0 |
| 33 | 0 | 0 | 21 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):965-965 NOLIN SL; GLICKSMAN A; LEWIS FA; YE LL; HOUCK GE; et al. EVIDENCE FOR A FAMILIAL FACTOR INVOLVED IN CGG REPEAT EXPANSION IN FRAGILE-X SYNDROME | 0 | 0 |
| 34 | 0 | 0 | 22 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1088-1088 CURLEY D; ZHONG N; WANG DW; JU W; DOBKIN C; et al. NEW INTRAGENIC ALU POLYMORPHISMS IN THE FRAGILE-X GENE | 0 | 0 |
| 35 | 0 | 0 | 23 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1218-1218 FALIKBORENSTEIN TC; YALON M; SHACHAK L; DAR C; BOROCHOWITZ Z; et al. LONG UNINTERRUPTED CGG REPEATS WITHIN THE FMR1 GENE - POSSIBLE MECHANISM FOR THE PREVALENCE OF THE FRAGILE-X SYNDROME AMONG TUNISIAN JEWS | 0 | 0 |
| 36 | 0 | 0 | 24 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1273-1273 MILA M; CASTELLVIBEL S; BARCELO A; SANCHEZ A; JIMENEZ D; et al. MUTATIONS IN THE CPG ISLAND OF THE FMR1 GENE - ARE THEY RESPONSIBLE FOR FRAGILE-X SYNDROME | 0 | 0 |
| 37 | 0 | 0 | 25 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1300-1300 PULKKINEN L; MANNERMAA A; KAJANOJA E; RYYNANANEN M; SAARIKOSKI S DELETION IN THE FMR1 GENE IN A FRAGILE-X-MALE | 0 | 0 |
| 38 | 0 | 0 | 26 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1344-1344 WILLEMSEN R; BAKKER C; MANDEL JL; DEVRIES B; DEVYS D; et al. RAPID SCREENING-TEST FOR FRAGILE-X SYNDROME | 0 | 0 |
| 39 | 0 | 0 | 27 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1359-1359 BAKKER C; DEGRAAFF E; ZHONG N; WILLEMSEN R; OOSTRA B INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF FMR1 PROTEIN IN A MALE-PATIENT WITH A LUNG-TUMOR | 0 | 0 |
| 40 | 0 | 0 | 28 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1395-1395 HART PS; OLSON SM; CRANDALL K; TARLETON J FRAGILE-X SYNDROME RESULTING FROM A 400 BASEPAIR DELETION WITHIN THE FMR1 GENE | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 41 | 0 | 0 | 29 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1407-1407 JOHNSON JP; CURRY C; MICEK M; LOUIE E; ABRAMS L; et al. TRANSMISSION OF STABLE AND UNSTABLE PREMUTATIONS FROM GREAT-GRANDMOTHER AND GREAT-GRANDFATHER RESPECTIVELY - LESSONS FOR GENETIC-COUNSELING IN FRAGILE-X SYNDROME FAMILIES | 0 | 0 |
| 42 | 0 | 0 | 30 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1603-1603 BUCHANAN JA; KLOCK RJ; DORAN K; KENNEDY D; WYATT P PRENATAL TEST FOR FRAGILE-X SYNDROME REVEALS APPARENT FMR1 GENE CONTRACTION | 0 | 0 |
| 43 | 0 | 0 | 31 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1676-1676 SHAPIRO LR; WILMOT PL; MARINELLO MJ NONINDUCED FRAGILE-X CHROMOSOMES DETECTED IN ROUTINE AMNIOTIC-FLUID CELL-CULTURE - DETERMINATION OF SIGNIFICANCE | 0 | 0 |
| 44 | 0 | 0 | 32 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1705-1705 DEVRIES BBA; VANDENOUWELAND AMW; MOHKAMSING S; HALLEY DJJ; TIBBEN A; et al. ACCEPTANCE OF SCREENING FOR THE FRAGILE-X SYNDROME AMONG 1878 MENTALLY-RETARDED INDIVIDUALS IN INSTITUTES AND SPECIAL SCHOOLS IN THE NETHERLANDS | 0 | 0 |
| 45 | 0 | 0 | 33 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1838-1838 EIGEL A; ZYGULSKA M; DOLSCHEID T; BOGDANOVA N; DWORNICZAK B; et al. FRAGILE-X PREMUTATION FREQUENCY IN NORTHERN THAILAND | 0 | 0 |
| 46 | 0 | 1 | 34 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1914-1914 GOONEWARDENA P; ZHANG J A SINGLE TUBE NONRADIOACTIVE PCR ASSAY FOR THE DETECTION OF THE FULL SPECTRUM OR FMR1 CGG REPEATS SEEN IN THE NORMAL, CARRIER AND FRAGILE-X SYNDROME INDIVIDUALS | 0 | 0 |
| 47 | 0 | 0 | 35 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1921-1921 JOHNSON DB; QUAN F; BUCHANNAN JA; POPOVICH BW ALLELIC SIZE LADDERS FCR THE ACCURATE SIZING OF TRINUCLEOTIDE REPEATS IN HUNTINGTON DISEASE AND FRAGILE-X SYNDROME | 0 | 0 |
| 48 | 0 | 0 | 36 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1941-1941 TSAI MS; CHIEN TY; YANG YL; CHEN HR; HWANG SM IDENTIFICATION OF THE NUMBER OF THE FRAGILE-X SYNDROME CGG REPEAT USING SILVER STAIN | 0 | 0 |
| 49 | 0 | 0 | 37 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1947-1947 BROWN CA; BRASINGTON CK; GRASS FS PATERNAL TRANSMISSION OF A FULL MUTATION IN THE FMR1 GENE - IDENTIFICATION OF PATERNAL CGG REPEAT SHES IN MULTIPLE TISSUES | 0 | 0 |
| 50 | 1 | 21 | 38 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):991-993 SHERMAN SL THE HIGH PREVALENCE OF FRAGILE-X PREMUTATION CARRIER FEMALES - IS THIS FREQUENCY UNIQUE TO THE FRENCH-CANADIAN POPULATION | 9 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 51 | 0 | 42 | 39 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):1006-1018 ROUSSEAU F; ROUILLARD P; MOREL ML; KHANDJIAN EW; MORGAN K PREVALENCE OF CARRIERS OF PREMUTATION-SIZE ALLELES OF THE FMRI GENE AND IMPLICATIONS FOR THE POPULATION-GENETICS OF THE FRAGILE-X SYNDROME | 86 | 114 |
| 52 | 0 | 27 | 40 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1408-1413 LOESCH DZ; HUGGINS R; PETROVIC V; SLATER H EXPANSION OF THE CGG REPEAT IN FRAGILE-X IN THE FMR1 GENE DEPENDS ON THE SEX OF THE OFFSPRING | 8 | 13 |
| 53 | 2 | 42 | 41 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1414-1425 ASHLEY AE; SHERMAN SL POPULATION-DYNAMICS OF A MEIOTIC MITOTIC EXPANSION MODEL FOR THE FRAGILE-X SYNDROME | 18 | 20 |
| 54 | 0 | 20 | 158 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(1):237-239 Antinolo G; Borrego S; Cabeza JC; Sanchez R; Sanchez J; et al. Reverse mutation in fragile X syndrome | 9 | 11 |
| 55 | 1 | 13 | 159 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(3):641-643 Brown WT; Zhong N; Dobkin C Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution | 7 | 12 |
| 56 | 1 | 21 | 160 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(5):906-913 Knight SJL; Ritchie RJ; Chakrabarti L; Cross G; Taylor GR; et al. A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom | 12 | 41 |
| 57 | 2 | 37 | 161 1996 AMERICAN JOURNAL OF HUMAN GENETICS 59(3):540-546 Vaisanen ML; Haataja R; Leisti L Decrease in the CGG(n) trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission | 5 | 9 |
| 58 | 9 | 38 | 162 1996 AMERICAN JOURNAL OF HUMAN GENETICS 59(6):1252-1261 Nolin SL; Lewis FA; Ye LL; Houck GE; Glicksman AE; et al. Familial transmission of the FMR1 CGG repeat | 43 | 54 |
| 59 | 4 | 41 | 304 1997 AMERICAN JOURNAL OF HUMAN GENETICS 60(1):103-112 FalikZaccai TC; Shachak E; Yalon M; Lis Z; Borochowitz Z; et al. Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype | 17 | 27 |
