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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 601 | 21 | 37 | 2077 2000 MOLECULAR BRAIN RESEARCH 80(1):17-25 Todd PK; Mack KJ Sensory stimulation increases cortical expression of the fragile X mental retardation protein in vivo | 17 | 17 |
| 602 | 10 | 17 | 2089 2000 PRENATAL DIAGNOSIS 20(8):611-614 Pesso R; Berkenstadt H; Cuckle H; Gak E; Peleg L; et al. Screening for fragile X syndrome in women of reproductive age | 13 | 17 |
| 603 | 5 | 37 | 2256 2002 CURRENT BIOLOGY 12(15):1331-1335 Inoue SB; Shimoda M; Nishinokubi I; Siomi MC; Okamura M; et al. A role for the Drosophila fragile X-related gene in circadian output | 13 | 17 |
| 604 | 3 | 25 | 177 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):195-207 SIMPSON NE; NEWMAN BJ; PARTINGTON MW FRAGILE-X SYNDROME .3. DERMATOGLYPHIC STUDIES IN MALES | 10 | 16 |
| 605 | 1 | 3 | 350 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):567-572 JACOBS PA; MAYER M; ABRUZZO MA STUDIES OF THE FRAGILE (X) SYNDROME IN POPULATIONS OF MENTALLY-RETARDED INDIVIDUALS IN HAWAII | 13 | 16 |
| 606 | 11 | 29 | 356 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):701-713 FRIEDMAN JM; HOWARDPEEBLES PN INHERITANCE OF FRAGILE-X SYNDROME - AN HYPOTHESIS | 10 | 16 |
| 607 | 6 | 13 | 399 1986 JOURNAL OF MEDICAL GENETICS 23(5):407-410 TUCKERMAN E; WEBB T; THAKE A REPLICATION STATUS OF FRAGILE X(Q27.3) IN 13 FEMALE HETEROZYGOTES | 12 | 16 |
| 608 | 17 | 36 | 427 1987 ANNALS OF HUMAN GENETICS 51:107-124 GIANNELLI F; MORRIS AH; GARRETT C; DAKER M; THURSTON C; et al. GENETIC-HETEROGENEITY OF X-LINKED MENTAL-RETARDATION WITH FRAGILE-X - ASSOCIATION OF TIGHT LINKAGE TO FACTOR-IX AND INCOMPLETE PENETRANCE IN MALES | 7 | 16 |
| 609 | 6 | 34 | 433 1987 BIOLOGICAL PSYCHIATRY 22(3):303-312 STCLAIR DM; BLACKWOOD DHR; OLIVER CJ; DICKENS P P3 ABNORMALITY IN FRAGILE-X SYNDROME | 5 | 16 |
| 610 | 16 | 30 | 459 1987 HUMAN GENETICS 76(2):165-172 BUCHANAN JA; BUCKTON KE; GOSDEN CM; NEWTON MS; CLAYTON JF; et al. 10 FAMILIES WITH FRAGILE-X SYNDROME - LINKAGE RELATIONSHIPS WITH 4 DNA PROBES FROM DISTAL-XQ | 9 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 611 | 6 | 10 | 551 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):665-672 NERI G; SANFILIPPO S; PAVONE L; MOLLICA F; BARBERI I; et al. THE FRAGILE-X IN SICILY - AN EPIDEMIOLOGICAL SURVEY | 10 | 16 |
| 612 | 16 | 24 | 594 1988 HUMAN GENETICS 80(4):375-378 VOELCKEL MA; MATTEI MG; NGUYEN C; PHILIP N; BIRG F; et al. DISSOCIATION BETWEEN MENTAL-RETARDATION AND FRAGILE SITE EXPRESSION IN A FAMILY WITH FRAGILE X-LINKED MENTAL-RETARDATION | 9 | 16 |
| 613 | 10 | 14 | 624 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):302-303 COHEN IL; BROWN WT; JENKINS EC; KRAWCZUN MS; FRENCH JH; et al. FRAGILE-X SYNDROME IN FEMALES WITH AUTISM | 13 | 16 |
| 614 | 9 | 32 | 691 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 |
| 615 | 24 | 44 | 700 1990 CLINICAL GENETICS 37(1):2-11 SUTHERLAND GR; MULLEY JC DIAGNOSTIC MOLECULAR-GENETICS OF THE FRAGILE-X | 14 | 16 |
| 616 | 9 | 21 | 711 1990 HUMAN GENETICS 85(6):590-594 YU WD; WENGER SL; STEELE MW X-CHROMOSOME IMPRINTING IN FRAGILE-X SYNDROME | 8 | 16 |
| 617 | 6 | 28 | 872 1991 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 21(4):503-516 HODAPP RM; DYKENS EM; ORT SI; ZELINSKY DG; LECKMAN JF CHANGING PATTERNS OF INTELLECTUAL STRENGTHS AND WEAKNESSES IN MALES WITH FRAGILE-X SYNDROME | 5 | 16 |
| 618 | 13 | 22 | 944 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):244-254 SNOW K; DOUD L; HAGERMAN R; HULL C; HIRST MC; et al. ANALYSIS OF MUTATIONS AT THE FRAGILE-X LOCUS USING THE DNA PROBE OX1.9 | 14 | 16 |
| 619 | 7 | 15 | 961 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1057-1062 WEBB T DELAYED REPLICATION OF XQ27 IN INDIVIDUALS WITH THE FRAGILE X-SYNDROME | 2 | 16 |
| 620 | 12 | 13 | 1207 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):497-500 SMITS A; SMEETS D; HAMEL B; DREESEN J; DEHAAN A; et al. PREDICTION OF MENTAL STATUS IN CARRIERS OF THE FRAGILE-X MUTATION USING CGG REPEAT LENGTH | 13 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 621 | 9 | 21 | 1210 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):513-516 DEELEN W; BAKKER C; HALLEY DJJ; OOSTRA BA CONSERVATION OF CGG REGION IN FMR1 GENE IN MAMMALS | 11 | 16 |
| 622 | 21 | 34 | 1238 1994 HUMAN GENETICS 94(4):395-400 MILA M; KRUYER H; GLOVER G; SANCHEZ A; CARBONELL P; et al. MOLECULAR ANALYSIS OF THE (CGG)(N) EXPANSION IN THE FMR-1 GENE IN 59 SPANISH FRAGILE-X SYNDROME FAMILIES | 15 | 16 |
| 623 | 1 | 3 | 1243 1994 HUMAN MOLECULAR GENETICS 3(3):521-521 JOKINEN E; SAKAI J; YAMAMOTO T; HOBBS HH CGG TRIPLE REPEAT POLYMORPHISM IN VLDL RECEPTOR (VLDL-R) GENE | 0 | 16 |
| 624 | 16 | 40 | 1417 1995 JOURNAL OF MEDICAL GENETICS 32(10):764-769 DEVRIES BBA; ROBINSON H; STOLTEDIJKSTRA I; GI CVTP; DIJKSTRA PF; et al. GENERAL OVERGROWTH IN THE FRAGILE-X SYNDROME - VARIABILITY IN THE PHENOTYPIC-EXPRESSION OF THE FMR1 GENE MUTATION | 6 | 16 |
| 625 | 42 | 70 | 1439 1995 SEMINARS IN CELL BIOLOGY 6(1):5-11 NELSON DL THE FRAGILE-X SYNDROMES | 4 | 16 |
| 626 | 18 | 21 | 1470 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 |
| 627 | 18 | 21 | 1480 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 |
| 628 | 22 | 31 | 1486 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 |
| 629 | 16 | 21 | 1489 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 |
| 630 | 15 | 26 | 1536 1996 HUMAN GENETICS 97(6):808-812 Haddad LA; MingroniNetto RC; ViannaMorgante AM; Pena SDJ A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males | 9 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 631 | 10 | 13 | 1550 1996 JOURNAL OF MEDICAL GENETICS 33(4):338-340 Mila M; CastellviBel S; Sanchez A; Lazaro C; Villa M; et al. Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene | 11 | 16 |
| 632 | 3 | 4 | 1559 1996 LANCET 348(9032):967-968 Willemsen R; Oosterwijk JC; Los FJ; Galjaard H; Oostra BA Prenatal diagnosis of fragile X syndrome | 11 | 16 |
| 633 | 21 | 32 | 1685 1997 JOURNAL OF MEDICAL GENETICS 34(8):627-631 Kunst CB; Leeflang EP; Iber JC; Arnheim N; Warren ST The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing | 3 | 16 |
| 634 | 11 | 33 | 1768 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 |
| 635 | 7 | 40 | 1769 1998 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 39(5):699-710 van Lieshout CFM; De Meyer RE; Curfs LMG; Fryns JP Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome | 4 | 16 |
| 636 | 17 | 36 | 1791 1998 NEUROPSYCHOLOGIA 36(11):1239-1246 Cornish KM; Munir F; Cross G The nature of the spatial deficit in young females with Fragile-X syndrome: A neuropsychological and molecular perspective | 12 | 16 |
| 637 | 11 | 20 | 1834 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):308-312 Fisch GS; Carpenter N; Holden JJA; Howard-Peebles PN; Maddalena A; et al. Longitudinal changes in cognitive and adaptive behavior in fragile X females: A prospective multicenter analysis | 10 | 16 |
| 638 | 15 | 30 | 1881 1999 CORTEX 35(2):263-271 Cornish KM; Munir F; Cross G Spatial cognition in males with Fragile-X syndrome: Evidence for a neuropsychological phenotype | 14 | 16 |
| 639 | 6 | 8 | 1940 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 |
