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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
Page 4: 1 (1246) 2 (77) 3 (47) 4 (34) 5 (25) 6 (19) 7 (14) 8 (11) 9 (9) 10 (7) 11 (5) 12 (4) 13 (3) 14 (2) 15 (1) 16 (1) 17 (0) 18 (0) 19 (0) 20 (0) 21 (0) 22 (0) 23 (0) 24 (0)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 301 | 60 | 138 | 1065 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 48(2):112-121 FISCH GS WHAT IS ASSOCIATED WITH THE FRAGILE-X SYNDROME | 21 | 34 |
| 302 | 10 | 13 | 1114 1993 JOURNAL OF MEDICAL GENETICS 30(2):94-96 SMITS APT; DREESEN JCFM; POST JG; SMEETS DFCM; DEDIESMULDERS C; SPAANSVANDERBIJL T; GOVAERTS LCP; WARREN ST; OOSTRA BA; VANOOST BA THE FRAGILE-X SYNDROME - NO EVIDENCE FOR ANY RECENT MUTATIONS | 27 | 34 |
| 303 | 16 | 21 | 1184 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):482-485 VANDENOUWELAND AMW; DEVRIES BBA; BAKKER PLG; DEELEN WH; DEGRAAFF E; VANHEMEL JO; OOSTRA BA; NIERMEIJER MF; HALLEY DJJ DNA DIAGNOSIS OF THE FRAGILE-X-SYNDROME IN A SERIES OF 236 MENTALLY-RETARDED SUBJECTS AND EVIDENCE FOR A REVERSAL OF MUTATION IN THE FMR-1 GENE | 26 | 34 |
| 304 | 18 | 65 | 1260 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1147-1155 FISCH GS; SNOW K; THIBODEAU SN; CHALIFAUX M; HOLDEN JJA; NELSON DL; HOWARDPEEBLES PN; MADDALENA A THE FRAGILE-X PREMUTATION IN CARRIERS AND ITS EFFECT ON MUTATION SIZE IN OFFSPRING | 24 | 34 |
| 305 | 2 | 13 | 86 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):861-868 UCHIDA IA; FREEMAN VCP; JAMRO H; PARTINGTON MW; SOLTAN HC ADDITIONAL EVIDENCE FOR FRAGILE-X ACTIVITY IN HETEROZYGOUS CARRIERS | 25 | 33 |
| 306 | 5 | 19 | 283 1985 HUMAN GENETICS 69(3):209-211 KRAWCZUN MS; JENKINS EC; BROWN WT ANALYSIS OF THE FRAGILE-X CHROMOSOME - LOCALIZATION AND DETECTION OF THE FRAGILE SITE IN HIGH-RESOLUTION PREPARATIONS | 19 | 33 |
| 307 | 8 | 22 | 539 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):543-550 HEILIG R; OBERLE I; ARVEILER B; HANAUER A; VIDAUD M; MANDEL JL IMPROVED DNA MARKERS FOR EFFICIENT ANALYSIS OF FRAGILE-X FAMILIES | 11 | 33 |
| 308 | 3 | 19 | 821 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):498-502 COHEN IL; VIETZE PM; SUDHALTER V; JENKINS EC; BROWN WT EFFECTS OF AGE AND COMMUNICATION LEVEL ON EYE CONTACT IN FRAGILE-X MALES AND NON-FRAGILE-X AUTISTIC MALES | 22 | 33 |
| 309 | 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 |
| 310 | 21 | 35 | 1594 1997 HUMAN MOLECULAR GENETICS 6(7):971-979 Moutou C; Vincent MC; Biancalana V; Mandel JL Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic | 18 | 33 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 311 | 27 | 47 | 1729 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):286-295 Kaufmann WE; Abrams MT; Chen WM; Reiss AL Genotype, molecular phenotype, and cognitive phenotype: Correlations in fragile X syndrome | 27 | 33 |
