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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 |
|---|---|---|---|---|---|
| 401 | 13 | 39 | 1910 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(4):278-282 Wisbeck JM; Huffman LC; Freund L; Gunnar MR; Davis EP; Reiss AL Cortisol and social stressors in children with fragile X: A pilot study | 8 | 10 |
| 402 | 27 | 39 | 1988 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(4):314-319 Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; Blasey C; Taylor A; Reiss A Neurobehavioral phenotype in carriers of the fragile X premutation | 5 | 5 |
| 403 | 17 | 39 | 2147 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(2):107-114 Fisch GS; Simensen RJ; Schroer RJ Longitudinal changes in cognitive and adaptive Behavior scores in children and adolescents with the fragile X mutation or autism | 2 | 2 |
| 404 | 17 | 39 | 2178 2002 NEUROBIOLOGY OF DISEASE 11(1):53-63 Schenck A; Van de Bor V; Bardoni B; Giangrande A Novel features of dFMR1, the Drosophila orthologue of the fragile X mental retardation protein | 3 | 3 |
| 405 | 28 | 39 | 2199 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(2):454-464 Nolin SL; Brown WT; Glicksman A; Houck GE; Gargano AD; Sullivan A; Biancalana V; Brondum-Nielsen K; Hjalgrim H; Holinski-Feder E; Kooy F; Longshore J; Macpherson J; Mandel JL; Matthijs G; Rousseau F; Steinbach P; Vaisanen ML; von Koskull H; Sherman SL Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles | 8 | 12 |
| 406 | 15 | 39 | 2233 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160 Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; Karadottir S; O'Brien A Receptive language skills of adolescents and young adults with Down or fragile X syndrome | 2 | 3 |
| 407 | 21 | 39 | 2300 2003 NEUROSCIENCE 120(4):1005-1017 Chen L; Yun SW; Seto J; Liu W; Toth M The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences | 3 | 3 |
| 408 | 20 | 39 | 2360 2004 NATURE NEUROSCIENCE 7(2):113-117 Jin P; Zarnescu DC; Ceman S; Nakamoto M; Mowrey J; Jongens TA; Nelson DL; Moses K; Warren ST Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway | 2 | 6 |
| 409 | 11 | 38 | 326 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):241-262 HAGERMAN RJ; JACKSON AW; LEVITAS A; BRADEN M; MCBOGG P; KEMPER M; MCGAVRAN L; BERRY R; MATUS I; HAGERMAN PJ ORAL FOLIC-ACID VERSUS PLACEBO IN THE TREATMENT OF MALES WITH THE FRAGILE-X SYNDROME | 18 | 26 |
| 410 | 17 | 38 | 469 1987 JOURNAL OF MEDICAL GENETICS 24(1):23-31 VEENEMA H; GERAEDTS JPM; BEVERSTOCK GC; PEARSON PL THE FRAGILE X-SYNDROME IN A LARGE FAMILY .1. CYTOGENETIC AND CLINICAL INVESTIGATIONS | 14 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 411 | 6 | 38 | 674 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):187-195 SUTHERS GK; HYLAND VJ; CALLEN DF; OBERLE I; ROCCHI M; THOMAS NS; MORRIS CP; SCHWARTZ CE; SCHMIDT M; ROPERS HH; BAKER E; OOSTRA BA; DAHL N; WILSON PJ; HOPWOOD JJ; SUTHERLAND GR PHYSICAL MAPPING OF NEW DNA PROBES NEAR THE FRAGILE-X MUTATION (FRAXA) BY USING A PANEL OF CELL-LINES | 26 | 64 |
| 412 | 16 | 38 | 835 1991 BIOESSAYS 13(5):243-251 JORDAN BR FRAGILE X-LINKED MENTAL-RETARDATION AND THE DIFFICULTIES OF REVERSE GENETICS | 1 | 1 |
| 413 | 17 | 38 | 951 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(6):1050-1056 GLASS IA; DELMASTRO RG; LANYON WG; RAEBURN JA; KILPATRICK MW; WEBB TP; CONNOR JM TIGHTLY LINKED POLYMORPHIC MARKERS FOR FRAGILE X-SYNDROME AND PRENATAL CYTOGENETIC DIAGNOSTIC EXPERIENCE | 0 | 0 |
