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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 3: 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 |
|---|---|---|---|---|---|
| 201 | 0 | 0 | 1980 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):667-667 Brown WT; Nolin S; Houck GE; Ding XH; Glicksman A; Li SH; Brooks S; Dobkin C; Jenkins EC The Fragile X Syndrome: Screening and prenatal diagnosis. | 0 | 0 |
| 202 | 5 | 10 | 1889 2000 GENETIC TESTING 4(3):241-242 Brown WT; Nolin SL Apparent FMR1 allele instability in non-Fragile X males - Invited commentary | 0 | 1 |
| 203 | 0 | 0 | 2085 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):347-347 Brown WT; Nolin SL; Dobkin CS; Houck GS; Glicksman A; Ding XD; Gargano AD; Crawford L; Gitcho N; Spence SJ; Geschwind DH; Agre Frequency of fragile X in multiplex autism: Testing the AGRE families. | 0 | 0 |
| 204 | 0 | 0 | 1707 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A103-A103 Brown WT; Rabe A; Durnas R; Haubenstock H; Dobkin C FMR1 knockout mouse shows a strain-specific severe learning impairment: A robust model for the fragile X syndrome. | 0 | 0 |
| 205 | 1 | 3 | 520 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):201-205 BROWN WT; RUDELLI RD; WISNIEWSKI HM FRAGILE-X SYNDROME - NEUROPATHOLOGY CENTER | 1 | 1 |
| 206 | 8 | 14 | 452 1987 HUMAN GENETICS 75(3):294-295 BROWN WT; SHERMAN SL; DOBKIN CS HYPOTHESIS REGARDING THE NATURE OF THE FRAGILE-X MUTATION - A REPLY | 3 | 5 |
| 207 | 6 | 10 | 482 1987 LANCET 1(8527):280-280 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; JENKINS EC RFLP FOR LINKAGE ANALYSIS OF FRAGILE-X SYNDROME | 21 | 35 |
| 208 | 0 | 0 | 440 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):587-587 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; JENKINS EC; CARPENTER N LINKAGE OF FLANKING PROBES IN 40 FRAGILE X-FAMILIES | 1 | 7 |
| 209 | 12 | 22 | 540 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):551-566 BROWN WT; YE W; GROSS AC; CHAN CB; DOBKIN CS; JENKINS EC MULTIPOINT LINKAGE OF 9 ANONYMOUS PROBES TO HPRT, FACTOR-IX, AND FRAGILE-X | 8 | 25 |
| 210 | 6 | 13 | 1395 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 | 6 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 211 | 0 | 0 | 1273 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):913-913 BROWN WT; ZHONG N; KAJANOJA E; SMITS B; CURLEY D; WANG D; JU W; HOUCK G; NOLIN S; RYYNANEN M FRAGILE-X FOUNDER CHROMOSOME EFFECTS AND NEW MUTATIONS | 0 | 0 |
| 212 | 0 | 0 | 1041 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):781-781 BROWN WT; ZHONG N; YE L; DOBKIN C FOUNDER FRAGILE-X CHROMOSOMES | 0 | 0 |
| 213 | 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 |
| 214 | 9 | 15 | 2062 2001 REVISTA DE NEUROLOGIA 33:S29-S32 Brun-Gasca C; Artigas-Pallares J Psycholinguistic aspects of fragile X chromosome syndrome | 0 | 1 |
| 215 | 14 | 47 | 2102 2002 AMERICAN JOURNAL OF NEURORADIOLOGY 23(10):1757-1766 Brunberg JA; Jacquemont S; Hagerman RJ; Berry-Kravis EM; Grigsby J; Leehey MA; Tassone F; Brown WT; Greco CM; Hagerman PJ Fragile X premutation carriers: Characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction | 11 | 19 |
