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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by NCR.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 501 | 11 | 35 | 2107 2002 ARCHIVES OF MEDICAL RESEARCH 33(2):128-135 Wang TS; Hsieh LJ; Hsu TY; Chung CH; Li SY DNA damage and repair in lymphoblastoid cell lines from normal donors and fragile X syndrome patients | 0 | 1 |
| 502 | 16 | 35 | 2167 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):168-173 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; Harris SW; Simon J; Church K; Bonnell J; Ognibene TC; McIntosh DN Influence of stimulants on electrodermal studies in fragile X syndrome | 1 | 1 |
| 503 | 25 | 35 | 2168 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):174-178 Kau ASM; Meyer WA; Kaufmann WE Early development in males with fragile X syndrome: A review of the literature | 2 | 3 |
| 504 | 19 | 35 | 2286 2003 JOURNAL OF NEUROGENETICS 17(2-3):223-230 Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; Romac S Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation | 0 | 0 |
| 505 | 5 | 35 | 2297 2003 NEURON 39(5):739-747 Jin P; Zarnescu DC; Zhang FP; Pearson CE; Lucchesi JC; Moses K; Warren ST RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila | 4 | 9 |
| 506 | 14 | 34 | 251 1985 AMERICAN JOURNAL OF MENTAL DEFICIENCY 90(2):119-123 DELACRUZ FF FRAGILE-X SYNDROME | 9 | 12 |
| 507 | 9 | 34 | 279 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 |
| 508 | 6 | 34 | 429 1987 BIOLOGICAL PSYCHIATRY 22(3):303-312 STCLAIR DM; BLACKWOOD DHR; OLIVER CJ; DICKENS P P3 ABNORMALITY IN FRAGILE-X SYNDROME | 5 | 16 |
| 509 | 16 | 34 | 583 1988 HUMAN GENETICS 78(4):338-342 CLAYTON JF; GOSDEN CM; HASTIE ND; EVANS HJ LINKAGE HETEROGENEITY AND FRAGILE-X | 4 | 8 |
| 510 | 5 | 34 | 650 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):422-426 DYKENS EM; HODAPP RM; ORT S; FINUCANE B; SHAPIRO LR; LECKMAN JF THE TRAJECTORY OF DEVELOPMENT IN MALES WITH FRAGILE-X SYNDROME | 31 | 50 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 511 | 7 | 34 | 732 1990 YALE JOURNAL OF BIOLOGY AND MEDICINE 63(4):293-299 BREGMAN JD; LECKMAN JF; ORT SI THYROID-FUNCTION IN FRAGILE-X SYNDROME MALES | 6 | 8 |
| 512 | 17 | 34 | 738 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(2):279-288 REISS AL; FREUND L; TSENG JE; JOSHI PK NEUROANATOMY IN FRAGILE-X FEMALES - THE POSTERIOR-FOSSA | 43 | 64 |
| 513 | 9 | 34 | 818 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):481-487 FISCH GS; ARINAMI T; FROSTERISKENIUS U; FRYNS JP; CURFS LM; BORGHGRAEF M; HOWARDPEEBLES PN; SCHWARTZ CE; SIMENSEN RJ; SHAPIRO LR RELATIONSHIP BETWEEN AGE AND IQ AMONG FRAGILE-X MALES - A MULTICENTER STUDY | 13 | 14 |
| 514 | 9 | 34 | 838 1991 CELL 64(4):861-866 BELL MV; HIRST MC; NAKAHORI Y; MACKINNON RN; ROCHE A; FLINT TJ; JACOBS PA; TOMMERUP N; TRANEBJAERG L; FROSTERISKENIUS U; KERR B; TURNER G; LINDENBAUM RH; WINTER R; PEMBREY M; THIBODEAU S; DAVIES KE PHYSICAL MAPPING ACROSS THE FRAGILE-X - HYPERMETHYLATION AND CLINICAL EXPRESSION OF THE FRAGILE-X SYNDROME | 118 | 222 |
