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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 401 | 20 | 52 | 2185 2002 NEURON 34(6):961-972 Morales J; Hiesinger PR; Schroeder AJ; Kume K; Verstreken P; Jackson FR; Nelson DL; Hassan BA Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain | 17 | 25 |
| 402 | 0 | 2 | 49 1982 ANNALES DE GENETIQUE 25(3):149-151 LEJEUNE J; LEGRAND N; LAFOURCADE J; RETHORE MO; RAOUL O; MAUNOURY C THE FRAGILE X - EFFECT OF TRIMETHOPRIME TREATMENT | 15 | 24 |
| 403 | 0 | 0 | 83 1982 PEDIATRICS 69(5):670-670 HARPEY JP TREATMENT OF FRAGILE-X | 19 | 24 |
| 404 | 6 | 21 | 396 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:27-39 GILLBERG C; PERSSON E; WAHLSTROM J THE AUTISM-FRAGILE-X SYNDROME (AFRAX) - A POPULATION-BASED STUDY OF 10 BOYS | 14 | 24 |
| 405 | 12 | 19 | 782 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):251-255 NOLIN SL; SNIDER DA; JENKINS EC; BROWN WT; KRAWCZUN M; STETKA D; HOUCK G; DOBKIN CS; STRONG G; SMITHDOBRANSKY G; VICTOR A; HUGHES K; KIMPTON D; LITTLE A; NAGARAJA U; KENEFICK B; SULLIVAN C FRAGILE-X SCREENING-PROGRAM IN NEW-YORK-STATE | 18 | 24 |
| 406 | 7 | 12 | 823 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):505-508 BRAINARD SS; SCHREINER RA; HAGERMAN RJ COGNITIVE PROFILES OF THE CARRIER FRAGILE-X WOMAN | 20 | 24 |
| 407 | 4 | 6 | 879 1991 LANCET 338(8772):957-958 DOBKIN CS; DING XH; JENKINS EC; KRAWCZUN MS; BROWN WT; GOONEWARDENA P; WILLNER J; BENSON C; HEITZ D; ROUSSEAU F PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 22 | 24 |
| 408 | 20 | 27 | 1022 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(7):723-726 STALEY LW; HULL CE; MAZZOCCO MMM; THIBODEAU SN; SNOW K; WILSON VL; TAYLOR A; MCGAVRAN L; WEINER D; RIDDLE J; OCONNOR R; HAGERMAN RJ MOLECULAR-CLINICAL CORRELATIONS IN CHILDREN AND ADULTS WITH FRAGILE X-SYNDROME | 21 | 24 |
| 409 | 28 | 64 | 1152 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 50(2):190-200 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H COGNITIVE-FUNCTIONING AND INFORMATION-PROCESSING OF ADULT MENTALLY-RETARDED MEN WITH FRAGILE-X SYNDROME | 17 | 24 |
| 410 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 411 | 24 | 59 | 1415 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):209-215 Chiurazzi P; Genuardi M; Kozak L; GiovannucciUzielli ML; Bussani C; DagnaBricarelli F; Grasso M; Perroni L; Sebastio G; Sperandeo MP; Oostra BA; Neri G Fragile X founder chromosomes in Italy: A few initial events and possible explanation for their heterogeneity | 11 | 24 |
| 412 | 28 | 43 | 1416 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):226-233 Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; Wang DW; Ju MN; Nolin S; Dobkin C; Ryynanen M; Brown WT Fragile X founder effects and new mutations in Finland | 9 | 24 |
| 413 | 24 | 61 | 1599 1997 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 27(4):415-435 Mazzocco MMM; Kates WR; Baumgardner TL; Freund LS; Reiss AL Autistic behaviors among girls with fragile X syndrome | 19 | 24 |
