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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 5: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 401 | 0 | 0 | 71 1982 JOURNAL OF MEDICAL GENETICS 19(1):64-64 DAKER MG; CHIDIAC P; FEAR CN; BERRY AC FRAGILE X-CHROMOSOME IN BROTHERS WITH NORMAL INTELLIGENCE, OR THE MAN WHO MIGHT HAVE BEEN A GENIUS | 0 | 2 |
| 402 | 0 | 0 | 2281 2003 JOURNAL OF MEDICAL GENETICS 40:S49-S49 Dalton A; Mills AC; Rigby A; Manly T; Hollis C; Turk J; Cornish K The neuropsychological phenotype of fragile X premutation males | 0 | 0 |
| 403 | 0 | 0 | 2037 2001 JOURNAL OF MEDICAL GENETICS 38:S40-S40 Daly E; Moore CJ; Schmitz N; Jacobs P; Davies K; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of Male Carriers of Fragile X Syndrome | 0 | 0 |
| 404 | 0 | 0 | 1989 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Daly E; Moore CJ; Schmitz N; Jacobs PA; Davis KE; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; A study of male carriers of Fragile X syndrome | 0 | 0 |
| 405 | 0 | 0 | 2248 2003 BIOLOGICAL PSYCHIATRY 53(8):49S-49S Daly EM; Moore CJ; Schmitz N; Morris R; Murphy KC; Murphy DG Expansion of CGG trinucleotide repeats: Effect on neuropsychology of male premutation carriers of Fragile X syndrome | 0 | 0 |
| 406 | 5 | 6 | 1937 2000 JOURNAL OF MOLECULAR DIAGNOSTICS 2(3):128-131 Daly TM; Rafii A; Martin RA; Zehnbauer BA Novel polymorphism in the FMR1 gene resulting in a "pseudodeletion" of FMR1 in a commonly used fragile X assay | 0 | 0 |
| 407 | 2 | 11 | 179 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):255-257 DANIEL A; EKBLOM L; PHILLIPS S FRAGILE-X EXPRESSION SUPPRESSED IN EITHER FUDR OR METHOTREXATE TREATED FIBROBLASTS BY PRETREATMENT WITH 5-AZACYTIDINE | 3 | 5 |
| 408 | 4 | 13 | 187 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 18(3):483-491 DANIEL A; EKBLOM L; PHILLIPS S CONSTITUTIVE FRAGILE SITES 1P31, 3P14, 6Q26, AND 16Q23 AND THEIR USE AS CONTROLS FOR FALSE-NEGATIVE RESULTS WITH THE FRAGILE(X) | 12 | 50 |
| 409 | 7 | 18 | 1223 1994 INTELLIGENCE 19(1):45-50 DANIELS JK; OWEN MJ; MCGUFFIN P; THOMPSON L; DETTERMAN DK; CHORNEY M; CHORNEY K; SMITH D; SKUDER P; VIGNETTI S; MCCLEARN GE; PLOMIN R IQ AND VARIATION IN THE NUMBER OF FRAGILE-X CGG REPEATS - NO ASSOCIATION IN A NORMAL SAMPLE | 2 | 9 |
| 410 | 0 | 0 | 355 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 25(1):186-187 DAR H; BAREL H; JAFFE M; WINTER ST THE FRAGILE-X SYNDROME - THE DILEMMA OF SELECTING PATIENTS FOR EXAMINATION | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 411 | 8 | 11 | 1359 1995 ISRAEL JOURNAL OF MEDICAL SCIENCES 31(5):323-325 DAR H; SCHAAP T; BAITOR H; BOROCHOWITZ Z; GELMANKOHAN Z; CHEMKE T; CHAKI R; COHEN H; FALIKBORENSTEIN Z; CHEMKE J ETHNIC DISTRIBUTION OF THE FRAGILE-X SYNDROME IN ISRAEL - EVIDENCE OF FOUNDER CHROMOSOMES() | 1 | 1 |
| 412 | 17 | 85 | 2005 2001 CELL 107(4):489-499 Darnell JC; Jensen KB; Jin P; Brown V; Warren ST; Darnell RB Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function | 48 | 116 |
| 413 | 18 | 32 | 2349 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):49-52 Darnell JC; Warren ST; Darnell RB The fragile X mental retardation protein, FMRP, recognizes G-quartets | 0 | 0 |