| 640 | 9 | 29 | 2033 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(9):6447-6452 Muller-Hartmann H; Deissler H; Naumann F; Schmitz B; Schroer J; et al. The human 20-kDa 5 '-(CGG)(n)-3 '-binding protein is targeted to the nucleus and affects the activity of the FMR1 promoter | 11 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 641 | 13 | 31 | 2193 2001 PRENATAL DIAGNOSIS 21(6):504-511 Apessos A; Abou-Sleiman PM; Harper JC; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 1 | 16 |
| 642 | 23 | 53 | 2318 2002 MOLECULAR AND CELLULAR BIOLOGY 22(24):8438-8447 Siomi MC; Higashijima K; Ishizuka A; Siomi H Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties | 14 | 16 |
| 643 | 9 | 27 | 331 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):273-289 FROSTERISKENIUS U; BODEKER K; OEPEN T; MATTHES R; PIPER U; et al. FOLIC-ACID TREATMENT IN MALES AND FEMALES WITH FRAGILE-(X)-SYNDROME | 10 | 15 |
| 644 | 2 | 9 | 386 1986 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 28(5):624-627 GILLBERG C; WAHLSTROM J; JOHANSSON R; TORNBLOM M; ALBERTSSONWIKLAND K FOLIC-ACID AS AN ADJUNCT IN THE TREATMENT OF CHILDREN WITH THE AUTISM FRAGILE-X SYNDROME (AFRAX) | 6 | 15 |
| 645 | 9 | 27 | 450 1987 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 29(6):711-719 THAKE A; TODD J; WEBB T; BUNDEY S CHILDREN WITH THE FRAGILE X-CHROMOSOME AT SCHOOLS FOR THE MILDLY MENTALLY-RETARDED | 11 | 15 |
| 646 | 7 | 33 | 458 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 |
| 647 | 11 | 25 | 484 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):589-592 GOLDFINE PE; MCPHERSON PM; HARDESTY VA; HEATH GA; BEAUREGARD LJ; et al. FRAGILE-X CHROMOSOME ASSOCIATED WITH PRIMARY LEARNING-DISABILITY | 12 | 15 |
| 648 | 1 | 3 | 503 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):1-17 NERI G; OPITZ JM; MIKKELSEN M; JACOBS PA; DAVIES K; et al. CONFERENCE REPORT - 3RD INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 6 | 15 |
| 649 | 7 | 16 | 549 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):641-654 SCHWARTZ CE; PHELAN MC; PULLIAM LH; WILKES G; VANNER LV; et al. FRAGILE-X SYNDROME - INCIDENCE, CLINICAL AND CYTOGENETIC FINDINGS IN THE BLACK AND WHITE-POPULATIONS OF SOUTH-CAROLINA | 12 | 15 |
| 650 | 5 | 12 | 559 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):753-765 SHERMAN SL; ROGATKO A; TURNER G RECURRENCE RISKS FOR RELATIVES IN FAMILIES WITH AN ISOLATED CASE OF THE FRAGILE X SYNDROME | 11 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 651 | 2 | 10 | 562 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):779-781 BUTLER MG; NAJJAR JL DO SOME PATIENTS WITH FRAGILE-X SYNDROME HAVE PRECOCIOUS PUBERTY | 13 | 15 |
| 652 | 11 | 25 | 811 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):391-395 LAIRD CD POSSIBLE ERASURE OF THE IMPRINT ON A FRAGILE-X CHROMOSOME WHEN TRANSMITTED BY A MALE | 8 | 15 |
| 653 | 7 | 15 | 829 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):503-504 CRONISTER A; HAGERMAN RJ; WITTENBERGER M; AMIRI K MENTAL IMPAIRMENT IN CYTOGENETICALLY POSITIVE FRAGILE-X FEMALES | 14 | 15 |
| 654 | 18 | 33 | 1211 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 | 9 | 15 |
| 655 | 7 | 41 | 1277 1994 NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY 24(6):413-426 FERRI R; MUSUMECI SA; ELIA M; DELGRACCO S; SCUDERI C; et al. BIT-MAPPED SOMATOSENSORY-EVOKED POTENTIALS IN THE FRAGILE-X SYNDROME | 7 | 15 |
| 656 | 14 | 20 | 1467 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 |
| 657 | 21 | 29 | 1542 1996 HUMAN MOLECULAR GENETICS 5(6):821-825 Mornet E; Chateau C; Hirst MC; Thepot F; Taillandier A; et al. Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline range | 6 | 15 |
| 658 | 19 | 35 | 1576 1996 SOMATIC CELL AND MOLECULAR GENETICS 22(6):435-441 Eberhart DE; Warren ST Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus | 7 | 15 |
| 659 | 11 | 14 | 1647 1997 CLINICAL GENETICS 52(4):211-215 Arvio M; Peippo M; Simola KOJ Applicability of a checklist for clinical screening of the fragile X syndrome | 10 | 15 |
| 660 | 12 | 36 | 1763 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):509-517 Mazzocco MMM; Baumgardner T; Freund LS; Reiss AL Social functioning among girls with fragile X or Turner syndrome and their sisters | 11 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 661 | 27 | 52 | 1800 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 |
| 662 | 9 | 21 | 2007 2000 EUROPEAN JOURNAL OF HUMAN GENETICS 8(4):247-252 Murray A; Ennis S; MacSwiney F; Webb J; Morton NE Reproductive and menstrual history of females with fragile X expansions | 11 | 15 |
| 663 | 6 | 32 | 2039 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 |
| 664 | 17 | 37 | 2121 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):16-27 Bailey DB; Hatton DD; Tassone F; Skinner M; Taylor AK Variability in FMRP and early development in males with fragile X syndrome | 16 | 15 |
| 665 | 34 | 53 | 2130 2001 BRAIN 124:1610-1618 Eliez S; Blasey CM; Freund LS; Hastie T; Reiss AL Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome | 9 | 15 |
| 666 | 16 | 17 | 2136 2001 CELL 107(5):555-557 Kaytor MD; Orr HT RNA targets of the fragile X protein | 6 | 15 |
| 667 | 29 | 45 | 2158 2001 HUMAN MOLECULAR GENETICS 10(16):1693-1699 Bontekoe CJM; Bakker CE; Nieuwenhuizen IM; van der Linde H; Lans H; et al. Instability of a (CGG)(98) repeat in the Fmr1 promoter | 12 | 15 |
| 668 | 8 | 71 | 2166 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(21):18605-18613 Bacolla A; Pradhan S; Larson JE; Roberts RJ; Wells RD Recombinant human DNA (cytosine-5) methyltransferase - III. Allosteric control, reaction order, and influence of plasmid topology and triplet repeat length on methylation of the fragile X CGG center dot CCG sequence | 0 | 15 |
| 669 | 14 | 46 | 2253 2002 BRAIN RESEARCH 927(1):8-17 Nielsen DM; Derber WJ; McClellan DA; Crnic LS Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndrome | 11 | 15 |
| 670 | 24 | 62 | 2416 2003 DEVELOPMENT 130(22):5543-5552 Lee A; Li WJ; Xu KY; Bogert BA; Su K; et al. Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1 | 10 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 671 | 21 | 53 | 2432 2003 HUMAN MOLECULAR GENETICS 12(24):3295-3305 Ceman S; O'Donnell WT; Reed M; Patton S; Pohl J; et al. Phosphorylation influences the translation state of FMRP-associated polyribosomes | 12 | 15 |
| 672 | 22 | 55 | 2531 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(4):460-469 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; et al. Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population | 6 | 15 |
| 673 | 12 | 37 | 2559 2004 JOURNAL OF NEUROSCIENCE 24(11):2648-2655 Antar LN; Afroz R; Dictenberg JB; Carroll RC; Bassell GJ Metabotropic glutamate receptor activation regulates Fragile X mental retardation protein and Fmr1 mRNA localization differentially in dendrites and at synapses | 10 | 15 |
| 674 | 2 | 5 | 66 1982 HUMAN GENETICS 61(3):254-255 EBERLE G; ZANKL M; ZANKL H THE EXPRESSION OF FRAGILE X-CHROMOSOMES IN MEMBERS OF THE SAME FAMILY AT DIFFERENT TIMES OF EXAMINATION | 12 | 14 |
| 675 | 0 | 4 | 79 1982 LANCET 1(8263):101-101 GARDNER AP; HOWELL RT; MCDERMOTT A FRAGILE-X CHROMOSOME - CONSISTENT DEMONSTRATION OF FRAGILE SITE IN FIBROBLAST-CULTURES | 10 | 14 |
| 676 | 6 | 36 | 191 1984 AMERICAN JOURNAL OF MEDICINE 77(4):602-611 BRANDA RF; ARTHUR DC; WOODS WG; DANZL TJ; KING RA FOLATE METABOLISM AND CHROMOSOMAL STABILITY IN THE FRAGILE-X SYNDROME | 5 | 14 |