| 414 | 11 | 27 | 1757 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):300-303 Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U; Ricotti G; Biondi C; Scarselli B; Vieri F; Scarnato P; Gori F; Sereni A Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data | 11 | 24 |
| 415 | 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 |
| 416 | 27 | 40 | 1865 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):195-203 Tassone F; Hagerman RJ; Chamberlain WD; Hagerman PJ Transcription of the FMR1 gene in individuals with fragile X syndrome | 16 | 24 |
| 417 | 0 | 4 | 26 1981 LANCET 2(8254):1055-1055 BROWN WT; MEZZACAPPA PM; JENKINS EC SCREENING FOR FRAGILE X SYNDROME BY TESTICULAR SIZE MEASUREMENT | 16 | 23 |
| 418 | 7 | 15 | 299 1985 JOURNAL OF NEUROGENETICS 2(3):231-237 FORSTERGIBSON CJ; MULLIGAN LM; PARTINGTON MW; SIMPSON NE; HOLDEN JJA; WHITE BN THE GENETIC-DISTANCE BETWEEN THE COAGULATION FACTOR-IX GENE AND THE LOCUS FOR THE FRAGILE-X SYNDROME - CLINICAL IMPLICATIONS | 13 | 23 |
| 419 | 8 | 19 | 414 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):909-914 WENGER SL; HENNESSEY JC; STEELE MW INCREASED SISTER CHROMATID EXCHANGE FREQUENCY AT XQ27-SITE IN AFFECTED FRAGILE-X MALES | 5 | 23 |
| 420 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 421 | 19 | 40 | 585 1988 HUMAN GENETICS 79(3):219-227 THIBODEAU SN; DORKINS HR; FAULK KR; BERRY R; SMITH ACM; HAGERMAN R; KING A; DAVIES KE LINKAGE ANALYSIS USING MULTIPLE DNA POLYMORPHIC MARKERS IN NORMAL-FAMILIES AND IN FAMILIES WITH FRAGILE-X SYNDROME | 13 | 23 |
| 422 | 0 | 0 | 640 1989 GENOMICS 5(4):797-801 VINCENT A; DAHL N; OBERLE I; HANAUER A; MANDEL JL; MALMGREN H; PETTERSSON U THE POLYMORPHIC MARKER DXS304 IS WITHIN 5-CENTIMORGANS OF THE FRAGILE-X LOCUS | 13 | 23 |
| 423 | 3 | 12 | 1142 1993 NEUROPEDIATRICS 24(4):211-213 REES M; DIEBOLD U; PARKER K; DOOSE H; GARDINER RM; WHITEHOUSE WP BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES AND THE FOCAL SHARP WAVE TRAIT IS NOT LINKED TO THE FRAGILE-X REGION | 6 | 23 |
| 424 | 9 | 30 | 1168 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):386-391 EINFELD SL; TONGE BJ; FLORIO T BEHAVIORAL AND EMOTIONAL DISTURBANCE IN FRAGILE-X-SYNDROME | 12 | 23 |
| 425 | 30 | 50 | 1414 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):203-208 Chiurazzi P; Macpherson J; Sherman S; Neri G Significance of linkage disequilibrium between the fragile X locus and its flanking markers | 9 | 23 |
| 426 | 9 | 15 | 1577 1997 CLINICAL GENETICS 52(3):147-154 Hecimovic S; Barisic I; Muller A; Petkovic I; Baric I; Ligutic I; Pavelic K Expand long PCR for fragile X mutation detection | 8 | 23 |
| 427 | 14 | 19 | 1591 1997 HUMAN GENETICS 100(5-6):564-568 Larsen LA; Gronskov K; NorgaardPedersen B; BrondumNielsen K; Hasholt L; Vuust J High-throughput analysis of fragile X (CGG)(n) alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis | 5 | 23 |