| 60 | 6 | 35 | 305 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(3):660-667 deVries BBA; vandenOuweland AMW; Mohkamsing S; Duivenvoorden HJ; Mol E; et al. Screening and diagnosis for the fragile X syndrome among the mentally retarded: An epidemiological and psychological survey | 44 | 80 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 61 | 0 | 0 | 306 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Fisch GS; Holden JJA; Chalifoux M; Carpenter NJ; Howard-Peebles PN; et al. Natural history of cognitive and adaptive behavior in young fragile X males and females: A 6-year prospective multicenter study. | 0 | 0 |
| 62 | 0 | 0 | 307 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Kenneson A; Cramer DW; Warren ST The fragile X premutation is not a major risk for early menopause. | 0 | 0 |
| 63 | 0 | 0 | 308 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A8-A8 Toth-Fejel S; Gunter K; McMilin K; Reifsteck C; Chen XN; et al. High rate of chromosome 11 structural mosaicism in chromosome 11 terminal deletions: fragile site expression and CGG repeat expansion at FRA11B as a genetic mechanism. | 0 | 0 |
| 64 | 0 | 0 | 309 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Brown VL; Small K; Lakkis L; Wilkinson KD; Warren ST Purification and characterization of the fragile X mental retardation protein. | 0 | 0 |
| 65 | 0 | 0 | 310 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Corbin F; Bouillon M; Rousseau F; Khandjian EW The fragile-X mental retardation protein is a mRNA chaperone associated with translating complexes. | 0 | 0 |
| 66 | 0 | 0 | 311 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A30-A30 Gunter C; Paradee W; Newman J; Sherman SL; Warren ST A novel biallelic polymorphism in the FMR1 gene shows strong linkage disequilibrium With CGG repeats and flanking microsatellite markers. | 1 | 1 |
| 67 | 0 | 0 | 312 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A33-A33 Ju W; Xu WM; Hwang YW; Brown WT; Zhong N Molecular pathogenetic studies of the fragile X syndrome: Double knockouts of FMR1 and FXR1 affect early development of Xenopus oocytes. | 0 | 0 |
| 68 | 0 | 0 | 313 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A100-A100 Hagerman RJ; Staley-Gane L; Linden MG; Tassone F; Hills J; et al. A compound heterozygous female with fragile X syndrome. | 0 | 0 |
| 69 | 0 | 0 | 314 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A109-A109 Perroni L; Grasso M; Garavelli L; Argusti A; Cavani S; et al. Three cases of high functioning fragile X males | 0 | 0 |
| 70 | 0 | 0 | 315 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A110-A110 Rhee LE; Hatcher SL; Robb KM; Towner DR Fragile X syndrome associated with birth defects. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 71 | 0 | 0 | 316 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A128-A128 Jenkins EC; Wen GY; Goldberg EM; Genovese M; Brown WT; et al. Fragile X chromosome longitudinal sections studied by transmission electron microscopy. | 0 | 0 |
| 72 | 0 | 0 | 317 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Osthus RC; DiMaio MS; Mahoney MJ; Bale AE Significance of borderline fragile X premutations. | 0 | 0 |
| 73 | 0 | 0 | 318 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Paradee W; Rasmussen D; Melikian H; Conn PJ; Warren ST Hippocampus-independent deficits in the Fragile X mouse. | 0 | 0 |
| 74 | 0 | 0 | 319 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A170-A170 Feng Y; Absher D; Brown V; Eberhart DE; Malter HE; et al. FMRP associates with polyribosomes as an mRNP and the I304N mutation causing severe fragile X syndrome abolishes this association. | 0 | 0 |
| 75 | 0 | 0 | 320 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A175-A175 Kaufmann WE; Abrams MT; Chen W; Reiss AL Genotype and molecular phenotype in fragile X syndrome. | 0 | 0 |
| 76 | 0 | 0 | 321 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A177-A177 Mangel L; Ternes T; Schmitz B; Doerfler W Characterization of new 5 '-(CGG)(n)-3 ' trinucleotide repeat-containing loci in the human genome. | 0 | 0 |
| 77 | 0 | 0 | 322 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A182-A182 Sandberg G; Schalling M Detection of methylated CpG sequences in the FMR-1 promoter using the sodium bisulfite method and expression studies after in vitro methylation and CGG repeat insert. | 0 | 0 |
| 78 | 0 | 0 | 323 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A192-A192 Staley-Gane L; Holloway SL; Flynn L; Logan L; Hageman RJ Assessment of patient agenda prior to genetic counseling for fragile X syndrome. | 0 | 0 |
| 79 | 0 | 0 | 324 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A219-A219 de Vries BBA; van den Ouweland AMW; Mohkamsing S; Duivenvoorden HJ; Halley DJJ; et al. A fragile X screening program in The Netherlands: prevalence of fragile X syndrome lower than previously considered, but the disorder is still underdiagnosed. | 0 | 0 |
| 80 | 0 | 0 | 325 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A303-A303 Ashley AE; Robinson H; Glicksman AE; Nolin SL; Schwartz C; et al. Identification of risk factors associated with instability of the FMR1 CGG repeat. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 81 | 0 | 0 | 326 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A304-A304 Bat O; Kimmel M; Axelrod DE; Chakraborty R Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease. | 0 | 0 |
| 82 | 0 | 0 | 327 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A306-A306 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the fragile X syndrome gene. | 1 | 1 |
| 83 | 0 | 0 | 328 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A313-A313 Layman LC; Moffitt DV; McDonough PG; Song M; Shamoun D; et al. Correlation and vertical transmission of fragile X syndrome and ovarian failure within a single family. | 0 | 0 |
| 84 | 0 | 0 | 329 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A316-A316 Nolin SL; Houck GE; Blumstein H; Ye LL; Dobkin CS; et al. Single cell analysis shows different FMR1 CGG repeat stability in sperm and lymphocytes of premutation males. | 1 | 2 |
| 85 | 0 | 0 | 330 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A321-A321 Tassone F; Hagerman RJ; Ikle D; Dyer PN; Lampe M; et al. FMRP expression as a potential prognostic indicator in fragile X syndrome. | 1 | 1 |
| 86 | 0 | 0 | 331 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A324-A324 Zhong N; Ju W; Xu WM; Liu B; Dobkin C; et al. Molecular pathogenetic studies of the fragile X syndrome: A candidate transcript targeted by the fragile X protein FMRP. | 0 | 0 |
| 87 | 0 | 0 | 332 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A330-A330 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; et al. Methylation analysis of the fragile X syndrome by PCR. | 0 | 0 |
| 88 | 0 | 0 | 333 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A389-A389 Ye LL; Ju W; Xu WM; Schupf N; Jenkins EC; et al. Distribution of apolipoprotein E genotypes in the fragile X syndrome, Batten disease, and Down syndrome populations. | 0 | 0 |