| 414 | 0 | 0 | 1548 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A330-A330 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; Popovich B; Prior TW; Arinami T; Ravine D; Ledbetter DH Methylation analysis of the fragile X syndrome by PCR. | 0 | 0 |
| 415 | 11 | 19 | 1587 1997 GENETIC TESTING 1(3):151-155 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; Prior TW; Popovich B; Rosser L; Arinami T; Ledbetter DH Methylation analysis of the fragile X syndrome by PCR | 2 | 3 |
| 416 | 8 | 10 | 1249 1994 MOLECULAR AND CELLULAR PROBES 8(3):241-244 DAVIDOW LS; BARBERIO D; CAO J; MCCORMICK I AN IMPROVED FRAGILE-X SOUTHERN BLOT PROBE WITHOUT THE CGGS ELIMINATES BACKGROUND BANDS | 0 | 0 |
| 417 | 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 |
| 418 | 7 | 11 | 884 1991 NATURE 351(6326):439-440 DAVIES K HUMAN-GENETICS - BREAKING THE FRAGILE-X | 2 | 7 |
| 419 | 1 | 5 | 271 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):612-612 DAVIES KE; HARPER K; MATTEI MG; MATTEI JF; VEENEMA H; TOMMERUP N; NIELSEN KB; MIKKELSEN M; BEIGHTON P; PEMBREY ME LINKAGE RELATIONSHIP OF DNA SEGMENT 52A (HGM7-DXS51) AND FACTOR-IX (HGM7-F9) TO FRAGILE-X MENTAL-RETARDATION (FRAXQ27) | 0 | 0 |
| 420 | 0 | 0 | 268 1985 CLINICAL GENETICS 28(5):422-423 DAVIES KE; OLD J; MCGLADE S; SPEER A; COUTELLE C; PEMBREY M; HARPER K LINKAGE OF RFLPS AROUND THE DMD AND BMD LOCI AND THE FRAGILE X-LOCUS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 421 | 0 | 0 | 603 1988 JOURNAL OF MEDICAL GENETICS 25(2):129-129 DAVIES KE; PATTERSON M; BELL M; KENWRICK SJ MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 422 | 0 | 0 | 1258 1995 AMERICAN JOURNAL OF EPIDEMIOLOGY 141(11):S50-S50 DAWSON DV; LACHIEWICZ AM BEHAVIORAL EPIDEMIOLOGY OF FRAGILE-X SYNDROME IN FEMALE PEDIATRIC POPULATIONS | 0 | 0 |
| 423 | 29 | 49 | 2142 2002 GENETICS AND MOLECULAR BIOLOGY 25(1):1-6 de Diego Y; Hmadcha A; Moron F; Lucas M; Carrasco M; Pintado E Fragile X founder effect and distribution of CGG repeats among the mentally retarded population of Andalusia, South Spain | 0 | 0 |
| 424 | 8 | 40 | 2069 2001 REVISTA DE NEUROLOGIA 33:S70-S76 de Diego-Otero Y Experimental therapeutic models for fragile X syndrome | 0 | 0 |
| 425 | 134 | 197 | 1686 1998 JOURNAL OF MEDICAL GENETICS 35(7):579-589 de Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF The fragile X syndrome | 28 | 50 |
| 426 | 0 | 0 | 1807 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-172 De Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF Fragile X syndrome: of POF and premutations | 0 | 0 |
| 427 | 16 | 22 | 1809 1999 JOURNAL OF MEDICAL GENETICS 36(6):467-470 de Vries BBA; Mohkamsing S; van den Ouweland AMW; Mol E; Gelsema K; van Rijn M; Tibben A; Halley DJJ; Duivenvoorden HJ; Oostra BA; Niermeijer MF; Collaborative Fragile X Study Grp Screening for the fragile X syndrome among the mentally retarded: a clinical study | 2 | 8 |
| 428 | 27 | 53 | 1955 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):255-263 de Vries BBA; Oostra BA The fragile X syndrome: A model for mental retardation | 0 | 0 |
| 429 | 28 | 41 | 2284 2003 JOURNAL OF MEDICAL GENETICS 40(7):535-539 de Vries BBA; Severijnen LA; Jacobs A; Olmer R; Halley DJJ; Oostra BA; Willemsen R FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics | 1 | 1 |