| 414 | 30 | 38 | 1151 1994 AMERICAN JOURNAL OF HUMAN GENETICS 55(2):225-237 ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; MALMGREN H; DAHL N; BARNICOAT A; MATHEW C; MORNET E; TEJADA I; MADDALENA A; SPIEGEL R; SCHINZEL A; MARCOS JAG; SCHORDERET DF; SCHAAP T; MACCIONI L; RUSSO S; JACOBS PA; SCHWARTZ C; MANDEL JL 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 | 119 | 165 |
| 415 | 15 | 38 | 1331 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):270-279 Belser RC; Sudhalter V Arousal difficulties in males with fragile X syndrome: A preliminary report | 20 | 24 |
| 416 | 12 | 38 | 1595 1997 HUMAN MOLECULAR GENETICS 6(9):1465-1472 Corbin F; Bouillon M; Fortin A; Morin S; Rousseau F; Khandjian EW The fragile X mental retardation protein is associated with poly(A)(+) mRNA in actively translating polyribosomes | 55 | 85 |
| 417 | 26 | 38 | 1597 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 | 6 | 9 |
| 418 | 12 | 38 | 1611 1997 JOURNAL OF MEDICAL GENETICS 34(11):907-911 vanRijn MA; deVries BBA; Tibben A; vandenOuweland AMW; Halley DJJ; Niermeijer MF DNA testing for fragile X syndrome: implications for parents and family | 3 | 4 |
| 419 | 21 | 38 | 1767 1999 ANNALES DE GENETIQUE 42(4):197-201 Arrieta I; Criado B; Martinez B; Telez M; Nunez T; Penagarikano O; Ortega B; Lostao CM A survey of fragile X syndrome in a sample from Spanish Basque country | 3 | 4 |
| 420 | 20 | 38 | 2252 2003 BRAIN TOPOGRAPHY 15(3):165-171 Castren M; Paakkonen A; Tarkka IM; Ryynanen M; Partanen J Augmentation of auditory N1 in children with fragile X syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 421 | 28 | 38 | 2317 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 128A(3):250-255 Penagarikano O; Gil A; Telez M; Ortega B; Flores P; Veiga I; Peixoto A; Criado B; Arrieta I A new insight into fragile X syndrome among Basque population | 0 | 0 |
| 422 | 5 | 37 | 84 1982 WESTERN JOURNAL OF MEDICINE 137(4):278-281 MOORE BC; GLOVER TW; KAISERMCCAW B; HECHT F FRAGILE X-LINKED MENTAL-RETARDATION AND MACRO-ORCHIDISM | 1 | 3 |
| 423 | 16 | 37 | 370 1986 CHILD STUDY JOURNAL 16(4):285-296 BURD L; KERBESHIAN J FRAGILE X-SYNDROME - DEVELOPMENTAL ASPECTS | 0 | 1 |
| 424 | 9 | 37 | 434 1987 CLINICAL GENETICS 32(3):179-186 BORGHGRAEF M; FRYNS JP; DIELKENS A; PYCK K; VANDENBERGHE H FRAGILE (X) SYNDROME - A STUDY OF THE PSYCHOLOGICAL PROFILE IN 23 PREPUBERTAL PATIENTS | 46 | 56 |
| 425 | 12 | 37 | 493 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 | 29 | 71 |
| 426 | 20 | 37 | 578 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(2):257-261 HO HZ; GLAHN TJ; HO JC THE FRAGILE-X SYNDROME | 2 | 3 |
| 427 | 18 | 37 | 672 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):175-180 BROWN WT INVITED EDITORIAL - THE FRAGILE-X - PROGRESS TOWARD SOLVING THE PUZZLE | 28 | 41 |
| 428 | 12 | 37 | 894 1991 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 88(19):8302-8306 POUSTKA A; DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; LEHRACH H PHYSICAL MAP OF HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 7 | 75 |
| 429 | 18 | 37 | 897 1991 SCIENCE 252(5009):1097-1102 OBERLE I; ROUSSEAU F; HEITZ D; KRETZ C; DEVYS D; HANAUER A; BOUE J; BERTHEAS MF; MANDEL JL INSTABILITY OF A 550 BASE PAIR DNA SEGMENT AND ABNORMAL METHYLATION IN FRAGILE X-SYNDROME | 394 | 835 |