| 89 | 0 | 0 | 334 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A407-A407 Sucharov CC; Varandas FR; Rondinelli E; Carakushansky G; Moura-Neto RS Establishment of a differential diagnostic of patients with Mental Retardation based on Southern-blot and PCR considering the frequency of Fragile X trinucleotide repeats from normal population in Rio de Janeiro, Brazil. | 0 | 0 |
| 90 | 0 | 0 | 335 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A407-A407 Taylor AK; Tassone F; Staley-Gane L; Hagerman RJ Identical premutation size in multiple tissues of a male fragile X carrier. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 91 | 13 | 44 | 336 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):961-967 Gronskov K; Hjalgrim H; Bjerager MO; BrondumNielsen K Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression | 5 | 6 |
| 92 | 13 | 43 | 337 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(6):1362-1369 Kenneson A; Cramer DW; Warren ST Fragile X premutations are not a major cause of early menopause | 13 | 22 |
| 93 | 11 | 42 | 429 1998 AMERICAN JOURNAL OF HUMAN GENETICS 63(3):776-785 Ashley-Koch AE; Robinson H; Glicksman AE; Nolin SL; Schwartz CE; et al. Examination of factors associated with instability of the FMR1 CGG repeat | 15 | 22 |
| 94 | 5 | 24 | 516 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(1):98-103 Willemsen R; Anar B; Otero YD; de Vries BBA; Hilhorst-Hofstee Y; et al. Noninvasive test for fragile X syndrome, using hair root analysis | 22 | 24 |
| 95 | 7 | 52 | 517 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(3):680-688 Nolin SL; Houck GE; Gargano AD; Blumstein H; Dobkin CS; et al. FMR1 CCG-repeat instability by single sperm and lymphocytes of fragile-X premutation males | 8 | 15 |
| 96 | 0 | 0 | 518 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A29-A29 Ceman S; Brown V; Warren ST Isolation of an FMRP-associated mRNP and the identification of nucleolin and the fragile X-related proteins as components of the complex. | 0 | 0 |
| 97 | 0 | 0 | 519 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A30-A30 Peier AM; McIlwain KL; Paylor R; Nelson DL FMR1 YAC transgenic mice: rescue of the FMRl knockout mouse and behavior of the CGG trinucleotide repeat. | 0 | 0 |
| 98 | 0 | 0 | 520 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A49-A49 Drasinover V; Ehrlich S; Magal N; Taub E; Libman V; et al. Increased transmission of the premutated allele compared to the normal allele in female carriers of the fragile X syndrome. | 0 | 0 |
| 99 | 0 | 0 | 521 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A68-A68 Fisch GS; Howard-Peebles PN; Carpenter N; Tarleton J; Simensen R; et al. Age-related features of genetic mutations producing cognitive impairment: the Fragile X mutation, NF1, and Williams Syndrome. | 0 | 0 |
| 100 | 0 | 0 | 522 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A103-A103 Brown WT; Rabe A; Durnas R; Haubenstock H; Dobkin C FMR1 knockout mouse shows a strain-specific severe learning impairment: A robust model for the fragile X syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 101 | 0 | 0 | 523 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A105-A105 Kenneson A; Hagedorn CH; Warren ST Quantitative studies of the fragile X mental retardation 1 (FMR1) gene product, FMRP. | 0 | 0 |
| 102 | 0 | 0 | 524 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A145-A145 Chernoff EJ; Nunes M; White B; McClellan J; Coll E; et al. Fragile X premutation status in a male with mental retardation. | 0 | 0 |
| 103 | 0 | 0 | 525 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A165-A165 Iqbal MA; Sakati N; Nester A; Ozand P Cytogenetic diagnosis of fragile X syndrome a study of 305 suspected cases in Saudi Arabia. | 0 | 0 |
| 104 | 0 | 0 | 526 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A214-A214 Falik-Zaccai TC; Shachak E; Borochowitz Z; Magal N; Zatz S; et al. Fragile X syndrome: Population carrier screening and implication for prenatal diagnosis. | 0 | 0 |
| 105 | 0 | 0 | 527 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A263-A263 Absher DM; Warren SR Functional studies of mammalian FMRP in yeast. | 0 | 0 |
| 106 | 0 | 0 | 528 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A266-A266 Burman RW; Popovich BW; Yates PA; Jacky PB; Schnell JL; et al. Fully expanded fragile X CGG repeats exhibit a length-and differentiation-dependent instability in cell hybrids that is independent of DNA methylation. | 0 | 0 |
| 107 | 0 | 0 | 529 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A268-A268 Crawford DC; Schwartz CE; Warren ST; Sherman SL Novel repeat structures identified in African-Americans represent a new mechanism leading to fragile X CGG repeat instability. | 0 | 0 |
| 108 | 0 | 0 | 530 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A269-A269 DiMarco SP; Ceman S; Torre E; Warren ST FMRP is a phosphoprotein and a substrate of the Fes non-receptor tryosine kinase. | 2 | 3 |
| 109 | 0 | 0 | 531 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A270-A270 El-Hazmi MF Fragile X mental retardation in syndrome in Saudi Arabia. | 0 | 0 |
| 110 | 0 | 0 | 532 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A279-A279 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson J; et al. Haplotype and AGG-interspersion analysis of FMR1(CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 111 | 0 | 0 | 533 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A403-A403 Xu B; School JM; Buroker NE; Scott CR; Chen SH High frequency of the FMR-1 INV10+14c/t polymorphism in Asians, and its association with the Fragile X Syndrome in Caucasians. | 0 | 1 |
| 112 | 0 | 0 | 534 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A464-A464 Nolin SL; Houck GE; Gargano AD; Li SY; Glicksman A; et al. Instability of FMR1 alleles with 40-60 CGG repeats. | 0 | 0 |
| 113 | 0 | 0 | 535 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A471-A471 Ventura KA; Fraer LM; Smith EE; Merrill AE; Treat KJ; et al. Transmission on a fragile X full mutation through a normal transmitting male. | 0 | 0 |
| 114 | 0 | 0 | 536 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A474-A474 Lazarou LP; Warburton S; Roberts CE; Lindley VH; Bartlett S; et al. Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male. | 0 | 0 |
| 115 | 0 | 0 | 537 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A493-A493 Tassone F; Hagerman RJ; Taylor AK; Mills JB; Wood S; et al. FMR1 mRNA expression levels in fragile X. | 0 | 0 |