| 428 | 31 | 40 | 1752 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):233-239 Taylor AK; Tassone F; Dyer PN; Hersch SM; Harris JB; Greenough WT; Hagerman RJ Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome | 15 | 23 |
| 429 | 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 |
| 430 | 0 | 6 | 3 1980 AMERICAN JOURNAL OF MEDICAL GENETICS 7(4):503-505 KAISERMCCAW B; HECHT F; CADIEN JD; MOORE BC FRAGILE X-LINKED MENTAL-RETARDATION | 14 | 22 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 431 | 4 | 23 | 60 1982 HUMAN GENETICS 61(2):113-117 NIELSEN KB; TOMMERUP N; DYGGVE HV; SCHOU C MACRO-ORCHIDISM AND FRAGILE-X IN MENTALLY-RETARDED MALES - CLINICAL, CYTOGENETIC, AND SOME HORMONAL INVESTIGATIONS IN MENTALLY-RETARDED MALES, INCLUDING 2 WITH THE FRAGILE SITE AT XQ28, FRA(X)(Q28) | 12 | 22 |
| 432 | 1 | 14 | 109 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(4):631-635 HOWARDPEEBLES PN; FINLEY WH SCREENING OF MENTALLY-RETARDED MALES FOR MACRO-ORCHIDISM AND THE FRAGILE-X CHROMOSOME | 16 | 22 |
| 433 | 2 | 11 | 184 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):303-310 WANG JCC; ERBE RW FOLATE METABOLISM IN CELLS FROM FRAGILE-X SYNDROME PATIENTS AND CARRIERS | 15 | 22 |
| 434 | 4 | 11 | 349 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):589-595 SANFILIPPO S; RAGUSA RM; MUSUMECI S; NERI G FRAGILE-X MENTAL-RETARDATION - PREVALENCE IN A GROUP OF INSTITUTIONALIZED PATIENTS IN ITALY AND DESCRIPTION OF A NOVEL EEG PATTERN | 15 | 22 |
| 435 | 3 | 11 | 368 1986 BRITISH JOURNAL OF PSYCHIATRY 148:655-657 PRIMROSE DA; ELMATMATI R; BOYD E; GOSDEN C; NEWTON M PREVALENCE OF THE FRAGILE-X SYNDROME IN AN INSTITUTION FOR THE MENTALLY-HANDICAPPED | 16 | 22 |
| 436 | 5 | 14 | 668 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(3):443-451 SVED JA; LAIRD CD POPULATION GENETIC CONSEQUENCES OF THE FRAGILE-X SYNDROME, BASED ON THE X-INACTIVATION IMPRINTING MODEL | 12 | 22 |
| 437 | 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 |
| 438 | 12 | 47 | 857 1991 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 33(9):776-788 FERRIER LJ; BASHIR AS; MERYASH DL; JOHNSTON J; WOLFF P CONVERSATIONAL SKILLS OF INDIVIDUALS WITH FRAGILE-X SYNDROME - A COMPARISON WITH AUTISM AND DOWN-SYNDROME | 18 | 22 |
| 439 | 6 | 9 | 1127 1993 LANCET 342(8878):1025-1026 WANG Q; GREEN E; BARNICOAT A; GARRETT D; MULLARKEY M; BOBROW M; MATHEW CG CYTOGENETIC VERSUS DNA DIAGNOSIS IN ROUTINE REFERRALS FOR FRAGILE-X SYNDROME | 15 | 22 |
| 440 | 15 | 18 | 1244 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(9):1316-1321 MERENSTEIN SA; SHYU V; SOBESKY WE; STALEY L; BERRYKRAVIS E; NELSON DL; LUGENBEEL KA; TAYLOR AK; PENNINGTON BF; HAGERMAN RJ FRAGILE-X SYNDROME IN A NORMAL IQ MALE WITH LEARNING AND EMOTIONAL-PROBLEMS | 18 | 22 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 441 | 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 |
| 442 | 15 | 21 | 1492 1996 JOURNAL OF MEDICAL GENETICS 33(5):376-378 Wang ZM; Taylor AK; Bridge JA FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 17 | 22 |