| 430 | 10 | 21 | 1805 1999 JOURNAL OF MEDICAL GENETICS 36(2):167-170 de Vries BBA; van den Boer-van den Berg HMA; Niermeijer MF; Tibben A Dilemmas in Counselling females with the fragile X syndrome | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 431 | 0 | 0 | 1542 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A219-A219 de Vries BBA; van den Ouweland AMW; Mohkamsing S; Duivenvoorden HJ; Halley DJJ; Sandkuijl LA; Oostra BA; Tibben A; Niermeijer MF A fragile X screening program in The Netherlands: prevalence of fragile X syndrome lower than previously considered, but the disorder is still underdiagnosed. | 0 | 0 |
| 432 | 1 | 4 | 128 1983 CLINICAL GENETICS 24(5):320-323 DEARCE MA TABLES FOR THE CYTOGENETIC STUDY OF FRAGILE X-CHROMOSOMES FOR DIAGNOSTIC PURPOSES | 11 | 17 |
| 433 | 3 | 6 | 205 1984 HUMAN GENETICS 68(4):346-347 DEARCE MA VERIFICATION OF LYONS HYPOTHESIS IN FRAGILE-X CARRIERS | 2 | 5 |
| 434 | 3 | 5 | 373 1986 CLINICAL GENETICS 29(2):95-95 DEARCE MA; HECHT F; SUTHERLAND GR; WEBB GC GUIDELINES FOR THE DIAGNOSIS OF FRAGILE X | 0 | 2 |
| 435 | 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 |
| 436 | 0 | 0 | 206 1984 IRISH JOURNAL OF MEDICAL SCIENCE 153(1):29-30 DEARCE MA; LAW E A SIMPLE STATISTICAL APPROACH TO AVOID FALSE POSITIVES IN THE CYTOGENETIC DIAGNOSIS OF FRAGILE X-CHROMOSOMES | 0 | 0 |
| 437 | 8 | 28 | 139 1983 IRISH JOURNAL OF MEDICAL SCIENCE 152(12):440-445 DEARCE MA; LAW E; MASTERSON JG NON-SPECIFIC X-LINKED MENTAL-RETARDATION WITH FRAGILE-X CHROMOSOME - SOMATIC FEATURES, CYTOGENETIC DIAGNOSIS AND ELEMENTS FOR GENETIC-COUNSELING | 1 | 3 |
| 438 | 2 | 4 | 430 1987 BRITISH JOURNAL OF PSYCHIATRY 150:700-702 DEB S; COWIE VA; TIMBERLAKE C A CASE OF MOSAICISM WITH FRAGILE-X AND FRAGILE-XXY COMPONENTS | 5 | 5 |
| 439 | 16 | 27 | 1133 1993 NATURE GENETICS 3(1):31-35 DEBOULLE K; VERKERK AJMH; REYNIERS E; VITS L; HENDRICKX J; VANROY B; VANDENBOS F; DEGRAAFF E; OOSTRA BA; WILLEMS PJ A POINT MUTATION IN THE FMR-1 GENE ASSOCIATED WITH FRAGILE-X MENTAL-RETARDATION | 131 | 262 |
| 440 | 0 | 0 | 2131 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Deelen WH; Jansen C; Ramlakhan SR; Labrijn-Marks I; Olmer R; Dooijes D; vanden Ouweland AMW; Halley DJJ Five years experience with DIG labeled probes on Southern blots applied in Fragile X diagnostics | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 441 | 29 | 43 | 1428 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):302-308 deGraaff E; deVries BBA; Willemsen R; vanHemel JO; Mohkamsing S; Oostra BA; vandenOuweland AMW The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells | 11 | 13 |
| 442 | 25 | 49 | 1357 1995 HUMAN MOLECULAR GENETICS 4(1):45-49 DEGRAAFF E; ROUILLARD P; WILLEMS PJ; SMITS APT; ROUSSEAU F; OOSTRA BA HOTSPOT FOR DELETIONS IN THE CGG REPEAT REGION OF FMR1 IN FRAGILE-X PATIENTS | 27 | 46 |
| 443 | 35 | 54 | 1262 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(3):609-618 DEGRAAFF E; WILLEMSEN R; ZHONG N; DEDIESMULDERS CEM; BROWN WT; FRELING G; OOSTRA B INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF THE FMR1 PROTEIN IN A MALE FRAGILE-X PATIENT WITH A LUNG-TUMOR | 22 | 31 |