| 116 | 7 | 40 | 652 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(1):6-15 Tassone F; Hagerman RJ; Taylor AK; Gane LW; Godfrey TE; et al. Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in the fragile-X syndrome | 62 | 96 |
| 117 | 6 | 28 | 653 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):413-418 Hundscheid RDL; Sistermans EA; Thomas CMG; Braat DDM; Straatman H; et al. Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations | 15 | 31 |
| 118 | 16 | 52 | 654 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):480-493 Crawford DC; Schwartz CE; Meadows KL; Newman JL; Taft LF; et al. Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population | 9 | 18 |
| 119 | 6 | 8 | 655 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):11-13 Sherman SL Premature ovarian failure among fragile X premutation carriers: Parent-of-origin effect? | 4 | 8 |
| 120 | 1 | 4 | 656 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):253-254 Murray A; Ennis S; Morton N No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers | 9 | 17 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 121 | 4 | 8 | 657 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):254-255 Vianna-Morgante AM; Costa SS Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X | 8 | 16 |
| 122 | 3 | 3 | 658 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):256-258 Hundscheid RDL; Thomas CMG; Braat DDM; Oostra BA; Smits APT Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X - Reply | 2 | 5 |
| 123 | 0 | 0 | 659 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Brown V; Ceman S; Jin P; Jin C; Wilkinson KD; et al. Messenger RNAs associated with the fragile X mental retardation protein in mouse brain. | 1 | 1 |
| 124 | 0 | 0 | 660 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Jin P; Feng Y; Brown V; Warren ST Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays. | 1 | 2 |
| 125 | 0 | 0 | 661 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):25-25 Crawford DC; Wilson B; Sherman SL Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool-PCR. | 0 | 0 |
| 126 | 0 | 0 | 662 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):26-26 Hagerman RJ; Tassone F; Leehey M; Hills J; Wilson R; et al. Cerebellar tremor and cerebellar cortical atrophy in older males with the fragile X premutation. | 0 | 0 |
| 127 | 0 | 0 | 663 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P; Oostra BA Differential reactivation of the FMR1 gene in fragile X patients cell lines. | 0 | 0 |
| 128 | 0 | 0 | 664 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Kenneson A; Zhang F; Warren ST Fragile X premutation alleles are associated with reduced FMRP levels due to a reduction of message translatability. | 0 | 0 |
| 129 | 0 | 0 | 665 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):57-57 Li MM; Nelson L; Bamshad M; Ward K Fragile X mosaics in a family with multiple mildly affected individuals. | 0 | 0 |
| 130 | 0 | 0 | 666 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):130-130 Khalifa M; Struthers J High frequency of Klinefelter syndrome among a large population of patients referred for Fragile X syndrome testing due to undiagnosed mental retardation. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 131 | 0 | 0 | 667 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):135-135 Harris SW; Brown KE; Hills JL; Tassone F; Hagerman PJ; et al. Adaptive functioning and molecular relationships in individuals with fragile X syndrome. | 0 | 0 |
| 132 | 0 | 0 | 668 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):184-184 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ Clinical and molecular correlations in individuals with a fragile X full mutation. | 0 | 0 |
| 133 | 0 | 0 | 669 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):200-200 Ceman SS; Kenneson A; Nelson R; Jin C; Lakkis L; et al. Development and characterization of a unique set of anti-FMRP antibodies using a novel strategy. | 0 | 0 |
| 134 | 0 | 0 | 670 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):236-236 Mathews DJ; Hudson R; Eichier E; Chakravarti A Sequence variation and linkage disequilibrium at the fragile X syndrome locus. | 0 | 0 |
| 135 | 0 | 0 | 671 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):238-238 Sullivan AK; Crawford DC; Meadows KL; Wilson B; Sherman SL Parent-child transmission of intermediate FMR1 CGG repeat alleles: Examination of factors associated with repeat instability. | 0 | 0 |
| 136 | 0 | 0 | 672 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):247-247 Brown NM; Friez MJ; Longshore JW; Stenzel TT Evaluation of an automated commercially available PCR kit for determination of Fragile X (FRAXA) normal, gray-zone and premutation allele sizes. | 0 | 0 |
| 137 | 0 | 0 | 673 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):248-248 Murphy KM; Nunes ME Comparison of child-only versus mother/child sample collection in Fragile X testing. | 0 | 0 |
| 138 | 0 | 0 | 674 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):254-254 Weinhaeusel A; Skarits C; Haas OA Methylation-sensitive PCR (MS-PCR) analysis of the fragile X (FRAXA) syndrome. | 0 | 0 |
| 139 | 0 | 0 | 675 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):348-348 Dyack S; Steele L; Koultchitski G; Yang Y; Weksberg R; et al. AGG interruptions in the CGG trinucleotide repeat tract of the FMR1 gene may contribute to stability of Fragile X premutations. | 0 | 0 |
| 140 | 0 | 0 | 676 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):360-360 Ramos FJ; Mila M; Ortilles M; Rife M; Tazon B; et al. Validity of the analysis of the FMRP expression in bloodsmears as a screening method for the Fragile X Syndrome. | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 141 | 0 | 0 | 677 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):364-364 Chen SH; Xu B; Shoof JM; Buroker NE; Scott CR Evidence for a stepwise expansion of the CGG repeats within the FMR1 gene. | 0 | 0 |
| 142 | 0 | 0 | 678 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 O'Donnell WT; Warren ST Investigating the cause of macroorchidism in fragile X syndrome using oligonucleotide microarrays. | 0 | 0 |
| 143 | 0 | 0 | 679 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 Nolin SL; Rousseau F; Houck GE; Gargano AD; Biancalana V; et al. FMR1 CGG expansion to full mutation: What is the lower limit in premutation females? | 0 | 0 |
| 144 | 0 | 0 | 680 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Raca G; Siyanova E; Mirkin S Janus effects of premutation size CGG repeats on gene expression. | 1 | 1 |
| 145 | 0 | 0 | 681 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Parades WJ; Warren ST Meiotic stability of a fragile X premutation CGG trinucleotide repeat in a mouse model. | 0 | 0 |