| 216 | 0 | 0 | 93 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A127-A127 BRYANT EM; GLADSTONE P; MARTIN GM EXPRESSION OF THE FRAGILE-X IN MOUSE-X HUMAN SOMATIC-CELL HYBRIDS | 2 | 2 |
| 217 | 0 | 0 | 6 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A99-A99 BRYANT EM; HOEHN H; MARTIN GM EXPRESSION OF THE FRAGILE X IN EUPLOID SOMATIC-CELL HYBRIDS | 3 | 3 |
| 218 | 1 | 10 | 133 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 |
| 219 | 16 | 30 | 455 1987 HUMAN GENETICS 76(2):165-172 BUCHANAN JA; BUCKTON KE; GOSDEN CM; NEWTON MS; CLAYTON JF; CHRISTIE S; HASTIE N 10 FAMILIES WITH FRAGILE-X SYNDROME - LINKAGE RELATIONSHIPS WITH 4 DNA PROBES FROM DISTAL-XQ | 9 | 16 |
| 220 | 0 | 0 | 1283 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1603-1603 BUCHANAN JA; KLOCK RJ; DORAN K; KENNEDY D; WYATT P PRENATAL TEST FOR FRAGILE-X SYNDROME REVEALS APPARENT FMR1 GENE CONTRACTION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 221 | 0 | 0 | 1605 1997 JOURNAL OF MEDICAL GENETICS 34:539-539 Buckingham A; Bell JA; Payne SJ; Masters K; Emmerson J; Holder SE Recurrence of Turner's syndrome in a fragile-X family | 0 | 0 |
| 222 | 0 | 0 | 764 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):289-289 BUCKLEY D; JALAL S; DEWALD G FRAGILE-X STUDIES - WHAT IS PRACTICAL | 0 | 0 |
| 223 | 0 | 0 | 1370 1995 JOURNAL OF MEDICAL GENETICS 32(2):154-154 BULLOCK S; FELIX CA; BUTTERWORTH MA; STEVENSON K; WILLIAMS D THE USE OF MOLECULAR DNA TESTING TO DISTINGUISH BETWEEN MUTATIONS AT THE FRAGILE-X A-SITES AND E-SITES | 0 | 0 |
| 224 | 0 | 0 | 1236 1994 JOURNAL OF MEDICAL GENETICS 31(2):173-173 BULLOCK S; LINDLEY V COMPLEMENTARY CYTOGENETIC AND MOLECULAR ANALYSIS OF A REFERRAL FOR FRAGILE-X TESTING | 0 | 0 |
| 225 | 0 | 0 | 1369 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 BULLOCK S; LINDLEY VH; STEVENSON K; COLE T MOLECULAR DNA TESTING OF A FAMILY MANIFESTING FRAGILE-X SYNDROME IN BOTH THE FRAX-A FULL MUTATION AND MOSAIC FORMS | 0 | 0 |
| 226 | 0 | 0 | 490 1987 PRACTITIONER 231(1431):910-& BUNDEY S THE FRAGILE X-SYNDROME | 1 | 1 |
| 227 | 6 | 13 | 693 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME | 1 | 1 |
| 228 | 3 | 4 | 1124 1993 LANCET 341(8847):770-770 BUNDEY S; NORMAN E POPULATION SCREENING FOR FRAGILE-X SYNDROME | 8 | 8 |
| 229 | 5 | 29 | 297 1985 JOURNAL OF MEDICAL GENETICS 22(4):258-266 BUNDEY S; WEBB TP; THAKE A; TODD J A COMMUNITY STUDY OF SEVERE MENTAL-RETARDATION IN THE WEST MIDLANDS AND THE IMPORTANCE OF THE FRAGILE X-CHROMOSOME IN ITS ETIOLOGY | 16 | 31 |
| 230 | 9 | 29 | 1795 1999 INTERNATIONAL JOURNAL OF BEHAVIORAL DEVELOPMENT 23(2):519-531 Burack JA; Shulman C; Katzir E; Schaap T; Brennan JM; Iarocci G; Wilansky P; Amir N Cognitive and behavioural development of Israeli males with fragile X and Down Syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 231 | 4 | 4 | 485 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 BURD L THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 232 | 16 | 37 | 370 1986 CHILD STUDY JOURNAL 16(4):285-296 BURD L; KERBESHIAN J FRAGILE X-SYNDROME - DEVELOPMENTAL ASPECTS | 0 | 1 |