| 430 | 25 | 37 | 959 1992 ANNALS OF MEDICINE 24(6):453-456 POUSTKA A FRAGILE-X SYNDROME - MOLECULAR ANALYSIS REVEALS A NEW MECHANISM OF MUTATION IN HUMAN GENETIC-DISEASES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 431 | 18 | 37 | 1081 1993 CLINICAL GENETICS 44(3):129-138 BUTLER MG; PRATESI R; WATSON MS; BREG WR; SINGH DN ANTHROPOMETRIC AND CRANIOFACIAL PATTERNS IN MENTALLY-RETARDED MALES WITH EMPHASIS ON THE FRAGILE-X SYNDROME | 4 | 8 |
| 432 | 14 | 37 | 1110 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 | 68 | 87 |
| 433 | 20 | 37 | 1143 1993 PEDIATRICS 91(2):321-329 FREUND LS; REISS AL; ABRAMS MT PSYCHIATRIC-DISORDERS ASSOCIATED WITH FRAGILE-X IN THE YOUNG FEMALE | 54 | 76 |
| 434 | 27 | 37 | 1183 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):474-481 HAGERMAN RJ; WILSON P; STALEY LW; LANG KA; FAN T; UHLHORN C; JEWELLSMART S; HULL C; DRISKO J; FLOM K; TAYLOR AK EVALUATION OF SCHOOL-CHILDREN AT HIGH-RISK FOR FRAGILE-X-SYNDROME UTILIZING BUCCAL CELL FMR-1 TESTING | 17 | 36 |
| 435 | 11 | 37 | 1243 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 | 21 | 31 |
| 436 | 20 | 37 | 1259 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1042-1051 QUAN F; ZONANA J; GUNTER K; PETERSON KL; MAGENIS RE; POPOVICH BW AN ATYPICAL CASE OF FRAGILE-X SYNDROME CAUSED BY A DELETION THAT INCLUDES THE FMRI GENE | 16 | 29 |
| 437 | 19 | 37 | 1332 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):280-292 Sobesky WE; Porter D; Pennington BF; Hagerman RJ Dimensions of shyness in fragile X females | 12 | 17 |
| 438 | 22 | 37 | 1364 1995 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 17(4):518-528 HINTON VJ; HALPERIN JM; DOBKIN CS; DING XH; BROWN WT; MIEZEJESKI CM COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X | 5 | 7 |
| 439 | 15 | 37 | 1397 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 | 4 | 9 |
| 440 | 13 | 37 | 1419 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):246-251 Godfraind JM; Reyniers E; DeBoulle K; DHooge R; DeDeyn PP; Bakker CE; Oostra BA; Kooy RF; Willems PJ Long-term potentiation in the hippocampus of fragile X knockout mice | 22 | 31 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 441 | 19 | 37 | 1455 1996 ARCHIVES DE PEDIATRIE 3(8):814-821 Mornet E; SimonBouy B Molecular biology of fragile X syndrome: Applications to genetic counselling and molecular diagnosis | 3 | 4 |
| 442 | 5 | 37 | 1488 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(38):22937-22940 Wang YH; Griffith J Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion | 1 | 22 |
| 443 | 10 | 37 | 1675 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(25):15521-15527 Brown V; Small K; Lakkis L; Feng Y; Gunter C; Wilkinson KD; Warren ST Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein | 36 | 62 |
| 444 | 18 | 37 | 1744 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):184-190 Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: Incidence, genetic variation, and stability | 7 | 18 |
| 445 | 20 | 37 | 1753 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):245-249 Reyniers E; Martin JJ; Cras P; Van Marck E; Handig I; Jorens HZJ; Oostra BA; Kooy RF; Willems PJ Postmortem examination of two fragile X brothers with an FMR1 full mutation | 14 | 19 |