| 515 | 16 | 34 | 989 1992 JOURNAL OF INHERITED METABOLIC DISEASE 15(4):532-538 HIRST MC; KNIGHT SM; NAKAHORI Y; ROCHE A; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 516 | 23 | 34 | 994 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 | 72 | 108 |
| 517 | 16 | 34 | 1016 1992 REMEDIAL AND SPECIAL EDUCATION 13(2):32-39 SANTOS KE FRAGILE X-SYNDROME - AN EDUCATORS ROLE IN IDENTIFICATION, PREVENTION, AND INTERVENTION | 0 | 2 |
| 518 | 22 | 34 | 1058 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(6):1217-1228 SNOW K; DOUD LK; HAGERMAN R; PERGOLIZZI RG; ERSTER SH; THIBODEAU SN ANALYSIS OF A CGG SEQUENCE AT THE FMR-I LOCUS IN FRAGILE-X FAMILIES AND IN THE GENERAL-POPULATION | 84 | 136 |
| 519 | 16 | 34 | 1083 1993 CURRENT BIOLOGY 3(11):783-786 TROTTIER Y; DEVYS D; MANDEL JL FRAGILE-X SYNDROME - AN EXPANDING STORY | 4 | 8 |
| 520 | 17 | 34 | 1129 1993 MEDICAL JOURNAL OF AUSTRALIA 158(7):482-485 SUTHERLAND GR; MULLEY JC; RICHARDS RI FRAGILE-X SYNDROME - THE MOST COMMON CAUSE OF FAMILIAL INTELLECTUAL HANDICAP | 1 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 521 | 16 | 34 | 1161 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):346-352 FISCH GS; HOLDEN JJA; SIMENSEN R; CARPENTER N; HOWARDPEEBLES PN; MADDALENA A; SANDGRUND A; JACQUES JR; MCGANN B FRAGILE-X-SYNDROME A PERVASIVE DEVELOPMENTAL DISABILITY - COGNITIVE-ABILITY AND ADAPTIVE-BEHAVIOR IN MATES WITH THE FULL MUTATION | 10 | 12 |
| 522 | 21 | 34 | 1216 1994 HUMAN GENETICS 94(4):395-400 MILA M; KRUYER H; GLOVER G; SANCHEZ A; CARBONELL P; CASTELLVIBEL S; VOLPINI V; ROSELL J; GABARRON J; LOPEZ I; VILLA M; BALLESTA F; ESTIVILL X MOLECULAR ANALYSIS OF THE (CGG)(N) EXPANSION IN THE FMR-1 GENE IN 59 SPANISH FRAGILE-X SYNDROME FAMILIES | 12 | 16 |
| 523 | 11 | 34 | 1385 1995 NUCLEIC ACIDS RESEARCH 23(11):1876-1881 MITCHELL JE; NEWBURY SF; MCCLELLAN JA COMPACT STRUCTURES OF D(CNG)(N) OLIGONUCLEOTIDES IN SOLUTION AND THEIR POSSIBLE RELEVANCE TO FRAGILE-X AND RELATED HUMAN GENETIC-DISEASES | 2 | 31 |
| 524 | 15 | 34 | 1400 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-14 Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; Fryns JP; Hagerman R; Jacobs PA; Mandel JL; Mulley J; Oostra B; Schwartz C; Sherman S; Willard H; Willems P Seventh International Workshop on the Fragile X and X-linked Mental Retardation | 2 | 4 |
| 525 | 7 | 34 | 1620 1997 NATURE STRUCTURAL BIOLOGY 4(9):712-716 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; Nilges M; Pastore A The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome | 5 | 40 |
| 526 | 20 | 34 | 1745 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):191-194 Zhong N; Ju WN; Xu WM; Ye LL; Shen Y; Wu GY; Chen SH; Jin RM; Hu XF; Yang AD; Liu XX; Poon P; Pang C; Zheng Y; Song L; Zhao P; Fu BJ; Gu HJ; Brown WT Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians | 6 | 10 |
| 527 | 19 | 34 | 1801 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:314-324 York A; von Fraunhofer N; Turk J; Sedgwick P Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators | 2 | 4 |
| 528 | 18 | 34 | 1967 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 | 7 |