| 146 | 0 | 0 | 682 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):415-415 Najmabadi H; Taghizadeh F; Teimourian SH; Karimi-Nejad R; Shafeghati Y; et al. Molecular analysis of Fragile X syndrome in Iranian population. | 0 | 0 |
| 147 | 0 | 0 | 683 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):428-428 Brown WT; Ding X; Idrissi AE; Scalia J; Glicksman A; et al. Fragile X transgene and embryonic lethality in mice. | 0 | 0 |
| 148 | 12 | 40 | 811 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(2):351-360 Toledano-Alhadef H; Basel-Vanagaite L; Magal N; Davidov B; Ehrlich S; et al. Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel | 13 | 22 |
| 149 | 11 | 34 | 812 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(3):504-515 Wohrle D; Salat U; Hameister H; Vogel W; Steinbach P Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells | 4 | 10 |
| 150 | 0 | 0 | 813 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; et al. Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 151 | 0 | 0 | 814 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):291-291 Thiele H; Peters H; Bahrke D; Hansmann I Homozygosity for a premutation of the FMR1 gene and normal phenotype in two sisters from a family with fragile X syndrome. | 0 | 0 |
| 152 | 0 | 0 | 815 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):352-352 Gantois I; Reyniers E; Kooy RF Identification of genes differentially expressed in the fragile X syndrome. | 0 | 0 |
| 153 | 0 | 0 | 816 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Naumann F; Muller-Hartmann H; Deissler H; Doerfler W Functional studies on the human 5 '-CGG-3 '-binding protein CGGBP1 (p20). | 0 | 0 |
| 154 | 0 | 0 | 817 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P Pharmacological reactivation of the FMR1 gene of the fragile X syndrome. | 0 | 0 |
| 155 | 0 | 0 | 818 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 |
| 156 | 0 | 0 | 819 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 |
| 157 | 0 | 0 | 820 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 |
| 158 | 0 | 0 | 821 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 |
| 159 | 0 | 0 | 822 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 |
| 160 | 0 | 0 | 823 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 161 | 0 | 0 | 824 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 |
| 162 | 0 | 0 | 825 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 |
| 163 | 0 | 0 | 826 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 |
| 164 | 0 | 0 | 827 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 |
| 165 | 0 | 0 | 934 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 |
| 166 | 0 | 0 | 935 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 |
| 167 | 0 | 0 | 936 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 |
| 168 | 0 | 0 | 937 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 |
| 169 | 0 | 0 | 938 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 |
| 170 | 0 | 0 | 939 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 171 | 0 | 0 | 940 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 |
| 172 | 0 | 0 | 941 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 |
| 173 | 0 | 0 | 942 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 |
| 174 | 0 | 0 | 943 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 |
| 175 | 0 | 0 | 944 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 |
| 176 | 0 | 0 | 945 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 |
| 177 | 0 | 0 | 946 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 |
| 178 | 0 | 0 | 947 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 |
| 179 | 0 | 0 | 948 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 |
| 180 | 0 | 0 | 949 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 181 | 3 | 37 | 950 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 |
| 182 | 15 | 39 | 1065 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 |
| 183 | 12 | 36 | 1066 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 |
| 184 | 0 | 0 | 1067 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 |
| 185 | 0 | 0 | 1068 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 |
| 186 | 0 | 0 | 1069 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 |
| 187 | 0 | 0 | 1070 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 |
| 188 | 0 | 0 | 1071 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 |
| 189 | 0 | 0 | 1072 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 |
| 190 | 0 | 0 | 1073 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 191 | 0 | 0 | 1074 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 |
| 192 | 0 | 0 | 1075 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 |
| 193 | 0 | 0 | 1076 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 |
| 194 | 0 | 0 | 1077 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 |
| 195 | 0 | 0 | 1078 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 |
| 196 | 0 | 0 | 1079 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):372-372 Reddy K Autism: Incidence of cytogenetic abnormality and fragile-X syndrome. | 0 | 0 |
| 197 | 0 | 0 | 1080 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 |
| 198 | 0 | 0 | 1081 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 |
| 199 | 0 | 0 | 1082 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 |
| 200 | 0 | 0 | 1083 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 201 | 0 | 0 | 1084 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 |
| 202 | 0 | 0 | 1085 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 |
| 203 | 0 | 0 | 1086 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 |
| 204 | 0 | 0 | 1087 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 |
| 205 | 0 | 0 | 1088 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 |
| 206 | 0 | 0 | 1089 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 |
| 207 | 35 | 80 | 1197 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):805-816 Hagerman PJ; Hagerman RJ The fragile-X premutation: A maturing perspective | 8 | 14 |
| 208 | 14 | 26 | 1198 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):1051-1056 Hagerman RJ; Leavitt BR; Farzin F; Jacquemont S; Greco CM; et al. Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation | 3 | 7 |
| 209 | 1 | 1 | 1199 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(2):352-352 Hagerman; Hagerman The fragile-X premutation: A maturing perspective (vol 74, pg 805, 2003) | 0 | 0 |
| 210 | 2 | 10 | 1200 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):730-731 Mandel JL Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 211 | 1 | 5 | 1201 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):731-732 Salomons GS; Ropers HH Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation - Reply | 0 | 0 |