| 443 | 30 | 43 | 1552 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(6):1362-1369 Kenneson A; Cramer DW; Warren ST Fragile X premutations are not a major cause of early menopause | 11 | 22 |
| 444 | 46 | 98 | 1772 1999 BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE 77(4):331-342 Khandjian EW Biology of the fragile X mental retardation protein, an RNA-binding protein | 12 | 22 |
| 445 | 14 | 43 | 1822 1999 RNA-A PUBLICATION OF THE RNA SOCIETY 5(9):1248-1258 Adinolfi S; Bagni C; Musco G; Gibson T; Mazzarella L; Pastore A Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains | 15 | 22 |
| 446 | 25 | 40 | 2144 2002 HUMAN MOLECULAR GENETICS 11(4):371-378 Dombrowski C; Levesque S; Morel ML; Rouillard P; Morgan K; Rousseau F Premutation and intermediate-size FMR1 alleles in 10,572 males from the general population: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles | 15 | 22 |
| 447 | 1 | 6 | 80 1982 NEW ENGLAND JOURNAL OF MEDICINE 306(25):1551-1552 POPOVICH B; VEKEMANS M; ROSENBLATT D; MONROE P FRAGILE-X | 17 | 21 |
| 448 | 5 | 25 | 147 1983 JOURNAL OF MEDICAL GENETICS 20(6):404-407 VEKEMANS M; POPOVICH B; ROSENBLATT D; MONROE P CHROMOSOMAL BREAKAGE IN NORMAL AND FRAGILE-X SUBJECTS USING LOW FOLATE CULTURE CONDITIONS | 12 | 21 |
| 449 | 5 | 19 | 163 1984 ACTA PSYCHIATRICA SCANDINAVICA 70(5):510-514 JORGENSEN OS; NIELSEN KB; ISAGER T; MOURIDSEN SE FRAGILE X-CHROMOSOME AMONG CHILD PSYCHIATRIC-PATIENTS WITH DISTURBANCES OF LANGUAGE AND SOCIAL RELATIONSHIPS - A PILOT-STUDY | 12 | 21 |
| 450 | 0 | 4 | 175 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):209-214 RHOADS FA FRAGILE-X SYNDROME IN HAWAII - A SUMMARY OF CLINICAL-EXPERIENCE | 10 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 451 | 2 | 11 | 193 1984 CLINICAL GENETICS 26(5):445-447 FRYNS JP; KLECZKOWSKA A; WOLFS I; VANDENBERGHE H KLINEFELTER SYNDROME AND 2 FRAGILE X-CHROMOSOMES | 15 | 21 |
| 452 | 5 | 25 | 210 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(2):197-204 AUGUST GJ; LOCKHART LH FAMILIAL AUTISM AND THE FRAGILE-X-CHROMOSOME | 10 | 21 |
| 453 | 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 |
| 454 | 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 |
| 455 | 17 | 44 | 495 1988 AMERICAN JOURNAL OF DISEASES OF CHILDREN 142(11):1216-1221 HAGERMAN R; BERRY R; JACKSON AW; CAMPBELL J; SMITH ACM; MCGAVRAN L INSTITUTIONAL SCREENING FOR THE FRAGILE-X SYNDROME | 12 | 21 |
| 456 | 32 | 50 | 546 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):655-663 FISCH GS; COHEN IL; JENKINS EC; BROWN WT SCREENING DEVELOPMENTALLY DISABLED MALE POPULATIONS FOR FRAGILE-X - THE EFFECT OF SAMPLE-SIZE | 17 | 21 |
| 457 | 15 | 17 | 1173 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):428-435 KOLEHMAINEN K POPULATION-GENETICS OF FRAGILE-X - A MULTIPLE ALLELE MODEL WITH VARIABLE RISK OF CGG REPEAT EXPANSION | 15 | 21 |
| 458 | 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 |