| 312 | 0 | 23 | 21 1981 JOURNAL OF MEDICAL GENETICS 18(5):366-373 PROOPS R; WEBB T THE FRAGILE X-CHROMOSOME IN THE MARTIN-BELL-RENPENNING SYNDROME AND IN MALES WITH OTHER FORMS OF FAMILIAL MENTAL-RETARDATION | 20 | 32 |
| 313 | 7 | 21 | 158 1983 PRENATAL DIAGNOSIS 3(2):131-137 WEBB T; GOSDEN CM; RODECK CH; HAMILL MA; EASON PE PRENATAL-DIAGNOSIS OF X-LINKED MENTAL-RETARDATION WITH FRAGILE (X) USING FETOSCOPY AND FETAL BLOOD-SAMPLING | 16 | 32 |
| 314 | 7 | 16 | 643 1989 HUMAN GENETICS 82(3):216-218 DAHL N; HAMMARSTROMHEEROMA K; GOONEWARDENA P; WADELIUS C; GUSTAVSON KH; HOLMGREN G; VANOMMEN GJB; PETTERSSON U ISOLATION OF A DNA PROBE OF POTENTIAL USE FOR DIAGNOSIS OF THE FRAGILE-X SYNDROME | 17 | 32 |
| 315 | 10 | 22 | 739 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(3):656-661 KREMER EJ; YU S; PRITCHARD M; NAGARAJA R; HEITZ D; LYNCH M; BAKER E; HYLAND VJ; LITTLE RD; WADA M; TONIOLO D; VINCENT A; ROUSSEAU F; SCHLESSINGER D; SUTHERLAND GR; RICHARDS RI ISOLATION OF A HUMAN DNA-SEQUENCE WHICH SPANS THE FRAGILE-X | 16 | 32 |
| 316 | 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 |
| 317 | 7 | 9 | 1007 1992 NATURE GENETICS 1(4):237-238 CHAKRAVARTI A FRAGILE-X FOUNDER EFFECT | 15 | 32 |
| 318 | 15 | 29 | 1118 1993 JOURNAL OF MEDICAL GENETICS 30(8):647-650 HIRST MC; KNIGHT SJL; CHRISTODOULOU Z; GREWAL PK; FRYNS JP; DAVIES KE ORIGINS OF THE FRAGILE-X SYNDROME MUTATION | 16 | 32 |
| 319 | 18 | 33 | 1242 1994 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 33(2):247-255 SOBESKY WE; HULL CE; HAGERMAN RJ SYMPTOMS OF SCHIZOTYPAL PERSONALITY-DISORDER IN FRAGILE-X WOMEN | 17 | 32 |
| 320 | 2 | 6 | 61 1982 HUMAN GENETICS 61(2):160-162 STEINBACH P; BARBI G; BOLLER T ON THE FREQUENCY OF TELOMERIC CHROMOSOMAL CHANGES INDUCED BY CULTURE CONDITIONS SUITABLE FOR FRAGILE-X EXPRESSION | 17 | 31 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 321 | 4 | 12 | 145 1983 JOURNAL OF MEDICAL GENETICS 20(4):286-289 VANROY BC; DESMEDT MC; RAES RA; DUMON JE; LEROY JG FRAGILE X TRAIT IN A LARGE KINDRED - TRANSMISSION ALSO THROUGH NORMAL MALES | 20 | 31 |
| 322 | 4 | 19 | 168 1984 AMERICAN JOURNAL OF HUMAN GENETICS 36(3):640-645 KNOLL JH; CHUDLEY AE; GERRARD JW FRAGILE (X) X-LINKED MENTAL-RETARDATION .2. FREQUENCY AND REPLICATION PATTERN OF FRAGILE (X) (Q28) IN HETEROZYGOTES | 20 | 31 |
| 323 | 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 |
| 324 | 2 | 7 | 304 1985 LANCET 1(8433):870-870 TOMMERUP N; SONDERGAARD F; TONNESEN T; KRISTENSEN M; ARVEILER B; SCHINZEL A 1ST TRIMESTER PRENATAL-DIAGNOSIS OF A MALE FETUS WITH FRAGILE-X | 20 | 31 |
| 325 | 9 | 24 | 613 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(5):697-705 REISS AL; FREUND L; VINOGRADOV S; HAGERMAN R; CRONISTER A PARENTAL INHERITANCE AND PSYCHOLOGICAL DISABILITY IN FRAGILE-X FEMALES | 26 | 31 |
| 326 | 8 | 19 | 659 1989 PEDIATRICS 83(4):547-552 SIMKO A; HORNSTEIN L; SOUKUP S; BAGAMERY N FRAGILE X-SYNDROME - RECOGNITION IN YOUNG-CHILDREN | 28 | 31 |