| 212 | 12 | 41 | 1337 2005 AMERICAN JOURNAL OF HUMAN GENETICS 76(2):302-311 Edamura KN; Leonard MR; Pearson CE Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells | 0 | 0 |
| 213 | 0 | 13 | 42 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 55(3):384-386 PRIOR TW; PAPP AC; SNYDER PJ; SEDRA MS; GUIDA M; et al. GERMLINE MOSAICISM AT THE FRAGILE-X LOCUS | 2 | 7 |
| 214 | 0 | 5 | 43 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 57(3):508-509 LAXOVA R FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 2 | 3 |
| 215 | 0 | 33 | 44 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 58(3):249-256 LOESCH DZ; HUGGINS RM; HOANG NH GROWTH IN STATURE IN FRAGILE-X FAMILIES - A MIXED LONGITUDINAL-STUDY | 12 | 14 |
| 216 | 0 | 21 | 45 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):426-430 MCCONKIEROSELL A; ROBINSON H; WAKE S; STALEY LW; HELLER K; et al. DISSEMINATION OF GENETIC RISK INFORMATION TO RELATIVES IN THE FRAGILE-X SYNDROME - GUIDELINES FOR GENETIC COUNSELORS | 7 | 8 |
| 217 | 0 | 9 | 46 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 59(4):526-526 SCHIANO CM; DEMB HB; BROWN WT LACK OF SIGNIFICANT ASSOCIATION BETWEEN SPINA-BIFIDA AND THE FRAGILE-X SYNDROME | 0 | 0 |
| 218 | 0 | 28 | 47 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(1):39-43 SPINELLI M; ROCHA ACD; GIACHETI CM; RICHIERICOSTA A WORD-FINDING DIFFICULTIES, VERBAL PARAPHASIAS, AND VERBAL DYSPRAXIA IN 10 INDIVIDUALS WITH FRAGILE-X-SYNDROME | 7 | 7 |
| 219 | 0 | 19 | 48 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(4):302-306 MUELLER OT; HARTSFIELD JK; AMAR MJA; GALLARDO LA; KOUSSEFF BG FRAGILE-X SYNDROME - DISCORDANT LEVELS OF CGG REPEAT MOSAICISM IN 2 BROTHERS | 2 | 5 |
| 220 | 0 | 92 | 49 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(6):480-493 Schapiro MB; Murphy DGM; Hagerman RJ; Azari NP; Alexander GE; et al. Adult fragile X syndrome: Neuropsychology, brain anatomy, and metabolism | 21 | 31 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 221 | 0 | 24 | 163 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 63(2):396-400 Giampietro PF; Haas BR; Lipper E; Gutman A; Zellers NJ; et al. Fragile X syndrome in two siblings with major congenital malformations | 0 | 1 |
| 222 | 0 | 0 | 164 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-1 Laing S; Robinson H; Wake S; Wright F; Turner G Normal males and their role in transmission of the fragile x syndrome. | 0 | 0 |
| 223 | 9 | 34 | 165 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-14 Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; et al. Seventh International Workshop on the Fragile X and X-linked Mental Retardation | 2 | 4 |
| 224 | 0 | 0 | 166 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):6-6 Maes B; Borghraef M; Fryns JP Presentation of a fragile-X screening list. | 0 | 0 |
| 225 | 0 | 0 | 167 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):14-14 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; et al. A rare example of a reverse mutation in a fragile X syndrome family. | 0 | 0 |
| 226 | 0 | 0 | 168 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):16-16 Murray A; Conway GS; Jacobs PA Premature ovarian failure and fragile X. | 0 | 0 |
| 227 | 0 | 0 | 169 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):17-17 Oostra BA; Willemsen R; Mandel JL; DeVries B; Devys D Rapid screening test for fragile X syndrome. | 0 | 0 |
| 228 | 0 | 0 | 170 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):18-18 Oostra B; DeGraaf E; Zhong N; Willemsen R Instability of the CGG repeat and expression of FMR1 protein in a male patient with a lung tumor. | 0 | 0 |
| 229 | 0 | 0 | 171 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):19-19 Shen Y; Zhu N; Huang D; Wu GY Studies on fragile X syndrome in the Chinese. | 0 | 0 |
| 230 | 0 | 0 | 172 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):25-25 deVries BBA; vandenOuweland AMW; Mohkamsing S; Halley DJJ; Tibben A; et al. Acceptance of screening for the fragile X syndrome among 1878 mentally retarded individuals in institutions and special schools in the Netherlands | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 231 | 1 | 21 | 173 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):27-30 Carrel L; Willard HF An assay for X inactivation based on differential methylation at the fragile X locus, FMR1 | 1 | 32 |
| 232 | 3 | 12 | 174 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):176-180 Perroni L; Grasso M; Argusti A; LoNigro C; Croci GF; et al. Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families | 6 | 7 |
| 233 | 1 | 12 | 175 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):181-183 Spence WC; Black SH; Fallon L; Maddalena A; Cummings E; et al. Molecular fragile X screening in normal populations | 13 | 18 |
| 234 | 0 | 10 | 176 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):187-190 Grasso M; Perroni L; Colella S; Piombo G; Argusti A; et al. Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome | 1 | 2 |
| 235 | 4 | 24 | 177 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):191-195 Brown WT; Nolin S; Houck G; Ding XH; Glicksman A; et al. Prenatal diagnosis and carrier screening for fragile X by PCR | 20 | 28 |
| 236 | 1 | 12 | 178 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):196-197 Turner G; Webb T; Wake S; Robinson; H Prevalence of fragile X syndrome | 153 | 235 |
| 237 | 1 | 11 | 179 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):198-202 Robinson H; Wake S; Wright F; Laing S; Turner G Informed choice in fragile X syndrome and its effects on prevalence | 9 | 11 |
| 238 | 10 | 50 | 180 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):203-208 Chiurazzi P; Macpherson J; Sherman S; Neri G Significance of linkage disequilibrium between the fragile X locus and its flanking markers | 18 | 25 |
| 239 | 3 | 59 | 181 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):209-215 Chiurazzi P; Genuardi M; Kozak L; GiovannucciUzielli ML; Bussani C; et al. Fragile X founder chromosomes in Italy: A few initial events and possible explanation for their heterogeneity | 17 | 26 |
| 240 | 2 | 45 | 182 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):220-225 Eichler EE; Nelson DL Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations | 14 | 18 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 241 | 5 | 43 | 183 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):226-233 Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; et al. Fragile X founder effects and new mutations in Finland | 14 | 26 |
