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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by LCS.
Page 1: 1 2 3 4 5 6 7 8 9
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1 | 11 | 40 | 846 1991 CELL 65(5):905-914 VERKERK AJMH; PIERETTI M; SUTCLIFFE JS; FU YH; KUHL DPA; et al. IDENTIFICATION OF A GENE (FMR-1) CONTAINING A CGG REPEAT COINCIDENT WITH A BREAKPOINT CLUSTER REGION EXHIBITING LENGTH VARIATION IN FRAGILE-X SYNDROME | 576 | 1282 |
| 2 | 18 | 37 | 905 1991 SCIENCE 252(5009):1097-1102 OBERLE I; ROUSSEAU F; HEITZ D; KRETZ C; DEVYS D; et al. INSTABILITY OF A 550 BASE PAIR DNA SEGMENT AND ABNORMAL METHYLATION IN FRAGILE X-SYNDROME | 440 | 846 |
| 3 | 12 | 23 | 848 1991 CELL 67(6):1047-1058 FU YH; KUHL DPA; PIZZUTI A; PIERETTI M; SUTCLIFFE JS; et al. VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX | 432 | 957 |
| 4 | 10 | 15 | 847 1991 CELL 66(4):817-822 PIERETTI M; ZHANG FP; FU YH; WARREN ST; OOSTRA BA; et al. ABSENCE OF EXPRESSION OF THE FMR-1 GENE IN FRAGILE-X SYNDROME | 333 | 598 |
| 5 | 3 | 9 | 906 1991 SCIENCE 252(5009):1179-1181 YU S; PRITCHARD M; KREMER E; LYNCH M; NANCARROW J; et al. FRAGILE-X GENOTYPE CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 295 | 542 |
| 6 | 15 | 28 | 892 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1673-1681 ROUSSEAU F; HEITZ D; BIANCALANA V; BLUMENFELD S; KRETZ C; et al. DIRECT DIAGNOSIS BY DNA ANALYSIS OF THE FRAGILE X-SYNDROME OF MENTAL-RETARDATION | 290 | 445 |
| 7 | 11 | 40 | 288 1985 HUMAN GENETICS 69(4):289-299 SHERMAN SL; JACOBS PA; MORTON NE; FROSTERISKENIUS U; HOWARDPEEBLES PN; et al. FURTHER SEGREGATION ANALYSIS OF THE FRAGILE-X SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES | 236 | 349 |
| 8 | 5 | 13 | 907 1991 SCIENCE 252(5013):1711-1714 KREMER EJ; PRITCHARD M; LYNCH M; YU S; HOLMAN K; et al. MAPPING OF DNA INSTABILITY AT THE FRAGILE-X TO A TRINUCLEOTIDE REPEAT SEQUENCE P(CCG)N | 218 | 584 |
| 9 | 20 | 36 | 1156 1993 NATURE GENETICS 4(4):335-340 DEVYS D; LUTZ Y; ROUYER N; BELLOCQ JP; MANDEL JL THE FMR-1 PROTEIN IS CYTOPLASMIC, MOST ABUNDANT IN NEURONS AND APPEARS NORMAL IN CARRIERS OF A FRAGILE X PREMUTATION | 201 | 294 |
| 10 | 11 | 12 | 1461 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 11 | 16 | 27 | 1150 1993 NATURE GENETICS 3(1):31-35 DEBOULLE K; VERKERK AJMH; REYNIERS E; VITS L; HENDRICKX J; et al. A POINT MUTATION IN THE FMR-1 GENE ASSOCIATED WITH FRAGILE-X MENTAL-RETARDATION | 145 | 270 |
| 12 | 15 | 56 | 1091 1993 CELL 74(2):291-298 SIOMI H; SIOMI MC; NUSSBAUM RL; DREYFUSS G THE PROTEIN PRODUCT OF THE FRAGILE-X GENE, FMR1, HAS CHARACTERISTICS OF AN RNA-BINDING PROTEIN | 141 | 334 |
| 13 | 30 | 38 | 1170 1994 AMERICAN JOURNAL OF HUMAN GENETICS 55(2):225-237 ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; MALMGREN H; et al. A MULTICENTER STUDY ON GENOTYPE-PHENOTYPE CORRELATIONS IN THE FRAGILE-X-SYNDROME, USING DIRECT DIAGNOSIS WITH PROBE STB-12.3 - THE FIRST 2,253 CASES | 129 | 172 |
| 14 | 9 | 34 | 845 1991 CELL 64(4):861-866 BELL MV; HIRST MC; NAKAHORI Y; MACKINNON RN; ROCHE A; et al. PHYSICAL MAPPING ACROSS THE FRAGILE-X - HYPERMETHYLATION AND CLINICAL EXPRESSION OF THE FRAGILE-X SYNDROME | 127 | 224 |
| 15 | 10 | 29 | 1705 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(10):5401-5404 Comery TA; Harris JB; Willems PJ; Oostra BA; Irwin SA; et al. Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits | 125 | 220 |
| 16 | 20 | 55 | 1122 1993 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 270(13):1569-1575 BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING XH; et al. RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST | 120 | 159 |
| 17 | 8 | 17 | 1149 1993 NATURE 363(6431):722-724 VERHEIJ C; BAKKER CE; DEGRAAFF E; KEULEMANS J; WILLEMSEN R; et al. CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME | 114 | 187 |
| 18 | 11 | 14 | 889 1991 NATURE 349(6310):624-626 VINCENT A; HEITZ D; PETIT C; KRETZ C; OBERLE I; et al. ABNORMAL PATTERN DETECTED IN FRAGILE-X PATIENTS BY PULSED-FIELD GEL-ELECTROPHORESIS | 112 | 165 |
| 19 | 20 | 33 | 1151 1993 NATURE GENETICS 3(1):36-43 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; et al. TISSUE SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE-X SYNDROME | 104 | 160 |
| 20 | 15 | 30 | 909 1992 AMERICAN JOURNAL OF HUMAN GENETICS 50(5):968-980 YU S; MULLEY J; LOESCH D; TURNER G; DONNELLY A; et al. FRAGILE-X SYNDROME - UNIQUE GENETICS OF THE HERITABLE UNSTABLE ELEMENT | 103 | 175 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 21 | 22 | 34 | 1073 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(6):1217-1228 SNOW K; DOUD LK; HAGERMAN R; PERGOLIZZI RG; ERSTER SH; et al. ANALYSIS OF A CGG SEQUENCE AT THE FMR-I LOCUS IN FRAGILE-X FAMILIES AND IN THE GENERAL-POPULATION | 102 | 140 |
| 22 | 18 | 58 | 1704 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(10):5395-5400 Weiler IJ; Irwin SA; Klintsova AY; Spencer CM; Brazelton AD; et al. Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation | 102 | 192 |
| 23 | 21 | 53 | 1228 1994 CELL 77(6):853-861 KUNST CB; WARREN ST CRYPTIC AND POLAR VARIATION OF THE FRAGILE-X REPEAT COULD RESULT IN PREDISPOSING NORMAL ALLELES | 101 | 244 |