| 327 | 1 | 14 | 914 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):78-86 MAZZOCCO MMM; HAGERMAN RJ; PENNINGTON BF PROBLEM-SOLVING LIMITATIONS AMONG CYTOGENETICALLY EXPRESSING FRAGILE-X WOMEN | 23 | 31 |
| 328 | 9 | 24 | 1169 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):392-399 LOESCH DZ; HAY DA; MULLEY J TRANSMITTING MALES AND CARRIER FEMALES IN FRAGILE-X - REVISITED | 21 | 31 |
| 329 | 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 |
| 330 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 331 | 11 | 34 | 1385 1995 NUCLEIC ACIDS RESEARCH 23(11):1876-1881 MITCHELL JE; NEWBURY SF; MCCLELLAN JA COMPACT STRUCTURES OF D(CNG)(N) OLIGONUCLEOTIDES IN SOLUTION AND THEIR POSSIBLE RELEVANCE TO FRAGILE-X AND RELATED HUMAN GENETIC-DISEASES | 2 | 31 |
| 332 | 13 | 37 | 1419 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):246-251 Godfraind JM; Reyniers E; DeBoulle K; DHooge R; DeDeyn PP; Bakker CE; Oostra BA; Kooy RF; Willems PJ Long-term potentiation in the hippocampus of fragile X knockout mice | 22 | 31 |
| 333 | 15 | 41 | 1436 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):356-361 Fisch GS; Simensen R; Tarleton J; Chalifoux M; Holden JJ; Carpenter N; HowardPeebles PN; Maddalena A Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: A prospective multicenter analysis | 24 | 31 |
| 334 | 18 | 36 | 1667 1998 HUMAN REPRODUCTION 13(5):1184-1187 Conway GS; Payne NN; Webb J; Murray A; Jacobs PA Fragile X premutation screening in women with premature ovarian failure | 8 | 31 |
| 335 | 13 | 40 | 2193 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99(11):7746-7750 Huber KM; Gallagher SM; Warren ST; Bear MF Altered synaptic plasticity in a mouse model of fragile X mental retardation | 16 | 31 |
| 336 | 0 | 0 | 11 1981 BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE 165(9):1197-1206 LEJEUNE J MONOCARBONS METABOLISM AND FRAGILE-X SYNDROME | 22 | 30 |
| 337 | 1 | 12 | 65 1982 HUMAN GENETICS 62(3):282-284 HOWELL RT; MCDERMOTT A REPLICATION STATUS OF THE FRAGILE X-CHROMOSOME, FRA(X) (Q27), IN 3 HETEROZYGOUS FEMALES | 21 | 30 |
| 338 | 20 | 36 | 982 1992 HUMAN GENETICS 90(1-2):55-61 ERSTER SH; BROWN WT; GOONEWARDENA P; DOBKIN CS; JENKINS EC; PERGOLIZZI RG POLYMERASE CHAIN-REACTION ANALYSIS OF FRAGILE X-MUTATIONS | 18 | 30 |
| 339 | 17 | 44 | 1167 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):378-385 SOBESKY WE; PENNINGTON BF; PORTER D; HULL CE; HAGERMAN RJ EMOTIONAL AND NEUROCOGNITIVE DEFICITS IN FRAGILE-X | 25 | 30 |
| 340 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 341 | 13 | 23 | 1637 1998 AMERICAN JOURNAL ON MENTAL RETARDATION 103(1):29-39 Bailey DB; Hatton DD; Skinner M Early developmental trajectories of males with fragile X syndrome | 28 | 30 |
| 342 | 10 | 33 | 1872 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(3):973-980 Sung YJ; Conti J; Currie JR; Brown WT; Denman RB RNAs that interact with the Fragile X syndrome RNA binding protein FMRP | 23 | 30 |