| 444 | 14 | 34 | 251 1985 AMERICAN JOURNAL OF MENTAL DEFICIENCY 90(2):119-123 DELACRUZ FF FRAGILE-X SYNDROME | 9 | 12 |
| 445 | 6 | 8 | 2365 2004 PRENATAL DIAGNOSIS 24(1):67-68 Delatycki MB; Sheffield LJ; Wake S; Cohen J Screening approach for Fragile X syndrome | 0 | 0 |
| 446 | 0 | 0 | 408 1986 RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS 12(4):442-444 DELGIUDICE E; POGGI V; SARTORIO R; CARROZZO R; ROMANO A; SIRONE P; FIORE M THE FRAGILE X-SYNDROME | 0 | 0 |
| 447 | 3 | 31 | 609 1988 SCHIZOPHRENIA RESEARCH 1(4):277-281 DELISI LE; REISS AL; WHITE BJ; GERSHON ES CYTOGENETIC STUDIES OF MALES WITH SCHIZOPHRENIA - SCREENING FOR THE FRAGILE X-CHROMOSOME AND OTHER CHROMOSOMAL-ABNORMALITIES | 1 | 36 |
| 448 | 0 | 0 | 152 1983 MEDICINA-BUENOS AIRES 43(6):756-756 DELREY G; COCO R INVESTIGATION OF FRAGILE X-CHROMOSOMES IN MEN WITH MENTAL-RETARDATION (RM) OF UNKNOWN CAUSE | 0 | 0 |
| 449 | 29 | 60 | 2234 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(5):314-326 Demark JL; Feldman MA; Holden JJA Behavioral relationship between autism and fragile X syndrome | 0 | 0 |
| 450 | 12 | 40 | 2309 2003 YONSEI MEDICAL JOURNAL 44(4):583-592 Demirhan O; Tastemir D; Diler RS; Firat S; Avei A A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 451 | 6 | 21 | 2112 2002 CELLULAR & MOLECULAR BIOLOGY LETTERS 7(3):877-883 Denman RB Methylation of the arginine-glycine-rich region in the fragile X mental retardation protein FMRP differentially affects RNA binding | 2 | 4 |
| 452 | 51 | 135 | 2323 2004 CELLULAR AND MOLECULAR LIFE SCIENCES 61(14):1714-1728 Denman RB; Dolzhanskaya N; Sung YJ Regulating a translational regulator: mechanisms cells use to control the activity of the fragile X mental retardation protein | 0 | 0 |
| 453 | 12 | 24 | 2109 2002 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 292(4):1063-1069 Denman RB; Sung YJ Species-specific and isoform-specific RNA binding of human and mouse fragile X mental retardation proteins | 5 | 6 |
| 454 | 3 | 10 | 721 1990 NEUROLOGY 40(2):378-380 DESAI HB; DONAT J; SHOKEIR MHK; MUNOZ DG AMYOTROPHIC LATERAL SCLEROSIS IN A PATIENT WITH FRAGILE X-SYNDROME | 5 | 7 |
| 455 | 0 | 1 | 212 1984 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 5(3):160-161 DESPOSITO F THE FRAGILE X-SYNDROME - DIAGNOSIS, BIOCHEMISTRY AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 456 | 14 | 17 | 1509 1996 PEDIATRICS 98(2):297-300 Desposito F; Cho S; Frias JL; Sherman J; Wappner RS; Wilson MG Health supervision for children with fragile X syndrome | 3 | 8 |
| 457 | 0 | 2 | 178 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):253-254 DEV VG; MIXON C 5-AZACYTIDINE DECREASES THE FREQUENCY OF FRAGILE-X EXPRESSION IN PERIPHERAL LYMPHOCYTE CULTURE | 4 | 6 |
| 458 | 6 | 20 | 819 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 | 6 | 8 |
| 459 | 10 | 27 | 1119 1993 JOURNAL OF MEDICAL GENETICS 30(9):761-766 DEVRIES BBA; FRYNS JP; BUTLER MG; CANZIANI F; WESBYVANSWAAY E; VANHEMEL JO; OOSTRA BA; HALLEY DJJ; NIERMEIJER MF CLINICAL AND MOLECULAR STUDIES IN FRAGILE-X PATIENTS WITH A PRADER-WILLI-LIKE PHENOTYPE | 18 | 33 |