| 242 | 0 | 20 | 184 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):234-238 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; et al. Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus | 9 | 15 |
| 243 | 3 | 20 | 185 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):241-245 Kooy RF; DHooge R; Reyniers E; Bakker CE; Nagels G; et al. Transgenic mouse model for the fragile X syndrome | 25 | 44 |
| 244 | 3 | 37 | 186 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):246-251 Godfraind JM; Reyniers E; DeBoulle K; DHooge R; DeDeyn PP; et al. Long-term potentiation in the hippocampus of fragile X knockout mice | 25 | 34 |
| 245 | 3 | 21 | 187 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):256-260 Sherman SL; Meadows KL; Ashley AE Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females | 13 | 16 |
| 246 | 4 | 28 | 188 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):261-265 Zhong N; Ju WN; Pietrofesa J; Wang DW; Dobkin C; et al. Fragile X ''gray zone'' alleles: AGG patterns, expansion risks, and associated haplotypes | 15 | 27 |
| 247 | 0 | 21 | 189 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):266-267 Wohrle D; Schwemmle S; Steinbach P DNA methylation and triplet repeat stability: New proposals addressing actual questions on the CGG repeat of fragile X syndrome | 11 | 18 |
| 248 | 1 | 17 | 190 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):270-273 MingroniNetto RC; Haddad LA; ViannaMorgante AM The number of CGG repeats of the FMR1 locus in premutated and fully mutated heterozygotes and their offspring: Implications for the origin of mosaicism | 5 | 6 |
| 249 | 0 | 13 | 191 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):274-277 Steyaert J; Borghgraef M; Legius E; Fryns JP Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene | 15 | 19 |
| 250 | 0 | 21 | 192 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):278-282 Lachiewicz AM; Spiridigliozzi GA; McConkieRosell A; Burgess D; Feng Y; et al. A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene | 9 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 251 | 3 | 35 | 193 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):287-292 Brown WT; Houck GE; Ding XH; Zhong N; Nolin S; et al. Reverse mutations in the fragile X syndrome | 11 | 18 |
| 252 | 2 | 20 | 194 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):293-295 Mannermaa A; Pulkkinen L; Kajanoja E; Ryynanen M; Saarikoski S Deletion in the FMR1 gene in a fragile-X male | 9 | 9 |
| 253 | 2 | 24 | 195 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):296-301 Dobkin CS; Nolin SL; Cohen I; Sudhalter V; Bialer MG; et al. Tissue differences in fragile X mosaics: Mosaicism in blood cells may differ greatly from skin | 9 | 11 |
| 254 | 3 | 43 | 196 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):302-308 deGraaff E; deVries BBA; Willemsen R; vanHemel JO; Mohkamsing S; et al. The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells | 12 | 13 |
| 255 | 2 | 21 | 197 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):309-312 Maddalena A; Yadvish KN; Spence WC; HowardPeebles PN A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood | 13 | 16 |
| 256 | 0 | 9 | 198 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):319-322 Fisch GS; Carpenter N; Maddalena A; Tarleton J; JulienInalsingh C; et al. Rater reliability of fragile X mutation size estimates: A multilaboratory analysis | 5 | 5 |
| 257 | 0 | 31 | 199 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):323-328 Mazzocco MMM; Holden JJA Neuropsychological profiles of three sisters homozygous for the fragile X premutation | 6 | 8 |
| 258 | 0 | 24 | 200 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):329-333 AllinghamHawkins DJ; Brown CA; Babul R; Chitayat D; Krekewich K; et al. Tissue-specific methylation differences and cognitive function in fragile X premutation females | 8 | 13 |
| 259 | 0 | 18 | 201 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):334-339 Franke P; Maier W; Hautzinger M; Weiffenbach O; Gansicke M; et al. Fragile-X carrier females: Evidence for a distinct psychopathological phenotype? | 23 | 32 |
| 260 | 1 | 29 | 202 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):340-345 Sobesky WE; Taylor AK; Pennington BF; Bennetto L; Porter D; et al. Molecular/clinical correlations in females with fragile X | 31 | 39 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 261 | 2 | 31 | 203 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):350-355 WrightTalamante C; Cheema A; Riddle JE; Luckey DW; Taylor AK; et al. A controlled study of longitudinal IQ changes in females and males with fragile X syndrome | 14 | 16 |
| 262 | 1 | 41 | 204 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):356-361 Fisch GS; Simensen R; Tarleton J; Chalifoux M; Holden JJ; et al. Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: A prospective multicenter analysis | 27 | 34 |
| 263 | 1 | 14 | 205 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):362-364 Fisch GS; Carpenter N; HowardPeebles PN; Maddalena A; Simensen R; et al. Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report | 1 | 3 |
| 264 | 2 | 21 | 206 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):365-369 Cohen IL; Nolin SL; Sudhalter V; Ding XH; Dobkin CS; et al. Mosaicism for the FMR1 gene influences adaptive skills development in fragile X-affected males | 15 | 16 |
| 265 | 1 | 7 | 207 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):370-372 Partington MW; Moore DY; Turner GM Confirmation of early menopause in fragile X carriers | 26 | 44 |
| 266 | 1 | 2 | 208 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):376-376 Burgess B; Partington M; Turner G; Robinson H Normal age of menarche in fragile X syndrome | 3 | 3 |
| 267 | 1 | 6 | 209 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):377-377 HowardPeebles PN Successful pregnancy in a fragile X carrier by donor egg | 2 | 3 |
| 268 | 0 | 7 | 210 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):378-381 Wingrove EJ; Norris J; Barton PL; Hagerman R Experiences and attitudes concerning genetic testing and insurance in a Colorado population: A survey of families diagnosed with fragile X syndrome | 0 | 9 |
| 269 | 1 | 18 | 211 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):395-398 Piussan C; Mathieu M; Berquin P; Fryns JP Fragile X mutation and FG syndrome-like phenotype | 1 | 4 |
| 270 | 0 | 19 | 212 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):404-407 Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; et al. Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 271 | 1 | 20 | 213 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):413-414 Loesch DZ Fragile X: Clinical associations | 0 | 0 |