| 24 | 1 | 6 | 408 1986 NEW ENGLAND JOURNAL OF MEDICINE 315(10):607-609 TURNER G; ROBINSON H; LAING S; PURVISSMITH S PREVENTIVE SCREENING FOR THE FRAGILE-X SYNDROME | 99 | 126 |
| 25 | 28 | 44 | 1154 1993 NATURE GENETICS 4(2):143-146 REYNIERS E; VITS L; DEBOULLE K; VANROY B; VANVELZEN D; et al. THE FULL MUTATION IN THE FMR-1 GENE OF MALE FRAGILE-X PATIENTS IS ABSENT IN THEIR SPERM | 96 | 170 |
| 26 | 23 | 52 | 1229 1994 CELL 78(1):23-33 BAKKER CE; VERHEIJ C; WILLEMSEN R; VANDERHELM R; OERLEMANS F; et al. FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION | 96 | 163 |
| 27 | 18 | 53 | 1543 1996 HUMAN MOLECULAR GENETICS 5(8):1083-1091 Eberhart DE; Malter HE; Feng Y; Warren ST The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals | 93 | 132 |
| 28 | 15 | 42 | 451 1987 GENETICS 117(3):587-599 LAIRD CD PROPOSED MECHANISM OF INHERITANCE AND EXPRESSION OF THE HUMAN FRAGILE-X SYNDROME OF MENTAL-RETARDATION | 92 | 167 |
| 29 | 10 | 39 | 838 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):289-294 HINTON VJ; BROWN WT; WISNIEWSKI K; RUDELLI RD ANALYSIS OF NEOCORTEX IN 3 MALES WITH THE FRAGILE-X SYNDROME | 92 | 134 |
| 30 | 23 | 41 | 1274 1994 NATURE GENETICS 8(1):88-94 EICHLER EE; HOLDEN JJA; POPOVICH BW; REISS AL; SNOW K; et al. LENGTH OF UNINTERRUPTED CGG REPEATS DETERMINES INSTABILITY IN THE FMR1 GENE | 92 | 243 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 31 | 26 | 47 | 1693 1997 MOLECULAR CELL 1(1):109-118 Feng Y; Absher D; Eberhart DE; Brown V; Malter HE; et al. FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association | 89 | 134 |
| 32 | 9 | 33 | 903 1991 SCIENCE 251(4998):1236-1239 HEITZ D; ROUSSEAU F; DEVYS D; SACCONE S; ABDERRAHIM H; et al. ISOLATION OF SEQUENCES THAT SPAN THE FRAGILE-X AND IDENTIFICATION OF A FRAGILE-X RELATED CPG ISLAND | 87 | 139 |
| 33 | 10 | 23 | 1018 1992 NATURE GENETICS 1(5):341-344 GEDEON AK; BAKER E; ROBINSON H; PARTINGTON MW; GROSS B; et al. FRAGILE-X SYNDROME WITHOUT CCG AMPLIFICATION HAS AN FMR1 DELETION | 87 | 138 |
| 34 | 34 | 42 | 1322 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 |
| 35 | 23 | 59 | 1689 1997 JOURNAL OF NEUROSCIENCE 17(5):1539-1547 Feng Y; Gutekunst CA; Eberhart DE; Yi H; Warren ST; et al. Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes | 85 | 145 |
| 36 | 23 | 34 | 1003 1992 JOURNAL OF MEDICAL GENETICS 29(11):794-801 HEITZ D; DEVYS D; IMBERT G; KRETZ C; MANDEL JL INHERITANCE OF THE FRAGILE-X SYNDROME - SIZE OF THE FRAGILE-X PREMUTATION IS A MAJOR DETERMINANT OF THE TRANSITION TO FULL MUTATION | 84 | 111 |
| 37 | 22 | 31 | 2156 2001 HUMAN MOLECULAR GENETICS 10(4):329-338 Laggerbauer B; Ostareck D; Keidel EM; Ostareck-Lederer A; Fischer U Evidence that fragile X mental retardation protein is a negative regulator of translation | 84 | 106 |
| 38 | 5 | 23 | 72 1982 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 12(3):303-308 BROWN WT; JENKINS EC; FRIEDMAN E; BROOKS J; WISNIEWSKI K; et al. AUTISM IS ASSOCIATED WITH THE FRAGILE-X SYNDROME | 82 | 124 |
| 39 | 12 | 32 | 249 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):709-717 PEMBREY ME; WINTER RM; DAVIES KE A PRE-MUTATION THAT GENERATES A DEFECT AT CROSSING OVER EXPLAINS THE INHERITANCE OF FRAGILE X MENTAL RETARDATION | 82 | 116 |
| 40 | 8 | 9 | 1421 1995 LANCET 345(8958):1147-1148 WILLEMSEN R; MOHKAMSING S; DEVRIES B; DEVYS D; VANDENOUWELAND A; et al. RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME | 81 | 101 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 41 | 30 | 48 | 1250 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):507-514 TAYLOR AK; SAFANDA JF; FALL MZ; QUINCE C; LANG KA; et al. MOLECULAR PREDICTORS OF COGNITIVE INVOLVEMENT IN FEMALE CARRIERS OF FRAGILE-X SYNDROME | 80 | 92 |
| 42 | 25 | 47 | 2134 2001 CELL 107(4):477-487 Brown V; Jin P; Ceman S; Darnell JC; O'Donnell WT; et al. Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome | 80 | 162 |
| 43 | 13 | 42 | 337 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):359-374 HAGERMAN RJ; JACKSON AW; LEVITAS A; RIMLAND B; BRADEN M AN ANALYSIS OF AUTISM IN 50 MALES WITH THE FRAGILE-X SYNDROME | 79 | 109 |
| 44 | 8 | 33 | 156 1983 NATURE 306(5944):701-704 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE OF FRAGILE X MENTAL-RETARDATION SYNDROME TO HEMOPHILIA-B AND TRANSMISSION THROUGH A NORMAL-MALE | 78 | 171 |
| 45 | 5 | 26 | 322 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):157-169 FRYNS JP THE FEMALE AND THE FRAGILE-X - A STUDY OF 144 OBLIGATE FEMALE CARRIERS | 78 | 103 |
| 46 | 8 | 20 | 1017 1992 NATURE GENETICS 1(4):257-260 RICHARDS RI; HOLMAN K; FRIEND K; KREMER E; HILLEN D; et al. EVIDENCE OF FOUNDER CHROMOSOMES IN FRAGILE-X SYNDROME | 78 | 158 |
| 47 | 7 | 52 | 238 1985 ACTA NEUROPATHOLOGICA 67(3-4):289-295 RUDELLI RD; BROWN WT; WISNIEWSKI K; JENKINS EC; LAUREKAMIONOWSKA M; et al. ADULT FRAGILE X-SYNDROME - CLINICO-NEUROPATHOLOGIC FINDINGS | 77 | 116 |
| 48 | 18 | 23 | 911 1992 AMERICAN JOURNAL OF HUMAN GENETICS 51(2):299-306 WOHRLE D; KOTZOT D; HIRST MC; MANCA A; KORN B; et al. A MICRODELETION OF LESS THAN 250 KB, INCLUDING THE PROXIMAL PART OF THE FMR-I GENE AND THE FRAGILE-X SITE, IN A MALE WITH THE CLINICAL PHENOTYPE OF FRAGILE-X SYNDROME | 77 | 122 |