| 459 | 6 | 29 | 1487 1996 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 26(3):287-301 Dykens E; Ort S; Cohen I; Finucane B; Spiridigliozzi G; Lachiewicz A; Reiss A; Freund L; Hagerman R; OConnor R Trajectories and profiles of adaptive behavior in males with fragile X syndrome: Multicenter studies | 17 | 21 |
| 460 | 21 | 25 | 1557 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(4):430-434 Hammond LS; Macias MM; Tarleton JC; Pai GS Fragile X syndrome and deletions in FMR1: New case and review of the literature | 13 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 461 | 17 | 54 | 1991 2001 AMERICAN JOURNAL OF PSYCHIATRY 158(7):1040-1051 Kwon H; Menon V; Eliez S; Warsofsky IS; White CD; Dyer-Friedman J; Taylor AK; Glover GH; Reiss AL Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavioral and molecular measures | 10 | 21 |
| 462 | 5 | 14 | 125 1983 CLINICAL GENETICS 23(4):311-317 GARDNER RJM; SMART RD; CORNELL JM; MERCKEL LM; BEIGHTON P THE FRAGILE X-CHROMOSOME IN A LARGE INDIAN KINDRED | 17 | 20 |
| 463 | 32 | 83 | 215 1984 JOURNAL OF MEDICAL GENETICS 21(2):84-91 DEARCE MA; KEARNS A THE FRAGILE X-SYNDROME - THE PATIENTS AND THEIR CHROMOSOMES | 9 | 20 |
| 464 | 2 | 11 | 219 1984 JOURNAL OF NERVOUS AND MENTAL DISEASE 172(9):549-551 KERBESHIAN J; BURD L; MARTSOLF J A FAMILY WITH FRAGILE-X SYNDROME | 7 | 20 |
| 465 | 0 | 5 | 346 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):557-562 UCHIDA IA; FREEMAN VCP; BASRUR PK THE FRAGILE-X IN CATTLE | 4 | 20 |
| 466 | 14 | 23 | 383 1986 EXPERIMENTAL CELL BIOLOGY 54(1):40-48 JENKINS EC; BROWN WT; BROOKS J; DUNCAN CJ; SANZ MM; SILVERMAN WP; LELE KP; MASIA A; KATZ E; LUBIN RA; NOLIN SL LOW-FREQUENCIES OF APPARENTLY FRAGILE X-CHROMOSOMES IN NORMAL CONTROL CULTURES - A POSSIBLE EXPLANATION | 16 | 20 |
| 467 | 5 | 13 | 541 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):567-580 MULLEY J; TURNER G; BAIN S; SUTHERLAND GR LINKAGE BETWEEN THE FRAGILE-X AND F9, DXS52 (ST14), DXS98 (4D-8) AND DXS105 (CX55.7) | 13 | 20 |
| 468 | 13 | 27 | 696 1990 CLINICAL GENETICS 37(5):341-346 BORGHGRAEF M; FRYNS JP; VANDENBERGHE H THE FEMALE AND THE FRAGILE X-SYNDROME - DATA ON CLINICAL AND PSYCHOLOGICAL FINDINGS IN 7 FRA(X) CARRIERS | 16 | 20 |
| 469 | 4 | 12 | 912 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):65-71 SUDHALTER V; MARANION M; BROOKS P EXPRESSIVE SEMANTIC DEFICIT IN THE PRODUCTIVE LANGUAGE OF MALES WITH FRAGILE-X SYNDROME | 18 | 20 |
| 470 | 26 | 42 | 1293 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1414-1425 ASHLEY AE; SHERMAN SL POPULATION-DYNAMICS OF A MEIOTIC MITOTIC EXPANSION MODEL FOR THE FRAGILE-X SYNDROME | 13 | 20 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 471 | 16 | 30 | 1306 1995 ARCHIVES OF DISEASE IN CHILDHOOD 72(1):33-37 SLANEY SF; WILKIE AOM; HIRST MC; CHARLTON R; MCKINLEY M; POINTON J; CHRISTODOULOU Z; HUSON SM; DAVIES KE DNA TESTING FOR FRAGILE-X SYNDROME IN SCHOOLS FOR LEARNING-DIFFICULTIES | 12 | 20 |
| 472 | 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 |