| 529 | 21 | 34 | 2008 2001 CELLULAR AND MOLECULAR NEUROBIOLOGY 21(1):29-38 Castren M; Haapasalo A; Oostra BA; Castren E Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons | 2 | 2 |
| 530 | 18 | 34 | 2033 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):409-417 Rogers SJ; Wehner EA; Hagerman R The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders | 9 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 531 | 26 | 34 | 2265 2003 GENETIC TESTING 7(4):303-308 Gasteiger M; Grasbon-Frod E; Neitzel B; Kooy F; Holinski-Feder E FMR1 gene deletion/reversion: A pitfall of fragile X carrier testing | 0 | 0 |
| 532 | 8 | 33 | 153 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 |
| 533 | 7 | 33 | 454 1987 HUMAN GENETICS 76(2):141-147 JOHANNISSON R; REHDER H; WENDT V; SCHWINGER E SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .1. HISTOLOGY - LIGHT AND ELECTRON-MICROSCOPY | 8 | 15 |
| 534 | 13 | 33 | 472 1987 JOURNAL OF MEDICAL GENETICS 24(7):413-421 VEENEMA H; CARPENTER NJ; BAKKER E; HOFKER MH; WARD AM; PEARSON PL THE FRAGILE-X SYNDROME IN A LARGE FAMILY .3. INVESTIGATIONS ON LINKAGE OF FLANKING DNA MARKERS WITH THE FRAGILE SITE-XQ27 | 17 | 38 |
| 535 | 2 | 33 | 647 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 | 30 | 47 |
| 536 | 12 | 33 | 670 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):738-743 ROCCHI M; ARCHIDIACONO N; RINALDI A; FILIPPI G; BARTOLUCCI G; FANCELLO GS; SINISCALCO M MENTAL-RETARDATION IN HETEROZYGOTES FOR THE FRAGILE-X MUTATION - EVIDENCE IN FAVOR OF AN X INACTIVATION-DEPENDENT EFFECT | 11 | 13 |
| 537 | 8 | 33 | 704 1990 HUMAN GENETICS 85(3):267-271 LI SY; LIN JK DIFFERENTIAL BLEOMYCIN SUSCEPTIBILITY IN CULTURED LYMPHOCYTES OF FRAGILE X-PATIENTS AND NORMAL INDIVIDUALS | 3 | 5 |
| 538 | 16 | 33 | 735 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(3):460-467 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; STEINBACH P; GLASS IA; SCHWARTZ CE; VANOOST BA; THIBODEAU SN; HAITES NE; OOSTRA BA; GINE R; CARBALLO M; MORRIS CP; HOPWOOD JJ; SUTHERLAND GR GENETIC-MAPPING OF NEW DNA PROBES AT XQ27 DEFINES A STRATEGY FOR DNA STUDIES IN THE FRAGILE-X SYNDROME | 30 | 47 |
| 539 | 2 | 33 | 816 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463 KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; SCHWARTZRICHSTEIN C; HONG G; BROWN WT DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS | 1 | 1 |
| 540 | 9 | 33 | 895 1991 SCIENCE 251(4998):1236-1239 HEITZ D; ROUSSEAU F; DEVYS D; SACCONE S; ABDERRAHIM H; LEPASLIER D; COHEN D; VINCENT A; TONIOLO D; DELLAVALLE G; JOHNSON S; SCHLESSINGER D; OBERLE I; MANDEL JL ISOLATION OF SEQUENCES THAT SPAN THE FRAGILE-X AND IDENTIFICATION OF A FRAGILE-X RELATED CPG ISLAND | 86 | 139 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 541 | 16 | 33 | 975 1992 EDUCATIONAL RESEARCH 34(3):221-228 GIBB C THE MOST COMMON-CAUSE OF LEARNING-DIFFICULTIES - A PROFILE OF FRAGILE-X SYNDROME AND ITS IMPLICATIONS FOR EDUCATION | 1 | 1 |
| 542 | 18 | 33 | 1010 1992 PEDIATRIC NEUROLOGY 8(4):272-274 WONG VCN; LAM STS FRAGILE X POSITIVITY IN CHINESE CHILDREN WITH AUTISTIC SPECTRUM DISORDER | 3 | 5 |