| 233 | 2 | 2 | 1440 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):376-376 Burgess B; Partington M; Turner G; Robinson H Normal age of menarche in fragile X syndrome | 3 | 3 |
| 234 | 27 | 44 | 1891 2000 GENETICS IN MEDICINE 2(4):242-248 Burman RW; Anoe KS; Popovich BW Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics | 1 | 2 |
| 235 | 0 | 0 | 1712 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A266-A266 Burman RW; Popovich BW; Yates PA; Jacky PB; Schnell JL; Turker MS Fully expanded fragile X CGG repeats exhibit a length-and differentiation-dependent instability in cell hybrids that is independent of DNA methylation. | 0 | 0 |
| 236 | 27 | 41 | 961 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(2):99-103 BURSZTEJN C; ALEMBIK Y; STOLL C; POUPIER G; FELLER L; HAMON J; TRIBOUT JL; GARDONE MC; DANIONGRILLIAT A FRAGILE-X SYNDROME ASSOCIATED WITH INFANTILE-AUTISM AND PSYCHOTIC DISORDERS | 0 | 2 |
| 237 | 11 | 19 | 2327 2004 EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY 112(2):189-191 Bussani C; Papi L; Sestini R; Baldinotti F; Bucciantini S; Bruni V; Scarselli G Premature ovarian failure and fragile X premutation: a study on 45 women | 0 | 0 |
| 238 | 6 | 12 | 700 1990 HUMAN GENETICS 84(2):216-217 BUTLER MG NO SIGNIFICANT RELATIONSHIP BETWEEN AGE AND FREQUENCY OF CHROMOSOME LESIONS IN MENTALLY-RETARDED INDIVIDUALS WITH OR WITHOUT THE FRAGILE X-SYNDROME | 1 | 4 |
| 239 | 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 |
| 240 | 3 | 4 | 517 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 241 | 10 | 23 | 1012 1992 PEDIATRICS 89(6):1059-1062 BUTLER MG; BRUNSCHWIG A; MILLER LK; HAGERMAN RJ STANDARDS FOR SELECTED ANTHROPOMETRIC MEASUREMENTS IN MALES WITH THE FRAGILE X-SYNDROME | 24 | 28 |
| 242 | 5 | 12 | 557 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):775-778 BUTLER MG; DEV VG; SHAH D; ULM JE; WILMOT PL; SHAPIRO LR THE USE OF EARLY SIMULTANEOUS PERCUTANEOUS UMBILICAL BLOOD-SAMPLING (PUBS) AND AMNIOCENTESIS FOR PRENATAL FRAGILE-X CHROMOSOME DIAGNOSIS | 0 | 0 |
| 243 | 2 | 15 | 556 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):767-773 BUTLER MG; FLETCHER M; GALE DD; MEANEY FJ; MCLEOD DR; FAGAN J; CARPENTER NJ METACARPOPHALANGEAL PATTERN PROFILE ANALYSIS IN FRAGILE-X SYNDROME | 4 | 8 |
| 244 | 0 | 0 | 622 1989 AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 78(2):200-200 BUTLER MG; HAYNES JL; ALLEN GA; SINGH DN ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT FRAGILE X-SYNDROME | 0 | 0 |
| 245 | 3 | 5 | 584 1988 HUMAN GENETICS 78(4):383-383 BUTLER MG; JOSEPH GM; RAMES LJ; CACHEIRO N; LOZZIO CB CHROMOSOME BREAKAGE IN CONTROL AND FRAGILE-X SUBJECTS USING FOLATE-DEFICIENT CULTURE CONDITIONS | 2 | 2 |
| 246 | 5 | 10 | 842 1991 CLINICAL GENETICS 39(5):347-354 BUTLER MG; MANGRUM T; GUPTA R; SINGH DN A 15-ITEM CHECKLIST FOR SCREENING MENTALLY-RETARDED MALES FOR THE FRAGILE X-SYNDROME | 28 | 32 |
| 247 | 2 | 10 | 558 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 |
| 248 | 8 | 9 | 1157 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):315-316 BUTLER MG; PRATESI R; VNENCAKJONES CL MOLECULAR-GENETIC SCREENING IN CYTOGENETICALLY NORMAL MENTALLY-RETARDED MALES WITH MANIFESTATIONS OF FRAGILE-X-SYNDROME | 2 | 3 |
| 249 | 15 | 26 | 1366 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:544-553 Butler MG; Pratesi R; VnencakJones CL Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome | 0 | 1 |
| 250 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 251 | 7 | 23 | 1112 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 | 8 |
| 252 | 16 | 27 | 1094 1993 HUMAN GENETICS 92(3):269-272 BUYLE S; REYNIERS E; VITS L; DEBOULLE K; HANDIG I; WUYTS FLE; DEELEN W; HALLEY DJJ; OOSTRA BA; WILLEMS PJ FOUNDER EFFECT IN A BELGIAN-DUTCH FRAGILE-X POPULATION | 19 | 29 |
| 253 | 2 | 4 | 111 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 | 12 |
| 254 | 3 | 52 | 2068 2001 REVISTA DE NEUROLOGIA 33:S65-S70 Calvani M; D'Iddio S; de Gaetano A; Mariotti P; Mosconi L; Pomponi MG; Tabolacci E; Torrioli MG; Vernacotola S; Neri G L-acetylcarnityne treatment on fragile X patients hyperactive behaviour | 0 | 0 |
| 255 | 8 | 33 | 153 1983 NATURE 306(5944):701-704 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE OF FRAGILE X MENTAL-RETARDATION SYNDROME TO HEMOPHILIA-B AND TRANSMISSION THROUGH A NORMAL-MALE | 78 | 171 |
| 256 | 0 | 0 | 197 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):432-432 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE BETWEEN THE LOCI FOR THE FRAGILE X MENTAL-RETARDATION AND HEMOPHILIA-B | 0 | 0 |
| 257 | 2 | 13 | 579 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(5):646-649 CAMMARATA S; ARCHIDIACONO N; ROMEO G; BENASSI G; GUARINO M; DALESSANDRO R PREVALENCE OF MENTAL-RETARDATION RELATED TO FRAGILE X SYNDROME AND OTHER CHROMOSOMAL-ABNORMALITIES IN THE REPUBLIC OF SAN MARINO | 0 | 2 |
| 258 | 3 | 24 | 203 1984 HUMAN GENETICS 67(1):99-102 CANTU ES; JACOBS PA FRAGILE (X) EXPRESSION - RELATIONSHIP TO THE CELL-CYCLE | 4 | 7 |
| 259 | 4 | 18 | 242 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(5):947-955 CANTU ES; NUSSBAUM RL; AIRHART SD; LEDBETTER DH FRAGILE (X) EXPRESSION INDUCED BY FUDR IS TRANSIENT AND INVERSELY RELATED TO LEVELS OF THYMIDYLATE SYNTHASE ACTIVITY | 3 | 5 |
| 260 | 9 | 32 | 685 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):442-447 CANTU ES; STONE JW; WING AA; LANGEE HR; WILLIAMS CA CYTOGENETIC SURVEY FOR AUTISTIC FRAGILE-X CARRIERS IN A MENTAL-RETARDATION CENTER | 5 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 261 | 4 | 8 | 1248 1994 MOLECULAR AND CELLULAR PROBES 8(2):177-180 CAO J; TARLETON J; BARBERIO D; DAVIDOW LS A SIMPLE FRAGILE-X PCR ASSAY WITH 7-DEAZAGUANINE-SUBSTITUTED DNA VISUALIZED BY ETHIDIUM-BROMIDE | 2 | 5 |
| 262 | 3 | 23 | 230 1984 PEDIATRICS 74(5):883-886 CARMI R; MERYASH DL; WOOD J; GERALD PS FRAGILE-X SYNDROME ASCERTAINED BY THE PRESENCE OF MACRO-ORCHIDISM IN A 5-MONTH-OLD INFANT | 4 | 6 |
| 263 | 0 | 0 | 2122 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:55-56 Carmichael B Fragile X Syndrome - its impact on families | 0 | 0 |
| 264 | 8 | 10 | 1800 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 |
| 265 | 7 | 20 | 791 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):311-318 CARPENTER NJ DNA LINKAGE ANALYSIS OF 26 FAMILIES WITH FRAGILE-X SYNDROME | 1 | 1 |
| 266 | 0 | 1 | 89 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 |
| 267 | 0 | 0 | 7 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A100-A100 CARPENTER NJ; LEICHTMAN LG; LOGAN A; SAY B FRAGILE X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 268 | 0 | 0 | 31 1981 PEDIATRIC RESEARCH 15(4):560-560 CARPENTER NJ; LEICHTMAN LG; SAY B STUDIES ON THE FRAGILE X-SYNDROME IN SUBJECTS WITH MENTAL-RETARDATION OF UNKNOWN ETIOLOGY | 0 | 0 |
| 269 | 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 |
| 270 | 7 | 22 | 942 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):312-319 CARPENTER NJ; SWARTZBOYD J; PRICHARD JK; LAM T LINKAGE AND RISK ASSESSMENT IN FRAGILE-X FAMILIES USING NEW DNA PROBES AT XQ27 | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 271 | 16 | 20 | 797 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):349-353 CARPENTER NJ; THIBODEAU SN; BROWN WT LINKAGE RELATIONSHIPS BETWEEN DXS105, DXS98, AND OTHER POLYMORPHIC DNA MARKERS FLANKING THE FRAGILE-X LOCUS | 2 | 3 |
| 272 | 6 | 10 | 418 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(3):731-732 CARPENTER NJ; VEENEMA H; BAKKER E; HOFKER MH; PEARSON PL A NEW DNA PROBE PROXIMAL TO AND CLOSELY LINKED TO FRAGILE-X | 4 | 4 |
| 273 | 2 | 12 | 2064 2001 REVISTA DE NEUROLOGIA 33:S37-S41 Carrasco M Informing members of families affected by fragile X syndrome of this diagnosis | 0 | 0 |
| 274 | 4 | 21 | 1407 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):27-30 Carrel L; Willard HF An assay for X inactivation based on differential methylation at the fragile X locus, FMR1 | 1 | 30 |
| 275 | 11 | 20 | 2115 2002 CURRENT BIOLOGY 12(24):R852-R854 Carthew RW RNA interference: The fragile X syndrome connection | 0 | 3 |
| 276 | 1 | 1 | 2293 2003 NATURE REVIEWS GENETICS 4(10):758-758 Casci T Fragile X: a class of its own | 0 | 0 |
| 277 | 1 | 1 | 2294 2003 NATURE REVIEWS NEUROSCIENCE 4(10):776-777 Casci T Neurological disorders - Fragile X: a class of its own | 0 | 0 |
| 278 | 2 | 10 | 1146 1993 SCIENTIST 7(19):16-16 CASKEY CT HOT PAPERS - MOLECULAR-GENETICS - VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX BY FU,Y.H., KUHL,D.P.A., PIZZUTI,A., ET-AL, AND AN UNSTABLE TRIPLET REPEAT IN A GENE-RELATED TO MYOTONIC MUSCULAR-DYSTROPHY BY FU,Y.H., PIZZUTI,A., FENWICK,R.G., ET-AL | 0 | 0 |
| 279 | 13 | 16 | 1228 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):552-553 CASKEY CT FRAGILE-X SYNDROME - IMPROVING UNDERSTANDING AND DIAGNOSIS | 2 | 2 |
| 280 | 3 | 6 | 1893 2000 HUMAN GENETICS 107(2):195-196 Castellvi-Bel S; Fernandez-Burriel M; Rife M; Jimenez D; Mallolas J; Sanchez A; Ramos F; Mila M Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 281 | 0 | 0 | 1045 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1136-1136 CASTELLVIBEL S; KRUYER H; BANCHS I; MILA M; ESTIVILL X NONRADIOACTIVE PCR OF THE CGG REPEAT OF THE FRAGILE-X GENE | 0 | 0 |
| 282 | 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 |
| 283 | 21 | 34 | 2008 2001 CELLULAR AND MOLECULAR NEUROBIOLOGY 21(1):29-38 Castren M; Haapasalo A; Oostra BA; Castren E Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons | 2 | 2 |
| 284 | 23 | 59 | 2179 2002 NEUROBIOLOGY OF DISEASE 11(1):221-229 Castren M; Lampinen KE; Miettinen R; Koponen E; Sipola I; Bakker CE; Oostra BA; Castren E BDNF regulates the expression of fragile X mental retardation protein mRNA in the hippocampus | 2 | 3 |
| 285 | 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 |
| 286 | 9 | 43 | 2139 2002 GENES & DEVELOPMENT 16(19):2491-2496 Caudy AA; Myers M; Hannon GJ; Hammond SM Fragile X-related protein and VIG associate with the RNA interference machinery | 14 | 66 |
| 287 | 0 | 0 | 1704 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A29-A29 Ceman S; Brown V; Warren ST Isolation of an FMRP-associated mRNP and the identification of nucleolin and the fragile X-related proteins as components of the complex. | 0 | 0 |
| 288 | 14 | 46 | 1816 1999 MOLECULAR AND CELLULAR BIOLOGY 19(12):7925-7932 Ceman S; Brown V; Warren ST Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex | 35 | 64 |
| 289 | 39 | 64 | 1579 1997 CURRENT OPINION IN NEUROLOGY 10(2):142-147 Chakrabarti L; Davies KE Fragile X syndrome | 2 | 4 |
| 290 | 7 | 9 | 1007 1992 NATURE GENETICS 1(4):237-238 CHAKRAVARTI A FRAGILE-X FOUNDER EFFECT | 15 | 32 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 291 | 12 | 28 | 1642 1998 CLINICAL GENETICS 53(3):179-183 Chan SY; Wong V DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome | 2 | 5 |
| 292 | 18 | 62 | 2249 2003 BMC MOLECULAR BIOLOGY 4 Chandler SP; Kansagra P; Hirst MC Fragile X (CGG)(n) repeats induce a transcriptional repression in cis upon a linked promoter: Evidence for a chromatin mediated effect | 0 | 2 |
| 293 | 1 | 2 | 837 1991 BRITISH MEDICAL JOURNAL 302(6789):1359-1359 CHARATAN F GENE FOR FRAGILE-X SYNDROME DISCOVERED | 0 | 0 |
| 294 | 0 | 0 | 1460 1996 BIOLOGICALS 24(3):210-210 Chehab FF; Wall J; Cai SP Lessons derived from the clinical molecular diagnosis of cystic fibrosis, thalassaemia, Fragile X and Huntington's disease | 0 | 0 |
| 295 | 15 | 43 | 2050 2001 NEUROSCIENCE 103(4):1043-1050 Chen L; Toth M Fragile X mice develop sensory hyperreactivity to auditory stimuli | 16 | 26 |
| 296 | 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 |
| 297 | 0 | 0 | 2088 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):384-384 Chen S; Schoof JM; Lemoine CJ; Gordon CL; Scott CR Prevalence survey of the Fragile X E syndrome referred for Fragile X syndrome testing in boys with mental retardation. | 0 | 0 |
| 298 | 6 | 10 | 1564 1997 ANNALS OF CLINICAL BIOCHEMISTRY 34:517-520 Chen TA; Lu XF; Che PK; Ho WKK Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects | 5 | 7 |
| 299 | 0 | 0 | 1495 1996 JOURNAL OF NEUROCHEMISTRY 67:S36-S36 Chen TA; Lu XF; Ilo WKK; Yi YH; Chen SQ; Chen Z Variation of the CGG repeat in FMR-1 gene in non retarded Chinese population and fragile X syndrome patients | 0 | 0 |
| 300 | 0 | 0 | 1494 1996 JOURNAL OF NEUROCHEMISTRY 67:S34-S34 Chen TA; Lu XF; Yi YH; Ho WKK Analysis of a CGG sequence at the FMR-1 locus in fragile X site by PCR-DGGE method. | 0 | 0 |
Page 3: 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)
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