| 49 | 16 | 36 | 1384 1995 EMBO JOURNAL 14(21):5358-5366 ZHANG Y; OCONNOR JP; SIOMI MC; SRINIVASAN S; DUTRA A; et al. THE FRAGILE-X MENTAL-RETARDATION SYNDROME PROTEIN INTERACTS WITH NOVEL HOMOLOGS FXR1 AND FXR2 | 77 | 121 |
| 50 | 10 | 32 | 1155 1993 NATURE GENETICS 4(3):244-251 ASHLEY CT; SUTCLIFFE JS; KUNST CB; LEINER HA; EICHLER EE; et al. HUMAN AND MURINE FMR-1 - ALTERNATIVE SPLICING AND TRANSLATIONAL INITIATION DOWNSTREAM OF THE CGG-REPEAT | 74 | 120 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 51 | 16 | 39 | 1227 1994 CELL 77(1):33-39 SIOMI H; CHOI MY; SIOMI MC; NUSSBAUM RL; DREYFUSS G ESSENTIAL ROLE FOR KH DOMAINS IN RNA-BINDING - IMPAIRED RNA-BINDING BY A MUTATION IN THE KH DOMAIN OF FMR1 THAT CAUSES FRAGILE-X SYNDROME | 74 | 266 |
| 52 | 42 | 81 | 1251 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):536-542 WARREN ST; NELSON DL ADVANCES IN MOLECULAR ANALYSIS OF FRAGILE-X SYNDROME | 74 | 129 |
| 53 | 17 | 85 | 2135 2001 CELL 107(4):489-499 Darnell JC; Jensen KB; Jin P; Brown V; Warren ST; et al. Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function | 74 | 149 |
| 54 | 23 | 47 | 1036 1993 AMERICAN JOURNAL OF HUMAN GENETICS 52(5):884-894 REISS AL; FREUND L; ABRAMS MT; BOEHM C; KAZAZIAN H NEUROBEHAVIORAL EFFECTS OF THE FRAGILE-X PREMUTATION IN ADULT WOMEN - A CONTROLLED-STUDY | 73 | 98 |
| 55 | 18 | 51 | 335 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):341-352 BROWN WT; JENKINS EC; COHEN IL; FISCH GS; WOLFSCHEIN EG; et al. FRAGILE-X AND AUTISM - A MULTICENTER SURVEY | 72 | 110 |
| 56 | 20 | 36 | 2190 2001 NUCLEIC ACIDS RESEARCH 29(11):2276-2283 Li ZZ; Zhang YY; Ku L; Wilkinson KD; Warren ST; et al. The fragile X mental retardation protein inhibits translation via interacting with mRNA | 72 | 93 |
| 57 | 14 | 37 | 1127 1993 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 14(5):328-335 MAZZOCCO MMM; PENNINGTON BF; HAGERMAN RJ THE NEUROCOGNITIVE PHENOTYPE OF FEMALE CARRIERS OF FRAGILE-X - ADDITIONAL EVIDENCE FOR SPECIFICITY | 71 | 90 |
| 58 | 4 | 11 | 397 1986 JOURNAL OF MEDICAL GENETICS 23(5):396-399 WEBB TP; BUNDEY S; THAKE A; TODD J THE FREQUENCY OF THE FRAGILE X-CHROMOSOME AMONG SCHOOLCHILDREN IN COVENTRY | 70 | 105 |
| 59 | 10 | 31 | 1564 1996 NATURE GENETICS 12(1):91-93 Khandjian EW; Corbin F; Woerly S; Rousseau F The fragile X mental retardation protein is associated with ribosomes | 70 | 101 |
| 60 | 13 | 38 | 1667 1997 HUMAN MOLECULAR GENETICS 6(9):1465-1472 Corbin F; Bouillon M; Fortin A; Morin S; Rousseau F; et al. The fragile X mental retardation protein is associated with poly(A)(+) mRNA in actively translating polyribosomes | 70 | 93 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 61 | 38 | 61 | 1174 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):298-308 HAGERMAN RJ; HULL CE; SAFANDA JF; CARPENTER I; STALEY LW; et al. HIGH FUNCTIONING FRAGILE-X MALES - DEMONSTRATION OF AN UNMETHYLATED FULLY EXPANDED FMR-1 MUTATION ASSOCIATED WITH PROTEIN EXPRESSION | 69 | 97 |
| 62 | 22 | 62 | 2147 2001 EMBO JOURNAL 20(17):4803-4813 Schaeffer C; Bardoni B; Mandel JL; Ehresmann B; Ehresmann C; et al. The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif | 66 | 97 |
| 63 | 38 | 118 | 365 1986 ANNUAL REVIEW OF GENETICS 20:109-145 NUSSBAUM RL; LEDBETTER DH FRAGILE-X SYNDROME - A UNIQUE MUTATION IN MAN | 65 | 112 |
| 64 | 11 | 20 | 880 1991 JOURNAL OF MEDICAL GENETICS 28(12):830-836 ROUSSEAU F; HEITZ D; OBERLE I; MANDEL JL SELECTION IN BLOOD-CELLS FROM FEMALE CARRIERS OF THE FRAGILE-X SYNDROME - INVERSE CORRELATION BETWEEN AGE AND PROPORTION OF ACTIVE X-CHROMOSOMES CARRYING THE FULL MUTATION | 64 | 86 |
| 65 | 23 | 41 | 1071 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(4):800-809 MCCONKIEROSELL A; LACHIEWICZ AM; SPIRIDIGLIOZZI GA; TARLETON J; SCHOENWALD S; et al. EVIDENCE THAT METHYLATION OF THE FMR-I LOCUS IS RESPONSIBLE FOR VARIABLE PHENOTYPIC-EXPRESSION OF THE FRAGILE-X SYNDROME | 64 | 99 |
| 66 | 19 | 23 | 1153 1993 NATURE GENETICS 4(2):140-142 WOHRLE D; HENNIG I; VOGEL W; STEINBACH P MITOTIC STABILITY OF FRAGILE-X MUTATIONS IN DIFFERENTIATED CELLS INDICATES EARLY POSTCONCEPTIONAL TRINUCLEOTIDE REPEAT EXPANSION | 64 | 122 |
| 67 | 18 | 29 | 1245 1994 HUMAN MOLECULAR GENETICS 3(9):1543-1551 SNOW K; TESTER DJ; KRUCKEBERG KE; SCHAID DJ; THIBODEAU SN SEQUENCE-ANALYSIS OF THE FRAGILE-X TRINUCLEOTIDE REPEAT - IMPLICATIONS FOR THE ORIGIN OF THE FRAGILE-X MUTATION | 64 | 115 |
| 68 | 5 | 10 | 878 1991 JOURNAL OF MEDICAL GENETICS 28(12):818-823 RICHARDS RI; HOLMAN K; KOZMAN H; KREMER E; LYNCH M; et al. FRAGILE-X SYNDROME - GENETIC LOCALIZATION BY LINKAGE MAPPING OF 2 MICROSATELLITE REPEATS FRAXAC1 AND FRAXAC2 WHICH IMMEDIATELY FLANK THE FRAGILE SITE | 63 | 102 |
| 69 | 6 | 11 | 893 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1720-1722 SUTHERLAND GR; GEDEON A; KORNMAN L; DONNELLY A; BYARD RW; et al. PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT DETECTION OF THE UNSTABLE DNA-SEQUENCE | 62 | 86 |
| 70 | 14 | 43 | 1383 1995 EMBO JOURNAL 14(11):2401-2408 SIOMI MC; SIOMI H; SAUER WH; SRINIVASAN S; NUSSBAUM RL; et al. FXR1, AN AUTOSOMAL HOMOLOG OF THE FRAGILE-X MENTAL-RETARDATION GENE | 62 | 102 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 71 | 22 | 40 | 1935 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 |