| 543 | 20 | 33 | 1134 1993 NATURE GENETICS 3(1):36-43 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; HOUSMAN DE; SCHALLING M TISSUE SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE-X SYNDROME | 91 | 154 |
| 544 | 18 | 33 | 1190 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):517-521 CHIURAZZI P; KOZAK L; NERI G UNSTABLE TRIPLETS AND THEIR MUTATIONAL MECHANISM - SIZE-REDUCTION OF THE CGG REPEAT VS GERMLINE MOSAICISM IN THE FRAGILE-X-SYNDROME | 7 | 15 |
| 545 | 16 | 33 | 1199 1994 AMERICAN JOURNAL ON MENTAL RETARDATION 98(4):455-462 KERBY DS; DAWSON BL AUTISTIC FEATURES, PERSONALITY, AND ADAPTIVE-BEHAVIOR IN MALES WITH THE FRAGILE-X SYNDROME AND NO AUTISM | 12 | 21 |
| 546 | 21 | 33 | 1220 1994 HUMAN MOLECULAR GENETICS 3(4):615-620 MEIJER H; DEGRAAFF E; MERCKX DML; JONGBLOED RJE; DEDIESMULDERS CEM; ENGELEN JJM; FRYNS JP; CURFS PMG; OOSTRA BA A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1 GENE CAUSES THE CLINICAL PHENOTYPE OF THE FRAGILE X SYNDROME | 46 | 78 |
| 547 | 18 | 33 | 1242 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(2):247-255 SOBESKY WE; HULL CE; HAGERMAN RJ SYMPTOMS OF SCHIZOTYPAL PERSONALITY-DISORDER IN FRAGILE-X WOMEN | 17 | 32 |
| 548 | 16 | 33 | 1296 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 |
| 549 | 17 | 33 | 1329 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):242-251 Freund LS; Peebles CD; Aylward E; Reiss AL Preliminary report on cognitive and adaptive behaviors of preschool-aged males with fragile X | 15 | 20 |
| 550 | 17 | 33 | 1355 1995 HUMAN GENETICS 96(3):323-329 DREESEN JCFM; GERAEDTS JPM; DUMOULIN JCM; EVERS JLH; PIETERS MHEC RS46(DXS548) GENOTYPING OF REPRODUCTIVE CELLS - APPROACHING PREIMPLANTATION TESTING OF THE FRAGILE-X SYNDROME | 2 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 551 | 9 | 33 | 1498 1996 KOREAN JOURNAL OF GENETICS 18(3):199-210 Choi SK; Kim HY; Paik YK Cytogenetic analysis of a Korean family with fragile X syndrome | 0 | 1 |
| 552 | 17 | 33 | 1516 1996 VARIATION IN THE HUMAN GENOME 197:119-126 Sutherland GR; Richards RI Unusual inheritance patterns due to dynamic mutation in fragile X syndrome | 0 | 0 |
| 553 | 20 | 33 | 1633 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 | 2 |
| 554 | 10 | 33 | 1678 1998 JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS 15(4):745-756 Chen X; Mariappan SVS; Moyzis RK; Bradbury EM; Gupta G Hairpin induced slippage and hyper-methylation of the fragile X DNA triplets | 4 | 16 |
| 555 | 19 | 33 | 1697 1998 OPTOMETRY AND VISION SCIENCE 75(12):856-859 Kranjc BS; Brezigar A; Peterlin B Bilateral macular dysplasia in fragile X syndrome | 0 | 0 |
| 556 | 18 | 33 | 1784 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(5):526-532 Kooy RF; Reyniers E; Verhoye M; Sijbers J; Bakker CE; Oostra BA; Willems PJ; Van der Linden A Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging | 7 | 20 |
| 557 | 21 | 33 | 1853 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 93(2):99-106 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson JN; Brondum-Nielsen K; Hasholt L; Norgaard-Pedersen B; Vuust J Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles | 2 | 6 |