| 677 | 0 | 4 | 221 1984 JOURNAL OF MEDICAL GENETICS 21(5):373-373 FITCHETT M; SEABRIGHT M DELETED X-CHROMOSOMES IN PATIENTS WITH THE FRAGILE X-SYNDROME | 10 | 14 |
| 678 | 3 | 11 | 230 1984 OBSTETRICS AND GYNECOLOGY 63(3):S19-S21 HOGGE WA; SCHONBERG SA; GLOVER TW; HECHT F; GOLBUS MS PRENATAL-DIAGNOSIS OF FRAGILE (X) SYNDROME | 7 | 14 |
| 679 | 6 | 18 | 266 1985 CLINICAL GENETICS 27(5):463-467 GUSTAVSON KH; DAHLBOM K; FLOOD A; HOLMGREN G; BLOMQUIST HK; et al. EFFECT OF FOLIC-ACID TREATMENT IN THE FRAGILE X-SYNDROME | 10 | 14 |
| 680 | 2 | 17 | 328 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):227-239 BERKOVITZ GD; WILSON DP; CARPENTER NJ; BROWN TR; MIGEON CJ GONADAL-FUNCTION IN MEN WITH THE MARTIN-BELL (FRAGILE-X) SYNDROME | 10 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 681 | 9 | 17 | 330 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):263-271 BROWN WT; COHEN IL; FISCH GS; WOLFSCHEIN EG; JENKINS VA; et al. HIGH-DOSE FOLIC-ACID TREATMENT OF FRAGILE-(X) MALES | 9 | 14 |
| 682 | 21 | 26 | 334 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):313-324 TOMMERUP N; AULA P; GUSTAVII B; HEIBERG A; HOLMGREN G; et al. 2ND TRIMESTER PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 7 | 14 |
| 683 | 9 | 31 | 362 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 |
| 684 | 5 | 36 | 415 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(2):184-187 HAGERMAN RJ; ALTSHULSTARK D; MCBOGG P RECURRENT OTITIS-MEDIA IN THE FRAGILE X-SYNDROME | 9 | 14 |
| 685 | 0 | 15 | 454 1987 HUMAN GENETICS 75(1):4-6 AMAROSE AP; HUTTENLOCHER PR; SPRUDZS RM; LAITSCH TJ; PETTENATI MJ A HERITABLE FRAGILE 12Q24.13 SEGREGATING IN A FAMILY WITH THE FRAGILE X-CHROMOSOME | 2 | 14 |
| 686 | 11 | 14 | 529 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):337-345 PURVISSMITH SG; LAING S; SUTHERLAND GR; BAKER E PRENATAL-DIAGNOSIS OF THE FRAGILE-X - THE AUSTRALASIAN EXPERIENCE | 0 | 14 |
| 687 | 2 | 6 | 602 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-460 LECOUTEUR A; RUTTER M; SUMMERS D; BUTLER L FRAGILE-X IN FEMALE AUTISTIC TWINS | 8 | 14 |
| 688 | 9 | 19 | 649 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(2):343-347 HO HH; KALOUSEK DK BRIEF REPORT - FRAGILE X-SYNDROME IN AUTISTIC BOYS | 10 | 14 |
| 689 | 4 | 16 | 817 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):418-420 LEDBETTER SA; SCHWARTZ CE; DAVIES KE; LEDBETTER DH NEW SOMATIC-CELL HYBRIDS FOR PHYSICAL MAPPING IN DISTAL XQ AND THE FRAGILE-X REGION | 0 | 14 |
| 690 | 9 | 34 | 825 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):481-487 FISCH GS; ARINAMI T; FROSTERISKENIUS U; FRYNS JP; CURFS LM; et al. RELATIONSHIP BETWEEN AGE AND IQ AMONG FRAGILE-X MALES - A MULTICENTER STUDY | 13 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 691 | 5 | 23 | 1074 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(1):81-87 BERRYKRAVIS E; SKLENA P DEMONSTRATION OF ABNORMAL CYCLIC-AMP PRODUCTION IN PLATELETS FROM PATIENTS WITH FRAGILE-X SYNDROME | 11 | 14 |
| 692 | 3 | 25 | 1152 1993 NATURE GENETICS 3(1):44-48 HANZLIK AJ; OSEMLAKHANZLIK MM; HAUSER MA; KURNIT DM A RECOMBINATION-BASED ASSAY DEMONSTRATES THAT THE FRAGILE-X SEQUENCE IS TRANSCRIBED WIDELY DURING DEVELOPMENT | 9 | 14 |
| 693 | 14 | 36 | 1182 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):358-363 HAY DA DOES IQ DECLINE WITH AGE IN FRAGILE-X A METHODOLOGICAL CRITIQUE | 13 | 14 |
| 694 | 12 | 21 | 1321 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 |
| 695 | 16 | 33 | 1327 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 |
| 696 | 18 | 31 | 1397 1995 HUMAN MOLECULAR GENETICS 4(9):1681-1684 QUAN F; GROMPE M; JAKOBS P; POPOVICH BW SPONTANEOUS DELETION IN THE FMR1 GENE IN A PATIENT WITH FRAGILE-X SYNDROME AND CHERUBISM | 9 | 14 |
| 697 | 12 | 30 | 1723 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):18-23 Guerreiro MM; Camargo EE; Kato M; Marques-De-Faria AP; Ciasca SM; et al. Fragile X syndrome - Clinical, electroencephalographic and neuroimaging characteristics | 8 | 14 |
| 698 | 4 | 66 | 1766 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(41):26998-27008 Parsons MA; Sinden RR; Izban MG Transcriptional properties of RNA polymerase II within triplet repeat-containing DNA from the human myotonic dystrophy and fragile X loci | 0 | 14 |
| 699 | 26 | 55 | 2021 2000 HUMAN MOLECULAR GENETICS 9(10):1487-1493 Tamanini F; Kirkpatrick LL; Schonkeren J; van Unen L; Bontekoe C; et al. The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins | 9 | 14 |
| 700 | 10 | 37 | 2233 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):923-932 Coffee B; Zhang FP; Ceman S; Warren ST; Reines D Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile X syndrome | 3 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 701 | 13 | 28 | 2239 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(2):140-146 Irwin SA; Idupulapati M; Gilbert ME; Harris JB; Chakravarti AB; et al. Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice | 11 | 14 |
| 702 | 15 | 44 | 2287 2002 HUMAN BRAIN MAPPING 16(4):206-218 Rivera SM; Menon V; White CD; Glaser B; Reiss AL Functional brain activation during arithmetic processing in females with fragile X Syndrome is related to FMRI protein expression | 7 | 14 |
| 703 | 8 | 27 | 2324 2002 NEUROBIOLOGY OF DISEASE 10(3):211-218 D'Agata V; Warren ST; Zhao WQ; Torre ER; Alkon DL; et al. Gene expression profiles in a transgenic animal model of fragile X syndrome | 0 | 14 |
| 704 | 28 | 41 | 2344 2002 RNA-A PUBLICATION OF THE RNA SOCIETY 8(12):1482-1488 Primerano B; Tassone F; Hagerman RJ; Hagerman P; Amaldi F; et al. Reduced FMR1 mRNA translation efficiency in Fragile X patients with premutations | 11 | 14 |
| 705 | 15 | 31 | 2389 2003 ANNALS OF NEUROLOGY 53(5):616-623 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; et al. Tremor and ataxia in fragile X premutation carriers: Blinded videotape study | 11 | 14 |
| 706 | 41 | 80 | 2480 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):805-816 Hagerman PJ; Hagerman RJ The fragile-X premutation: A maturing perspective | 8 | 14 |
| 707 | 8 | 46 | 70 1982 JOHNS HOPKINS MEDICAL JOURNAL 151(5):231-237 PYERITZ RE; STAMBERG J; THOMAS GH; BELL BB; ZAHKA KG; et al. THE MARKER XQ28 SYNDROME (FRAGILE-X SYNDROME) IN A RETARDED MAN WITH MITRAL-VALVE PROLAPSE | 8 | 13 |
| 708 | 2 | 8 | 78 1982 LANCET 1(8263):100-100 SUTHERLAND GR; JACKY PB PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 6 | 13 |
| 709 | 2 | 4 | 114 1983 ANNALES DE GENETIQUE 26(3):147-149 CALVAMERCADO MP; MAUNOURY C; RETHORE MO; LEJEUNE J FRAGILE-X AND INHIBITION OF DIHYDROFOLATE-REDUCTASE - COMPARED EFFECTS OF 2 ANTIBIOTICS - TRIMETHOPRIME AND PYRIMETHAMINE | 6 | 13 |
| 710 | 3 | 20 | 183 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):259-273 HOLDEN JJA; WANG HS; WHITE BN THE FRAGILE-X SYNDROME .4. PROGRESS TOWARDS THE IDENTIFICATION OF LINKED RESTRICTION FRAGMENT LENGTH VARIANTS (RFLVS) | 4 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 711 | 4 | 11 | 192 1984 ANNALES DE GENETIQUE 27(4):230-232 LEJEUNE J; RETHORE MO; DEBLOIS MC; RAVEL A ASSAY OF FOLIC-ACID TREATMENT IN FRAGILE-X SYNDROME | 8 | 13 |
| 712 | 0 | 0 | 220 1984 JOURNAL OF MEDICAL GENETICS 21(4):299-299 PEMBREY ME; WINTER RM; DAVIES KE A PERMUTATION THAT GENERATES THE DEFINITIVE MUTATION BY RECOMBINATION EXPLAINS THE INHERITANCE OF THE MARTIN-BELL SYNDROME (FRAGILE-X) | 9 | 13 |