| 446 | 14 | 37 | 1866 2000 AMERICAN JOURNAL ON MENTAL RETARDATION 105(4):286-299 Kau ASM; Reider EE; Payne L; Meyer WA; Freund L Early behavior signs of psychiatric phenotypes in fragile X syndrome | 2 | 4 |
| 447 | 20 | 37 | 1867 2000 ANNALES DE GENETIQUE 43(1):29-34 Gonzalez-del Angel A; Vidal S; Saldana Y; del Castillo V; Alcantara MA; Macias M; Luna JP; Orozco L Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico | 2 | 3 |
| 448 | 20 | 37 | 1949 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 | 15 | 17 |
| 449 | 17 | 37 | 1992 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 | 13 | 12 |
| 450 | 18 | 37 | 2007 2001 CELL 107(5):591-603 Zhang YQ; Bailey AM; Matthies HJG; Renden RB; Smith MA; Speese SD; Rubin GM; Broadie K Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function | 36 | 71 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 451 | 10 | 37 | 2093 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 | 2 | 7 |
| 452 | 5 | 37 | 2114 2002 CURRENT BIOLOGY 12(15):1331-1335 Inoue SB; Shimoda M; Nishinokubi I; Siomi MC; Okamura M; Nakamura A; Kobayashi S; Ishida N; Siomi H A role for the Drosophila fragile X-related gene in circadian output | 9 | 13 |
| 453 | 11 | 37 | 2340 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 | 0 | 0 |
| 454 | 0 | 36 | 110 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 |
| 455 | 6 | 36 | 188 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 |
| 456 | 11 | 36 | 399 1986 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 25(5):641-644 WRIGHT HH; YOUNG SR; EDWARDS JG; ABRAMSON RK; DUNCAN J FRAGILE X-SYNDROME IN A POPULATION OF AUTISTIC-CHILDREN | 16 | 21 |
| 457 | 5 | 36 | 411 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 |
| 458 | 17 | 36 | 423 1987 ANNALS OF HUMAN GENETICS 51:107-124 GIANNELLI F; MORRIS AH; GARRETT C; DAKER M; THURSTON C; SMITH CAB GENETIC-HETEROGENEITY OF X-LINKED MENTAL-RETARDATION WITH FRAGILE-X - ASSOCIATION OF TIGHT LINKAGE TO FACTOR-IX AND INCOMPLETE PENETRANCE IN MALES | 7 | 16 |
| 459 | 3 | 36 | 484 1987 NEUROPSYCHOLOGIA 25(6):881-891 GRIGSBY JP; KEMPER MB; HAGERMAN RJ DEVELOPMENTAL GERSTMANN SYNDROME WITHOUT APHASIA IN FRAGILE-X SYNDROME | 16 | 27 |
| 460 | 10 | 36 | 521 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 461 | 18 | 36 | 707 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 |
| 462 | 20 | 36 | 982 1992 HUMAN GENETICS 90(1-2):55-61 ERSTER SH; BROWN WT; GOONEWARDENA P; DOBKIN CS; JENKINS EC; PERGOLIZZI RG POLYMERASE CHAIN-REACTION ANALYSIS OF FRAGILE X-MUTATIONS | 18 | 30 |
| 463 | 29 | 36 | 1024 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 | 27 | 38 |
| 464 | 19 | 36 | 1138 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 | 169 | 277 |
| 465 | 14 | 36 | 1163 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):358-363 HAY DA DOES IQ DECLINE WITH AGE IN FRAGILE-X A METHODOLOGICAL CRITIQUE | 12 | 13 |
| 466 | 27 | 36 | 1328 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):230-241 Brun C; Obiols JE; Cheema A; OConnor R; Riddle J; DiMaria M; WrightTalamante C; Hagerman R Longitudinal IQ changes in fragile X females | 1 | 1 |
| 467 | 16 | 36 | 1347 1995 EMBO JOURNAL 14(21):5358-5366 ZHANG Y; OCONNOR JP; SIOMI MC; SRINIVASAN S; DUTRA A; NUSSBAUM RL; DREYFUSS G THE FRAGILE-X MENTAL-RETARDATION SYNDROME PROTEIN INTERACTS WITH NOVEL HOMOLOGS FXR1 AND FXR2 | 63 | 111 |