| 343 | 18 | 32 | 1883 2000 EPILEPSIA 41(1):19-23 Musumeci SA; Bosco P; Calabrese G; Bakker C; De Sarro GB; Elia M; Ferri R; Oostra BA Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome | 23 | 30 |
| 344 | 55 | 93 | 2117 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 | 18 | 30 |
| 345 | 4 | 16 | 177 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):241-252 SOUDEK D; PARTINGTON MW; LAWSON JS THE FRAGILE-X SYNDROME .1. FAMILIAL VARIATION IN THE PROPORTION OF LYMPHOCYTES WITH THE FRAGILE SITE IN MALES | 24 | 29 |
| 346 | 2 | 8 | 213 1984 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 5(4):201-203 KERBESHIAN J; BURD L; MARTSOLF JT FRAGILE X-SYNDROME ASSOCIATED WITH TOURETTE SYMPTOMATOLOGY IN A MALE WITH MODERATE MENTAL-RETARDATION AND AUTISM | 4 | 29 |
| 347 | 4 | 14 | 386 1986 HUMAN GENETICS 73(4):309-312 ARINAMI T; KONDO I; NAKAJIMA S FREQUENCY OF THE FRAGILE X-SYNDROME IN JAPANESE MENTALLY-RETARDED MALES | 23 | 29 |
| 348 | 6 | 45 | 397 1986 JOURNAL OF MENTAL DEFICIENCY RESEARCH 30:129-148 MADISON LS; GEORGE C; MOESCHLER JB COGNITIVE-FUNCTIONING IN THE FRAGILE-X SYNDROME - A STUDY OF INTELLECTUAL, MEMORY AND COMMUNICATION-SKILLS | 24 | 29 |
| 349 | 1 | 1 | 783 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):256-259 LAING S; PARTINGTON M; ROBINSON H; TURNER G CLINICAL SCREENING SCORE FOR THE FRAGILE-X (MARTIN-BELL) SYNDROME | 25 | 29 |
| 350 | 3 | 21 | 820 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):493-497 SUDHALTER V; SCARBOROUGH HS; COHEN IL SYNTACTIC DELAY AND PRAGMATIC DEVIANCE IN THE LANGUAGE OF FRAGILE-X MALES | 21 | 29 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 351 | 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 |
| 352 | 11 | 25 | 1172 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):405-411 ZHONG N; YE LL; DOBKIN C; BROWN WT FRAGILE-X FOUNDER CHROMOSOME EFFECTS - LINKAGE DISEQUILIBRIUM OR MICROSATELLITE HETEROGENEITY | 17 | 29 |
| 353 | 20 | 37 | 1259 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1042-1051 QUAN F; ZONANA J; GUNTER K; PETERSON KL; MAGENIS RE; POPOVICH BW AN ATYPICAL CASE OF FRAGILE-X SYNDROME CAUSED BY A DELETION THAT INCLUDES THE FMRI GENE | 16 | 29 |
| 354 | 28 | 92 | 1301 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 60(6):480-493 Schapiro MB; Murphy DGM; Hagerman RJ; Azari NP; Alexander GE; Miezejeski CM; Hinton VJ; Horwitz B; Haxby JV; Kumar A; White B; Grady CL Adult fragile X syndrome: Neuropsychology, brain anatomy, and metabolism | 19 | 29 |
| 355 | 9 | 28 | 1825 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):413-418 Hundscheid RDL; Sistermans EA; Thomas CMG; Braat DDM; Straatman H; Kiemeney LALM; Oostra BA; Smits APT Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations | 14 | 29 |
| 356 | 16 | 41 | 1900 2000 HUMAN REPRODUCTION 15(1):197-202 Marozzi A; Vegetti W; Manfredini E; Tibiletti MG; Testa G; Crosignani PG; Ginelli E; Meneveri R; Dalpra L Association between idiopathic premature ovarian failure and fragile X premutation | 10 | 29 |