| 72 | 10 | 20 | 897 1991 NUCLEIC ACIDS RESEARCH 19(16):4355-4359 NAKAHORI Y; KNIGHT SJL; HOLLAND J; SCHWARTZ C; ROCHE A; et al. MOLECULAR HETEROGENEITY OF THE FRAGILE-X SYNDROME | 61 | 91 |
| 73 | 10 | 15 | 941 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):208-216 DEVYS D; BIANCALANA V; ROUSSEAU F; BOUE J; MANDEL JL; et al. ANALYSIS OF FULL FRAGILE-X MUTATIONS IN FETAL TISSUES AND MONOZYGOTIC TWINS INDICATE THAT ABNORMAL METHYLATION AND SOMATIC HETEROGENEITY ARE ESTABLISHED EARLY IN DEVELOPMENT | 61 | 92 |
| 74 | 4 | 31 | 840 1991 ANNALS OF NEUROLOGY 29(1):26-32 REISS AL; AYLWARD E; FREUND LS; JOSHI PK; BRYAN RN NEUROANATOMY OF FRAGILE-X-SYNDROME - THE POSTERIOR-FOSSA | 60 | 114 |
| 75 | 46 | 64 | 1858 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):250-261 Tassone F; Hagerman RJ; Ikle DN; Dyer PN; Lampe M; et al. FMRP expression as a potential prognostic indicator in fragile X syndrome | 60 | 67 |
| 76 | 7 | 32 | 564 1988 ARCHIVES OF GENERAL PSYCHIATRY 45(1):25-30 REISS AL; HAGERMAN RJ; VINOGRADOV S; ABRAMS M; KING RJ PSYCHIATRIC DISABILITY IN FEMALE CARRIERS OF THE FRAGILE X-CHROMOSOME | 59 | 93 |
| 77 | 13 | 27 | 523 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):191-200 KEMPER MB; HAGERMAN RJ; ALTSHULSTARK D COGNITIVE PROFILES OF BOYS WITH THE FRAGILE-X SYNDROME | 58 | 77 |
| 78 | 21 | 31 | 1021 1992 PEDIATRICS 89(3):395-400 HAGERMAN RJ; JACKSON C; AMIRI K; SILVERMAN AC; OCONNOR R; et al. GIRLS WITH FRAGILE-X SYNDROME - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 58 | 81 |
| 79 | 13 | 23 | 1035 1993 AMERICAN JOURNAL OF HUMAN GENETICS 52(2):297-304 OUDET C; MORNET E; SERRE JL; THOMAS F; LENTESZENGERLING S; et al. LINKAGE DISEQUILIBRIUM BETWEEN THE FRAGILE-X MUTATION AND 2 CLOSELY LINKED CA REPEATS SUGGESTS THAT FRAGILE-X CHROMOSOMES ARE DERIVED FROM A SMALL NUMBER OF FOUNDER CHROMOSOMES | 58 | 112 |
| 80 | 20 | 37 | 1161 1993 PEDIATRICS 91(2):321-329 FREUND LS; REISS AL; ABRAMS MT PSYCHIATRIC-DISORDERS ASSOCIATED WITH FRAGILE-X IN THE YOUNG FEMALE | 58 | 80 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 81 | 17 | 57 | 1563 1996 MOLECULAR AND CELLULAR BIOLOGY 16(7):3825-3832 Siomi MC; Zhang Y; Siomi H; Dreyfuss G Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them | 58 | 109 |
| 82 | 22 | 42 | 1695 1997 NATURE GENETICS 15(2):165-169 Malter HE; Iber JC; Willemsen R; deGraaff E; Tarleton JC; et al. Characterization of the full fragile X syndrome mutation in fetal gametes | 58 | 89 |
| 83 | 0 | 3 | 194 1984 CLINICAL GENETICS 25(2):131-134 FRYNS JP; JACOBS J; KLECZKOWSKA A; VANDENBERGHE H THE PSYCHOLOGICAL PROFILE OF THE FRAGILE X-SYNDROME | 57 | 75 |
| 84 | 20 | 37 | 2137 2001 CELL 107(5):591-603 Zhang YQ; Bailey AM; Matthies HJG; Renden RB; Smith MA; et al. Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function | 57 | 98 |
| 85 | 1 | 4 | 31 1981 LANCET 2(8258):1292-1292 JENKINS EC; BROWN WT; DUNCAN CJ; BROOKS J; BENYISHAY M; et al. FEASIBILITY OF FRAGILE X-CHROMOSOME PRENATAL-DIAGNOSIS DEMONSTRATED | 56 | 77 |
| 86 | 8 | 32 | 108 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):699-712 CHUDLEY AE; KNOLL J; GERRARD JW; SHEPEL L; MCGAHEY E; et al. FRAGILE (X) X-LINKED MENTAL-RETARDATION .1. RELATIONSHIP BETWEEN AGE AND INTELLIGENCE AND THE FREQUENCY OF EXPRESSION OF FRAGILE (X)(Q28) | 56 | 80 |
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| 88 | 27 | 46 | 1246 1994 HUMAN MOLECULAR GENETICS 3(9):1553-1560 HIRST MC; GREWAL PK; DAVIES KE PRECURSOR ARRAYS FOR TRIPLET REPEAT EXPANSION AT THE FRAGILE-X LOCUS | 56 | 108 |
| 89 | 9 | 24 | 241 1985 AMERICAN JOURNAL OF DISEASES OF CHILDREN 139(7):674-678 HAGERMAN R; KEMPER M; HUDSON M LEARNING-DISABILITIES AND ATTENTIONAL PROBLEMS IN BOYS WITH THE FRAGILE X-SYNDROME | 55 | 72 |
| 90 | 12 | 22 | 916 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):35-46 REISS AL; FREUND L BEHAVIORAL-PHENOTYPE OF FRAGILE-X SYNDROME - DSM-III-R AUTISTIC BEHAVIOR IN MALE-CHILDREN | 55 | 74 |
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| 96 | 32 | 85 | 482 1987 JOURNAL OF PEDIATRICS 110(6):821-831 CHUDLEY AE; HAGERMAN RJ FRAGILE-X SYNDROME | 53 | 80 |
| 97 | 0 | 0 | 28 1981 LANCET 1(8223):780-780 DAKER MG; CHIDIAC P; FEAR CN; BERRY AC FRAGILE X IN A NORMAL-MALE - A CAUTIONARY TALE | 52 | 84 |
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| 103 | 7 | 17 | 1024 1992 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 89(9):4215-4217 MORTON NE; MACPHERSON JN POPULATION-GENETICS OF THE FRAGILE-X SYNDROME - MULTIALLELIC MODEL FOR THE FMR1 LOCUS | 51 | 79 |
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| 108 | 2 | 35 | 39 1982 AMERICAN JOURNAL OF DISEASES OF CHILDREN 136(5):392-398 CARPENTER NJ; LEICHTMAN LG; SAY B FRAGILE X-LINKED MENTAL-RETARDATION - A SURVEY OF 65 PATIENTS WITH MENTAL-RETARDATION OF UNKNOWN ORIGIN | 49 | 65 |
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| 114 | 8 | 10 | 1007 1992 LANCET 339(8788):271-272 PERGOLIZZI RG; ERSTER SH; GOONEWARDENA P; BROWN WT DETECTION OF FULL FRAGILE-X MUTATION | 48 | 69 |
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| 120 | 12 | 21 | 793 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):283-287 HAGERMAN RJ; AMIRI K; CRONISTER A FRAGILE-X CHECKLIST | 47 | 64 |