| 473 | 12 | 14 | 1496 1996 JOURNAL OF PEDIATRICS 129(4):611-614 Giangreco CA; Steele MW; Aston CE; Cummins JH; Wenger SL A simplified six-item checklist for screening for fragile X syndrome in the pediatric population | 10 | 20 |
| 474 | 15 | 24 | 1702 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(1):98-103 Willemsen R; Anar B; Otero YD; de Vries BBA; Hilhorst-Hofstee Y; Smits A; van Looveren E; Willems PJ; Galjaard H; Oostra BA Noninvasive test for fragile X syndrome, using hair root analysis | 18 | 20 |
| 475 | 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 |
| 476 | 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 |
| 477 | 68 | 116 | 1862 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(2):153-163 Bardoni B; Mandel JL; Fisch GS FMR1 gene and fragile X syndrome | 10 | 20 |
| 478 | 57 | 117 | 1945 2000 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 6(2):96-106 Mazzocco MMM Advances in research on the fragile X syndrome | 18 | 20 |
| 479 | 28 | 40 | 1966 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(2):351-360 Toledano-Alhadef H; Basel-Vanagaite L; Magal N; Davidov B; Ehrlich S; Drasinover V; Taub E; Halpern GJ; Ginott N; Shohat M Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel | 12 | 20 |
| 480 | 99 | 154 | 2020 2001 GENETICS IN MEDICINE 3(5):359-371 Crawford DC; Acuna JM; Sherman SL FMR1 and the fragile X syndrome: Human genome epidemiology review | 13 | 20 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 481 | 8 | 28 | 2028 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(6):4357-4364 Kumari D; Usdin K Interaction of the transcription factors USF1, USF2, and alpha-Pal/Nrf-1 with the FMR1 promoter - Implications for Fragile X mental retardation syndrome | 12 | 20 |
| 482 | 1 | 9 | 150 1983 LANCET 1(8335):1221-1222 RUDELLI RD; JENKINS EC; WISNIEWSKI K; MORETZ R; BYRNE J; BROWN WT TESTICULAR SIZE IN FETAL FRAGILE X SYNDROME | 14 | 19 |
| 483 | 6 | 24 | 234 1984 SOMATIC CELL AND MOLECULAR GENETICS 10(4):409-413 WARREN ST; DAVIDSON RL EXPRESSION OF FRAGILE X-CHROMOSOME IN HUMAN RODENT SOMATIC-CELL HYBRIDS | 14 | 19 |
| 484 | 9 | 23 | 243 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(5):956-964 HOWARDPEEBLES PN; FRIEDMAN JM UNAFFECTED CARRIER MALES IN FAMILIES WITH FRAGILE-X SYNDROME | 14 | 19 |
| 485 | 2 | 6 | 350 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):611-617 JACOBS PA; SHERMAN S; TURNER G; WEBB T THE FRAGILE(X) SYNDROME - THE MUTATION PROBLEM | 14 | 19 |
| 486 | 3 | 23 | 352 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):685-699 HOEGERMAN SF; RARY JM SPECULATION ON THE ROLE OF TRANSPOSABLE ELEMENTS IN HUMAN GENETIC-DISEASE WITH PARTICULAR ATTENTION TO ACHONDROPLASIA AND THE FRAGILE-X SYNDROME | 10 | 19 |
| 487 | 10 | 20 | 420 1987 AMERICAN JOURNAL OF MENTAL DEFICIENCY 91(5):445-449 ROGERS RC; SIMENSEN RJ FRAGILE-X SYNDROME - A COMMON ETIOLOGY OF MENTAL-RETARDATION | 13 | 19 |