| 357 | 6 | 13 | 182 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):289-297 BROWN WT; JENKINS EC; FRIEDMAN E; BROOKS J; COHEN IL; DUNCAN C; HILL AL; MALIK MN; MORRIS V; WOLF E; WISNIEWSKI K; FRENCH JH FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 20 | 28 |
| 358 | 7 | 26 | 256 1985 ARCHIVES OF DISEASE IN CHILDHOOD 60(11):1001-1007 THAKE A; TODD J; BUNDEY S; WEBB T IS IT POSSIBLE TO MAKE A CLINICAL-DIAGNOSIS OF THE FRAGILE X-SYNDROME IN A BOY | 22 | 28 |
| 359 | 6 | 25 | 300 1985 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 48(2):150-153 FINELLI PF; PUESCHEL SM; PADREMENDOZA T; OBRIEN MM NEUROLOGICAL FINDINGS IN PATIENTS WITH THE FRAGILE-X SYNDROME | 19 | 28 |
| 360 | 3 | 18 | 322 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):189-194 LOEHR JP; SYNHORST DP; WOLFE RR; HAGERMAN RJ AORTIC ROOT DILATATION AND MITRAL-VALVE PROLAPSE IN THE FRAGILE-X SYNDROME | 19 | 28 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 361 | 8 | 25 | 333 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):353-358 MCGILLIVRAY BC; HERBST DS; DILL FJ; SANDERCOCK HJ; TISCHLER B INFANTILE-AUTISM - AN OCCASIONAL MANIFESTATION OF FRAGILE-(X) MENTAL-RETARDATION | 19 | 28 |
| 362 | 12 | 24 | 357 1986 AMERICAN JOURNAL OF PSYCHIATRY 143(1):71-73 FISCH GS; COHEN IL; WOLF EG; BROWN WT; JENKINS EC; GROSS A AUTISM AND THE FRAGILE X-SYNDROME | 19 | 28 |
| 363 | 7 | 30 | 678 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 35(1):28-35 GRIGSBY JP; KEMPER MB; HAGERMAN RJ; MYERS CS NEUROPSYCHOLOGICAL DYSFUNCTION AMONG AFFECTED HETEROZYGOUS FRAGILE-X FEMALES | 22 | 28 |
| 364 | 28 | 73 | 690 1990 BIOLOGICAL PSYCHIATRY 27(2):223-240 REISS AL; FREUND L FRAGILE X-SYNDROME | 22 | 28 |
| 365 | 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 |
| 366 | 22 | 51 | 1121 1993 JOURNAL OF PEDIATRICS 122(2):169-185 TARLETON JC; SAUL RA MOLECULAR GENETIC ADVANCES IN FRAGILE X-SYNDROME | 14 | 28 |
| 367 | 12 | 21 | 1192 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):527-534 LEVINSON G; MADDALENA A; PALMER FT; HARTON GL; BICK DP; HOWARDPEEBLES PN; BLACK SH; SCHULMAN JD IMPROVED SIZING OF FRAGILE-X CCG REPEATS BY NESTED POLYMERASE CHAIN-REACTION | 15 | 28 |
| 368 | 19 | 41 | 1200 1994 AMERICAN JOURNAL ON MENTAL RETARDATION 98(5):567-579 LACHIEWICZ AM; SPIRIDIGLIOZZI GA; GULLION CM; RANSFORD SN; RAO K ABERRANT BEHAVIORS OF YOUNG BOYS WITH FRAGILE X-SYNDROME | 26 | 28 |
| 369 | 12 | 18 | 1433 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):334-339 Franke P; Maier W; Hautzinger M; Weiffenbach O; Gansicke M; Iwers B; Poustka F; Schwab SG; Froster U Fragile-X carrier females: Evidence for a distinct psychopathological phenotype? | 19 | 28 |
| 370 | 27 | 51 | 1685 1998 JOURNAL OF MEDICAL GENETICS 35(2):103-111 Wohrle D; Salat U; Glaser D; Mucke J; Meisel-Stosiek M; Schindler D; Vogel W; Steinbach P Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats | 15 | 28 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 371 | 0 | 9 | 201 1984 HUMAN GENETICS 65(4):400-401 FRYNS JP; KLECZKOWSKA A; KUBIEN E; PETIT P; VANDENBERGHE H INACTIVATION PATTERN OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 18 | 27 |