| 713 | 11 | 29 | 244 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(3):543-552 ROSENBLATT DS; DUSCHENES EA; HELLSTROM FV; GOLICK MS; VEKEMANS MJJ; et al. FOLIC-ACID BLINDED TRIAL IN IDENTICAL-TWINS WITH FRAGILE-X SYNDROME | 9 | 13 |
| 714 | 14 | 34 | 254 1985 AMERICAN JOURNAL OF MENTAL DEFICIENCY 90(2):119-123 DELACRUZ FF FRAGILE-X SYNDROME | 10 | 13 |
| 715 | 6 | 28 | 296 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(2):87-90 VARLEY CK; HOLM VA; EREN MO COGNITIVE AND PSYCHIATRIC VARIABILITY IN 3 BROTHERS WITH FRAGILE X-SYNDROME | 10 | 13 |
| 716 | 43 | 97 | 364 1986 ANNALS OF THE NEW YORK ACADEMY OF SCIENCES 477:129-150 BROWN WT; JENKINS EC; KRAWCZUN MS; WISNIEWSKI K; RUDELLI R; et al. THE FRAGILE-X SYNDROME | 10 | 13 |
| 717 | 7 | 12 | 381 1986 CLINICAL GENETICS 30(4):249-254 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; et al. ANALYSIS OF FRAGILE X-MENTAL RETARDATION FAMILIES USING FLANKING POLYMORPHIC DNA PROBES | 7 | 13 |
| 718 | 4 | 7 | 495 1987 PRENATAL DIAGNOSIS 7(3):197-202 SUTHERLAND GR; BAKER E; PURVISSMITH S; HOCKEY A; KRUMINS E; et al. PRENATAL-DIAGNOSIS OF THE FRAGILE-X USING THYMIDINE INDUCTION | 5 | 13 |
| 719 | 0 | 18 | 514 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):77-82 PHELAN MC; STEVENSON RE; COLLINS JL; TRENT HE FRAGILE-X SYNDROME AND NEOPLASIA | 7 | 13 |
| 720 | 4 | 16 | 516 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):99-107 FILIPPI G; PECILE V; RINALDI A; SINISCALCO M FRAGILE-X MUTATION AND KLINEFELTER SYNDROME - A REAPPRAISAL | 9 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 721 | 22 | 61 | 531 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):355-368 MCKINLEY MJ; KEARNEY LU; NICOLAIDES KH; GOSDEN CM; WEBB TP; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME BY PLACENTAL (CHORIONIC VILLI) BIOPSY CULTURE | 8 | 13 |
| 722 | 12 | 33 | 676 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):738-743 ROCCHI M; ARCHIDIACONO N; RINALDI A; FILIPPI G; BARTOLUCCI G; et al. MENTAL-RETARDATION IN HETEROZYGOTES FOR THE FRAGILE-X MUTATION - EVIDENCE IN FAVOR OF AN X INACTIVATION-DEPENDENT EFFECT | 11 | 13 |
| 723 | 6 | 17 | 686 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(2):265-267 MOORE PSJ; CHUDLEY AE; WINTER JSD TRUE PRECOCIOUS PUBERTY IN A GIRL WITH THE FRAGILE X-SYNDROME | 10 | 13 |
| 724 | 1 | 14 | 697 1990 BRAIN & DEVELOPMENT 12(1):128-130 WAHLSTROM J; WITTENGERSTROM I; MELLQUIST L; ANVRET M; ODEN A THE RETT SYNDROME RELATED TO FRAGILE-X(P22) IN CAFFEINE-INDUCED LYMPHOCYTE CULTURE | 0 | 13 |
| 725 | 18 | 36 | 713 1990 JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME 72A(6):889-896 DAVIDS JR; HAGERMAN RJ; EILERT RE ORTHOPEDIC ASPECTS OF FRAGILE-X SYNDROME | 0 | 13 |
| 726 | 18 | 35 | 865 1991 GENOMICS 10(3):576-582 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; et al. LINKAGE HOMOGENEITY NEAR THE FRAGILE-X LOCUS IN NORMAL AND FRAGILE-X FAMILIES | 9 | 13 |
| 727 | 7 | 16 | 868 1991 HUMAN GENETICS 87(3):369-372 HULSEBOS TJM; OOSTRA BA; BROERSEN S; SMITS A; VANOOST BA; et al. NEW DISTAL MARKER CLOSELY LINKED TO THE FRAGILE-X LOCUS | 4 | 13 |
| 728 | 9 | 23 | 871 1991 JOURNAL OF ABNORMAL CHILD PSYCHOLOGY 19(3):253-262 EINFELD S; HALL W; LEVY F HYPERACTIVITY AND THE FRAGILE X SYNDROME | 12 | 13 |
| 729 | 5 | 17 | 1087 1993 BIOLOGICAL PSYCHIATRY 33(3):213-216 JEFFRIES FM; REISS AL; BROWN WT; MEYERS DA; GLICKSMAN AC; et al. BIPOLAR SPECTRUM DISORDER AND FRAGILE-X SYNDROME - A FAMILY STUDY | 4 | 13 |
| 730 | 20 | 26 | 1092 1993 CLINICAL GENETICS 43(1):34-38 HORI T; YAMAUCHI M; SEKI N; TSUJI S; IKUKO K HERITABLE UNSTABLE DNA-SEQUENCES AND HYPERMETHYLATION ASSOCIATED WITH FRAGILE-X SYNDROME IN JAPANESE FAMILIES | 11 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 731 | 38 | 84 | 1106 1993 GENETIC COUNSELING 4(4):245-263 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H FRAGILE-X SYNDROME AND AUTISM - A PREVALENT ASSOCIATION OR A MISINTERPRETED CONNECTION | 6 | 13 |
| 732 | 6 | 7 | 1139 1993 LANCET 341(8841):373-374 PALOMAKI GE; HADDOW JE IS IT TIME FOR POPULATION-BASED PRENATAL SCREENING FOR FRAGILE-X | 10 | 13 |
| 733 | 21 | 27 | 1323 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 |
| 734 | 40 | 75 | 1365 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):252-269 Cohen IL Behavioral profiles of autistic and nonautistic fragile X males | 12 | 13 |
| 735 | 7 | 8 | 1379 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):405-407 Holden JJA; Chalifoux M; Wing M; JulienInalsingh C; Lawson JS; et al. Distribution and frequency of FMR1 CGG repeat numbers in the general population | 6 | 13 |
| 736 | 14 | 35 | 1419 1995 JOURNAL OF MEDICAL GENETICS 32(12):925-929 KIRCHGESSNER CU; WARREN ST; WILLARD HF X INACTIVATION OF THE FMR1 FRAGILE-X MENTAL-RETARDATION GENE | 5 | 13 |
| 737 | 29 | 43 | 1479 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 |
| 738 | 14 | 24 | 1483 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 |
| 739 | 8 | 29 | 1621 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 |
| 740 | 5 | 11 | 1839 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):327-328 Braat DDM; Smits APT; Thomas CMG Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: A pilot study | 10 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 741 | 13 | 65 | 1886 1999 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 41(9):625-632 Hatton DD; Bailey DB; Hargett-Beck MQ; Skinner M; Clark RD Behavioral style of young boys with fragile X syndrome | 9 | 13 |
| 742 | 27 | 42 | 1967 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(4):229-236 Lachiewicz AM; Dawson DV; Spiridigliozzi GA Physical characteristics of young boys with fragile X syndrome: Reasons for difficulties in making a diagnosis in young males | 12 | 13 |
| 743 | 7 | 25 | 2160 2001 HUMAN REPRODUCTION 16(3):457-462 Hundscheid RDL; Braat DDM; Kiemeney LALM; Smits APT; Thomas CMG Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives | 8 | 13 |
| 744 | 26 | 47 | 2187 2001 NEUROPSYCHOLOGY 15(2):290-299 Bennetto L; Pennington BF; Porter D; Taylor AK; Hagerman RJ Profile of cognitive functioning in women with the fragile X mutation | 10 | 13 |
| 745 | 30 | 56 | 2437 2003 JOURNAL OF BIOLOGICAL CHEMISTRY 278(18):15669-15678 Sung YJ; Dolzhanskaya N; Nolin SL; Brown T; Currie JR; et al. The fragile X mental retardation protein FMRP binds elongation factor 1A mRNA and negatively regulates its translation in vivo | 8 | 13 |
| 746 | 22 | 45 | 2473 2003 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 100(24):14374-14378 Todd PK; Mack KJ; Malter JS The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95 | 8 | 13 |
| 747 | 36 | 60 | 2477 2003 TRENDS IN GENETICS 19(3):148-154 Kooy RF Of mice and the fragile X syndrome | 10 | 13 |
| 748 | 1 | 7 | 33 1981 NEW ENGLAND JOURNAL OF MEDICINE 305(22):1348-1348 NIELSEN KB; TOMMERUP N; DYGGVE H; SCHOU C MACROORCHIDISM, MENTAL-RETARDATION, AND THE FRAGILE-X | 8 | 12 |
| 749 | 1 | 7 | 84 1982 PEDIATRICS 69(5):668-669 RHOADS FA X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME | 11 | 12 |
| 750 | 5 | 26 | 90 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):869-878 POPOVICH BW; ROSENBLATT DS; COOPER BA; VEKEMANS M INTRACELLULAR FOLATE DISTRIBUTION IN CULTURED FIBROBLASTS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 8 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 751 | 1 | 10 | 136 1983 CYTOGENETICS AND CELL GENETICS 35(3):223-225 BRYANT EM; MARTIN GM; HOEHN H FRAGILE-X EXPRESSION STUDIED BY CLONAL ANALYSIS AND SOMATIC-CELL HYBRIDIZATION | 9 | 12 |