| 488 | 2 | 8 | 526 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):347-354 SHAPIRO LR; WILMOT PL; MURPHY PD; BREG WR EXPERIENCE WITH MULTIPLE APPROACHES TO THE PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - AMNIOTIC-FLUID, CHORIONIC VILLI, FETAL BLOOD AND MOLECULAR METHODS | 12 | 19 |
| 489 | 3 | 13 | 600 1988 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 29(4):447-451 GILLBERG C; OHLSON VA; WAHLSTROM J; STEFFENBURG S; BLIX K MONOZYGOTIC FEMALE TWINS WITH AUTISM AND THE FRAGILE-X SYNDROME (AFRAX) | 9 | 19 |
| 490 | 5 | 14 | 701 1990 HUMAN GENETICS 84(3):263-266 ROUSSEAU F; VINCENT A; OBERLE I; MANDEL JL NEW INFORMATIVE POLYMORPHISM AT THE DXS304 LOCUS, A CLOSE DISTAL MARKER FOR THE FRAGILE X-LOCUS | 4 | 19 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 491 | 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 |
| 492 | 13 | 21 | 934 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):217-223 KNIGHT SJL; HIRST MC; ROCHE A; CHRISTODOULOU Z; HUSON SM; WINTER R; FITCHETT M; MCKINLEY MJ; LINDENBAUM RH; NAKAHORI Y; DAVIES KE MOLECULAR STUDIES OF THE FRAGILE-X SYNDROME | 10 | 19 |
| 493 | 5 | 22 | 960 1992 ANNALS OF NEUROLOGY 31(1):22-26 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE-X SYNDROME | 13 | 19 |
| 494 | 11 | 27 | 1147 1993 SOMATIC CELL AND MOLECULAR GENETICS 19(4):393-404 LUO SY; ROBINSON JC; REISS AL; MIGEON BR DNA METHYLATION OF THE FRAGILE-X LOCUS IN SOMATIC AND GERM-CELLS DURING FETAL DEVELOPMENT - RELEVANCE TO THE FRAGILE-X SYNDROME AND X-INACTIVATION | 6 | 19 |
| 495 | 13 | 19 | 1217 1994 HUMAN GENETICS 94(5):479-483 HAATAJA R; VAISANEN ML; LI MY; RYYNANEN M; LEISTI J THE FRAGILE-X SYNDROME IN FINLAND - DEMONSTRATION OF A FOUNDER EFFECT BY ANALYSIS OF MICROSATELLITE HAPLOTYPES | 11 | 19 |
| 496 | 7 | 13 | 1423 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):274-277 Steyaert J; Borghgraef M; Legius E; Fryns JP Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene | 15 | 19 |
| 497 | 15 | 64 | 1590 1997 HUMAN GENETICS 100(3-4):407-414 Lavedan CN; Garrett L; Nussbaum RL Trinucleotide repeats (CGG)(22)TGG(CGG)(43)TGG(CGG)(21) from the fragile X gene remain stable in transgenic mice | 9 | 19 |
| 498 | 21 | 51 | 1600 1997 JOURNAL OF CLINICAL INVESTIGATION 100(2):331-338 Jakala P; Hanninen T; Ryynanen M; Laakso M; Partanen K; Mannermaa A; Soininen H Fragile-X: Neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes | 12 | 19 |
| 499 | 3 | 6 | 1736 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):322-325 Allingham-Hawkins SJ; Babul-Hirji R; Chitayat D; Holden JJA; Yang KT; Lee C; Hudson R; Gorwill H; Nolin SL; Glicksman A; Jenkins EC; Brown WT; Howard-Peebles PN; Becchi C; Cummings E; Fallon L; Seitz S; Black SH; Vianna-Morgante AM; Costa SS; Otto PA; Mingroni-Netto RC; Murray A; Webb J; MacSwinney F; Dennis N; Jacobs PA; Syrrou M; Georgiou I; Patsalis PC; Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data | 10 | 19 |
| 500 | 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 |
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