| 468 | 18 | 36 | 1667 1998 HUMAN REPRODUCTION 13(5):1184-1187 Conway GS; Payne NN; Webb J; Murray A; Jacobs PA Fragile X premutation screening in women with premature ovarian failure | 8 | 31 |
| 469 | 12 | 36 | 1674 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 | 8 | 11 |
| 470 | 20 | 36 | 1690 1998 JOURNAL OF PEDIATRICS 133(3):363-365 Meyer GA; Blum NJ; Hitchcock W; Fortina P Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 471 | 17 | 36 | 1695 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 | 10 | 14 |
| 472 | 4 | 36 | 1756 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):272-276 Currie JR; Brown WT KH domain-containing proteins of yeast: Absence of a fragile X gene homologue | 0 | 4 |
| 473 | 17 | 36 | 1771 1999 BIOCHEMICAL JOURNAL 343:517-523 Tamanini F; van Unen L; Bakker C; Sacchi N; Galjaard H; Oostra BA; Hoogeveen AT Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P | 15 | 20 |
| 474 | 21 | 36 | 1934 2000 JOURNAL OF MEDICAL GENETICS 37(1):77-79 Beresford RG; Tatlidil C; Riddell DC; Welch JP; Ludman MD; Neumann PE; Greer WL Absence of fragile X syndrome in Nova Scotia | 4 | 4 |
| 475 | 18 | 36 | 2051 2001 NUCLEIC ACIDS RESEARCH 29(11):2276-2283 Li ZZ; Zhang YY; Ku L; Wilkinson KD; Warren ST; Feng Y The fragile X mental retardation protein inhibits translation via interacting with mRNA | 46 | 67 |
| 476 | 10 | 36 | 2055 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98(13):7101-7106 Greenough WT; Klintsova AY; Irwin SA; Galvez R; Bates KE; Weiler IJ Synaptic regulation of protein synthesis and the fragile X protein | 30 | 49 |
| 477 | 18 | 36 | 2056 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 | 20 | 38 |
| 478 | 3 | 36 | 2100 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(4):381-387 Steinhausen HC; von Gontard A; Spohr HL; Hauffa BP; Eiholzer U; Backes M; Willms J; Malin Z Behavioral phenotypes in four mental retardation syndromes: Fetal alcohol syndrome, Prader-Willi syndrome, fragile X syndrome, and tuberosis sclerosis | 0 | 0 |
| 479 | 16 | 36 | 2187 2002 NUCLEIC ACIDS RESEARCH 30(14):3278-3285 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; Neri G Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 3 | 6 |
| 480 | 18 | 36 | 2200 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(4):869-878 Jacquemont S; Hagerman RJ; Leehey M; Grigsby J; Zhang L; Brunberg JA; Greco C; Des Portes V; Jardini T; Levine R; Berry-Kravis E; Brown WT; Schaeffer S; Kissel J; Tassone F; Hagerman PJ Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates | 10 | 19 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 481 | 25 | 36 | 2251 2003 BRAIN RESEARCH 972(1-2):9-15 Segal M; Kreher U; Greenberger V; Braun K Is fragile X mental retardation protein involved in activity-induced plasticity of dendritic spines? | 0 | 1 |
| 482 | 8 | 36 | 2303 2003 PEDIATRICS 111(2):407-416 Bailey DB; Skinner D; Sparkman KL Discovering fragile X syndrome: Family experiences and perceptions | 4 | 4 |
| 483 | 6 | 36 | 2336 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(1):21-27 Mirrett PL; Bailey DB; Roberts JE; Hatton DD Developmental screening and detection of developmental delays in infants and toddlers with fragile X syndrome | 0 | 0 |
| 484 | 2 | 35 | 36 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 | 48 | 65 |