| 460 | 13 | 20 | 1493 1996 JOURNAL OF MEDICAL GENETICS 33(12):1007-1010 deVries BBA; Jansen CCAM; Duits AA; Verheij C; Willemsen R; vanHemel JO; vandenOuweland AMW; Niermeijer MF; Oostra BA; Halley DJJ Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family | 31 | 38 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 461 | 1 | 2 | 1239 1994 JOURNAL OF MEDICAL GENETICS 31(10):820-820 DEVRIES BBA; NIERMEIJER MF THE PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X PATIENTS - A DESIGNATION FACILITATING CLINICAL (AND MOLECULAR) DIFFERENTIAL-DIAGNOSIS | 1 | 6 |
| 462 | 16 | 40 | 1373 1995 JOURNAL OF MEDICAL GENETICS 32(10):764-769 DEVRIES BBA; ROBINSON H; STOLTEDIJKSTRA I; GI CVTP; DIJKSTRA PF; VANDOOM J; HALLEY DJJ; OOSTRA BA; TURNER G; NIERMEIJER MF GENERAL OVERGROWTH IN THE FRAGILE-X SYNDROME - VARIABILITY IN THE PHENOTYPIC-EXPRESSION OF THE FMR1 GENE MUTATION | 6 | 15 |
| 463 | 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 |
| 464 | 0 | 0 | 1285 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1705-1705 DEVRIES BBA; VANDENOUWELAND AMW; MOHKAMSING S; HALLEY DJJ; TIBBEN A; OOSTRA BA; GALJAARD H; NIERMEIJER MF ACCEPTANCE OF SCREENING FOR THE FRAGILE-X SYNDROME AMONG 1878 MENTALLY-RETARDED INDIVIDUALS IN INSTITUTES AND SPECIAL SCHOOLS IN THE NETHERLANDS | 0 | 0 |
| 465 | 0 | 0 | 1406 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):25-25 deVries BBA; vandenOuweland AMW; Mohkamsing S; Halley DJJ; Tibben A; Oostra BA; Galjaard H; Niermeijer MF Acceptance of screening for the fragile X syndrome among 1878 mentally retarded individuals in institutions and special schools in the Netherlands | 0 | 0 |
| 466 | 9 | 31 | 1089 1993 EUROPEAN JOURNAL OF HUMAN GENETICS 1(1):72-79 DEVRIES BBA; WIEGERS AM; DEGRAAFF E; VERKERK AJMH; VANHEMEL JO; HALLEY DJJ; FRYNS JP; CURFS LMG; NIERMEIJER MF; OOSTRA BA MENTAL STATUS AND FRAGILE-X EXPRESSION IN RELATION TO FMR-1 GENE MUTATION | 36 | 48 |
| 467 | 9 | 20 | 1232 1994 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 38:1-8 DEVRIES LBA; HALLEY DJJ; OOSTRA BA; NIERMEIJER MF THE FRAGILE-X SYNDROME - A GROWING GENE CAUSING FAMILIAL INTELLECTUAL DISABILITY | 1 | 2 |
| 468 | 10 | 15 | 933 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):208-216 DEVYS D; BIANCALANA V; ROUSSEAU F; BOUE J; MANDEL JL; OBERLE I ANALYSIS OF FULL FRAGILE-X MUTATIONS IN FETAL TISSUES AND MONOZYGOTIC TWINS INDICATE THAT ABNORMAL METHYLATION AND SOMATIC HETEROGENEITY ARE ESTABLISHED EARLY IN DEVELOPMENT | 58 | 89 |
| 469 | 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 |
| 470 | 16 | 32 | 955 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(6):816-821 DEWALD GW; BUCKLEY DD; SPURBECK JL; JALAL SM CYTOGENETIC GUIDELINES FOR FRAGILE-X STUDIES TESTED IN ROUTINE PRACTICE | 3 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 471 | 0 | 0 | 2358 2004 MOVEMENT DISORDERS 19:S359-S360 Di Maria E; Grasso M; Abbruzzese G; Mandich P; Ratto S; Sciolla R The role for Fragile X premutation in essential tremor and spinocerebellar ataxia: Findings from two cohorts of Italian patients | 0 | 0 |
| 472 | 0 | 0 | 2216 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):555-555 Di Maria E; Grasso M; Pigullo S; Faravelli F; Abbruzzese G; Barone P; Martinelli P; Ratto S; Sciolla R; Bellone E; Dagna-Bricarelli F; Ajmar F; Mandich P Further evidence that a tremor/ataxia syndrome may occur in Fragile X premutation carriers: findings from two clinical series. | 0 | 0 |