| 272 | 3 | 25 | 214 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):428-433 Meadows KL; Pettay D; Newman J; Hersey J; Ashley AE; et al. Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population | 13 | 27 |
| 273 | 1 | 1 | 215 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(3):527-527 Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; ConstantinouDeltas CD; et al. Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus (vol 64, pg 234, 1996) | 0 | 0 |
| 274 | 0 | 3 | 216 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 65(4):355-356 Seemanova E Fragile X syndrome in incestuous families | 0 | 0 |
| 275 | 1 | 1 | 217 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 66(1):118-118 Perroni L; Grasso M; Argusti A; Nigro CL; Croci GF; et al. Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families (vol 64, pg 176, 1996) | 0 | 0 |
| 276 | 0 | 28 | 218 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 67(1):77-80 Simon EW; Finucane BM Facial emotion identification in males with fragile X syndrome | 6 | 6 |
| 277 | 0 | 29 | 338 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(1):62-69 McConkieRosell A; Spiridigliozzi GA; Iafolla T; Tarleton J; Lachiewicz AM Carrier testing in the fragile X syndrome: Attitudes and opinions of obligate carriers | 7 | 13 |
| 278 | 0 | 14 | 339 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(4):445-449 Wen GY; Jenkins EC; Yao XL; Yoon D; Brown WT; et al. Transmission electron microscopy of chromosomes by longitudinal section preparation: Application to fragile X chromosome analysis | 3 | 5 |
| 279 | 1 | 11 | 340 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 69(1):114-116 Martin NG; Healey SC; Pangan TS; Heath AC; Turner G Do mothers of dizygotic twins have earlier menopause? A role for fragile X? | 5 | 12 |
| 280 | 4 | 13 | 341 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(2):245-246 Healey SC; Duffy DL; Martin NG; Turner G Is fragile X syndrome a risk factor for dizygotic twinning? | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 281 | 9 | 25 | 342 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(4):430-434 Hammond LS; Macias MM; Tarleton JC; Pai GS Fragile X syndrome and deletions in FMR1: New case and review of the literature | 15 | 22 |
| 282 | 5 | 51 | 343 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 73(4):463-469 Ritchie RJ; Chakrabarti L; Knight SJL; Harding RM; Davies KE Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28 | 2 | 6 |
| 283 | 0 | 39 | 344 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 74(2):167-171 Miezejeski CM; Heaney G; Belser R; Brown WT; Jenkins EC; et al. Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation | 0 | 0 |
| 284 | 0 | 0 | 345 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 74(6):568-568 Bleiweiss H; Pollini A; Goldemberg A; Schuarzberg C; Staszauer M; et al. Treatment of patients with fragile X syndrome and psychiatric abnormalities. | 0 | 0 |
| 285 | 3 | 39 | 430 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 75(3):277-282 Jara L; Aspillaga M; Avendano I; Obreque V; Blanco R; et al. Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population | 6 | 7 |
| 286 | 1 | 1 | 431 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 78(4):397-399 Ritchie RJ; Chakrabarti L; Knight SJL; Harding RM; Davies KE Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28. (vol 73, pg 463, 1997) | 0 | 0 |
| 287 | 7 | 33 | 432 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 79(3):200-204 Bonaventure G; Torrado M; Barreiro C; Chertkoff L Fragile X founder effects in Argentina | 0 | 4 |
| 288 | 0 | 0 | 433 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 81(6):452-453 Oostra BA Fragile X syndrome is caused by a fragile gene. | 0 | 0 |
| 289 | 0 | 0 | 434 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 81(6):552-552 von Gontard A; Backes M; Schreck J; Genc B; Doerfler W Behavioural phenotype of the fragile-X-syndrome. | 0 | 0 |
| 290 | 8 | 53 | 538 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(1):25-30 Abrams MT; Kaufmann WE; Rousseau F; Oostra BA; Wolozin B; et al. FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome | 8 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 291 | 3 | 20 | 539 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(3):206-211 McConkie-Rosell A; Spiridigliozzi GA; Rounds K; Dawson DV; Sullivan JA; et al. Parental attitudes regarding carrier testing in children at risk for fragile X syndrome | 2 | 7 |
| 292 | 0 | 5 | 540 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(2):140-141 Hjalgrim H; Jacobsen TB; Norgaard K; Lou HC; Brondum-Nielsen K; et al. Frontal-subcortical hypofunction in the fragile X syndrome | 5 | 8 |
| 293 | 18 | 61 | 541 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):221-236 Holden JJA; Percy M; Allingham-Hawkins D; Brown WT; Chiurazzi P; et al. Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997 | 1 | 4 |
| 294 | 3 | 35 | 542 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):248-252 Weiler IJ; Greenough WT Synaptic synthesis of the Fragile X protein: Possible involvement in synapse maturation and elimination | 31 | 44 |
| 295 | 3 | 23 | 543 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):253-256 Fisch GS; Holden JJK; Carpenter NJ; Howard-Peebles PN; Maddalena A; et al. Age-related language characteristics of children and adolescents with fragile X syndrome | 7 | 8 |
| 296 | 5 | 26 | 544 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):257-263 Fisch GS; Carpenter NJ; Holden JJA; Simensen R; Howard-Peebles PN; et al. Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: Growth, development, and profiles | 10 | 10 |
| 297 | 5 | 54 | 545 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):268-279 Miller LJ; McIntosh DN; McGrath J; Shyu V; Lampe M; et al. Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report | 32 | 41 |
| 298 | 1 | 9 | 546 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):281-285 Teisl JT; Reiss AL; Mazzocco MMM Maximizing the sensitivity of a screening questionnaire for determining fragile X at-risk status | 2 | 2 |
| 299 | 9 | 47 | 547 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):286-295 Kaufmann WE; Abrams MT; Chen WM; Reiss AL Genotype, molecular phenotype, and cognitive phenotype: Correlations in fragile X syndrome | 30 | 36 |
| 300 | 2 | 13 | 548 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):296-297 Ferri R; Del Gracco S; Elia M; Musumeci SA; Pettinato S Heart rate variability and autonomic function during sleep in fragile X syndrome | 0 | 0 |