| 752 | 3 | 15 | 389 1986 HUMAN GENETICS 73(1):20-22 ABRUZZO MA; PETTAY D; MAYER M; JACOBS PA THE EFFECT OF CAFFEINE ON FRAGILE-X EXPRESSION | 9 | 12 |
| 753 | 14 | 52 | 402 1986 JOURNAL OF PEDIATRIC PSYCHOLOGY 11(1):91-102 MADISON LS; MOSHER GA; GEORGE CH FRAGILE-X SYNDROME - DIAGNOSIS AND RESEARCH | 0 | 12 |
| 754 | 4 | 7 | 455 1987 HUMAN GENETICS 75(3):269-271 WINTER RM POPULATION-GENETICS IMPLICATIONS OF THE PREMUTATION HYPOTHESIS FOR THE GENERATION OF THE FRAGILE X-MENTAL RETARDATION GENE | 11 | 12 |
| 755 | 16 | 41 | 472 1987 JOURNAL OF MEDICAL GENETICS 24(1):14-22 CONNOR JM; PIRRIT LA; YATES JRW; CROSSLEY JA; IMRIE SJ; et al. LINKAGE ANALYSIS USING MULTIPLE XQ DNA POLYMORPHISMS IN NORMAL-FAMILIES, FAMILIES WITH THE FRAGILE X-SYNDROME, AND OTHER FAMILIES WITH X-LINKED CONDITIONS | 7 | 12 |
| 756 | 4 | 18 | 546 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):613-623 WARREN ST; ZHANG F; SUTCLIFFE JS; PETERS JF STRATEGY FOR MOLECULAR-CLONING OF THE FRAGILE-X SITE DNA | 7 | 12 |
| 757 | 9 | 27 | 915 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):28-34 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; et al. LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X MALES - CLINICAL-EVIDENCE OF MORE THAN ONE MUTATION | 12 | 12 |
| 758 | 10 | 18 | 918 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):56-60 EINFELD S; HALL W BEHAVIOR PHENOTYPE OF THE FRAGILE X SYNDROME | 6 | 12 |
| 759 | 25 | 46 | 949 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):299-306 CLARKE A; BRADLEY D; GILLESPIE K; REES D; HOLLAND A; et al. FRAGILE-X MENTAL-RETARDATION AND THE IDURONATE SULFATASE LOCUS - TESTING LAIRD MODEL OF FRA(X) INHERITANCE | 7 | 12 |
| 760 | 5 | 25 | 962 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(5):543-550 LOESCH DZ; HAY DA; SHEFFIELD LJ FRAGILE-X FAMILY WITH UNUSUAL DIGITAL AND FACIAL ABNORMALITIES, CLEFT-LIP AND PALATE, AND EPILEPSY | 8 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 761 | 16 | 34 | 1180 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):346-352 FISCH GS; HOLDEN JJA; SIMENSEN R; CARPENTER N; HOWARDPEEBLES PN; et al. FRAGILE-X-SYNDROME A PERVASIVE DEVELOPMENTAL DISABILITY - COGNITIVE-ABILITY AND ADAPTIVE-BEHAVIOR IN MATES WITH THE FULL MUTATION | 11 | 12 |
| 762 | 17 | 18 | 1206 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):490-496 MADDALENA A; HICKS BD; SPENCE WC; LEVINSON G; HOWARDPEEBLES PN PRENATAL-DIAGNOSIS IN KNOWN FRAGILE-X CARRIERS | 7 | 12 |
| 763 | 1 | 16 | 1226 1994 CANCER RESEARCH 54(19):5212-5216 LEE ST; MCGLENNEN RC; LITZ CE CLONAL DETERMINATION BY THE FRAGILE-X (FMR1) AND PHOSPHOGLYCERATE KINASE (PGK) GENES IN HEMATOLOGICAL MALIGNANCIES | 1 | 12 |
| 764 | 19 | 28 | 1237 1994 HUMAN GENETICS 93(2):143-147 VAISANEN ML; KAHKONEN M; LEISTI J DIAGNOSIS OF FRAGILE-X SYNDROME BY DIRECT MUTATION ANALYSIS | 10 | 12 |
| 765 | 10 | 23 | 1254 1994 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 24(4):473-485 MAZZOCCO MMM; PENNINGTON BF; HAGERMAN RJ SOCIAL COGNITION SKILLS AMONG FEMALES WITH FRAGILE-X | 9 | 12 |
| 766 | 8 | 35 | 1372 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):336-344 Hagerman RJ; Riddle JE; Roberts LS; Breese K; Fulton M Survey of the efficacy of clonidine in fragile X syndrome | 12 | 12 |
| 767 | 6 | 13 | 1442 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 |
| 768 | 14 | 34 | 1538 1996 HUMAN GENETICS 98(4):409-414 Schmucker B; Ballhausen WG; Pfeiffer RA Mosaicism of a microdeletion of 486 bp involving the CGG repeat of the FMR1 gene due to misalignment of GTT tandem repeats at chi-like elements flanking both breakpoints and a full mutation | 5 | 12 |
| 769 | 12 | 14 | 1567 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 770 | 3 | 11 | 1623 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 771 | 7 | 10 | 1682 1997 JOURNAL OF MEDICAL GENETICS 34(3):250-251 Willemsen R; Los F; Mohkamsing S; vandenOuweland A; Deelen W; et al. Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal | 10 | 12 |
| 772 | 27 | 67 | 1900 1999 HUMAN MOLECULAR GENETICS 8(12):2293-2302 Burman RW; Popovich BW; Jacky PB; Turker MS Fully expanded FMR1 CGG repeats exhibit a length-and differentiation-dependent instability in cell hybrids that is independent of DNA methylation | 9 | 12 |
| 773 | 16 | 22 | 1919 1999 JOURNAL OF MEDICAL GENETICS 36(6):467-470 de Vries BBA; Mohkamsing S; van den Ouweland AMW; Mol E; Gelsema K; et al. Screening for the fragile X syndrome among the mentally retarded: a clinical study | 4 | 12 |
| 774 | 30 | 59 | 1974 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):150-156 Backes M; Genc B; Schreck J; Doerfler W; Lehmkuhl G; et al. Cognitive and behavioral profile of fragile X boys: Correlations to molecular data | 8 | 12 |
| 775 | 13 | 43 | 2122 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):28-38 Belser RC; Sudhalter V Conversational characteristics of children with fragile X syndrome: Repetitive speech | 9 | 12 |
| 776 | 3 | 21 | 2146 2001 ELECTROPHORESIS 22(6):1188-1193 Sung WC; Lee GB; Tzeng CC; Chen SH Plastic microchip electrophoresis for genetic screening: The analysis of polymerase chain reactions products of fragile X (CGG)n alleles | 0 | 12 |
| 777 | 18 | 33 | 2475 2003 RNA-A PUBLICATION OF THE RNA SOCIETY 9(10):1198-1207 Ramos A; Hollingworth D; Pastore A G-quartet-dependent recognition between the FMRP RGG box and RNA | 7 | 12 |
| 778 | 1 | 15 | 37 1981 PEDIATRICS 68(4):594-595 GERALD PS X-LINKED MENTAL-RETARDATION AND THE FRAGILE-X SYNDROME | 5 | 11 |
| 779 | 2 | 7 | 65 1982 HUMAN GENETICS 61(2):163-164 EBERLE G; ZANKL H; ZANKL M CO-CULTIVATION STUDIES WITH CELLS OF PATIENTS BEARING FRAGILE-X CHROMOSOMES | 7 | 11 |
| 780 | 8 | 23 | 129 1983 CLINICAL GENETICS 23(6):436-440 SILVERMAN W; LUBIN R; JENKINS EC; BROWN WT THE STRENGTH OF ASSOCIATION BETWEEN FRAGILE(X) CHROMOSOME PRESENCE AND MENTAL-RETARDATION | 8 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 781 | 0 | 18 | 376 1986 CLINICAL ENDOCRINOLOGY 24(3):327-333 OHARE JP; OBRIEN IAD; ARENDT J; ASTLEY P; RATCLIFFE W; et al. DOES MELATONIN DEFICIENCY CAUSE THE ENLARGED GENITALIA OF THE FRAGILE-X SYNDROME | 9 | 11 |
| 782 | 5 | 13 | 419 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):987-990 MULLEY JC; SUTHERLAND GR FRAGILE-X TRANSMISSION AND THE DETERMINATION OF CARRIER PROBABILITIES FOR GENETIC-COUNSELING | 0 | 11 |
| 783 | 4 | 11 | 463 1987 HUMAN GENETICS 77(1):92-94 ARINAMI T; KONDO I; HAMAGUCHI H; TAMURA K; HIRANO T A FRAGILE-X FEMALE WITH DOWN-SYNDROME | 8 | 11 |
| 784 | 10 | 24 | 501 1988 AMERICAN JOURNAL OF HUMAN GENETICS 43(1):46-51 ARINAMI T; SATO M; NAKAJIMA S; KONDO I AUDITORY BRAIN-STEM RESPONSES IN THE FRAGILE-X SYNDROME | 8 | 11 |
| 785 | 3 | 8 | 535 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):401-406 FRYNS JP; VANDENBERGHE H INACTIVATION PATTERN OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 7 | 11 |
| 786 | 6 | 7 | 650 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(3):473-476 BOLTON P; RUTTER M; BUTLER L; SUMMERS D FEMALES WITH AUTISM AND THE FRAGILE-X | 7 | 11 |
| 787 | 1 | 5 | 659 1989 LANCET 2(8657):279-279 SCHEPIS C; PALAZZO R; RAGUSA RM; SPINA E; BARLETTA C ASSOCIATION OF CUTIS VERTICIS GYRATA WITH FRAGILE-X SYNDROME AND FRAGILITY OF CHROMOSOME-12 | 0 | 11 |