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| 121 | 10 | 30 | 1006 1992 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 31(6):1141-1148 MAZZOCCO MMM; HAGERMAN RJ; CRONISTERSILVERMAN A; PENNINGTON BF SPECIFIC FRONTAL-LOBE DEFICITS AMONG WOMEN WITH THE FRAGILE-X GENE | 47 | 62 |
| 122 | 21 | 64 | 197 1984 CLINICAL GENETICS 26(6):497-528 FRYNS JP THE FRAGILE X-SYNDROME - A STUDY OF 83 FAMILIES | 45 | 78 |
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| 126 | 0 | 29 | 71 1982 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 12(3):295-301 MERYASH DL; SZYMANSKI LS; GERALD PS INFANTILE-AUTISM ASSOCIATED WITH THE FRAGILE-X SYNDROME | 44 | 71 |
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| 132 | 3 | 15 | 132 1983 CLINICAL GENETICS 24(6):393-398 BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G; NORDENSON I; PALSSONSTRAE U FRAGILE X-SYNDROME IN MILDLY MENTALLY-RETARDED CHILDREN IN A NORTHERN SWEDISH COUNTY - A PREVALENCE STUDY | 43 | 68 |
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| 179 | 6 | 24 | 721 1990 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 29(2):214-219 HODAPP RM; DYKENS EM; HAGERMAN RJ; SCHREINER R; LACHIEWICZ AM; et al. DEVELOPMENTAL IMPLICATIONS OF CHANGING TRAJECTORIES OF IQ IN MALES WITH FRAGILE-X SYNDROME | 32 | 45 |
| 180 | 11 | 16 | 1118 1993 HUMAN MOLECULAR GENETICS 2(11):1973-1974 TARLETON J; RICHIE R; SCHWARTZ C; RAO K; AYLSWORTH AS; et al. AN EXTENSIVE DE-NOVO DELETION REMOVING FMR1 IN A PATIENT WITH MENTAL-RETARDATION AND THE FRAGILE X-SYNDROME PHENOTYPE | 32 | 51 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 181 | 30 | 49 | 1540 1996 HUMAN MOLECULAR GENETICS 5(3):319-330 Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; et al. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome | 32 | 51 |
| 182 | 140 | 197 | 1779 1998 JOURNAL OF MEDICAL GENETICS 35(7):579-589 de Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF The fragile X syndrome | 32 | 52 |
| 183 | 16 | 54 | 1828 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 |
| 184 | 12 | 23 | 406 1986 NATURE 324(6093):161-163 LEDBETTER DH; LEDBETTER SA; NUSSBAUM RL IMPLICATIONS OF FRAGILE-X EXPRESSION IN NORMAL MALES FOR THE NATURE OF THE MUTATION | 31 | 56 |
| 185 | 21 | 44 | 623 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):187-193 EINFELD S; MOLONY H; HALL W AUTISM IS NOT ASSOCIATED WITH THE FRAGILE-X SYNDROME | 31 | 53 |
| 186 | 2 | 33 | 652 1989 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 30(6):845-856 COHEN IL; VIETZE PM; SUDHALTER V; JENKINS EC; BROWN WT PARENT CHILD DYADIC GAZE PATTERNS IN FRAGILE-X MALES AND IN NON-FRAGILE-X MALES WITH AUTISTIC DISORDER | 31 | 49 |
| 187 | 4 | 22 | 670 1989 SCIENCE 246(4935):1298-1300 SUTHERS GK; CALLEN DF; HYLAND VJ; KOZMAN HM; BAKER E; et al. A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 31 | 66 |
| 188 | 4 | 23 | 813 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):400-403 JACKY PB; AHUJA YR; ANYANEYEBOA K; BREG WR; CARPENTER NJ; et al. GUIDELINES FOR THE PREPARATION AND ANALYSIS OF THE FRAGILE-X CHROMOSOME IN LYMPHOCYTES | 31 | 44 |
| 189 | 6 | 20 | 1112 1993 HUMAN GENETICS 92(5):431-436 ARINAMI T; ASANO M; KOBAYASHI K; YANAGI H; HAMAGUCHI H DATA ON THE CGG REPEAT AT THE FRAGILE X-SITE IN THE NONRETARDED JAPANESE POPULATION AND FAMILY SUGGEST THE PRESENCE OF A SUBGROUP OF NORMAL ALLELES PREDISPOSING TO MUTATE | 31 | 42 |
| 190 | 26 | 49 | 1396 1995 HUMAN MOLECULAR GENETICS 4(1):45-49 DEGRAAFF E; ROUILLARD P; WILLEMS PJ; SMITS APT; ROUSSEAU F; et al. HOTSPOT FOR DELETIONS IN THE CGG REPEAT REGION OF FMR1 IN FRAGILE-X PATIENTS | 31 | 46 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 191 | 18 | 29 | 1485 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 |
| 192 | 13 | 20 | 1552 1996 JOURNAL OF MEDICAL GENETICS 33(12):1007-1010 deVries BBA; Jansen CCAM; Duits AA; Verheij C; Willemsen R; et al. Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family | 31 | 38 |
| 193 | 17 | 28 | 1762 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):499-508 Bailey DB; Mesibov GB; Hatton DD; Clark RD; Roberts JE; et al. Autistic behavior in young boys with fragile X syndrome | 31 | 40 |
| 194 | 6 | 35 | 1825 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 |
| 195 | 60 | 93 | 2259 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):284-293 Bardoni B; Mandel JL Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes | 31 | 39 |
| 196 | 4 | 12 | 339 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):393-401 REISS AL; FEINSTEIN C; TOOMEY KE; GOLDSMITH B; ROSENBAUM K; et al. PSYCHIATRIC DISABILITY ASSOCIATED WITH THE FRAGILE-X CHROMOSOME | 30 | 45 |
| 197 | 12 | 37 | 497 1987 SCIENCE 237(4813):420-423 WARREN ST; ZHANG FP; LICAMELI GR; PETERS JF THE FRAGILE-X SITE IN SOMATIC-CELL HYBRIDS - AN APPROACH FOR MOLECULAR-CLONING OF FRAGILE SITES | 30 | 71 |
| 198 | 5 | 23 | 701 1990 CLINICAL GENETICS 37(3):167-172 SUTHERLAND GR; BAKER E THE COMMON FRAGILE SITE IN BAND Q27 OF THE HUMAN X-CHROMOSOME IS NOT COINCIDENT WITH THE FRAGILE-X | 30 | 43 |
| 199 | 16 | 33 | 742 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(3):460-467 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; et al. GENETIC-MAPPING OF NEW DNA PROBES AT XQ27 DEFINES A STRATEGY FOR DNA STUDIES IN THE FRAGILE-X SYNDROME | 30 | 47 |