| 558 | 16 | 33 | 1857 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):123-129 Hjalgrim H; Hansen BF; Brondum-Nielsen K; Nolting D; Kjaer I Aspects of skeletal development in fragile X syndrome fetuses | 2 | 3 |
| 559 | 22 | 33 | 1864 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):189-194 Sherman SL Premature ovarian failure in the fragile X syndrome | 12 | 24 |
| 560 | 10 | 33 | 1872 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 | 23 | 30 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 561 | 20 | 33 | 1881 2000 CLINICAL GENETICS 58(2):111-115 Kallinen J; Heinonen S; Mannermaa A; Ryynanen M Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation | 3 | 5 |
| 562 | 16 | 33 | 2027 2001 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 31(2):165-174 Bailey DB; Hatton DD; Skinner M; Mesibov G Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome | 11 | 15 |
| 563 | 18 | 33 | 2260 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):206-212 Hagerman PJ; Greco CM; Hagerman RJ A cerebellar tremor/ataxia syndrome among fragile X premutation carriers | 2 | 3 |
| 564 | 0 | 32 | 52 1982 CANADIAN MEDICAL ASSOCIATION JOURNAL 127(2):123-126 LARBRISSEAU A; JEAN P; MESSIER B; RICHER CL FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 6 | 9 |
| 565 | 8 | 32 | 105 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):699-712 CHUDLEY AE; KNOLL J; GERRARD JW; SHEPEL L; MCGAHEY E; ANDERSON J FRAGILE (X) X-LINKED MENTAL-RETARDATION .1. RELATIONSHIP BETWEEN AGE AND INTELLIGENCE AND THE FREQUENCY OF EXPRESSION OF FRAGILE (X)(Q28) | 56 | 80 |
| 566 | 12 | 32 | 246 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 |
| 567 | 14 | 32 | 280 1985 HELVETICA PAEDIATRICA ACTA 40(2-3):133-152 SCHINZEL A; LARGO RH THE FRAGILE X-SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL AND CYTOGENETIC FINDINGS IN 16 PREPUBERTAL BOYS AND IN 4 OF THEIR 5 FAMILIES | 4 | 8 |
| 568 | 15 | 32 | 335 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):375-380 HAGERMAN RJ; CHUDLEY AE; KNOLL JH; JACKSON AW; KEMPER M; AHMAD R AUTISM IN FRAGILE-X FEMALES | 32 | 46 |
| 569 | 12 | 32 | 559 1988 AMERICAN JOURNAL ON MENTAL RETARDATION 92(5):436-446 COHEN IL; FISCH GS; SUDHALTER V; WOLFSCHEIN EG; HANSON D; HAGERMAN R; JENKINS EC; BROWN WT SOCIAL GAZE, SOCIAL AVOIDANCE, AND REPETITIVE BEHAVIOR IN FRAGILE X-MALES - A CONTROLLED-STUDY | 50 | 71 |
| 570 | 7 | 32 | 560 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 | 56 | 91 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 571 | 7 | 32 | 576 1988 CYTOGENETICS AND CELL GENETICS 47(4):177-180 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M FRAGILE-X EXPRESSION IN THYMIDINE-PROTOTROPHIC AND AUXOTROPHIC HUMAN-MOUSE SOMATIC-CELL HYBRIDS UNDER LOW AND HIGH THYMIDYLATE STRESS CONDITIONS | 1 | 3 |
| 572 | 17 | 32 | 582 1988 HUMAN GENETICS 78(3):201-205 BROWN WT; GROSS A; CHAN C; JENKINS EC; MANDEL JL; OBERLE I; ARVEILER B; NOVELLI G; THIBODEAU S; HAGERMAN R; SUMMERS K; TURNER G; WHITE BN; MULLIGAN L; FORSTERGIBSON C; HOLDEN JJA; ZOLL B; KRAWCZAK M; GOONEWARDENA P; GUSTAVSON KH; PETTERSSON U; HOLMGREN G; SCHWARTZ C; HOWARDPEEBLES PN; MURPHY P; BREG WR; VEENEMA H; CARPENTER NJ MULTILOCUS ANALYSIS OF THE FRAGILE-X SYNDROME | 33 | 49 |