| 788 | 35 | 45 | 1113 1993 HUMAN GENETICS 92(5):491-498 STEINBACH P; WOHRLE D; TARIVERDIAN G; KENNERKNECHT I; BARBI G; et al. MOLECULAR ANALYSIS OF MUTATIONS IN THE GENE FMR-1 SEGREGATING IN FRAGILE X-FAMILIES | 7 | 11 |
| 789 | 2 | 3 | 1140 1993 LANCET 341(8847):769-770 BONTHRON D; STRAIN L POPULATION SCREENING FOR FRAGILE-X SYNDROME | 10 | 11 |
| 790 | 17 | 32 | 1175 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):309-314 CHIURAZZI P; DEGRAAFF E; NG J; VERKERK AJMH; WOLFSON S; et al. NO APPARENT INVOLVEMENT OF THE FMR1 GENE IN 5 PATIENTS WITH PHENOTYPIC MANIFESTATIONS OF THE FRAGILE-X-SYNDROME | 7 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 791 | 7 | 13 | 1179 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):339-345 FISCH GS; NELSON DL; SNOW K; THIBODEAU SN; CHALIFOUX M; et al. RELIABILITY OF DIAGNOSTIC-ASSESSMENT OF NORMAL AND PREMUTATION STATUS IN THE FRAGILE-X-SYNDROME USING DNA TESTING | 9 | 11 |
| 792 | 58 | 91 | 1233 1994 EUROPEAN JOURNAL OF CLINICAL INVESTIGATION 24(1):1-10 ROUSSEAU F THE FRAGILE-X SYNDROME - IMPLICATIONS OF MOLECULAR-GENETICS FOR THE CLINICAL SYNDROME | 8 | 11 |
| 793 | 17 | 27 | 1416 1995 JOURNAL OF MEDICAL GENETICS 32(3):236-239 MACPHERSON JN; CURTIS G; CROLLA JA; DENNIS N; MIGEON B; et al. UNUSUAL (CGG)(N) EXPANSION AND RECOMBINATION IN A FAMILY WITH FRAGILE-X AND DIGEORGE-SYNDROME | 5 | 11 |
| 794 | 71 | 117 | 1433 1995 PEDIATRIC RESEARCH 38(5):629-637 OOSTRA BA; HALLEY DJJ COMPLEX BEHAVIOR OF SIMPLE REPEATS - THE FRAGILE-X SYNDROME | 8 | 11 |
| 795 | 14 | 20 | 1441 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 |
| 796 | 4 | 11 | 1462 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 |
| 797 | 12 | 21 | 1475 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 |
| 798 | 17 | 24 | 1478 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 |
| 799 | 27 | 53 | 1821 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 |
| 800 | 5 | 6 | 1838 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):326-326 Vianna-Morgante AM Twinning and premature ovarian failure in premutation fragile X carriers | 10 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 801 | 11 | 14 | 1843 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):347-349 Chiurazzi P; Pomponi MG; Sharrock A; Macpherson J; Lormeau S; et al. DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature | 4 | 11 |
| 802 | 18 | 31 | 1845 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):179-183 Pang CP; Poon PMK; Chen QL; Lai KYC; Yin CH; et al. Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients | 8 | 11 |
| 803 | 20 | 34 | 1847 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):191-194 Zhong N; Ju WN; Xu WM; Ye LL; Shen Y; et al. Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians | 7 | 11 |
| 804 | 4 | 11 | 1862 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):306-308 Syrrou M; Georgiou I; Patsalis PC; Bouba I; Adonakis G; et al. Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction | 2 | 11 |
| 805 | 8 | 10 | 1910 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:47-53 Carmichael B; Pembrey M; Turner G; Barnicoat A Diagnosis of fragile-X syndrome: the experiences of parents | 9 | 11 |
| 806 | 2 | 29 | 1987 2000 BEHAVIOR RESEARCH METHODS INSTRUMENTS & COMPUTERS 32(1):5-10 Boccia ML; Roberts JE Behavior and autonomic nervous system function assessed via heart period measures: The case of hyperarousal in boys with fragile X syndrome | 8 | 11 |
| 807 | 42 | 62 | 2022 2000 HUMAN MOLECULAR GENETICS 9(12):1759-1769 Crawford DC; Zhang FP; Wilson B; Warren ST; Sherman SL Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability | 7 | 11 |
| 808 | 35 | 55 | 2023 2000 HUMAN MOLECULAR GENETICS 9(19):2909-2918 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 | 3 | 11 |
| 809 | 13 | 39 | 2038 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(4):278-282 Wisbeck JM; Huffman LC; Freund L; Gunnar MR; Davis EP; et al. Cortisol and social stressors in children with fragile X: A pilot study | 9 | 11 |
| 810 | 32 | 45 | 2085 2000 NUCLEIC ACIDS RESEARCH 28(7):1535-1541 Weisman-Shomer P; Cohen E; Fry M Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures | 6 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 811 | 66 | 100 | 2139 2001 CLINICAL GENETICS 60(6):399-408 Oostra BA; Chiurazzi P The fragile X gene and its function | 5 | 11 |
| 812 | 22 | 39 | 2467 2003 NEUROSCIENCE 120(4):1005-1017 Chen L; Yun SW; Seto J; Liu W; Toth M The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences | 10 | 11 |
| 813 | 0 | 24 | 8 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(5):752-761 MARENI C; MIGEON BR FRAGILE-X SYNDROME - SEARCH FOR PHENOTYPIC MANIFESTATIONS AT LOCI FOR HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE | 7 | 10 |
| 814 | 1 | 9 | 285 1985 HUMAN GENETICS 69(3):206-208 MAYER M; ABRUZZO MA; JACOBS PA; YEE SC A CYTOGENETIC STUDY OF A POPULATION OF RETARDED FEMALES WITH SPECIAL REFERENCE TO THE FRAGILE (X) SYNDROME | 4 | 10 |
| 815 | 2 | 7 | 311 1985 PRENATAL DIAGNOSIS 5(3):229-231 ROCCHI M; PECILE V; ARCHIDIACONO N; MONNI G; DUMEZ Y; et al. PRENATAL-DIAGNOSIS OF THE FRAGILE-X IN MALE MONOZYGOTIC TWINS - DISCORDANT EXPRESSION OF THE FRAGILE SITE IN AMNIOCYTES | 5 | 10 |
| 816 | 5 | 11 | 323 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):171-178 SIMPSON NE DERMATOGLYPHIC INDEXES OF MALES WITH THE FRAGILE-X SYNDROME AND OF THE FEMALE HETEROZYGOTES | 6 | 10 |
| 817 | 2 | 7 | 378 1986 CLINICAL GENETICS 29(3):191-195 HECHT F; FRYNS JP; VLIETINCK RF; VANDENBERGHE H GENETIC-CONTROL OVER FRAGILE X-CHROMOSOME EXPRESSION | 9 | 10 |
| 818 | 3 | 4 | 521 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):165-168 BUTLER MG; ALLEN GA; SINGH DN; CARPENTER NJ; HALL BD PHOTOANTHROPOMETRIC ANALYSIS OF INDIVIDUALS WITH THE FRAGILE-X SYNDROME | 6 | 10 |
| 819 | 8 | 12 | 552 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):673-679 HOLMGREN G; BLOMQUIST HK; DRUGGE U; GUSTAVSON KH FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY DEMONSTRATING APPARENT PATERNAL TRANSMISSION FROM THE 18TH-CENTURY | 10 | 10 |
| 820 | 2 | 5 | 554 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):693-696 LAIRD CD FRAGILE-X MUTATION PROPOSED TO BLOCK COMPLETE REACTIVATION IN FEMALES OF AN INACTIVE X-CHROMOSOME | 7 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 821 | 8 | 13 | 558 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):735-739 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; et al. MARTIN-BELL SYNDROME IN GREECE, WITH REPORT OF ANOTHER 47,XXY FRAGILE X PATIENT | 7 | 10 |
| 822 | 0 | 0 | 875 1991 JOURNAL OF MEDICAL GENETICS 28(12):809-810 JACOBS PA THE FRAGILE-X SYNDROME | 6 | 10 |
| 823 | 9 | 18 | 884 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):831-834 HILTON DK; MARTIN CA; HEFFRON WM; HALL BD; JOHNSON GL IMIPRAMINE TREATMENT OF ADHD IN A FRAGILE-X CHILD | 5 | 10 |
| 824 | 16 | 19 | 954 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):333-338 GABARRON J; LOPEZ I; GLOVER G; CARBONELL P FRAGILE-X SCREENING-PROGRAM IN A SPANISH REGION | 9 | 10 |
| 825 | 1 | 3 | 1141 1993 LANCET 341(8847):770-770 HOWARDPEEBLES PN; MADDALENA A; BLACK SH; SCHULMAN JD POPULATION SCREENING FOR FRAGILE-X SYNDROME | 9 | 10 |