| 473 | 0 | 1 | 1457 1996 ARCHIVES OF MEDICAL RESEARCH 27(3):427-427 DiazGallardo Molecular characterization of the fragile-x syndrome in the Mexican population (vol 26, pg S77, 1995) | 0 | 0 |
| 474 | 11 | 19 | 1308 1995 ARCHIVES OF MEDICAL RESEARCH 26:S77-S83 DiazGallardo MY; BarrosNunez P; Diaz CA; Hernandez A; GomezEspinel I; Leal CA; Fragoso R; Figuera L; GarciaCruz D; RamirezDuenas ML; Cantu JM Molecular characterization of the fragile-X syndrome in the Mexican population | 2 | 4 |
| 475 | 10 | 25 | 888 1991 NUCLEIC ACIDS RESEARCH 19(10):2567-2572 DIETRICH A; KIOSCHIS P; MONACO AP; GROSS B; KORN B; WILLIAMS SV; SHEER D; HEITZ D; OBERLE I; TONIOLO D; WARREN ST; LEHRACH H; POUSTKA A MOLECULAR-CLONING AND ANALYSIS OF THE FRAGILE X-REGION IN MAN | 23 | 45 |
| 476 | 0 | 2 | 851 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; LEHRACH H; POUSTKA A A PHYSICAL MAP OF THE HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 0 | 0 |
| 477 | 0 | 0 | 850 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DJABALI M; NGUYEN C; BIUNNO I; IKEDA JE; OOSTRA BA; MATTEI MG; JORDAN BR LASER MICRODISSECTION OF THE FRAGILE-X REGION ALLOWS ISOLATION OF COSMID CLONES CONTAINING CONSERVED SEQUENCES | 0 | 0 |
| 478 | 9 | 23 | 859 1991 GENOMICS 10(4):1053-1060 DJABALI M; NGUYEN C; BIUNNO I; OOSTRA BA; MATTEI MG; IKEDA JE; JORDAN BR LASER MICRODISSECTION OF THE FRAGILE X REGION - IDENTIFICATION OF COSMID CLONES AND OF CONSERVED SEQUENCES IN THIS REGION | 1 | 25 |
| 479 | 6 | 11 | 1740 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):338-341 Dobkin C; Ding XH; Li SY; Houck G; Nolin SL; Glicksman A; Zhong N; Jenkins EC; Brown WT Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection | 2 | 3 |
| 480 | 0 | 0 | 1979 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):635-635 Dobkin CS; Ding X; Brown WT; El Idrissi A Reduced hippocampal GABAa receptors and increased kainic acid seizure susceptibility in the fragile X mouse. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 481 | 0 | 0 | 2089 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):505-505 Dobkin CS; Ding XH; Houck GE; Mitchell E; Brown WT; Nolin SL A rare Eag I polymorphism that may confound fragile X diagnosis. | 0 | 0 |
| 482 | 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 |
| 483 | 1 | 5 | 802 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):378-379 DOBKIN CS; DRISCOLL MC; FERRANDO C POLYMERASE CHAIN-REACTION DETECTION OF THE DDE-I POLYMORPHISM IN THE FACTOR-IX GENE FOR FRAGILE-X LINKAGE ANALYSIS | 0 | 3 |
| 484 | 17 | 24 | 1427 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):296-301 Dobkin CS; Nolin SL; Cohen I; Sudhalter V; Bialer MG; Ding XH; Jenkins EC; Zhong N; Brown WT Tissue differences in fragile X mosaics: Mosaicism in blood cells may differ greatly from skin | 9 | 11 |
| 485 | 9 | 26 | 2245 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 305(2):434-441 Dolzhanskaya N; Sung YJ; Conti J; Currie JR; Denman RB The fragile X mental retardation protein interacts with U-rich RNAs in a yeast three-hybrid system | 2 | 3 |