| 200 | 16 | 19 | 940 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):197-207 ROUSSEAU F; HEITZ D; BIANCALANA V; OBERLE I; MANDEL JL ON SOME TECHNICAL ASPECTS OF DIRECT DNA DIAGNOSIS OF THE FRAGILE-X SYNDROME | 30 | 48 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 201 | 17 | 44 | 1186 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):378-385 SOBESKY WE; PENNINGTON BF; PORTER D; HULL CE; HAGERMAN RJ EMOTIONAL AND NEUROCOGNITIVE DEFICITS IN FRAGILE-X | 30 | 34 |
| 202 | 13 | 23 | 1719 1998 AMERICAN JOURNAL ON MENTAL RETARDATION 103(1):29-39 Bailey DB; Hatton DD; Skinner M Early developmental trajectories of males with fragile X syndrome | 30 | 32 |
| 203 | 28 | 47 | 1830 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 |
| 204 | 20 | 50 | 1899 1999 HUMAN MOLECULAR GENETICS 8(5):863-869 Tamanini F; Bontekoe C; Bakker CE; van Unen L; Anar B; et al. Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations | 30 | 39 |
| 205 | 5 | 21 | 474 1987 JOURNAL OF MEDICAL GENETICS 24(1):32-38 VEENEMA H; VEENEMA T; GERAEDTS JPM THE FRAGILE X-SYNDROME IN A LARGE FAMILY .2. PSYCHOLOGICAL INVESTIGATIONS | 29 | 40 |
| 206 | 30 | 58 | 625 1989 AMERICAN JOURNAL OF ORTHOPSYCHIATRY 59(1):142-152 HAGERMAN RJ; SOBESKY WE PSYCHOPATHOLOGY IN FRAGILE-X-SYNDROME | 29 | 41 |
| 207 | 18 | 37 | 678 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):175-180 BROWN WT INVITED EDITORIAL - THE FRAGILE-X - PROGRESS TOWARD SOLVING THE PUZZLE | 29 | 41 |
| 208 | 5 | 9 | 885 1991 LANCET 338(8772):956-957 HIRST M; KNIGHT S; DAVIES K; CROSS G; OCRAFT K; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 29 | 35 |
| 209 | 29 | 36 | 1034 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1236-1241 HULL C; HAGERMAN RJ A STUDY OF THE PHYSICAL, BEHAVIORAL, AND MEDICAL PHENOTYPE, INCLUDING ANTHROPOMETRIC MEASURES, OF FEMALES WITH FRAGILE-X SYNDROME | 29 | 39 |
| 210 | 16 | 21 | 1204 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):482-485 VANDENOUWELAND AMW; DEVRIES BBA; BAKKER PLG; DEELEN WH; DEGRAAFF E; et al. DNA DIAGNOSIS OF THE FRAGILE-X-SYNDROME IN A SERIES OF 236 MENTALLY-RETARDED SUBJECTS AND EVIDENCE FOR A REVERSAL OF MUTATION IN THE FMR-1 GENE | 29 | 35 |
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| 211 | 24 | 29 | 1569 1996 PEDIATRICS 97(1):122-126 Hagerman RJ; Staley LW; OConner R; Lugenbeel K; Nelson D; et al. Learning-disabled males with a fragile X CGG expansion in the upper premutation size range | 29 | 40 |
| 212 | 28 | 40 | 1981 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):195-203 Tassone F; Hagerman RJ; Chamberlain WD; Hagerman PJ Transcription of the FMR1 gene in individuals with fragile X syndrome | 29 | 34 |
| 213 | 0 | 19 | 16 1981 CLINICAL GENETICS 19(2):101-110 GUSTAVSON KH; HOLMGREN G; BLOMQUIST HK; MIKKELSEN M; NORDENSON I; et al. FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 2 SWEDISH FAMILIES | 28 | 42 |
| 214 | 16 | 49 | 519 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):123-142 PROUTY LA; ROGERS RC; STEVENSON RE; DEAN JH; PALMER KK; et al. FRAGILE-X SYNDROME - GROWTH, DEVELOPMENT, AND INTELLECTUAL FUNCTION | 28 | 36 |
| 215 | 10 | 36 | 525 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):213-225 WOLFF PH; GARDNER J; LAPPEN J; PACCIA J; MERYASH D VARIABLE EXPRESSION OF THE FRAGILE-X SYNDROME IN HETEROZYGOUS FEMALES OF NORMAL INTELLIGENCE | 28 | 35 |
| 216 | 8 | 19 | 665 1989 PEDIATRICS 83(4):547-552 SIMKO A; HORNSTEIN L; SOUKUP S; BAGAMERY N FRAGILE X-SYNDROME - RECOGNITION IN YOUNG-CHILDREN | 28 | 31 |
| 217 | 19 | 66 | 675 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):696-719 LAIRD CD; LAMB MM; THORNE JL 2 PROGENITOR CELLS FOR HUMAN OOGONIA INFERRED FROM PEDIGREE DATA AND THE X-INACTIVATION IMPRINTING MODEL OF THE FRAGILE-X SYNDROME | 28 | 34 |
| 218 | 5 | 10 | 849 1991 CLINICAL GENETICS 39(5):347-354 BUTLER MG; MANGRUM T; GUPTA R; SINGH DN A 15-ITEM CHECKLIST FOR SCREENING MENTALLY-RETARDED MALES FOR THE FRAGILE X-SYNDROME | 28 | 32 |
| 219 | 14 | 20 | 1000 1992 JOURNAL OF MEDICAL GENETICS 29(6):368-374 MULLEY JC; YU S; GEDEON AK; DONNELLY A; TURNER G; et al. EXPERIENCE WITH DIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X | 28 | 39 |
| 220 | 18 | 52 | 1090 1993 CELL 73(7):1403-1409 HANSEN RS; CANFIELD TK; LAMB MM; GARTLER SM; LAIRD CD ASSOCIATION OF FRAGILE-X SYNDROME WITH DELAYED REPLICATION OF THE FMR1 GENE | 28 | 127 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 221 | 19 | 41 | 1221 1994 AMERICAN JOURNAL ON MENTAL RETARDATION 98(5):567-579 LACHIEWICZ AM; SPIRIDIGLIOZZI GA; GULLION CM; RANSFORD SN; RAO K ABERRANT BEHAVIORS OF YOUNG BOYS WITH FRAGILE X-SYNDROME | 28 | 33 |
| 222 | 19 | 65 | 1286 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 |
| 223 | 17 | 29 | 1681 1997 JOURNAL OF MEDICAL GENETICS 34(1):1-5 Morton JE; Bundey S; Webb TP; MacDonald F; Rindl PM; et al. Fragile X syndrome is less common than previously estimated | 28 | 47 |
| 224 | 20 | 52 | 2332 2002 NEURON 34(6):961-972 Morales J; Hiesinger PR; Schroeder AJ; Kume K; Verstreken P; et al. Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain | 28 | 37 |