| 826 | 9 | 16 | 1181 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):353-357 FISCH GS; SIMENSEN R; ARINAMI T; BORGHGRAEF M; FRYNS JP LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X FEMALES - A PRELIMINARY MULTICENTER ANALYSIS | 9 | 10 |
| 827 | 13 | 56 | 1524 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:689-697 Liu Q; Siomi H; Siomi MC; Fischer U; Zhang Y; et al. Molecular characterization of the protein products of the fragile X syndrome gene and the survival of motor neurons gene | 2 | 10 |
| 828 | 26 | 38 | 1669 1997 HUMAN MUTATION 10(5):393-399 Wang YC; Lin ML; Lin SJ; Li YC; Li SY Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome | 7 | 10 |
| 829 | 32 | 57 | 1675 1997 JOURNAL OF INHERITED METABOLIC DISEASE 20(2):139-151 Hoogeveen AT; Oostra BA The fragile X syndrome | 6 | 10 |
| 830 | 31 | 107 | 1731 1998 CURRENT OPINION IN GENETICS & DEVELOPMENT 8(2):245-253 Tapscott SJ; Klesert TR; Widrow RJ; Stoger R; Laird CD Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes | 1 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 831 | 13 | 26 | 1827 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 |
| 832 | 16 | 23 | 1887 1999 DIAGNOSTIC MOLECULAR PATHOLOGY 8(3):152-156 Tzeng CC; Cho WC; Kuo PL; Chen RM Pilot fragile X screening in normal population of Taiwan | 7 | 10 |
| 833 | 20 | 50 | 2032 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(3):2231-2238 Weisman-Shomer P; Naot Y; Fry M Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins | 7 | 10 |
| 834 | 21 | 34 | 2095 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 |
| 835 | 23 | 55 | 2123 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(3):216-230 Roberts JE; Mirrett P; Burchinal M Receptive and expressive communication development of young males with fragile X syndrome | 6 | 10 |
| 836 | 37 | 73 | 2140 2001 COGNITIVE NEUROPSYCHOLOGY 18(1):1-18 Simon JA; Keenan JM; Pennington BF; Taylor AK; Hagerman RJ Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence | 8 | 10 |
| 837 | 2 | 13 | 2182 2001 MOLECULAR AND CELLULAR ENDOCRINOLOGY 183:S77-S85 Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; et al. PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome | 0 | 10 |
| 838 | 11 | 20 | 2257 2002 CURRENT BIOLOGY 12(24):R852-R854 Carthew RW RNA interference: The fragile X syndrome connection | 3 | 10 |
| 839 | 8 | 61 | 2297 2002 JOURNAL OF COGNITIVE NEUROSCIENCE 14(2):160-171 Tamm L; Menon V; Johnston CK; Hessl DR; Reiss AL fMRI study of cognitive interference processing in females with fragile X syndrome | 6 | 10 |
| 840 | 33 | 95 | 2619 2004 TRENDS IN NEUROSCIENCES 27(7):370-377 Bear MF; Huber KM; Warren ST The mGIuR theory of fragile X mental retardation | 8 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 841 | 0 | 9 | 26 1981 LANCET 1(8219):556-557 SOUDEK D; MCGREGOR T SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 6 | 9 |
| 842 | 0 | 32 | 55 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 |
| 843 | 0 | 1 | 92 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A82-A82 CARPENTER NJ; BARBER DH; JONES M; LINDLEY W; CARR C CONTROLLED 6-MONTH STUDY OF ORAL FOLIC-ACID THERAPY IN BOYS WITH FRAGILE X-LINKED MENTAL-RETARDATION | 0 | 9 |
| 844 | 2 | 13 | 107 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):1270-1275 MIXON JC; DEV VG FRAGILE-X EXPRESSION IS DECREASED BY 5-AZACYTIDINE AND S-ADENOSYLHOMOCYSTEINE | 5 | 9 |
| 845 | 9 | 17 | 116 1983 ANNALES DE GENETIQUE 26(4):247-250 TEJADA I; BOUE J; GILGENKRANTZ S PRENATAL-DIAGNOSIS OF FRAGILE X-CHROMOSOME ON AMNIOTIC-FLUID CELLS | 6 | 9 |
| 846 | 3 | 11 | 130 1983 CLINICAL GENETICS 24(3):153-155 NIELSEN KB; TOMMERUP N; FRIIS B; HJELT K; HIPPE E FOLIC-ACID METABOLISM IN A PATIENT WITH FRAGILE-X | 0 | 9 |
| 847 | 8 | 23 | 137 1983 HUMAN GENETICS 64(1):39-41 FONATSCH C; SCHWINGER E FREQUENCY OF FRAGILE-X CHROMOSOMES, FRA(X), IN LYMPHOCYTES IN RELATION TO BLOOD-STORAGE TIME AND CULTURE TECHNIQUES | 6 | 9 |
| 848 | 0 | 4 | 170 1984 AMERICAN JOURNAL OF HUMAN GENETICS 36(1):227-229 MIEZEJESKI CM; JENKINS EC; HILL AL; WISNIEWSKI K; BROWN WT VERBAL VS NONVERBAL ABILITY, FRAGILE-X SYNDROME, AND HETEROZYGOUS CARRIERS | 8 | 9 |
| 849 | 2 | 10 | 207 1984 HUMAN GENETICS 68(2):189-190 REIDY JA; CHEN ATL FOLIC-ACID AND CHROMOSOME BREAKAGE .2. A METHIONINE EFFECT SIMILAR TO THAT IN FRAGILE-X EXPRESSION | 1 | 9 |
| 850 | 6 | 16 | 234 1984 PRENATAL DIAGNOSIS 4(1):61-66 WILSON MG; MARCHESE CA PRENATAL-DIAGNOSIS OF FRAGILE-X IN A HETEROZYGOUS FEMALE FETUS AND POSTNATAL FOLLOW-UP | 5 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 851 | 13 | 28 | 287 1985 HUMAN GENETICS 69(3):218-223 VONKOSKULL H; AULA P; AMMALA P; NORDSTROM AM; RAPOLA J IMPROVED TECHNIQUE FOR THE EXPRESSION OF FRAGILE-X IN CULTURED AMNIOTIC-FLUID CELLS | 5 | 9 |
| 852 | 24 | 48 | 414 1986 TRENDS IN NEUROSCIENCES 9(2):58-62 PEMBREY ME; WINTER RM; DAVIES KE FRAGILE X MENTAL-RETARDATION - CURRENT CONTROVERSIES | 7 | 9 |
| 853 | 7 | 17 | 423 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 28(1):13-15 CHUDLEY AE; DEVONFLINDT R; HAGERMAN RJ COGNITIVE VARIABILITY IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 854 | 14 | 26 | 460 1987 HUMAN GENETICS 76(4):344-347 ARINAMI T; KONDO I; NAKAJIMA S; HAMAGUCHI H FREQUENCY OF THE FRAGILE X-SYNDROME IN INSTITUTIONALIZED MENTALLY-RETARDED FEMALES IN JAPAN | 7 | 9 |
| 855 | 16 | 23 | 534 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):393-399 FISCH GS; COHEN IL; GROSS AC; JENKINS V; JENKINS EC; et al. FOLIC-ACID TREATMENT OF FRAGILE-X MALES - A FURTHER STUDY | 4 | 9 |
| 856 | 4 | 9 | 633 1989 BRITISH HEART JOURNAL 61(3):289-291 SREERAM N; WREN C; BHATE M; ROBERTSON P; HUNTER S CARDIAC ABNORMALITIES IN THE FRAGILE X-SYNDROME | 6 | 9 |
| 857 | 0 | 3 | 669 1989 SCIENCE 243(4888):171-172 BARNES DM FRAGILE-X SYNDROME AND ITS PUZZLING GENETICS | 3 | 9 |
| 858 | 24 | 65 | 712 1990 HUMAN GENETICS 85(6):659-665 WOHRLE D; FRYNS JP; STEINBACH P FRAGILE-X EXPRESSION AND FRAGILE-X INACTIVATION .1. THE EXPRESSION OF THE FRAGILE SITE AT XQ27.3 IS NOT SUPPRESSED ON INACTIVE X-CHROMOSOMES SEPARATED FROM THE ACTIVE HOMOLOG | 7 | 9 |
| 859 | 10 | 28 | 820 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):440-444 KUPKE KG; SORENG AL; MULLER U ORIGIN OF THE SUPERNUMERARY X-CHROMOSOME IN A PATIENT WITH FRAGILE-X AND KLINEFELTER SYNDROME | 7 | 9 |
| 860 | 6 | 20 | 826 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):488-492 DEVONFLINDT R; BYBEL B; CHUDLEY AE; LOPES F SHORT-TERM-MEMORY AND COGNITIVE VARIABILITY IN ADULT FRAGILE-X FEMALES | 7 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 861 | 0 | 0 | 898 1991 OPTOMETRY AND VISION SCIENCE 68(8):634-640 MAINO DM; WESSON M; SCHLANGE D; CIBIS G; MAINO JH OPTOMETRIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 862 | 0 | 3 | 926 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):116-119 STEYAERT J; BORGHGRAEF M; GAULTHIER C; FRYNS JP; VANDENBERGHE H COGNITIVE PROFILE IN ADULT, NORMAL INTELLIGENT FEMALE FRAGILE-X CARRIERS | 6 | 9 |
| 863 | 7 | 11 | 959 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(5):905-912 MACPHERSON J; HARVEY J; CURTIS G; WEBB T; HEITZ D; et al. A REINVESTIGATION OF 33 FRAGILE(X) FAMILIES USING PROBE STB12.3 | 7 | 9 |
| 864 | 6 | 25 | 988 1992 GENOMICS 12(4):818-821 LAVAL SH; BLAIR HJ; HIRST MC; DAVIES KE; BOYD Y MAPPING OF FMR1, THE GENE IMPLICATED IN FRAGILE X-LINKED MENTAL-RETARDATION, ON THE MOUSE X-CHROMOSOME | 0 | 9 |