| 573 | 9 | 32 | 685 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):442-447 CANTU ES; STONE JW; WING AA; LANGEE HR; WILLIAMS CA CYTOGENETIC SURVEY FOR AUTISTIC FRAGILE-X CARRIERS IN A MENTAL-RETARDATION CENTER | 5 | 16 |
| 574 | 7 | 32 | 784 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):260-268 BUTLER MG; ALLEN GA; HAYNES JL; SINGH DN; WATSON MS; BREG WR ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT THE FRAGILE-X SYNDROME | 16 | 22 |
| 575 | 16 | 32 | 955 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(6):816-821 DEWALD GW; BUCKLEY DD; SPURBECK JL; JALAL SM CYTOGENETIC GUIDELINES FOR FRAGILE-X STUDIES TESTED IN ROUTINE PRACTICE | 3 | 7 |
| 576 | 17 | 32 | 1156 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):309-314 CHIURAZZI P; DEGRAAFF E; NG J; VERKERK AJMH; WOLFSON S; FISCH GS; KOZAK L; NERI G; OOSTRA BA NO APPARENT INVOLVEMENT OF THE FMR1 GENE IN 5 PATIENTS WITH PHENOTYPIC MANIFESTATIONS OF THE FRAGILE-X-SYNDROME | 6 | 10 |
| 577 | 22 | 32 | 1561 1997 ANNALES DE GENETIQUE 40(3):139-144 Gerard B; LeHeuzey MF; Brunie G; Lewine P; Saiag MC; Cacheux V; DaSilva F; Dugas M; MourenSimeoni MC; Elion J; Grandchamp B Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children | 3 | 7 |
| 578 | 16 | 32 | 1792 1999 HUMAN MUTATION 14(1):71-79 Panagopoulos I; Lassen C; Kristoffersson U; Aman P A methylation PCR approach for detection of fragile X syndrome | 3 | 4 |
| 579 | 18 | 32 | 1883 2000 EPILEPSIA 41(1):19-23 Musumeci SA; Bosco P; Calabrese G; Bakker C; De Sarro GB; Elia M; Ferri R; Oostra BA Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome | 23 | 30 |
| 580 | 6 | 32 | 1911 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(5):315-321 Bailey DB; Skinner D; Hatton D; Roberts J Family experiences and factors associated with the diagnosis of fragile X syndrome | 12 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 581 | 8 | 32 | 1948 2000 MOLECULAR BRAIN RESEARCH 75(2):337-341 Valentine G; Chakravarty S; Sarvey J; Bramham C; Herkenham M Fragile X (fmr1) mRNA expression is differentially regulated in two adult models of activity-dependent gene expression | 6 | 9 |
| 582 | 15 | 32 | 1987 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(3):226-230 Schultz-Pedersen S; Hasle H; Olsen JH; Friedrich U Evidence of decreased risk of cancer in individuals with fragile X | 0 | 2 |
| 583 | 26 | 32 | 1996 2001 ANNALS OF CLINICAL BIOCHEMISTRY 38:264-271 Saha S; Karmakar P; Chatterjee C; Banerjee D; Das S; Dasgupta UB Fragile X syndrome in Calcutta, India | 1 | 3 |
| 584 | 12 | 32 | 2097 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 110(1):36-44 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Carrier testing in fragile X syndrome: When to tell and test | 0 | 0 |
| 585 | 15 | 32 | 2186 2002 NEUROPSYCHOLOGIA 40(8):1343-1349 Wilding J; Cornish K; Munir F Further delineation of the executive deficit in males with fragile-X syndrome | 4 | 4 |
| 586 | 7 | 32 | 2279 2003 JOURNAL OF INTELLECTUAL & DEVELOPMENTAL DISABILITY 28(2):135-144 Richdale AL A descriptive analysis of sleep behaviour in children with Fragile X | 0 | 0 |
| 587 | 18 | 32 | 2349 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):49-52 Darnell JC; Warren ST; Darnell RB The fragile X mental retardation protein, FMRP, recognizes G-quartets | 0 | 0 |
| 588 | 8 | 31 | 143 1983 JOURNAL OF MEDICAL GENETICS 20(3):169-178 MCDERMOTT A; WALTERS R; HOWELL RT; GARDNER A FRAGILE X-CHROMOSOME - CLINICAL AND CYTOGENETIC STUDIES ON CASES FROM 7 FAMILIES | 13 | 18 |
| 589 | 9 | 31 | 359 1986 ANNALS OF HUMAN GENETICS 50:385-398 LOESCH DZ DERMATOGLYPHIC FINDINGS IN FRAGILE X-SYNDROME - A CAUSAL HYPOTHESIS POINTS TO X-Y INTERCHANGE | 9 | 14 |
| 590 | 17 | 31 | 431 1987 BRITISH MEDICAL JOURNAL 295(6598):564-565 KINNELL HG FRAGILE X-SYNDROME - AN IMPORTANT PREVENTABLE CAUSE OF MENTAL HANDICAP | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 591 | 8 | 31 | 498 1988 AMERICAN JOURNAL OF HUMAN GENETICS 43(5):684-688 PATTERSON M; BELL M; KRESS W; DAVIES KE; FROSTERISKENIUS U LINKAGE STUDIES IN A LARGE FRAGILE X-FAMILY | 10 | 23 |
| 592 | 5 | 31 | 567 1988 CANCER 62(11):2383-2386 CUNNINGHAM M; DICKERMAN JD FRAGILE-X SYNDROME AND ACUTE LYMPHOBLASTIC-LEUKEMIA | 3 | 3 |
| 593 | 17 | 31 | 572 1988 CLINICAL GENETICS 33(6):410-417 VEENEMA H; BEVERSTOCK GC; DEKONING T; PEARSON PL; VANDEKAMP JJP THE FRAGILE X-CHROMOSOME - AN EVALUATION OF THE RESULTS IN A ROUTINE CYTOGENETIC LABORATORY IN THE PERIOD 1981-1986 | 1 | 3 |
| 594 | 3 | 31 | 609 1988 SCHIZOPHRENIA RESEARCH 1(4):277-281 DELISI LE; REISS AL; WHITE BJ; GERSHON ES CYTOGENETIC STUDIES OF MALES WITH SCHIZOPHRENIA - SCREENING FOR THE FRAGILE X-CHROMOSOME AND OTHER CHROMOSOMAL-ABNORMALITIES | 1 | 36 |
| 595 | 2 | 31 | 629 1989 CLINICAL GENETICS 36(1):15-24 MERYASH DL PERCEPTION OF BURDEN AMONG AT-RISK WOMEN OF RAISING A CHILD WITH FRAGILE-X SYNDROME | 2 | 7 |
| 596 | 14 | 31 | 793 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):322-327 GOONEWARDENA P; BROWN WT; GROSS AC; FERRANDO C; DOBKIN C; ROMANO V; BOSCO P; CERATTO N; PETTERSSON U; DAHL N LINKAGE ANALYSIS OF THE FRAGILE-X SYNDROME USING A NEW DNA MARKER U6.2 DEFINING LOCUS DXS304 | 1 | 1 |
| 597 | 14 | 31 | 827 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(2):234-243 CIANCHETTI C; SANNIOFANCELLO G; FRATTA AL; MANCONI F; ORANO A; PISCHEDDA MP; PRUNA D; SPINICCI G; ARCHIDIACONO N; FILIPPI G NEUROPSYCHOLOGICAL, PSYCHIATRIC, AND PHYSICAL MANIFESTATIONS IN 149 MEMBERS FROM 18 FRAGILE-X FAMILIES | 16 | 19 |
| 598 | 4 | 31 | 833 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 | 54 | 110 |
| 599 | 24 | 31 | 906 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):5-27 MANDEL JL; HAGERMAN R; FROSTER U; BROWN WT; JENKINS EC; JACOBS P; TURNER G; LUBS H; NERI G 5TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 5 | 8 |
| 600 | 21 | 31 | 1011 1992 PEDIATRICS 89(3):395-400 HAGERMAN RJ; JACKSON C; AMIRI K; SILVERMAN AC; OCONNOR R; SOBESKY W GIRLS WITH FRAGILE-X SYNDROME - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 57 | 79 |
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