| 225 | 0 | 11 | 147 1983 JOURNAL OF MEDICAL GENETICS 20(4):280-285 HARRISON CJ; JACK EM; ALLEN TD; HARRIS R THE FRAGILE X - A SCANNING ELECTRON-MICROSCOPE STUDY | 27 | 54 |
| 226 | 9 | 47 | 258 1985 ANNALS OF NEUROLOGY 18(6):665-669 WISNIEWSKI KE; FRENCH JH; FERNANDO S; BROWN WT; JENKINS EC; et al. FRAGILE X-SYNDROME - ASSOCIATED NEUROLOGICAL ABNORMALITIES AND DEVELOPMENTAL-DISABILITIES | 27 | 43 |
| 227 | 11 | 17 | 879 1991 JOURNAL OF MEDICAL GENETICS 28(12):824-829 HIRST MC; NAKAHORI Y; KNIGHT SJL; SCHWARTZ C; THIBODEAU SN; et al. GENOTYPE PREDICTION IN THE FRAGILE-X SYNDROME | 27 | 36 |
| 228 | 15 | 30 | 973 1992 ARCHIVES OF GENERAL PSYCHIATRY 49(1):54-60 FREUND LS; REISS AL; HAGERMAN R; VINOGRADOV S CHROMOSOME FRAGILITY AND PSYCHOPATHOLOGY IN OBLIGATE FEMALE CARRIERS OF THE FRAGILE X-CHROMOSOME | 27 | 47 |
| 229 | 7 | 26 | 1123 1993 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 23(1):135-145 DYKENS EM; HODAPP RM; ORT SI; LECKMAN JF TRAJECTORY OF ADAPTIVE-BEHAVIOR IN MALES WITH FRAGILE X-SYNDROME | 27 | 37 |
| 230 | 10 | 13 | 1131 1993 JOURNAL OF MEDICAL GENETICS 30(2):94-96 SMITS APT; DREESEN JCFM; POST JG; SMEETS DFCM; DEDIESMULDERS C; et al. THE FRAGILE-X SYNDROME - NO EVIDENCE FOR ANY RECENT MUTATIONS | 27 | 35 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 231 | 15 | 41 | 1487 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 |
| 232 | 6 | 30 | 1929 1999 NATURE GENETICS 22(1):98-101 Coffee B; Zhang FP; Warren ST; Reines D Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells | 27 | 102 |
| 233 | 11 | 33 | 1989 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(3):973-980 Sung YJ; Conti J; Currie JR; Brown WT; Denman RB RNAs that interact with the Fragile X syndrome RNA binding protein FMRP | 27 | 35 |
| 234 | 19 | 36 | 2195 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98(15):8844-8849 Schenck A; Bardoni B; Moro A; Bagni C; Mandel JL A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P | 27 | 51 |
| 235 | 15 | 79 | 2282 2002 GENES & DEVELOPMENT 16(19):2497-2508 Ishizuka A; Siomi MC; Siomi H A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins | 27 | 91 |
| 236 | 2 | 3 | 67 1982 HUMAN GENETICS 61(3):262-263 FRYNS JP; VANDENBERGHE H TRANSMISSION OF FRAGILE (X)(Q27) FROM NORMAL MALE(S) | 26 | 36 |
| 237 | 2 | 16 | 175 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):159-174 MERYASH DL; CRONK CE; SACHS B; GERALD PS AN ANTHROPOMETRIC STUDY OF MALES WITH THE FRAGILE-X SYNDROME | 26 | 43 |
| 238 | 9 | 34 | 282 1985 EUROPEAN JOURNAL OF PEDIATRICS 143(4):269-275 LARGO RH; SCHINZEL A DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN 13 BOYS WITH FRAGILE X-SYNDROME | 26 | 37 |
| 239 | 5 | 17 | 314 1985 TRENDS IN GENETICS 1(4):108-112 SUTHERLAND GR THE ENIGMA OF THE FRAGILE-X CHROMOSOME | 26 | 43 |
| 240 | 4 | 17 | 425 1987 AMERICAN JOURNAL OF MENTAL DEFICIENCY 92(2):234-236 DYKENS EM; HODAPP RM; LECKMAN JF STRENGTHS AND WEAKNESSES IN THE INTELLECTUAL-FUNCTIONING OF MALES WITH FRAGILE-X SYNDROME | 26 | 47 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 241 | 9 | 24 | 617 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(5):697-705 REISS AL; FREUND L; VINOGRADOV S; HAGERMAN R; CRONISTER A PARENTAL INHERITANCE AND PSYCHOLOGICAL DISABILITY IN FRAGILE-X FEMALES | 26 | 31 |
| 242 | 11 | 24 | 627 1989 AMERICAN JOURNAL ON MENTAL RETARDATION 93(4):406-411 WOLFF PH; GARDNER J; PACCIA J; LAPPEN J THE GREETING BEHAVIOR OF FRAGILE X-MALES | 26 | 39 |
| 243 | 6 | 38 | 680 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):187-195 SUTHERS GK; HYLAND VJ; CALLEN DF; OBERLE I; ROCCHI M; et al. PHYSICAL MAPPING OF NEW DNA PROBES NEAR THE FRAGILE-X MUTATION (FRAXA) BY USING A PANEL OF CELL-LINES | 26 | 64 |
| 244 | 36 | 54 | 1288 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 |
| 245 | 71 | 125 | 1335 1995 ANNUAL REVIEW OF NEUROSCIENCE 18:77-99 WARREN ST; ASHLEY CT TRIPLET REPEAT EXPANSION MUTATIONS - THE EXAMPLE OF FRAGILE-X SYNDROME | 26 | 58 |
| 246 | 3 | 7 | 1490 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 |
| 247 | 20 | 32 | 2006 2000 EPILEPSIA 41(1):19-23 Musumeci SA; Bosco P; Calabrese G; Bakker C; De Sarro GB; et al. Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome | 26 | 35 |
| 248 | 10 | 43 | 2281 2002 GENES & DEVELOPMENT 16(19):2491-2496 Caudy AA; Myers M; Hannon GJ; Hammond SM Fragile X-related protein and VIG associate with the RNA interference machinery | 26 | 109 |
| 249 | 19 | 36 | 2349 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(4):869-878 Jacquemont S; Hagerman RJ; Leehey M; Grigsby J; Zhang L; et al. Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates | 26 | 44 |
| 250 | 2 | 13 | 89 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):861-868 UCHIDA IA; FREEMAN VCP; JAMRO H; PARTINGTON MW; SOLTAN HC ADDITIONAL EVIDENCE FOR FRAGILE-X ACTIVITY IN HETEROZYGOUS CARRIERS | 25 | 33 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 251 | 4 | 16 | 173 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):111-121 HAGERMAN RJ; VANHOUSEN K; SMITH ACM; MCGAVRAN L CONSIDERATION OF CONNECTIVE-TISSUE DYSFUNCTION IN THE FRAGILE-X SYNDROME | 25 | 35 |
| 252 | 4 | 14 | 390 1986 HUMAN GENETICS 73(4):309-312 ARINAMI T; KONDO I; NAKAJIMA S FREQUENCY OF THE FRAGILE X-SYNDROME IN JAPANESE MENTALLY-RETARDED MALES | 25 | 30 |