| 486 | 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 |
| 487 | 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 |
| 488 | 0 | 0 | 1705 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A49-A49 Drasinover V; Ehrlich S; Magal N; Taub E; Libman V; Shohat T; Shohat M Increased transmission of the premutated allele compared to the normal allele in female carriers of the fragile X syndrome. | 0 | 0 |
| 489 | 17 | 33 | 1355 1995 HUMAN GENETICS 96(3):323-329 DREESEN JCFM; GERAEDTS JPM; DUMOULIN JCM; EVERS JLH; PIETERS MHEC RS46(DXS548) GENOTYPING OF REPRODUCTIVE CELLS - APPROACHING PREIMPLANTATION TESTING OF THE FRAGILE-X SYNDROME | 2 | 7 |
| 490 | 2 | 4 | 828 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(4):523-523 DREESEN JCFM; SMITS A; BRUNNER H RISK CALCULATIONS IN THE FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 491 | 8 | 14 | 1092 1993 HUMAN GENETICS 91(1):80-82 DREESEN JCFM; VANDENHURK JAJM; SMITS APT; VANDENOUWELAND AMW; MARKSLAG PWB; VANOOST BA DXS539, A POLYMORPHIC DNA MARKER PROXIMAL OF THE FRAGILE-X GENE | 0 | 2 |
| 492 | 0 | 0 | 1001 1992 M S-MEDECINE SCIENCES 8(8):878-878 DREYFUSS JC CLINICAL FRAGILE-X SYNDROME DUE TO TOTAL OR PARTIAL GENE DELETION | 0 | 0 |
| 493 | 5 | 8 | 1870 2000 AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE 30(1):86-88 Driscoll G; Clark J; Elakis G; Turner G Early menopause in a family carrying a fragile X premutation | 1 | 3 |
| 494 | 3 | 4 | 962 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(5):477-477 DROUIN V; VANNIER JP; MOIROT H; MITROFANOFF P; TRON P WILMS-TUMOR AND FRAGILE-X SYNDROME | 1 | 1 |
| 495 | 7 | 11 | 798 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):363-366 DRUGGE U; BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY OF POSSIBLY AFFECTED INDIVIDUALS IN THE 19TH-CENTURY | 2 | 2 |
| 496 | 3 | 3 | 947 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):353-354 DRUGGE U; HOLMGREN G; SONBLOMQUIST HK; DAHL N; GUSTAVSON KH; MALMGREN H STUDY OF INDIVIDUALS POSSIBLY AFFECTED WITH THE FRAGILE-X SYNDROME IN A LARGE SWEDISH FAMILY IN THE 18TH TO 20TH CENTURIES | 7 | 7 |
| 497 | 6 | 19 | 401 1986 MUTATION RESEARCH 173(3):201-205 DUNCAN AMV ENHANCED SENSITIVITY OF LYMPHOBLASTOID-CELLS FROM INDIVIDUALS CARRYING THE MUTATION FOR THE FRAGILE X-SYNDROME TO THE CLASTOGENIC EFFECTS OF FUDR | 2 | 3 |
| 498 | 0 | 0 | 1653 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:116-116 Duran M; Valverde L; Molina M; Onaindia ML; Tejada MI Carrier screening for fragile X by PCR in females: comparison with obligated carriers | 0 | 0 |
| 499 | 0 | 0 | 1845 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):348-348 Dyack S; Steele L; Koultchitski G; Yang Y; Weksberg R; Ray PN; Pearson CE AGG interruptions in the CGG trinucleotide repeat tract of the FMR1 gene may contribute to stability of Fragile X premutations. | 0 | 0 |
| 500 | 13 | 25 | 2158 2002 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 41(3):237-244 Dyer-Friedman J; Glaser B; Hessl D; Johnston C; Huffman LC; Taylor A; Wisbeck J; Reiss AL Genetic and environmental influences on the cognitive outcomes of children with fragile X syndrome | 5 | 5 |
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