| 485 | 3 | 35 | 233 1984 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES 81(24):7855-7859 SZABO P; PURRELLO M; ROCCHI M; ARCHIDIACONO N; ALHADEFF B; FILIPPI G; TONIOLO D; MARTINI G; LUZZATTO L; SINISCALCO M CYTOLOGICAL MAPPING OF THE HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE DISTAL TO THE FRAGILE-X SITE SUGGESTS A HIGH-RATE OF MEIOTIC RECOMBINATION ACROSS THIS SITE | 17 | 71 |
| 486 | 19 | 35 | 675 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(3):395-402 SOOD R; MULLIGAN LM; POON R; WHITE BN; HOLDEN JJA GENETIC-MAPPING OF 2 NEW DNA MARKERS IN XQ26-Q28 RELATIVE TO THE FRAGILE-X SYNDROME LOCUS | 3 | 7 |
| 487 | 18 | 35 | 858 1991 GENOMICS 10(3):576-582 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; STEINBACH P; GLASS IA; SCHWARTZ CE; VANOOST BA; THIBODEAU SN; HAITES NE; OOSTRA BA; SCHINZEL A; CARBALLO M; MORRIS CP; HOPWOOD JJ; SUTHERLAND GR LINKAGE HOMOGENEITY NEAR THE FRAGILE-X LOCUS IN NORMAL AND FRAGILE-X FAMILIES | 9 | 13 |
| 488 | 17 | 35 | 1057 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(5):1064-1073 LOESCH DZ; HUGGINS R; HAY DA; GEDEON AK; MULLEY JC; SUTHERLAND GR GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE-X SYNDROME - A FAMILY STUDY | 43 | 60 |
| 489 | 8 | 35 | 1336 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 | 10 | 10 |
| 490 | 13 | 35 | 1375 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 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 491 | 23 | 35 | 1389 1995 PRENATAL DIAGNOSIS 15(9):801-807 CASTELLVIBEL S; MILA M; SOLER A; CARRIO A; SANCHEZ A; VILLA M; JIMENEZ MD; ESTIVILL X PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - (CGG)(N) EXPANSION AND METHYLATION OF CHORIONIC VILLUS SAMPLES | 2 | 6 |
| 492 | 21 | 35 | 1425 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):287-292 Brown WT; Houck GE; Ding XH; Zhong N; Nolin S; Glicksman A; Dobkin C; Jenkins EC Reverse mutations in the fragile X syndrome | 9 | 18 |
| 493 | 17 | 35 | 1515 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 | 6 | 14 |
| 494 | 22 | 35 | 1527 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(3):660-667 deVries BBA; vandenOuweland AMW; Mohkamsing S; Duivenvoorden HJ; Mol E; Gelsema K; vanRijn M; Halley DJJ; Sandkuijl LA; Oostra BA; Tibben A; Niermeijer MF Screening and diagnosis for the fragile X syndrome among the mentally retarded: An epidemiological and psychological survey | 35 | 70 |
| 495 | 25 | 35 | 1571 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739 Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families | 2 | 2 |
| 496 | 21 | 35 | 1594 1997 HUMAN MOLECULAR GENETICS 6(7):971-979 Moutou C; Vincent MC; Biancalana V; Mandel JL Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic | 18 | 33 |
| 497 | 7 | 35 | 1615 1997 JOURNAL OF THEORETICAL BIOLOGY 188(1):53-67 Bat O; Kimmel M; Axelrod DE Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease | 1 | 4 |
| 498 | 6 | 35 | 1724 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 | 27 | 42 |
| 499 | 19 | 35 | 1732 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):302-307 Parvari R; Mumm S; Galil A; Manor E; Bar-David Y; Carmi R Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth | 2 | 6 |
| 500 | 26 | 35 | 1854 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(3):232-236 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; Hagerman PJ Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA | 16 | 23 |
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