| 253 | 6 | 45 | 401 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:129-148 MADISON LS; GEORGE C; MOESCHLER JB COGNITIVE-FUNCTIONING IN THE FRAGILE-X SYNDROME - A STUDY OF INTELLECTUAL, MEMORY AND COMMUNICATION-SKILLS | 25 | 31 |
| 254 | 12 | 44 | 533 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):377-392 HAGERMAN RJ; MURPHY MA; WITTENBERGER MD A CONTROLLED TRIAL OF STIMULANT MEDICATION IN CHILDREN WITH THE FRAGILE-X SYNDROME | 25 | 51 |
| 255 | 7 | 17 | 740 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(1):108-116 ROUSSEAU F; VINCENT A; RIVELLA S; HEITZ D; TRIBOLI C; et al. 4 CHROMOSOMAL BREAKPOINTS AND 4 NEW PROBES MARK OUT A 10-CM REGION ENCOMPASSING THE FRAGILE-X LOCUS (FRAXA) | 25 | 48 |
| 256 | 1 | 1 | 790 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):256-259 LAING S; PARTINGTON M; ROBINSON H; TURNER G CLINICAL SCREENING SCORE FOR THE FRAGILE-X (MARTIN-BELL) SYNDROME | 25 | 29 |
| 257 | 83 | 119 | 974 1992 BRITISH JOURNAL OF PSYCHIATRY 160:24-35 TURK J THE FRAGILE-X SYNDROME - ON THE WAY TO A BEHAVIORAL-PHENOTYPE | 25 | 46 |
| 258 | 10 | 23 | 1022 1992 PEDIATRICS 89(6):1059-1062 BUTLER MG; BRUNSCHWIG A; MILLER LK; HAGERMAN RJ STANDARDS FOR SELECTED ANTHROPOMETRIC MEASUREMENTS IN MALES WITH THE FRAGILE X-SYNDROME | 25 | 29 |
| 259 | 9 | 24 | 1188 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):392-399 LOESCH DZ; HAY DA; MULLEY J TRANSMITTING MALES AND CARRIER FEMALES IN FRAGILE-X - REVISITED | 25 | 34 |
| 260 | 4 | 11 | 1212 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):522-526 CHONG SS; EICHLER EE; NELSON DL; HUGHES MR ROBUST AMPLIFICATION AND ETHIDIUM-VISIBLE DETECTION OF THE FRAGILE-X-SYNDROME CGG REPEAT USING PFU POLYMERASE | 25 | 42 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 261 | 11 | 37 | 1267 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(2):256-264 DORN MB; MAZZOCCO MMM; HAGERMAN RJ BEHAVIORAL AND PSYCHIATRIC-DISORDERS IN ADULT MALE CARRIERS OF FRAGILE-X | 25 | 33 |
| 262 | 10 | 20 | 1468 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 |
| 263 | 13 | 37 | 1469 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 |
| 264 | 13 | 24 | 1510 1996 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 225(1):27-33 Willemsen R; Bontekoe C; Tamanini F; Galjaard H; Hoogeveen A; et al. Association of FMRP with ribosomal precursor particles in the nucleolus | 25 | 30 |
| 265 | 1 | 20 | 51 1982 AMERICAN JOURNAL OF MEDICAL GENETICS 13(2):139-148 BROOKWELL R; DANIEL A; TURNER G; FISHBURN J THE FRAGILE X(Q27) FORM OF X-LINKED MENTAL-RETARDATION - FUDR AS AN INDUCING AGENT FOR FRA(X)(Q27) EXPRESSION IN LYMPHOCYTES, FIBROBLASTS, AND AMNIOCYTES | 24 | 49 |
| 266 | 4 | 16 | 180 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):241-252 SOUDEK D; PARTINGTON MW; LAWSON JS THE FRAGILE-X SYNDROME .1. FAMILIAL VARIATION IN THE PROPORTION OF LYMPHOCYTES WITH THE FRAGILE SITE IN MALES | 24 | 29 |
| 267 | 56 | 112 | 483 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):463-471 BREGMAN JD; DYKENS E; WATSON M; ORT SI; LECKMAN JF FRAGILE-X SYNDROME - VARIABILITY OF PHENOTYPIC-EXPRESSION | 24 | 41 |
| 268 | 7 | 30 | 684 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 35(1):28-35 GRIGSBY JP; KEMPER MB; HAGERMAN RJ; MYERS CS NEUROPSYCHOLOGICAL DYSFUNCTION AMONG AFFECTED HETEROZYGOUS FRAGILE-X FEMALES | 24 | 29 |
| 269 | 3 | 18 | 738 1990 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 87(10):3856-3860 WARREN ST; KNIGHT SJL; PETERS JF; STAYTON CL; CONSALEZ GG; et al. ISOLATION OF THE HUMAN CHROMOSOMAL BAND XQ28 WITHIN SOMATIC-CELL HYBRIDS BY FRAGILE X-SITE BREAKAGE | 24 | 69 |
| 270 | 1 | 14 | 922 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):78-86 MAZZOCCO MMM; HAGERMAN RJ; PENNINGTON BF PROBLEM-SOLVING LIMITATIONS AMONG CYTOGENETICALLY EXPRESSING FRAGILE-X WOMEN | 24 | 32 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 271 | 14 | 29 | 1753 1998 HUMAN MOLECULAR GENETICS 7(13):2121-2128 Khandjian EW; Bardoni B; Corbin F; Sittler A; Giroux S; et al. Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis | 24 | 33 |
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| 285 | 4 | 12 | 148 1983 JOURNAL OF MEDICAL GENETICS 20(4):286-289 VANROY BC; DESMEDT MC; RAES RA; DUMON JE; LEROY JG FRAGILE X TRAIT IN A LARGE KINDRED - TRANSMISSION ALSO THROUGH NORMAL MALES | 22 | 32 |
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| 287 | 7 | 26 | 259 1985 ARCHIVES OF DISEASE IN CHILDHOOD 60(11):1001-1007 THAKE A; TODD J; BUNDEY S; WEBB T IS IT POSSIBLE TO MAKE A CLINICAL-DIAGNOSIS OF THE FRAGILE X-SYNDROME IN A BOY | 22 | 28 |
| 288 | 12 | 30 | 500 1988 AMERICAN JOURNAL OF HUMAN GENETICS 42(2):380-389 ARVEILER B; OBERLE I; VINCENT A; HOFKER MH; PEARSON PL; et al. GENETIC-MAPPING OF THE XQ27-Q28 REGION - NEW RFLP MARKERS USEFUL FOR DIAGNOSTIC APPLICATIONS IN FRAGILE-X AND HEMOPHILIA-B FAMILIES | 22 | 61 |
| 289 | 28 | 73 | 696 1990 BIOLOGICAL PSYCHIATRY 27(2):223-240 REISS AL; FREUND L FRAGILE X-SYNDROME | 22 | 28 |
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| 291 | 4 | 6 | 886 1991 LANCET 338(8772):957-958 DOBKIN CS; DING XH; JENKINS EC; KRAWCZUN MS; BROWN WT; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 22 | 24 |
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