| 865 | 6 | 26 | 1076 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(4):415-422 LOESCH DZ; HUGGINS RM; CHIN WF EFFECT OF FRAGILE-X ON PHYSICAL AND INTELLECTUAL TRAITS ESTIMATED BY PEDIGREE ANALYSIS | 7 | 9 |
| 866 | 0 | 0 | 1119 1993 INTERNATIONAL JOURNAL OF HEMATOLOGY 57(1):9-14 MIMURO J; MURAMATSU S; KANEKO M; YOSHITAKE S; IIJIMA K; et al. AN ABNORMAL PROTEIN-C (PROTEIN-C YONAGO) WITH AN AMINO-ACID SUBSTITUTION OF GLY FOR ARG-15 CAUSED BY A SINGLE BASE MUTATION OF C TO G IN CODON-57 (CGG-]GGG) - DETERIORATED CALCIUM-DEPENDENT CONFORMATION OF THE GAMMA-CARBOXYGLUTAMIC ACID DOMAIN RELEVANT TO A THROMBOTIC TENDENCY | 0 | 9 |
| 867 | 7 | 23 | 1129 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:131-142 BUTLER MG; SINGH DN CLINICAL AND CYTOGENETIC SURVEY OF INSTITUTIONALIZED MENTALLY-RETARDED PATIENTS WITH EMPHASIS ON THE FRAGILE-X SYNDROME | 4 | 9 |
| 868 | 0 | 3 | 1217 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):382-382 HOWARDPEEBLES PN; MADDALENA A; SPENCE WC; LEVINSON G; FALLON L; et al. FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 5 | 9 |
| 869 | 7 | 18 | 1247 1994 INTELLIGENCE 19(1):45-50 DANIELS JK; OWEN MJ; MCGUFFIN P; THOMPSON L; DETTERMAN DK; et al. IQ AND VARIATION IN THE NUMBER OF FRAGILE-X CGG REPEATS - NO ASSOCIATION IN A NORMAL SAMPLE | 2 | 9 |
| 870 | 20 | 28 | 1395 1995 HUMAN GENETICS 96(5):577-584 ELALEEM AA; BOHM I; TEMTAMY S; ELAWADY M; AWADALLA M; et al. DIRECT MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME IN A SAMPLE OF EGYPTIAN AND GERMAN PATIENTS USING NONRADIOACTIVE PCR AND SOUTHERN BLOT FOLLOWED BY CHEMILUMINESCENT DETECTION | 6 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 871 | 1 | 22 | 1401 1995 JOURNAL OF BACTERIOLOGY 177(7):1915-1917 FUTO S; SETO Y; MITSUSE S; MORI Y; SUZUKI T; et al. MOLECULAR-CLONING OF A 46-KILODALTON SURFACE-ANTIGEN (P46) GENE FROM MYCOPLASMA-HYOPNEUMONIAE - DIRECT EVIDENCE OF CGG CODON USAGE FOR ARGININE | 0 | 9 |
| 872 | 23 | 37 | 1408 1995 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 17(4):518-528 HINTON VJ; HALPERIN JM; DOBKIN CS; DING XH; BROWN WT; et al. COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X | 5 | 9 |
| 873 | 8 | 12 | 1418 1995 JOURNAL OF MEDICAL GENETICS 32(11):907-908 PINTADO E; DEDIEGO Y; HMADCHA A; CARRASCO M; SIERRA J; et al. INSTABILITY OF THE CGG REPEAT AT THE FRAXA LOCUS AND VARIABLE PHENOTYPIC-EXPRESSION IN A LARGE FRAGILE-X PEDIGREE | 2 | 9 |
| 874 | 18 | 37 | 1444 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 |
| 875 | 16 | 20 | 1477 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 |
| 876 | 0 | 7 | 1493 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 |
| 877 | 64 | 95 | 1517 1996 CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA 5(4):895-& Hagerman RJ Fragile X syndrome | 1 | 9 |
| 878 | 35 | 63 | 1571 1996 PRENATAL DIAGNOSIS 16(13):1199-1211 Sutherland GR; Mulley JC Fragile X syndrome and Fragile XE mental retardation | 3 | 9 |
| 879 | 8 | 10 | 1643 1997 BRITISH MEDICAL JOURNAL 315(7117):1223-1226 Turner G; Robinson H; Wake S; Laing S; Partington M Case finding for the fragile X syndrome and its consequences | 5 | 9 |
| 880 | 16 | 23 | 1664 1997 HUMAN GENETICS 101(2):214-218 Hirst MC; Arinami T; Laird CD Sequence analysis of long FMR1 arrays in the Japanese population: insights into the generation of long (CGG)(n) tracts | 4 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 881 | 10 | 39 | 1760 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(4):321-328 Mazzocco MMM; Pulsifer M; Fiumara A; Cocuzza M; Nigro F; et al. Brief report: Autistic behaviors among children with fragile X or Rett syndrome: Implications for the classification of pervasive developmental disorder | 4 | 9 |
| 882 | 2 | 13 | 1797 1998 STEROIDS 63(1):2-4 Joseph DR The rat androgen-binding protein (ABP/SHBG) gene contains triplet repeats similar to unstable triplets: Evidence that the ABP/SHBG and the fragile X-related 2 genes overlap | 0 | 9 |
| 883 | 12 | 18 | 1918 1999 JOURNAL OF MEDICAL GENETICS 36(3):253-257 Helderman-van den Enden ATJM; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; et al. Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities | 3 | 9 |
| 884 | 20 | 43 | 1922 1999 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 38(10):1294-1301 Murphy DGM; Mentis MJ; Pietrini P; Grady CL; Moore CJ; et al. Premutation female carriers of fragile X syndrome: A pilot study on brain anatomy and metabolism | 8 | 9 |
| 885 | 4 | 46 | 1990 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 278(3):833-838 Patel PK; Bhavesh NS; Hosur RV Cation-dependent conformational switches in d-TGGCGGC containing two triplet repeats of Fragile X Syndrome: NMR observations | 4 | 9 |
| 886 | 11 | 52 | 1992 2000 BRAIN AND COGNITION 44(3):387-401 Munir F; Cornish KM; Wilding J Nature of the working memory deficit in Fragile-X syndrome | 8 | 9 |
| 887 | 8 | 32 | 2076 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 | 7 | 9 |
| 888 | 20 | 55 | 2115 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(1):81-90 Sun HT; Cohen S; Kaufmann WE Annexin-1 is abnormally expressed in fragile X syndrome: Two-dimensional electrophoresis study in lymphocytes | 4 | 9 |
| 889 | 27 | 39 | 2117 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(4):314-319 Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; et al. Neurobehavioral phenotype in carriers of the fragile X premutation | 8 | 9 |
| 890 | 45 | 85 | 2132 2001 BRAIN RESEARCH BULLETIN 56(3-4):375-382 Bardoni B; Schenck A; Mandel JL The Fragile X mental retardation protein | 6 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 891 | 10 | 13 | 2213 2001 SCIENCE 294(5551):2487-2488 Moine H; Mandel JL Biomedicine - Do G quartets orchestrate fragile X pathology? | 4 | 9 |
| 892 | 0 | 44 | 2293 2002 JOURNAL OF BIOLOGICAL CHEMISTRY 277(23):21041-21049 Vargason JM; Ho PS The effect of cytosine methylation on the structure and geometry of the Holliday junction - The structure of d(CCGGTACm(5)CGG) at 1.5 angstrom resolution | 0 | 9 |
| 893 | 33 | 52 | 2316 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):179-186 Keysor CS; Mazzocco MMM A developmental approach to understanding fragile X syndrome in females | 8 | 9 |
| 894 | 19 | 36 | 2334 2002 NUCLEIC ACIDS RESEARCH 30(14):3278-3285 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; et al. Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 3 | 9 |
| 895 | 19 | 43 | 2343 2002 PSYCHONEUROENDOCRINOLOGY 27(7):855-872 Hessl D; Glaser B; Dyer-Friedman J; Blasey C; Hastie T; et al. Cortisol and behavior in fragile X syndrome | 6 | 9 |
| 896 | 0 | 9 | 27 1981 LANCET 1(8219):557-557 EBERLE G; ZANKL H; ZANKL M SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 4 | 8 |
| 897 | 1 | 30 | 38 1982 AMERICAN JOURNAL OF DISEASES OF CHILDREN 136(5):389-391 TOWNES PL FRAGILE-X SYNDROME - A JIGSAW PUZZLE WITH PICTURE EMERGING | 6 | 8 |
| 898 | 0 | 5 | 62 1982 HUMAN GENETICS 60(1):80-81 ZANKL H; EBERLE G METHODS OF INCREASING THE VISIBILITY OF FRAGILE-X CHROMOSOMES | 5 | 8 |
| 899 | 0 | 36 | 113 1983 AMERICAN JOURNAL OF MENTAL DEFICIENCY 87(4):372-376 PUESCHEL SM; HAYS RM; MENDOZA T FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MINOR CONGENITAL-ANOMALIES, MACRO-ORCHIDISM, AND FRAGILE X-CHROMOSOME | 6 | 8 |
| 900 | 0 | 4 | 154 1983 LANCET 2(8364):1427-1427 KINNELL HG; BANU SP INSTITUTIONAL PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |