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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by journal name.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1201 | 2 | 8 | 263 1985 CLINICAL GENETICS 27(2):118-121 HIRTH L; SINGH S; SCHILLING S; MULLER E; GOEDDE HW DERMATOGLYPHIC FINDINGS IN PATIENTS WITH FRAGILE X-CHROMOSOME | 2 | 6 |
| 1202 | 0 | 0 | 264 1985 CLINICAL GENETICS 27(3):307-307 FRYNS JP THE FRAGILE-X SYNDROME - A STUDY OF 83 INDEX-PATIENTS AND THEIR FAMILIES | 0 | 1 |
| 1203 | 0 | 0 | 265 1985 CLINICAL GENETICS 27(3):334-335 SCHMIDT A PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME | 2 | 4 |
| 1204 | 6 | 18 | 266 1985 CLINICAL GENETICS 27(5):463-467 GUSTAVSON KH; DAHLBOM K; FLOOD A; HOLMGREN G; BLOMQUIST HK; et al. EFFECT OF FOLIC-ACID TREATMENT IN THE FRAGILE X-SYNDROME | 10 | 14 |
| 1205 | 4 | 8 | 267 1985 CLINICAL GENETICS 27(5):520-521 WEBB GC DETECTION OF THE FRAGILE X-CHROMOSOME AND OTHER FRAGILE SITES | 5 | 6 |
| 1206 | 5 | 14 | 268 1985 CLINICAL GENETICS 27(6):529-534 WEBB TP CO-CULTIVATION STUDIES IN THE EXPRESSION OF FRAGILE(X) (Q27) IN LYMPHOCYTES | 1 | 2 |
| 1207 | 4 | 11 | 269 1985 CLINICAL GENETICS 28(2):97-99 ABUELO D; CASTREE K; PUESCHEL S; PADREMENDOZA T; ZOLNIERZ K FREQUENCY OF FRAGILE X-CHROMOSOME IN NORMAL FEMALES | 2 | 5 |
| 1208 | 3 | 6 | 270 1985 CLINICAL GENETICS 28(5):399-400 SOUDEK D DECREASE OF FRAGILE X-FREQUENCY IN STORED-BLOOD SAMPLES - INDIVIDUAL VARIABILITY | 1 | 1 |
| 1209 | 0 | 0 | 271 1985 CLINICAL GENETICS 28(5):422-423 DAVIES KE; OLD J; MCGLADE S; SPEER A; COUTELLE C; et al. LINKAGE OF RFLPS AROUND THE DMD AND BMD LOCI AND THE FRAGILE X-LOCUS | 0 | 0 |
| 1210 | 0 | 0 | 272 1985 CLINICAL GENETICS 28(5):449-449 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; et al. FRAGILE X-SYNDROME AND MENTAL-RETARDATION IN GREECE | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1211 | 3 | 5 | 377 1986 CLINICAL GENETICS 29(2):95-95 DEARCE MA; HECHT F; SUTHERLAND GR; WEBB GC GUIDELINES FOR THE DIAGNOSIS OF FRAGILE X | 0 | 2 |
| 1212 | 2 | 7 | 378 1986 CLINICAL GENETICS 29(3):191-195 HECHT F; FRYNS JP; VLIETINCK RF; VANDENBERGHE H GENETIC-CONTROL OVER FRAGILE X-CHROMOSOME EXPRESSION | 9 | 10 |
| 1213 | 0 | 0 | 379 1986 CLINICAL GENETICS 29(5):462-462 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; et al. STUDIES ON FRAGILE X-MENTAL RETARDATION BY THE USE OF DNA PROBES | 1 | 1 |
| 1214 | 2 | 4 | 380 1986 CLINICAL GENETICS 29(5):475-475 TOMMERUP N THE FRAGILE X-CHROMOSOME - PRENATAL-DIAGNOSIS | 1 | 3 |
| 1215 | 7 | 12 | 381 1986 CLINICAL GENETICS 30(4):249-254 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; et al. ANALYSIS OF FRAGILE X-MENTAL RETARDATION FAMILIES USING FLANKING POLYMORPHIC DNA PROBES | 7 | 13 |
| 1216 | 4 | 5 | 382 1986 CLINICAL GENETICS 30(4):346-347 SOUDEK D FRAGILE-X - EXPERIENCE OF A LABORATORY | 3 | 3 |
| 1217 | 9 | 37 | 438 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 | 47 | 57 |
| 1218 | 6 | 13 | 574 1988 CLINICAL GENETICS 33(3):169-175 LOESCH DZ DISCRIMINANT-ANALYSIS OF DERMATOGLYPHIC MEASUREMENTS IN FRAGILE-X MALES AND FEMALES | 0 | 1 |
| 1219 | 1 | 13 | 575 1988 CLINICAL GENETICS 33(5):349-355 MERYASH DL; ABUELO D COUNSELING NEEDS AND ATTITUDES TOWARD PRENATAL-DIAGNOSIS AND ABORTION IN FRAGILE-X FAMILIES | 5 | 17 |
| 1220 | 17 | 31 | 576 1988 CLINICAL GENETICS 33(6):410-417 VEENEMA H; BEVERSTOCK GC; DEKONING T; PEARSON PL; VANDEKAMP JJP THE FRAGILE X-CHROMOSOME - AN EVALUATION OF THE RESULTS IN A ROUTINE CYTOGENETIC LABORATORY IN THE PERIOD 1981-1986 | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1221 | 0 | 0 | 577 1988 CLINICAL GENETICS 33(6):464-464 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 0 | 0 |
| 1222 | 7 | 21 | 578 1988 CLINICAL GENETICS 34(4):265-271 ANVRET M; GILLBERG C; WAHLSTROM J; ALBERTSSONWIKLAND K; DAVIES K INFANTILE-AUTISM, FRAGILE (X) (Q27.3) AND RFLP ANALYSIS IN AN EXTENDED SWEDISH FAMILY | 2 | 4 |
| 1223 | 2 | 31 | 634 1989 CLINICAL GENETICS 36(1):15-24 MERYASH DL PERCEPTION OF BURDEN AMONG AT-RISK WOMEN OF RAISING A CHILD WITH FRAGILE-X SYNDROME | 2 | 7 |
| 1224 | 9 | 14 | 635 1989 CLINICAL GENETICS 36(1):25-30 TUCKERMAN E; WEBB T THE INACTIVATION OF THE FRAGILE X-CHROMOSOME IN FEMALE CARRIERS OF THE MARTIN-BELL SYNDROME AS STUDIED BY 2 DIFFERENT METHODS | 4 | 6 |
| 1225 | 24 | 44 | 700 1990 CLINICAL GENETICS 37(1):2-11 SUTHERLAND GR; MULLEY JC DIAGNOSTIC MOLECULAR-GENETICS OF THE FRAGILE-X | 14 | 16 |
| 1226 | 5 | 23 | 701 1990 CLINICAL GENETICS 37(3):167-172 SUTHERLAND GR; BAKER E THE COMMON FRAGILE SITE IN BAND Q27 OF THE HUMAN X-CHROMOSOME IS NOT COINCIDENT WITH THE FRAGILE-X | 30 | 43 |
| 1227 | 13 | 27 | 702 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 | 17 | 20 |
| 1228 | 5 | 10 | 849 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 |
| 1229 | 15 | 22 | 977 1992 CLINICAL GENETICS 42(1):22-26 MARTINEZ F; BADIA L; PRIETO F A FRAGILE-X FAMILY WITH HIGH PENETRANCE IN FEMALES - RISK HETEROGENEITY | 0 | 2 |
| 1230 | 20 | 26 | 1092 1993 CLINICAL GENETICS 43(1):34-38 HORI T; YAMAUCHI M; SEKI N; TSUJI S; IKUKO K HERITABLE UNSTABLE DNA-SEQUENCES AND HYPERMETHYLATION ASSOCIATED WITH FRAGILE-X SYNDROME IN JAPANESE FAMILIES | 11 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1231 | 7 | 7 | 1093 1993 CLINICAL GENETICS 43(3):157-159 MORNET E; JOKIC M; BOGYO A; TEJADA I; DELUCHAT C; et al. AFFECTED SIBS WITH FRAGILE-X SYNDROME EXHIBIT AN AGE-DEPENDENT DECREASE IN THE SIZE OF THE FRAGILE-X FULL MUTATION | 8 | 8 |
| 1232 | 4 | 14 | 1094 1993 CLINICAL GENETICS 44(2):82-88 LOESCH DZ; SAMPSON ML EFFECT OF THE FRAGILE-X ANOMALY ON BODY PROPORTIONS ESTIMATED BY PEDIGREE ANALYSIS | 3 | 3 |
| 1233 | 7 | 11 | 1095 1993 CLINICAL GENETICS 44(2):109-110 BODURTHA J; JACKSONCOOK C; MADDALENA A; PISERCHIO J; WALLER R 46XY/47XYY MOSAICISM AND FRAGILE-X | 3 | 4 |
| 1234 | 18 | 37 | 1096 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 |
| 1235 | 16 | 20 | 1097 1993 CLINICAL GENETICS 44(4):169-172 YAMAUCHI M; NAGATA S; SEKI N; TOYAMA Y; HARADA N; et al. PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT-DETECTION OF THE DYNAMIC MUTATION DUE TO AN UNSTABLE DNA-SEQUENCE | 2 | 5 |
| 1236 | 10 | 23 | 1230 1994 CLINICAL GENETICS 45(4):175-180 SCHRANDERSTUMPEL C; GERVER WJ; MEYER H; ENGELEN J; MULDER H; et al. PRADER-WILLI-LIKE PHENOTYPE IN FRAGILE-X SYNDROME | 4 | 17 |
| 1237 | 6 | 7 | 1231 1994 CLINICAL GENETICS 45(4):186-189 LOPEZPAJARES I; DELICADO A; PASCUALCASTROVIEJO I; LOPEZMARTIN V; MORENO F; et al. FRAGILE-X SYNDROME WITH EXTRA MICROCHROMOSOME | 0 | 1 |
| 1238 | 18 | 26 | 1644 1997 CLINICAL GENETICS 51(1):1-6 Loesch DZ; Petrovic V; Francis DI; Oertel R; Slater H ''Reduction'' of CGG trinucleotide expansion from mother to offspring in seven fragile-X families | 4 | 7 |
| 1239 | 1 | 9 | 1645 1997 CLINICAL GENETICS 51(1):71-74 Behjati F; Mullarkey M; Bergbaum A; Berry AC; Docherty Z Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation | 0 | 6 |
| 1240 | 9 | 15 | 1646 1997 CLINICAL GENETICS 52(3):147-154 Hecimovic S; Barisic I; Muller A; Petkovic I; Baric I; et al. Expand long PCR for fragile X mutation detection | 8 | 23 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1241 | 11 | 14 | 1647 1997 CLINICAL GENETICS 52(4):211-215 Arvio M; Peippo M; Simola KOJ Applicability of a checklist for clinical screening of the fragile X syndrome | 10 | 15 |
| 1242 | 12 | 28 | 1726 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 |
| 1243 | 8 | 10 | 1727 1998 CLINICAL GENETICS 53(3):200-201 Mornet E; Chateau C; Simon-Bouy B; Serre JL The intermediate alleles of the fragile X CGG repeat in patients with mental retardation | 3 | 7 |
| 1244 | 19 | 30 | 1728 1998 CLINICAL GENETICS 54(4):309-314 Russo S; Briscioli V; Cogliati F; Macchi M; Lalatta F; et al. An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutation | 0 | 1 |
| 1245 | 0 | 2 | 1729 1998 CLINICAL GENETICS 54(4):365-365 Toro-Sola MA Fragile X and Rett syndromes in Puerto Rico | 0 | 0 |
| 1246 | 7 | 12 | 1730 1998 CLINICAL GENETICS 54(4):366-367 Vatta S; Cigui I; Demori E; Morgutti M; Pecile V; et al. Fragile X syndrome, mental retardation and macroorchidism | 3 | 3 |
| 1247 | 34 | 44 | 1879 1999 CLINICAL GENETICS 55(5):346-351 Tassone F; Longshore J; Zunich J; Steinbach P; Salat U; et al. Tissue-specific methylation differences in a fragile X premutation carrier | 2 | 4 |
| 1248 | 8 | 12 | 1880 1999 CLINICAL GENETICS 56(1):98-99 Millan JM; Martinez F; Cadroy A; Gandia J; Casquero M; et al. Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain | 2 | 3 |
| 1249 | 6 | 13 | 2000 2000 CLINICAL GENETICS 57(6):456-458 Lisik M The comparison of anthropometric variables in mentally retarded boys with and without fragile X syndrome | 0 | 0 |
| 1250 | 24 | 33 | 2001 2000 CLINICAL GENETICS 58(2):111-115 Kallinen J; Heinonen S; Mannermaa A; Ryynanen M Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1251 | 66 | 100 | 2139 2001 CLINICAL GENETICS 60(6):399-408 Oostra BA; Chiurazzi P The fragile X gene and its function | 5 | 11 |
| 1252 | 9 | 18 | 2255 2002 CLINICAL GENETICS 61(1):13-20 O'Connell CD; Atha DH; Jakupciak JP; Richie KI Standardization of PCR amplification for fragile X trinucleotide repeat measurements | 0 | 3 |
| 1253 | 4 | 6 | 2409 2003 CLINICAL GENETICS 64(1):54-56 Rogers C; Partington MW; Turner GM Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome | 3 | 4 |
| 1254 | 0 | 1 | 2410 2003 CLINICAL GENETICS 64(2):106-108 Leavitt BR Something lost in the translation: 'premutations' in the FMR1 gene cause Fragile X tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 1255 | 11 | 21 | 1522 1996 CLINICAL OBSTETRICS AND GYNECOLOGY 39(4):772-782 Finucane B Should all pregnant women be offered carrier testing for fragile X syndrome? | 1 | 1 |
| 1256 | 4 | 13 | 850 1991 CLINICAL PEDIATRICS 30(5):318-321 HO HH; EAVES LC; PAYNE E VARIABILITY OF DEVELOPMENT IN 3 SIBLINGS WITH FRAGILE-X SYNDROME | 0 | 1 |
| 1257 | 0 | 0 | 20 1981 CLINICAL RESEARCH 29(1):A134-A134 HERBST DS; GERRARD JW; DUNN HG; DILL FJ; KALOUSEK DK; et al. NONSPECIFIC X-LINKED MENTAL-RETARDATION, MACRO-ORCHIDISM AND THE FRAGILE X-CHROMOSOME MARKER | 0 | 0 |
| 1258 | 0 | 0 | 56 1982 CLINICAL RESEARCH 30(2):A291-A291 BROWN WT; JENKINS EC; FRIEDMAN E; WISNIEWSKI K; FRENCH JH THE FRAGILE X-SYNDROME - A GENETIC CAUSE OF AUTISM | 0 | 0 |
| 1259 | 0 | 0 | 57 1982 CLINICAL RESEARCH 30(2):A292-A292 JENKINS EC; BROWN WT; DUNCAN CJ; BROOKS J DEMONSTRATION OF THE FRAGILE X-CHROMOSOME IN AMNIOTIC-FLUID CELLS | 1 | 2 |
| 1260 | 0 | 0 | 58 1982 CLINICAL RESEARCH 30(5):A890-A890 KRUMDIECK CL; HOWARDPEEBLES PN THE ORIGIN OF THE FRAGILE X IN HUMAN-CHROMOSOMES - AN HYPOTHESIS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1261 | 0 | 0 | 59 1982 CLINICAL RESEARCH 30(5):A891-A891 MIXON C; DEV V EFFECT OF FUDR AND METHIONINE ON THE EXPRESSION OF FRAGILE X IN A LYMPHOBLASTOID CELL-LINE | 1 | 1 |
| 1262 | 0 | 0 | 133 1983 CLINICAL RESEARCH 31(2):A290-A290 BRANDA RF; ARTHUR DC; KING RA FRAGILE X PATIENTS HAVE NORMAL FOLATE METABOLISM | 2 | 2 |
| 1263 | 0 | 1 | 134 1983 CLINICAL RESEARCH 31(2):A290-A290 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; et al. FOLIC-ACID THERAPY OF FRAGILE-X SYNDROME | 0 | 0 |
| 1264 | 0 | 1 | 135 1983 CLINICAL RESEARCH 31(5):A897-A897 HOWARDPEEBLES PN NORMAL-MALE TRANSMISSION OF THE FRAGILE-X - THE COUNSELING DILEMMA | 0 | 0 |
| 1265 | 0 | 0 | 198 1984 CLINICAL RESEARCH 32(5):A884-A884 FRIEDMAN JM; HOWARDPEEBLES PN A THEORETICAL-MODEL FOR UNAFFECTED CARRIER MALES IN FRAGILE-X FAMILIES | 0 | 0 |
| 1266 | 0 | 0 | 199 1984 CLINICAL RESEARCH 32(5):A885-A885 HOLMAN GH; ALLEN SM; TUCKER DA; TAWATER BA SEIZURES AND UNUSUAL VISUAL EVOKED-RESPONSES IN FRAGILE-X CARRIERS | 0 | 0 |
| 1267 | 0 | 0 | 383 1986 CLINICAL RESEARCH 34(1):A34-A34 VANDYKE DL; WEISS L MATERNAL EFFECT ON INTELLIGENCE IN FRAGILE-X MALES AND FEMALES - AN HYPOTHESIS | 0 | 0 |
| 1268 | 0 | 0 | 384 1986 CLINICAL RESEARCH 34(1):A114-A114 LOEHR JP; SYNHORST DP; HAGERMAN RJ; WOLFE RR CARDIOVASCULAR-ABNORMALITIES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1269 | 0 | 0 | 439 1987 CLINICAL RESEARCH 35(1):A60-A60 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE-X (FRA-X) EXPRESSION IN THE PRESENCE OF 5-FLOURO-2'-DEOXYURIDINE (FDUMP) | 0 | 0 |
| 1270 | 0 | 0 | 440 1987 CLINICAL RESEARCH 35(1):A60-A60 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1271 | 0 | 0 | 441 1987 CLINICAL RESEARCH 35(1):A211-A211 HAGERMAN RJ; JACKSON AW; BERRY R; CAMPBELL J; STILLMAN E; et al. PREDICTORS OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1272 | 0 | 0 | 579 1988 CLINICAL RESEARCH 36(1):A207-A207 BIXENMAN H; HECHT F; LOCKWOOD D; HECHT BK NEW COMMON FRAGILE SITE AT XQ27.3 CONFOUNDED WITH FRAGILE-X | 0 | 0 |
| 1273 | 0 | 0 | 636 1989 CLINICAL RESEARCH 37(1):A170-A170 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; et al. LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 0 | 0 |
| 1274 | 0 | 0 | 703 1990 CLINICAL RESEARCH 38(1):A164-A164 HAGERMAN R; AMIRI K; CRONISTER A; WITTENBERGER M; SCHREINER R; et al. FRAGILE-X GIRLS - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 0 | 0 |
| 1275 | 0 | 0 | 851 1991 CLINICAL RESEARCH 39(1):A1-A1 GOLDSON E; HAGERMAN RJ TEMPERAMENT AND THE FRAGILE-X SYNDROME | 2 | 2 |
| 1276 | 0 | 0 | 852 1991 CLINICAL RESEARCH 39(3):A722-A722 BERRYKRAVIS E; HODGES C DEFECTIVE CYCLIC-AMP PRODUCTION IN TISSUES FROM PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1277 | 3 | 13 | 2002 2000 CLINICAL RHEUMATOLOGY 19(4):262-264 Granel B; Ravix V; Pedeillier K; Serratrice J; Disdier P; et al. A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjogren's syndrome: A preliminary report | 0 | 0 |
| 1278 | 38 | 77 | 978 1992 CLINICAL SCIENCE 83(3):255-264 HIRST MC; KNIGHT SJL; BELL MV; SUPER M; DAVIES KE THE FRAGILE-X SYNDROME | 3 | 3 |
| 1279 | 45 | 78 | 1355 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-& Brown WT Perspectives and molecular diagnosis of the fragile X syndrome | 2 | 2 |
| 1280 | 51 | 120 | 2507 2004 CNS DRUGS 18(11):687-703 Tsiouris JA; Brown WT Neuropsychiatric symptoms of fragile X syndrome - Pathophysiology and pharmacotherapy | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1281 | 37 | 73 | 2140 2001 COGNITIVE NEUROPSYCHOLOGY 18(1):1-18 Simon JA; Keenan JM; Pennington BF; Taylor AK; Hagerman RJ Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence | 8 | 10 |
| 1282 | 24 | 47 | 2508 2004 COGNITIVE NEUROPSYCHOLOGY 21(6):579-596 Keenan JM; Simon JA Inference deficits in women with Fragile X Syndrome: A problem in working memory | 0 | 0 |
| 1283 | 9 | 45 | 385 1986 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 51:195-203 MANDEL JL; ARVEILER B; CAMERINO G; HANAUER A; HEILIG R; et al. GENETIC-MAPPING OF THE HUMAN X-CHROMOSOME - LINKAGE ANALYSIS OF THE Q26-Q28 REGION THAT INCLUDES THE FRAGILE X-LOCUS AND ISOLATION OF EXPRESSED SEQUENCES | 4 | 36 |
| 1284 | 40 | 74 | 1523 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:679-687 Eberhart DE; Warren ST The molecular basis of fragile X syndrome | 7 | 8 |
| 1285 | 13 | 56 | 1524 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:689-697 Liu Q; Siomi H; Siomi MC; Fischer U; Zhang Y; et al. Molecular characterization of the protein products of the fragile X syndrome gene and the survival of motor neurons gene | 2 | 10 |
| 1286 | 1 | 22 | 442 1987 COLLEGIUM ANTROPOLOGICUM 11(2):305-316 LOESCH DZ FACTOR-ANALYSIS OF RIDGE-PATTERNS AND HAND MEASUREMENTS IN NORMAL AND FRAGILE-X MALES | 0 | 2 |
| 1287 | 9 | 25 | 2141 2001 COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING 4(3):265-272 Murray J; Cuckle H Cystic fibrosis and fragile X syndrome: The arguments for antenatal screening | 1 | 2 |
| 1288 | 9 | 28 | 853 1991 COMPREHENSIVE PSYCHIATRY 32(1):83-87 TRANEBAERG L; ORUM A MAJOR DEPRESSIVE DISORDER AS A PROMINENT BUT UNDERESTIMATED FEATURE OF FRAGILE-X SYNDROME | 2 | 4 |
| 1289 | 10 | 13 | 979 1992 COMPTES RENDUS DES SEANCES DE LA SOCIETE DE BIOLOGIE ET DE SES FILIALES 186(4):363-370 BELDJORD C; RICHARD L FRAGILE-X SYNDROME - AN HERITABLE UNSTABLE ELEMENT | 0 | 0 |
| 1290 | 0 | 1 | 1525 1996 CONTEMPORARY PSYCHOLOGY 41(5):488-489 McGraw KO Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1291 | 15 | 30 | 1881 1999 CORTEX 35(2):263-271 Cornish KM; Munir F; Cross G Spatial cognition in males with Fragile-X syndrome: Evidence for a neuropsychological phenotype | 14 | 16 |
| 1292 | 17 | 34 | 1098 1993 CURRENT BIOLOGY 3(11):783-786 TROTTIER Y; DEVYS D; MANDEL JL FRAGILE-X SYNDROME - AN EXPANDING STORY | 4 | 8 |
| 1293 | 5 | 37 | 2256 2002 CURRENT BIOLOGY 12(15):1331-1335 Inoue SB; Shimoda M; Nishinokubi I; Siomi MC; Okamura M; et al. A role for the Drosophila fragile X-related gene in circadian output | 13 | 17 |
| 1294 | 11 | 20 | 2257 2002 CURRENT BIOLOGY 12(24):R852-R854 Carthew RW RNA interference: The fragile X syndrome connection | 3 | 10 |
| 1295 | 16 | 47 | 2509 2004 CURRENT BIOLOGY 14(12):1025-1034 Xu KY; Bogert BA; Li WJ; Su K; Lee A; et al. The fragile X-related gene affects the crawling behavior of Drosophila larvae by regulating the mRNA level of the DEG/ENaC protein pickpocket1 | 2 | 3 |
| 1296 | 20 | 37 | 2510 2004 CURRENT BIOLOGY 14(20):1863-1870 Pan LY; Zhang YQ; Woodruff E; Broadie K The Drosophila fragile X gene negatively regulates neuronal elaboration and synaptic differentiation | 2 | 2 |
| 1297 | 31 | 107 | 1731 1998 CURRENT OPINION IN GENETICS & DEVELOPMENT 8(2):245-253 Tapscott SJ; Klesert TR; Widrow RJ; Stoger R; Laird CD Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes | 1 | 10 |
| 1298 | 38 | 51 | 2258 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):278-283 Hagerman RJ; Hagerman PJ The fragile X premutation: into the phenotypic fold | 15 | 25 |
| 1299 | 60 | 93 | 2259 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):284-293 Bardoni B; Mandel JL Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes | 31 | 39 |
| 1300 | 42 | 64 | 1648 1997 CURRENT OPINION IN NEUROLOGY 10(2):142-147 Chakrabarti L; Davies KE Fragile X syndrome | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1301 | 69 | 87 | 2411 2003 CURRENT OPINION IN PEDIATRICS 15(6):559-566 Chiurazzi P; Neri G; Oostra BA Understanding the biological underpinnings of fragile X syndrome | 2 | 5 |
| 1302 | 35 | 50 | 1882 1999 CURRENT OPINION IN PSYCHIATRY 12(5):573-578 Harris SW; Hagerman RJ Fragile X syndrome: new developments | 2 | 2 |
| 1303 | 65 | 94 | 2142 2001 CURRENT OPINION IN PSYCHIATRY 14(5):443-449 Eliez S; Feinstein C The fragile X syndrome: bridging the gap from gene to behavior | 0 | 1 |
| 1304 | 66 | 84 | 2260 2002 CYTOGENETIC AND GENOME RESEARCH 99(1-4):257-264 Oostra BA; Willemsen R The X chromosome and fragile X mental retardation | 2 | 3 |
| 1305 | 43 | 136 | 2412 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):65-76 Greene E; Handa V; Kumari D; Usdin K Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia | 0 | 0 |
| 1306 | 97 | 168 | 2413 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):111-123 Bakker CE; Oostra BA Understanding fragile X syndrome: insights from animal models | 4 | 5 |
| 1307 | 11 | 59 | 2414 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):140-146 Fleming K; Riser DK; Kumari D; Usdin K Instability of the fragile X syndrome repeat in mice: the effect of age, diet and mutations in genes that affect DNA replication, recombination and repair proficiency | 0 | 0 |
| 1308 | 19 | 33 | 2415 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):206-212 Hagerman PJ; Greco CM; Hagerman RJ A cerebellar tremor/ataxia syndrome among fragile X premutation carriers | 4 | 7 |
| 1309 | 16 | 38 | 2511 2004 CYTOGENETIC AND GENOME RESEARCH 105(2-4):448-454 Errijgers V; Kooy RF Genetic modifiers in mice: the example of the fragile X mouse model | 0 | 0 |
| 1310 | 1 | 10 | 136 1983 CYTOGENETICS AND CELL GENETICS 35(3):223-225 BRYANT EM; MARTIN GM; HOEHN H FRAGILE-X EXPRESSION STUDIED BY CLONAL ANALYSIS AND SOMATIC-CELL HYBRIDIZATION | 9 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1311 | 0 | 0 | 200 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 |
| 1312 | 0 | 0 | 201 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):587-587 SNYDER FF; LIN CC; HARASYM CA; JAMRO HK; KUSHNIG ML; et al. EVIDENCE FOR CLOSE ASSOCIATION BETWEEN THE FRAGILE X(Q27-28)-CHROMOSOME SITE AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) BUT NOT WITH HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE (HPRT) | 3 | 3 |
| 1313 | 2 | 5 | 273 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):606-606 CONNOR JM; COLGAN JM; CROSSLEY JA; IMRIE SJ; YATES JRW; et al. MULTIPOINT LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE X-SYNDROME AND FAMILIES WITH HEMOPHILIA-B | 0 | 0 |
| 1314 | 1 | 5 | 274 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):612-612 DAVIES KE; HARPER K; MATTEI MG; MATTEI JF; VEENEMA H; et al. LINKAGE RELATIONSHIP OF DNA SEGMENT 52A (HGM7-DXS51) AND FACTOR-IX (HGM7-F9) TO FRAGILE-X MENTAL-RETARDATION (FRAXQ27) | 0 | 0 |
| 1315 | 0 | 0 | 275 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):645-645 GOONEWARDENA P; TOLUN A; GUSTAVSON KH; HOLMGREN G; LINDSTEN J; et al. STUDIES ON THE FRAGILE-X MENTAL-RETARDATION SYNDROME, DUCHENNE MUSCULAR-DYSTROPHY AND X-LINKED RETINITIS PIGMENTOSA IN SWEDISH FAMILIES, BY THE USE OF DNA PROBES | 0 | 0 |
| 1316 | 0 | 5 | 276 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):653-653 HOLDEN JJA; MULLIGAN LM; FORSTERGIBSON C; SIMPSON NE; WHITE BN; et al. APPLICATION OF FLANKING DNA PROBES TO CARRIER DETECTION IN THE FRAGILE-X SYNDROME | 0 | 2 |
| 1317 | 0 | 0 | 277 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):715-715 OBERLE I; ARVEILER B; MATTEI MG; MATTEI JF; BOUE J; et al. LINKAGE ANALYSIS OF THE FRAGILE X-MENTAL RETARDATION SYNDROME WITH FLANKING POLYMORPHIC DNA MARKERS | 2 | 5 |
| 1318 | 0 | 4 | 278 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):726-726 PURRELLO M; ALHADEFF B; ROCCHI M; ARCHIDIACONO N; DRAYNA D; et al. RELATIVE POSITIVE OF POLYMORPHIC DNA LOCI OF THE HUMAN X-CHROMOSOME LONG ARM SUBTELOMERIC REGION WITH RESPECT TO THE FRAGILE X SITE (FRAXQ27) | 1 | 4 |
| 1319 | 1 | 2 | 279 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):788-788 ZOLL B; ARNEMANN J; KRAWCZAK M; COOPER DN; PESCIA G; et al. THE LOCI FOR FRAGILE X-MENTAL RETARDATION SYNDROME AND COAGULATION FACTOR-IX ARE NOT CLOSELY LINKED | 0 | 0 |
| 1320 | 12 | 23 | 443 1987 CYTOGENETICS AND CELL GENETICS 44(2-3):118-122 LIN MS; SHIMANUKI K; WILSON MG EXPRESSION OF FRAGILE-X IN HUMAN-MOUSE SOMATIC-CELL HYBRIDS | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1321 | 0 | 0 | 444 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):587-587 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; et al. LINKAGE OF FLANKING PROBES IN 40 FRAGILE X-FAMILIES | 1 | 7 |
| 1322 | 0 | 0 | 445 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):594-594 CLAYTON JF; GOSDEN CM; HASTIE N; EVANS HJ MULTIPOINT ANALYSIS AND FRAGILE-X | 0 | 0 |
| 1323 | 0 | 0 | 446 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):598-598 CONNOR JM; OSMAN H; STEFANI L; NEVIN NC; HOFKER M LINKAGE ANALYSIS IN FAMILIES WITH THE FRAGILE-X SYNDROME USING CX55-7 (DXS105) | 0 | 2 |
| 1324 | 0 | 0 | 447 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):622-622 GOSDEN C; BUCHANAN J; NEWTON M; KESTON M; WRIGHT AF; et al. FRAGILE-X SYNDROME - NEW LINKAGE DATA IN 10 FAMILIES | 0 | 0 |
| 1325 | 0 | 0 | 448 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):688-689 SCHWARTZ C; PATTERSON M; DAVIES K; TRUNCA C; TRASK B; et al. THE USE OF DISTAL DELETIONS OF XQ TO ORDER LOCI BETWEEN FACTOR-IX AND THE FRAGILE-X SITE (XQ27.3) | 1 | 2 |
| 1326 | 0 | 0 | 449 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):690-690 SENIOR J; KILPATRICK M; WEBB T LINKAGE STUDIES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 1327 | 7 | 32 | 580 1988 CYTOGENETICS AND CELL GENETICS 47(4):177-180 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M FRAGILE-X EXPRESSION IN THYMIDINE-PROTOTROPHIC AND AUXOTROPHIC HUMAN-MOUSE SOMATIC-CELL HYBRIDS UNDER LOW AND HIGH THYMIDYLATE STRESS CONDITIONS | 1 | 3 |
| 1328 | 6 | 24 | 581 1988 CYTOGENETICS AND CELL GENETICS 48(3):142-147 FANTES J; GOSDEN J; PIPER J USE OF AN ALPHOID SATELLITE SEQUENCE TO LOCATE THE X-CHROMOSOME AUTOMATICALLY, WITH PARTICULAR REFERENCE TO IDENTIFICATION OF THE FRAGILE-X | 0 | 4 |
| 1329 | 2 | 10 | 637 1989 CYTOGENETICS AND CELL GENETICS 50(2-3):172-173 SAUER SM; PHELAN MC; RICHER CL; SCHWARTZ CE PHYSICAL MAPPING OF PROBES PROXIMAL TO THE FRAGILE-X LOCUS (FRAX) CONFIRMS THE ORDER F9-DXS105 (CX55.7)-DXS98 (4D8)-FRAXA | 1 | 1 |
| 1330 | 0 | 0 | 638 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):982-982 DAHL N; MALMSTROM H; HAMMARSTROMHEEROMA K; WADELIUS C; GUSTAVSON KH; et al. ISOLATION OF A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA) | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1331 | 0 | 0 | 639 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1007-1007 GOONEWARDENA P; GROSS AC; FERRANDO CJ; BROWN T; DAHL N; et al. ANONYMOUS DNA PROBE U6.2 (DXS304) FROM XQ MAPS DISTAL TO THE DXS98 LOCUS AND SHOWS CLOSE LINKAGE TO THE FRAGILE-X SYNDROME | 0 | 1 |
| 1332 | 0 | 0 | 640 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1009-1009 GROSS AC; FERRANDO CJ; BROWN WT LINKAGE DATA FOR FRAGILE-X AND 3 DISTAL MARKERS | 0 | 1 |
| 1333 | 0 | 0 | 641 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1086-1087 SUTHERLAND GR; BAKER E THE COMMON FRAGILE SITE (FRAXD) IS AT XQ27.2 AND CAN BE DISTINGUISHED FROM THE FRAGILE-X (FRAXA) AT XQ27.3 | 2 | 8 |
| 1334 | 0 | 0 | 642 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1089-1090 THIBODEAU SN; SCHAID D; BREN G; BLOOMFIELD J; BELL MV; et al. GENETIC-MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 0 | 1 |
| 1335 | 0 | 1 | 643 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1100-1101 WAHLSTROM J; WITTENGERSTROM I; ANVRET M; ODEN A; JOHANNESSON T; et al. RETT SYNDROME RELATED TO FRAGILE X(P22) IN CAFFEINE-INDUCED LYMPHOCYTES CULTURES | 0 | 2 |
| 1336 | 0 | 2 | 854 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 HOWARDPEEBLES PN FRAGILE X SCREENING VS FAMILY STUDIES (ESPECIALLY IN FEMALES) - LABORATORY PROCEDURES GUIDELINES | 0 | 0 |
| 1337 | 0 | 0 | 855 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 SHAPIRO LR; EALLONARDO SJ; WILMOT PL INTERNAL CONTROL FOR SUCCESSFUL INDUCTION OF THE FRAGILE X-CHROMOSOME - OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION ELIMINATED | 1 | 1 |
| 1338 | 2 | 9 | 856 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2054-2055 BOUVET A; BASRUR PK A MARKER FRAGILE X-CHROMOSOME ASSOCIATED WITH BALDY CALF SYNDROME | 1 | 1 |
| 1339 | 0 | 0 | 857 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DJABALI M; NGUYEN C; BIUNNO I; IKEDA JE; OOSTRA BA; et al. LASER MICRODISSECTION OF THE FRAGILE-X REGION ALLOWS ISOLATION OF COSMID CLONES CONTAINING CONSERVED SEQUENCES | 0 | 0 |
| 1340 | 0 | 2 | 858 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2062-2062 DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; LEHRACH H; et al. A PHYSICAL MAP OF THE HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1341 | 2 | 5 | 859 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2065-2065 GRAHAM CA; GRIER DG; CLARKSON M; STEWART FJ; NEVIN NC LINKAGE ANALYSIS IN FRAGILE-X SYNDROME | 0 | 0 |
| 1342 | 2 | 5 | 860 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2067-2067 HIRST M; NAKAHORI Y; KNIGHT S; ROCHE A; RAUT C; et al. A YAC CONTIG ACROSS THE FRAGILE-X REGION DERIVED FROM CHROMOSOME MICRODISSECTION MARKERS | 0 | 0 |
| 1343 | 0 | 0 | 861 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2076-2076 LYNCH M; KREMER EJ; PRITCHARD MA; YU S; BAKER E; et al. THE FRAGILE-X GENOTYPE IS CHARACTERIZED BY AN UNSTABLE REGION OF DNA | 0 | 0 |
| 1344 | 0 | 4 | 862 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2082-2082 POUSTKA A; DIETRICH A; KIOSCHIS P; KORN B; GROSS B; et al. MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| 1345 | 1 | 3 | 863 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2085-2085 RIGGINS GJ; SHERMAN SL; OOSTRA BA; FEITELL D; SUTCLIFFE JS; et al. A HIGHLY POLYMORPHIC DINUCLEOTIDE REPEAT, DXS 548, IS TIGHTLY LINKED TO THE FRAGILE-X SITE | 1 | 2 |
| 1346 | 0 | 0 | 980 1992 CYTOGENETICS AND CELL GENETICS 60(3-4):265-265 SHAPIRO LR; WILMOT PL; ANDREE LE PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X CHROMOSOME - FEASIBILITY AND SPEED OF INSITU CLONAL METHOD IN AMNIOTIC-FLUID CELL TISSUE-CULTURE | 0 | 0 |
| 1347 | 0 | 0 | 981 1992 CYTOGENETICS AND CELL GENETICS 60(3-4):266-266 JACKY PB; JENKINS EC FRAGILE-X CYTOGENETIC GUIDELINES REVIEWED - RELEVANCE TO FRA(X) MOLECULAR GENETIC-STUDIES AND TO APPROPRIATENESS OF CHROMOSOME-STUDIES IN ALL CASES OF DEVELOPMENTAL DELAY - A DISCUSSION | 0 | 0 |
| 1348 | 0 | 0 | 1099 1993 CYTOGENETICS AND CELL GENETICS 63(4):252-252 LUTHARDT F; SKOGERBOE K; SHADOAN P; DINNO N IDENTIFICATION OF DE-NOVO DEL(Y)(Q11.23) IN A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE USING A Y-CHROMOSOME COCKTAIL PROBE (DYZ1, DYZ3) | 0 | 0 |
| 1349 | 0 | 0 | 1100 1993 CYTOGENETICS AND CELL GENETICS 63(4):254-254 OSTROWSKI RS; GRASS FS; LOVETTJELLEMA J AN INVESTIGATION OF THE FRAGILE-X SITE AS IT RELATES TO CHROMOSOME OVERLAP IN CULTURED HUMAN WHITE BLOOD-CELLS | 0 | 0 |
| 1350 | 0 | 0 | 1101 1993 CYTOGENETICS AND CELL GENETICS 63(4):256-256 JACKY PB; BERRY TL; LAMB OA; LANGLOIS MI; OLSON CL; et al. ARE FRAGILE-X CHROMOSOME-STUDIES DEAD | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1351 | 1 | 1 | 1102 1993 CYTOGENETICS AND CELL GENETICS 64(3-4):187-187 SCHMIDT M X-CHROMOSOME INACTIVATION PATTERN IN INTERSTITIAL DELETIONS OF THE FRAGILE X-REGION | 0 | 0 |
| 1352 | 0 | 0 | 1356 1995 CYTOGENETICS AND CELL GENETICS 69(1-2):116-116 HOWARDPEEBLES PN IT IS TIME TO ABANDON THE CYTOGENETIC FRAGILE-X TEST | 0 | 0 |
| 1353 | 0 | 0 | 1649 1997 CYTOGENETICS AND CELL GENETICS 77(1-2):P250-P250 Malarchuk S; Li S; Wertelecki W; Bychkova A; Livshits L Analysis of patients with fragile X syndrome in Ukraine. | 0 | 0 |
| 1354 | 0 | 0 | 1650 1997 CYTOGENETICS AND CELL GENETICS 77(1-2):P287-P287 Tengstrom C; Ikonen A; Kaski M; Autio S High resolution banding and fragile X - screening in persons with mild mental retardation. | 0 | 0 |
| 1355 | 0 | 0 | 1883 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):137-138 Arrieta I; Criado B; Martinez B; Telez M; Fiores P; et al. Molecular and cytogenetic analysis of the fragile X syndrome in a sample from Basque Country: are the Basques a population with a low risk of developing the syndrome? | 0 | 0 |
| 1356 | 0 | 0 | 1884 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):165-165 Sofocleous C; Mavrou A; Fryssira H; Kolialexi A; Tsenghi C; et al. FMRP (Fragile X Mental Retardation Protein) studies in mentally retarded children in Greece | 0 | 0 |
| 1357 | 0 | 0 | 1885 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):167-167 Tayel SM; Al-Naggar RL; Ali FE; Al-Awadi SA Two-step fragile X screening program in mentally retarded males | 0 | 0 |
| 1358 | 1 | 6 | 2003 2000 CYTOGENETICS AND CELL GENETICS 89(1-2):11-13 Bardoni B; Giglio S; Schenck A; Rocchi M; Mandel JL Assignment of NUFIP1 (Nuclear FMRP Interacting Protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12 | 2 | 2 |
| 1359 | 1 | 12 | 704 1990 CYTOMETRY 11(1):73-79 PIPER J; FANTES J; GOSDEN J; JI L AUTOMATIC DETECTION OF FRAGILE X-CHROMOSOMES USING AN X-CENTROMERE PROBE | 0 | 4 |
| 1360 | 24 | 62 | 2416 2003 DEVELOPMENT 130(22):5543-5552 Lee A; Li WJ; Xu KY; Bogert BA; Su K; et al. Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1 | 10 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1361 | 152 | 233 | 2417 2003 DEVELOPMENT AND PSYCHOPATHOLOGY 15(4):927-968 Reiss AL; Dant CC The behavioral neurogenetics of fragile X syndrome: Analyzing gene-brain-behavior relationships in child developmental psychopathologies | 0 | 0 |
| 1362 | 0 | 0 | 2418 2003 DEVELOPMENTAL BIOLOGY 259(2):528-529 Qin M; Kang J; Smith CB Increased local rates of cerebral protein synthesis in fragile X knockout mice. | 0 | 0 |
| 1363 | 18 | 58 | 2512 2004 DEVELOPMENTAL BIOLOGY 270(2):290-307 Zhang YQ; Matthies HJG; Mancuso J; Andrews HK; Woodruff E; et al. The Drosophila fragile X-related gene regulates axoneme differentiation during spermatogenesis | 3 | 3 |
| 1364 | 19 | 64 | 1232 1994 DEVELOPMENTAL BRAIN DYSFUNCTION 7(2-3):155-164 HAGERMAN RJ; FULTON MJ; LEAMAN A; RIDDLE J; HAGERMAN K; et al. A SURVEY OF FLUOXETINE THERAPY IN FRAGILE-X SYNDROME | 17 | 19 |
| 1365 | 9 | 23 | 1357 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):167-184 Hagerman R; Staley L; Brown WT; Taylor A; Meadow K; et al. Conference summary: Fourth International Conference on Fragile X and X-linked Mental Retardation sponsored by the National Fragile X Foundation | 0 | 0 |
| 1366 | 0 | 0 | 1358 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):185-186 Nommensen D Report of the Executive Director of the National Fragile X Foundation | 0 | 0 |
| 1367 | 32 | 75 | 1359 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):187-198 Abrams MT; Reiss AL Quantitative brain imaging studies of fragile X syndrome | 2 | 3 |
| 1368 | 46 | 131 | 1360 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):199-217 Binstock TC Fragile X and the amygdala: Cognitive, interpersonal, emotional, and neuroendocrine considerations | 4 | 4 |
| 1369 | 3 | 16 | 1361 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):218-222 Musumeci SA; Ferri R; Elia M; DalGracco S; Scuderi C; et al. Sleep neurophysiology in fragile X patients | 2 | 3 |
| 1370 | 10 | 22 | 1362 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):223-229 King RA; Hagerman R; Houghton M Ocular findings in fragile X syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1371 | 27 | 36 | 1363 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):230-241 Brun C; Obiols JE; Cheema A; OConnor R; Riddle J; et al. Longitudinal IQ changes in fragile X females | 1 | 1 |
| 1372 | 17 | 33 | 1364 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 | 17 | 22 |
| 1373 | 40 | 75 | 1365 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):252-269 Cohen IL Behavioral profiles of autistic and nonautistic fragile X males | 12 | 13 |
| 1374 | 15 | 38 | 1366 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):270-279 Belser RC; Sudhalter V Arousal difficulties in males with fragile X syndrome: A preliminary report | 21 | 26 |
| 1375 | 19 | 37 | 1367 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):280-292 Sobesky WE; Porter D; Pennington BF; Hagerman RJ Dimensions of shyness in fragile X females | 14 | 19 |
| 1376 | 26 | 41 | 1368 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):293-301 Jenkins EC; Houck GE; Ding XH; Li SY; StarkHouck SL; et al. An update on fragile X prenatal diagnosis: End of the cytogenetic testing era | 1 | 1 |
| 1377 | 18 | 26 | 1369 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):302-309 Holden JJA; Chalifoux M; Wing M; JulienInalsingh C; Scott E; et al. Distribution and frequency of FMR1 CGG repeat number in institutionalized developmentally disabled individuals | 0 | 2 |
| 1378 | 12 | 21 | 1370 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):319-326 Wake SA; Robinson H Assessment of counselling of normal males and normal transmitting male carriers identified in fragile X families | 0 | 0 |
| 1379 | 10 | 25 | 1371 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):327-335 Roy JC; Johnsen J; Breese K; Hagerman R Fragile X syndrome: What is the impact of diagnosis on families? | 3 | 6 |
| 1380 | 8 | 35 | 1372 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):336-344 Hagerman RJ; Riddle JE; Roberts LS; Breese K; Fulton M Survey of the efficacy of clonidine in fragile X syndrome | 12 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1381 | 2 | 23 | 1373 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):345-352 Rattazzi MC Protein therapy in fragile X syndrome - A brief overview of principles, potentials and problems | 0 | 0 |
| 1382 | 0 | 7 | 1374 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):359-362 Lin JFH Introduction to fragile X syndrome for parents | 0 | 0 |
| 1383 | 0 | 0 | 1375 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):363-366 Glass L Females with fragile X: A parent's perspective | 0 | 0 |
| 1384 | 6 | 9 | 1376 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):370-379 Holden JJA Workshop for family and friends .1. The fragile X gene and its mutations | 0 | 0 |
| 1385 | 0 | 0 | 1377 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):390-395 McConkieRosell A; Robinson H; Wake S; Staley L; Heller K; et al. Educating extended family members about the inheritance of the fragile X syndrome | 0 | 1 |
| 1386 | 7 | 18 | 1378 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):396-404 Mazzocco MMM; Lachiewicz AM; Kovar CG; Freund LS; Baumgardner TL; et al. Psychological and emotional studies of the fragile X mutation - A workshop summary | 0 | 0 |
| 1387 | 7 | 8 | 1379 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):405-407 Holden JJA; Chalifoux M; Wing M; JulienInalsingh C; Lawson JS; et al. Distribution and frequency of FMR1 CGG repeat numbers in the general population | 6 | 13 |
| 1388 | 5 | 9 | 1380 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410 HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; et al. Fragile X screening in pediatric and obstetrical patients | 2 | 2 |
| 1389 | 0 | 0 | 1381 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):411-416 [Anon] 4th International Fragile X and X-Linked Mental Retardation Conference - Albuquerque, NM, USA, June 8-12, 1994 - Abstracts | 0 | 0 |
| 1390 | 16 | 52 | 2629 2005 DEVELOPMENTAL CELL 8(1):43-52 Zarnescu DC; Jin P; Betschinger J; Nakamoto M; Wang Y; et al. Fragile X protein functions with Lgl and the PAR complex in flies and mice | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1391 | 9 | 43 | 2630 2005 DEVELOPMENTAL CELL 8(3):331-342 Costa A; Wang Y; Dockendorff TC; Erdjument-Bromage H; Tempst P; et al. The Drosophila fragile X protein functions as a negative regulator in the orb autoregulatory pathway | 0 | 0 |
| 1392 | 0 | 0 | 60 1982 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 24(2):252-253 SERGOVICH F; POZSONYI J; HINTON GG RECENT ADVANCES IN MENTAL-RETARDATION - THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1393 | 0 | 0 | 280 1985 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 27(1):95-96 PUESCHEL SM; FINELLI PV NEUROLOGICAL INVESTIGATIONS IN PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1394 | 2 | 9 | 386 1986 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 28(5):624-627 GILLBERG C; WAHLSTROM J; JOHANSSON R; TORNBLOM M; ALBERTSSONWIKLAND K FOLIC-ACID AS AN ADJUNCT IN THE TREATMENT OF CHILDREN WITH THE AUTISM FRAGILE-X SYNDROME (AFRAX) | 6 | 15 |
| 1395 | 9 | 27 | 450 1987 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 29(6):711-719 THAKE A; TODD J; WEBB T; BUNDEY S CHILDREN WITH THE FRAGILE X-CHROMOSOME AT SCHOOLS FOR THE MILDLY MENTALLY-RETARDED | 11 | 15 |
| 1396 | 20 | 37 | 582 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(2):257-261 HO HZ; GLAHN TJ; HO JC THE FRAGILE-X SYNDROME | 2 | 3 |
| 1397 | 2 | 13 | 583 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(5):646-649 CAMMARATA S; ARCHIDIACONO N; ROMEO G; BENASSI G; GUARINO M; et al. PREVALENCE OF MENTAL-RETARDATION RELATED TO FRAGILE X SYNDROME AND OTHER CHROMOSOMAL-ABNORMALITIES IN THE REPUBLIC OF SAN MARINO | 0 | 2 |
| 1398 | 12 | 47 | 864 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 | 21 | 25 |
| 1399 | 23 | 48 | 982 1992 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 34(9):826-832 GOLDSON E; HAGERMAN RJ THE FRAGILE-X SYNDROME | 3 | 3 |
| 1400 | 16 | 28 | 1103 1993 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 35(6):532-539 BARNICOAT AJ; DOCHERTY Z; BOBROW M WHERE HAVE ALL THE FRAGILE-X BOYS GONE | 4 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1401 | 12 | 14 | 1732 1998 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 40(1):62-64 Gringras P; Barnicoat A Retesting for fragile X syndrome in cytogenetically normal males | 1 | 3 |
| 1402 | 13 | 65 | 1886 1999 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 41(9):625-632 Hatton DD; Bailey DB; Hargett-Beck MQ; Skinner M; Clark RD Behavioral style of young boys with fragile X syndrome | 9 | 13 |
| 1403 | 23 | 46 | 2004 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774 Sheldon L; Turk J Monozygotic boys with fragile X syndrome | 1 | 2 |
| 1404 | 0 | 1 | 2143 2001 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 43(2):142-142 [Anon] Monozygotic boys with fragile X syndrome (vol 42, pg 768, 2000) | 0 | 0 |
| 1405 | 17 | 25 | 2261 2002 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 44(11):724-728 Berry-Kravis E Epilepsy in fragile X syndrome | 5 | 6 |
| 1406 | 1 | 33 | 2631 2005 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 47(2):94-104 Weiskop S; Richdale A; Matthews J Behavioural treatment to reduce sleep problems in children with autism or fragile X syndrome | 0 | 0 |
| 1407 | 16 | 86 | 2144 2001 DEVELOPMENTAL PSYCHOBIOLOGY 39(2):107-123 Roberts JE; Boccia ML; Bailey DB; Hatton DD; Skinner M Cardiovascular indices of physiological arousal in boys with fragile X syndrome | 7 | 7 |
| 1408 | 42 | 139 | 2262 2002 DEVELOPMENTAL PSYCHOBIOLOGY 40(3):323-338 Churchill JD; Grossman AW; Irwin SA; Galvez R; Klintsova AY; et al. A converging-methods approach to fragile X syndrome | 2 | 8 |
| 1409 | 14 | 57 | 2263 2002 DEVELOPMENTAL PSYCHOBIOLOGY 41(2):133-146 Keysor CS; Mazzocco MMM; McLeod DR; Hoehn-Saric R Physiological arousal in females with fragile X or Turner syndrome | 1 | 2 |
| 1410 | 60 | 94 | 1526 1996 DEVELOPMENTAL PSYCHOLOGY 32(3):416-424 Hagerman RJ Biomedical advances in developmental psychology: The case of fragile X syndrome | 3 | 8 |
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| 1411 | 5 | 41 | 2513 2004 DEVELOPMENTAL SCIENCE 7(1):116-130 Scerif G; Cornish K; Wilding J; Driver J; Karmiloff-Smith A Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome | 1 | 1 |
| 1412 | 13 | 16 | 1382 1995 DIAGNOSTIC MOLECULAR PATHOLOGY 4(3):158-161 NABER SP MOLECULAR DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| 1413 | 10 | 16 | 1651 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; et al. A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol | 1 | 2 |
| 1414 | 1 | 1 | 1652 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(5):304-304 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; et al. Five-year experience with Fragile X-testing - Setting laboratory standards of practice and a cost-effective protocol (vol 6, pg 161, 1997) | 0 | 0 |
| 1415 | 16 | 23 | 1887 1999 DIAGNOSTIC MOLECULAR PATHOLOGY 8(3):152-156 Tzeng CC; Cho WC; Kuo PL; Chen RM Pilot fragile X screening in normal population of Taiwan | 7 | 10 |
| 1416 | 12 | 27 | 2145 2001 DIAGNOSTIC MOLECULAR PATHOLOGY 10(1):34-40 Tzeng CC; Lin SJ; Chen YJ; Kuo PL; Jong YJ; et al. An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome | 1 | 3 |
| 1417 | 9 | 44 | 281 1985 DISEASE MARKERS 3(1):9-25 JACOBS PA; SHERMAN SL THE FRAGILE(X) - A MARKER FOR THE MARTIN-BELL SYNDROME | 6 | 8 |
| 1418 | 16 | 24 | 983 1992 DISEASE MARKERS 10(1):1-5 KNIGHT SJL; HIRST MC; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 1 |
| 1419 | 16 | 33 | 984 1992 EDUCATIONAL RESEARCH 34(3):221-228 GIBB C THE MOST COMMON-CAUSE OF LEARNING-DIFFICULTIES - A PROFILE OF FRAGILE-X SYNDROME AND ITS IMPLICATIONS FOR EDUCATION | 1 | 1 |
| 1420 | 0 | 1 | 2632 2005 EDUCATIONAL REVIEW 57(2):258-260 Reid G Educating children with Fragile X syndrome | 0 | 0 |
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| 1421 | 3 | 21 | 2146 2001 ELECTROPHORESIS 22(6):1188-1193 Sung WC; Lee GB; Tzeng CC; Chen SH Plastic microchip electrophoresis for genetic screening: The analysis of polymerase chain reactions products of fragile X (CGG)n alleles | 0 | 12 |
| 1422 | 14 | 43 | 1383 1995 EMBO JOURNAL 14(11):2401-2408 SIOMI MC; SIOMI H; SAUER WH; SRINIVASAN S; NUSSBAUM RL; et al. FXR1, AN AUTOSOMAL HOMOLOG OF THE FRAGILE-X MENTAL-RETARDATION GENE | 62 | 102 |
| 1423 | 16 | 36 | 1384 1995 EMBO JOURNAL 14(21):5358-5366 ZHANG Y; OCONNOR JP; SIOMI MC; SRINIVASAN S; DUTRA A; et al. THE FRAGILE-X MENTAL-RETARDATION SYNDROME PROTEIN INTERACTS WITH NOVEL HOMOLOGS FXR1 AND FXR2 | 77 | 121 |
| 1424 | 16 | 39 | 1527 1996 EMBO JOURNAL 15(19):5408-5414 Fridell RA; Benson RE; Hua J; Bogerd HP; Cullen BR A nuclear role for the fragile X mental retardation protein | 35 | 67 |
| 1425 | 0 | 43 | 2005 2000 EMBO JOURNAL 19(17):4745-4758 Yaremchuk A; Cusack S; Tukalo M Crystal structure of a eukaryote/archaeon-like prolyl-tRNA synthetase and its complex with tRNA(Pro)(CGG) | 0 | 31 |
| 1426 | 22 | 62 | 2147 2001 EMBO JOURNAL 20(17):4803-4813 Schaeffer C; Bardoni B; Mandel JL; Ehresmann B; Ehresmann C; et al. The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif | 66 | 97 |
| 1427 | 17 | 55 | 2514 2004 EMBO JOURNAL 23(16):3346-3355 Rackham O; Brown CM Visualization of RNA-protein interactions in living cells: FMRP and IMP1 interact on mRNAs | 3 | 4 |
| 1428 | 0 | 0 | 202 1984 EMERGENCY MEDICINE 16(15):103-& [Anon] IN SEARCH OF THE FRAGILE-X | 0 | 0 |
| 1429 | 8 | 26 | 1733 1998 EPIGENETICS 214:280-290 Laird; Pillus; Hirst; Bestor; Jaenisch; et al. Rules of DNA methylation in humans inferred from the fragile X gene, FMR1 - Final general discussion | 0 | 0 |
| 1430 | 9 | 28 | 584 1988 EPILEPSIA 29(1):41-47 MUSUMECI SA; COLOGNOLA RM; FERRI R; GIGLI GL; PETRELLA MA; et al. FRAGILE-X SYNDROME - A PARTICULAR EPILEPTOGENIC EEG PATTERN | 17 | 38 |
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| 1431 | 0 | 0 | 1385 1995 EPILEPSIA 36:S1-S1 KLUGER G; BOHM I; LAUB MC; WALDENMEIER C; STUHRMANNSPANGENBERG M EEG IN CHILDREN WITH FRAGILE-X PREMUTATION | 0 | 0 |
| 1432 | 0 | 0 | 1386 1995 EPILEPSIA 36:S244-S244 SINGH R; SUTHERLAND G; MANSON J SEIZURES WITH EPILEPTOGENIC EEG PATTERN IN 2 SISTERS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1433 | 22 | 54 | 1888 1999 EPILEPSIA 40(8):1092-1099 Musumeci SA; Hagerman RJ; Ferri R; Bosco P; Dalla Bernardina B; et al. Epilepsy and EEG findings in males with fragile X syndrome | 10 | 19 |
| 1434 | 20 | 32 | 2006 2000 EPILEPSIA 41(1):19-23 Musumeci SA; Bosco P; Calabrese G; Bakker C; De Sarro GB; et al. Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome | 26 | 35 |
| 1435 | 14 | 24 | 2419 2003 EUROPEAN CHILD & ADOLESCENT PSYCHIATRY 12(4):172-177 Sabaratnam M; Murthy NV; Wijeratne A; Buckingham A; Payne S Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome - A prospective ten-year follow-up study | 0 | 1 |
| 1436 | 58 | 91 | 1233 1994 EUROPEAN JOURNAL OF CLINICAL INVESTIGATION 24(1):1-10 ROUSSEAU F THE FRAGILE-X SYNDROME - IMPLICATIONS OF MOLECULAR-GENETICS FOR THE CLINICAL SYNDROME | 8 | 11 |
| 1437 | 9 | 31 | 1104 1993 EUROPEAN JOURNAL OF HUMAN GENETICS 1(1):72-79 DEVRIES BBA; WIEGERS AM; DEGRAAFF E; VERKERK AJMH; VANHEMEL JO; et al. MENTAL STATUS AND FRAGILE-X EXPRESSION IN RELATION TO FMR-1 GENE MUTATION | 36 | 48 |
| 1438 | 20 | 27 | 1528 1996 EUROPEAN JOURNAL OF HUMAN GENETICS 4(1):8-12 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; et al. Unexpected inheritance of the (CGG)(n) trinucleotide expansion in a fragile X syndrome family | 5 | 6 |
| 1439 | 13 | 28 | 1653 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(2):89-93 FulchignoniLataud MC; Olchwang S; Serre JL The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients | 1 | 6 |
| 1440 | 21 | 33 | 1654 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(5):293-298 Bontekoe CJM; deGraaff E; Nieuwenhuizen IM; Willemsen R; Oostra BA FMR1 premutation allele (CGG)(81) is stable in mice | 16 | 18 |
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| 1441 | 0 | 0 | 1734 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:44-44 Tamanini F; van Unen L; Bontekoe C; Bakker; Willemsen R; et al. Oligomerization and intracellular transport of the Fragile X Mental Retardation Protein | 0 | 0 |
| 1442 | 0 | 0 | 1735 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:63-63 Weinhausel A; Skarits C; Wolschek M; Haas OA Diagnostic evaluation of the fragile X syndrome with methylation-sensitive PCR (MS-PCR) | 0 | 0 |
| 1443 | 0 | 0 | 1736 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:103-103 Syrrou M; Yapijakis C; Bouba I; Georgiou I; Patsalis PC; et al. Intra-population variation of CAG and CGG trinucleotide repeats in X-linked androgen receptor and FMR-1 genes in the Hellenic population | 0 | 0 |
| 1444 | 0 | 0 | 1737 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:107-107 Peixoto A; Santos R; Seruca R; Amorim A; Castedo S Haplotype analysis in fragile X and normal Portuguese populations | 0 | 0 |
| 1445 | 0 | 0 | 1738 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 |
| 1446 | 0 | 0 | 1739 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:144-144 Patsalis P; Sismani C; Hettinger JA; Boumba I; Georgiou I; et al. Population-based molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes: incidence, genetic variation and stability | 0 | 0 |
| 1447 | 0 | 0 | 1740 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:159-159 Strelnikov V; Nemstova M; Demina N; Galkina V; Kuleshov N; et al. DNA testing for fragile X syndrome | 0 | 0 |
| 1448 | 23 | 30 | 1741 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6(5):518-522 Peixoto A; dos Santos MR; Seruca R; Amorim A; Castedo S Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype | 2 | 2 |
| 1449 | 14 | 23 | 1889 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(2):212-216 Ryynanen M; Heinonen S; Makkonen M; Kajanoja E; Mannermaa A; et al. Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies | 13 | 18 |
| 1450 | 18 | 33 | 1890 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(5):526-532 Kooy RF; Reyniers E; Verhoye M; Sijbers J; Bakker CE; et al. Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging | 9 | 21 |
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| 1451 | 21 | 34 | 1891 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(7):771-777 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Brondum-Nielsen K; et al. Analysis of FMR1 (CGG)(n) alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia | 3 | 5 |
| 1452 | 9 | 21 | 2007 2000 EUROPEAN JOURNAL OF HUMAN GENETICS 8(4):247-252 Murray A; Ennis S; MacSwiney F; Webb J; Morton NE Reproductive and menstrual history of females with fragile X expansions | 11 | 15 |
| 1453 | 13 | 17 | 2148 2001 EUROPEAN JOURNAL OF HUMAN GENETICS 9(9):724-727 Larsen LA; Vuust J; Nystad M; Evseeva I; Van Ghelue M; et al. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia | 1 | 3 |
| 1454 | 0 | 0 | 2264 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:55-56 Carmichael B Fragile X Syndrome - its impact on families | 0 | 0 |
| 1455 | 0 | 0 | 2265 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:63-63 Hagerman PJ; Greco CM; Tassone F; Chudley A; Del Bigio MR; et al. Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers | 0 | 0 |
| 1456 | 0 | 0 | 2266 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Afifi HH; Abdel-Aleem AK; Shaheen OO Fragile X syndrome: clinical and behavioral study. | 0 | 0 |
| 1457 | 0 | 0 | 2267 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Loesch DZ Effect of prennutation in the FMR1 gene on cognitive and physical phenotype in fragile X assessed by pedigree analysis. | 0 | 0 |
| 1458 | 0 | 0 | 2268 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:227-227 Steinbach P; Jakubiczka S; Bettecken T X inactivation and fragile X methylation in human placentas | 0 | 0 |
| 1459 | 0 | 0 | 2269 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-228 Tzeng C; Chen W; Huang K Prevalence of fragile-X female carrier in Taiwan is lower than expected | 0 | 0 |
| 1460 | 0 | 0 | 2270 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-229 Biancalana V; Beldjord C; de Martinville B; Bieth E; Blayau M; et al. 5 years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study of 22 laboratories in France. | 0 | 0 |
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| 1461 | 0 | 0 | 2271 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Deelen WH; Jansen C; Ramlakhan SR; Labrijn-Marks I; Olmer R; et al. Five years experience with DIG labeled probes on Southern blots applied in Fragile X diagnostics | 0 | 0 |
| 1462 | 0 | 0 | 2272 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Hasanzad M; Amini SH; Taghizadeh F; Teimourian S; Karimi-Nejad R; et al. Analysis of FMR 1 methylation in Fragile X syndrome in Iranian population | 0 | 0 |
| 1463 | 0 | 0 | 2273 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Gryschenko NV; Malarchuk SG; Livshits LA CGG-repeat expansion and metilation status of the promotor region of FMR1 gene analysis in the Fragile-X sindrome patients from Ukraine | 0 | 0 |
| 1464 | 0 | 0 | 2274 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Zalfa F; Primerano B; Lauro C; Giorgi M; Moro A; et al. Towards an understanding of the Fragile X syndrome: FMRP is translated at the synapses where it acts as a translational regulator | 0 | 0 |
| 1465 | 0 | 0 | 2275 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Gantois I; Reyniers E; Kooy F Differential gene expression in the fragile X mouse model | 0 | 0 |
| 1466 | 2 | 2 | 2276 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Bardoni B; Schenck A; van de Bor V; Giangrande A; Mandel J Drosophila as a model to study the physiological pathway in which FMRP (Fragile X Mental Retardation Protein) is involved | 0 | 0 |
| 1467 | 0 | 0 | 2277 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-232 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; et al. Quantitative analysis of DNA demethylation and trascriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 0 | 0 |
| 1468 | 0 | 0 | 2278 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:232-232 McKelvie KB; Reynolds A; Tassone F; Taylor AK; Hagerman RJ Evidence for skewed X chromosome inactivation in females with the fragile X full mutation | 0 | 0 |
| 1469 | 0 | 0 | 2279 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:323-323 Wilson R; Epstein JH; McKelvie K; Grisgby J; Nagamoto H; et al. Psychological and neuropsychological findings in adults with the premutation and full mutation for Fragile X Syndrome | 0 | 0 |
| 1470 | 0 | 0 | 2280 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:323-323 O'Connor R; Riley K; Epstein J; Wilson R; McKelvie K; et al. Analysis of ADHD subtypes in Fragile X syndrome | 0 | 0 |
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| 1471 | 0 | 0 | 1742 1998 EUROPEAN JOURNAL OF NEUROSCIENCE 10:429-429 Castren M; Haapasalo AK; Oostra BE; Castren E Subcellular localization of FMRP and its mutated form I304N in PC12 cells and rat hippocampal neurons | 0 | 0 |
| 1472 | 0 | 0 | 2008 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:104-104 Braun K; Segal M FMRP involvement in the formation of functional synaptic connections among cultured hippocampal neurons | 0 | 0 |
| 1473 | 0 | 0 | 2009 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:305-305 Beckel-Mitchener AC; Weiler IJ; Klintsova AY; Harms L; Belt B; et al. Analysis of protein synthesis in Fragile X knockout mice | 0 | 0 |
| 1474 | 0 | 18 | 2010 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12(1):381-384 Miller WJ; Skinner JA; Foss GS; Davies KE Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain | 0 | 7 |
| 1475 | 11 | 19 | 2515 2004 EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY 112(2):189-191 Bussani C; Papi L; Sestini R; Baldinotti F; Bucciantini S; et al. Premature ovarian failure and fragile X premutation: a study on 45 women | 0 | 0 |
| 1476 | 0 | 0 | 203 1984 EUROPEAN JOURNAL OF PEDIATRICS 141(4):265-265 LARGO RH; SCHINZEL A DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN BOYS WITH THE FRAGILE-X SYNDROME | 1 | 4 |
| 1477 | 9 | 34 | 282 1985 EUROPEAN JOURNAL OF PEDIATRICS 143(4):269-275 LARGO RH; SCHINZEL A DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN 13 BOYS WITH FRAGILE X-SYNDROME | 26 | 37 |
| 1478 | 1 | 1 | 985 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(6):469-470 MUNDLOS S FRAGILE-X SOLVED | 0 | 0 |
| 1479 | 1 | 1 | 986 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(8):617-617 MUNDLOS S GIRLS WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 1480 | 10 | 27 | 705 1990 EUROPEAN NEUROLOGY 30(1):32-37 RAIMONDI E; LENTI C; ROMAGNONI M; NEGRI R; GAMBINI E; et al. FRAGILE-X MENTAL-RETARDATION IN A LARGE 5-GENERATION FAMILY - A CLINICAL AND CYTOGENETIC STUDY | 0 | 0 |
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| 1481 | 21 | 44 | 1529 1996 EUROPEAN PSYCHIATRY 11(5):227-232 Barbe B; Franke P; Maier W; Leboyer M Fragile X syndrome .1. An overview on its genetic mechanism | 0 | 0 |
| 1482 | 58 | 71 | 1530 1996 EUROPEAN PSYCHIATRY 11(5):233-243 Franke P; Barbe B; Leboyer M; Maier W Fragile X syndrome .2. Cognitive and behavioral correlates of mutations of the FMR-1 gene | 5 | 6 |
| 1483 | 14 | 23 | 387 1986 EXPERIMENTAL CELL BIOLOGY 54(1):40-48 JENKINS EC; BROWN WT; BROOKS J; DUNCAN CJ; SANZ MM; et al. LOW-FREQUENCIES OF APPARENTLY FRAGILE X-CHROMOSOMES IN NORMAL CONTROL CULTURES - A POSSIBLE EXPLANATION | 16 | 20 |
| 1484 | 0 | 28 | 1892 1999 EXPERIMENTAL CELL RESEARCH 251(2):388-400 Yano H; Wang BE; Ahmad I; Zhang JZ; Abo T; et al. Identification of (CAG)(n) and (CGG)(n) repeat-binding proteins, CAGERs expressed in mature neurons of the mouse brain | 0 | 5 |
| 1485 | 24 | 40 | 2011 2000 EXPERIMENTAL CELL RESEARCH 258(1):162-170 Bakker CE; Otero YD; Bontekoe C; Raghoe P; Luteijn T; et al. Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse | 22 | 31 |
| 1486 | 28 | 61 | 2420 2003 EXPERIMENTAL CELL RESEARCH 289(1):95-107 Bardoni B; Willemsen R; Weiler IJ; Schenck A; Severijnen LA; et al. NUFIP 1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosome | 6 | 7 |
| 1487 | 35 | 49 | 2516 2004 EXPERIMENTAL NEUROLOGY 189(2):343-353 Schrier M; Severijnen LA; Reis S; Rife M; van't Padje S; et al. Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cells | 0 | 0 |
| 1488 | 0 | 0 | 1387 1995 FASEB JOURNAL 9(6):A1324-A1324 MITAS M; YU A; DILL J; HAWORTH IS HAIRPIN PROPERTIES OF SINGLE-STRANDED-DNA CONTAINING G+C-RICH TRIPLET REPEATS - (CTG)(15) AND (CGG)(15) | 0 | 0 |
| 1489 | 0 | 0 | 1388 1995 FASEB JOURNAL 9(6):A1324-A1324 SMITH SS; LAAYOUN A; BAKER DJ; KHO MR RECOGNITION OF TELOMERE-LIKE STRUCTURES FROM THE HUMAN C-HA-RAS GENE AND THE TRINUCLEOTIDE REPEAT OF THE FMR-1 GENE OF FRAGILE-X BY HUMAN DNA METHYLTRANSFERASE | 0 | 0 |
| 1490 | 0 | 0 | 1531 1996 FASEB JOURNAL 10(6):D30-D30 Kramer PR; Pearson CE; Sinden RR Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines. | 0 | 0 |
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| 1491 | 0 | 0 | 1743 1998 FASEB JOURNAL 12(8):A1322-A1322 Warren ST The molecular basis of Fragile X syndrome | 0 | 0 |
| 1492 | 0 | 0 | 1893 1999 FASEB JOURNAL 13(5):A703-A703 Greenough WT; Weiler IJ; Angenstein F; Klintsova A; Bauchwitz R Synthesis of the fragile X mental retardation protein at synapses: Possible role in synaptic development and plasticity | 0 | 0 |
| 1493 | 0 | 0 | 2149 2001 FASEB JOURNAL 15(4):A710-A710 Lenert P; Stunz LL; Krieg AM; Ashman RF Down-regulation of CgG-induced B cell NF-kappa B, AP-1 and NF-IL-6 inhibitory oligonucleotides (ODN) | 0 | 0 |
| 1494 | 19 | 26 | 2633 2005 FEBS JOURNAL 272(3):872-878 Pozdnyakova I; Regan L New insights into Fragile X syndrome - Relating genotype to phenotype at the molecular level | 0 | 0 |
| 1495 | 0 | 16 | 1105 1993 FEBS LETTERS 333(3):248-250 BEHNKRAPPA A; MOLLENHAUER J; DOERFLER W TRIPLET REPEAT SEQUENCES IN HUMAN DNA CAN BE DETECTED BY HYBRIDIZATION TO A SYNTHETIC (5'-CGG-3')(17) OLIGODEOXYRIBONUCLEOTIDE | 0 | 3 |
| 1496 | 0 | 1 | 388 1986 FEDERATION PROCEEDINGS 45(3):702-702 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE X EXPRESSION IN THE PRESENCE OF 5-FLUORO-2'-DEOXYURIDINE (FUDR) | 0 | 0 |
| 1497 | 0 | 0 | 2517 2004 FERTILITY AND STERILITY 82:S246-S247 Malcov M; Carmon A; Mey-Raz N; Ben Yosef D; Lessing JB; et al. Preimplantation genetic diagnosis for fragile X syndrome in Israel | 0 | 0 |
| 1498 | 27 | 48 | 1655 1997 FOLIA HISTOCHEMICA ET CYTOBIOLOGICA 35(3):135-141 Szot M The fragile X syndrome | 0 | 0 |
| 1499 | 0 | 0 | 2 1976 GASTROENTEROLOGY 70(5):875-875 SILVA LCD; SETTE H; ANTONACIO F; STRASSMAN P; LOPES JD COMMERCIAL GAMMAGLOBULIN (CGG) AS A POSSIBLE VEHICLE OF TRANSMISSION OF HB-S AG IN FAMILIAL CLUSTERING | 0 | 0 |
| 1500 | 21 | 34 | 2518 2004 GENE 343(2):231-238 Guduric-Fuchs J; Mohrlen F; Frohme M; Frank U A fragile X mental retardation-like gene in a cnidarian | 0 | 0 |