| 372 | 2 | 10 | 305 1985 LANCET 1(8433):871-871 OBERLE I; MANDEL JL; BOUE J; MATTEI MG; MATTEI JF POLYMORPHIC DNA MARKERS IN PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 14 | 27 |
| 373 | 17 | 42 | 330 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):297-311 JENKINS EC; BROWN WT; WILSON MG; LIN MS; ALFI OS; WASSMAN ER; BROOKS J; DUNCAN CJ; MASIA A; KRAWCZUN MS THE PRENATAL DETECTION OF THE FRAGILE-X CHROMOSOME - REVIEW OF RECENT EXPERIENCE | 17 | 27 |
| 374 | 3 | 36 | 484 1987 NEUROPSYCHOLOGIA 25(6):881-891 GRIGSBY JP; KEMPER MB; HAGERMAN RJ DEVELOPMENTAL GERSTMANN SYNDROME WITHOUT APHASIA IN FRAGILE-X SYNDROME | 16 | 27 |
| 375 | 9 | 27 | 651 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):427-430 DYKENS EM; HODAPP RM; LECKMAN JF ADAPTIVE AND MALADAPTIVE FUNCTIONING OF INSTITUTIONALIZED AND NONINSTITUTIONALIZED FRAGILE-X MALES | 16 | 27 |
| 376 | 6 | 44 | 702 1990 HUMAN GENETICS 84(4):347-352 SCHMIDT M; CERTOMA A; DUSART D; KALITSIS P; LEVERSHA M; FOWLER K; SHEFFIELD L; JACK I; DANKS DM UNUSUAL X-CHROMOSOME INACTIVATION IN A MENTALLY-RETARDED GIRL WITH AN INTERSTITIAL DELETION XQ27 - IMPLICATIONS FOR THE FRAGILE X-SYNDROME | 7 | 27 |
| 377 | 11 | 18 | 913 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):72-77 LACHIEWICZ AM ABNORMAL BEHAVIORS OF YOUNG GIRLS WITH FRAGILE-X SYNDROME | 20 | 27 |
| 378 | 12 | 16 | 1178 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):454-457 TROTTIER Y; IMBERT G; POUSTKA A; FRYNS JP; MANDEL JL MALE WITH TYPICAL FRAGILE-X PHENOTYPE IS DELETED FOR PART OF THE FMR1 GENE AND FOR ABOUT 100 KB OF UPSTREAM REGION | 15 | 27 |
| 379 | 1 | 2 | 1195 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):380-381 PARK V; HOWARDPEEBLES P; SHERMAN S; TAYLOR A; WULFSBERG E POLICY STATEMENT - AMERICAN-COLLEGE-OF-MEDICAL-GENETICS - FRAGILE-X-SYNDROME - DIAGNOSTIC AND CARRIER TESTING | 16 | 27 |
| 380 | 10 | 20 | 1371 1995 JOURNAL OF MEDICAL GENETICS 32(3):170-173 WANG Q; GREEN E; BOBROW M; MATHEW CG A RAPID, NONRADIOACTIVE SCREENING-TEST FOR FRAGILE-X MUTATIONS AT THE FRAXA AND FRAXE LOCI | 15 | 27 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 381 | 13 | 29 | 1664 1998 HUMAN MOLECULAR GENETICS 7(13):2121-2128 Khandjian EW; Bardoni B; Corbin F; Sittler A; Giroux S; Heitz D; Tremblay S; Pinset C; Montarras D; Rousseau F; Mandel JL Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis | 17 | 27 |
| 382 | 8 | 17 | 149 1983 JOURNAL OF MENTAL DEFICIENCY RESEARCH 27(SEP):211-226 NIELSEN KB DIAGNOSIS OF THE FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL FINDINGS IN 27 MALES WITH THE FRAGILE SITE AT XQ28 | 18 | 26 |
| 383 | 11 | 38 | 326 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):241-262 HAGERMAN RJ; JACKSON AW; LEVITAS A; BRADEN M; MCBOGG P; KEMPER M; MCGAVRAN L; BERRY R; MATUS I; HAGERMAN PJ ORAL FOLIC-ACID VERSUS PLACEBO IN THE TREATMENT OF MALES WITH THE FRAGILE-X SYNDROME | 18 | 26 |
| 384 | 11 | 41 | 467 1987 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 17(4):457-468 PAUL R; DYKENS E; LECKMAN JF; WATSON M; BREG WR; COHEN DJ A COMPARISON OF LANGUAGE CHARACTERISTICS OF MENTALLY-RETARDED ADULTS WITH FRAGILE-X SYNDROME AND THOSE WITH NONSPECIFIC MENTAL-RETARDATION AND AUTISM | 19 | 26 |
| 385 | 24 | 53 | 876 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):825-830 PIVEN J; GAYLE J; LANDA R; WZOREK M; FOLSTEIN S THE PREVALENCE OF FRAGILE-X IN A SAMPLE OF AUTISTIC INDIVIDUALS DIAGNOSED USING A STANDARDIZED INTERVIEW | 7 | 26 |
| 386 | 33 | 48 | 967 1992 CHROMOSOMA 101(7):381-387 OOSTRA BA; VERKERK AJMH THE FRAGILE X-SYNDROME - ISOLATION OF THE FMR-1 GENE AND CHARACTERIZATION OF THE FRAGILE-X MUTATION | 11 | 26 |
| 387 | 13 | 28 | 1198 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 54(4):378-383 THOMPSON NM; GULLEY ML; ROGENESS GA; CLAYTON RJ; JOHNSON C; HAZELTON B; CHO CG; ZELLMER VT NEUROBEHAVIORAL CHARACTERISTICS OF CGG AMPLIFICATION STATUS IN FRAGILE-X FEMALES | 17 | 26 |
| 388 | 19 | 28 | 1421 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):261-265 Zhong N; Ju WN; Pietrofesa J; Wang DW; Dobkin C; Brown WT Fragile X ''gray zone'' alleles: AGG patterns, expansion risks, and associated haplotypes | 15 | 26 |
| 389 | 5 | 55 | 1483 1996 HUMAN GENETICS 98(2):151-157 Kramer PR; Pearson CE; Sinden RR Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines | 2 | 26 |
| 390 | 24 | 41 | 1526 1997 AMERICAN JOURNAL OF HUMAN GENETICS 60(1):103-112 FalikZaccai TC; Shachak E; Yalon M; Lis Z; Borochowitz Z; Macpherson JN; Nelson DL; Eichler EE Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype | 15 | 26 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 391 | 88 | 136 | 1765 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 88(1):11-24 Kaufmann WE; Reiss AL Molecular and cellular genetics of fragile X syndrome | 15 | 26 |
| 392 | 12 | 23 | 1821 1999 PRENATAL DIAGNOSIS 19(13):1223-1230 Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; Vandervorst M; Van Steirteghem A; Liebaers I Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG | 2 | 26 |
| 393 | 15 | 43 | 2050 2001 NEUROSCIENCE 103(4):1043-1050 Chen L; Toth M Fragile X mice develop sensory hyperreactivity to auditory stimuli | 16 | 26 |
| 394 | 5 | 17 | 292 1985 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 15(3):335-338 PUESCHEL SM; HERMAN R; GRODEN G SCREENING-CHILDREN WITH AUTISM FOR FRAGILE-X SYNDROME AND PHENYLKETONURIA | 15 | 25 |
| 395 | 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 |
| 396 | 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 |
| 397 | 16 | 24 | 1411 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):191-195 Brown WT; Nolin S; Houck G; Ding XH; Glicksman A; Li SY; StarkHouck S; Brophy P; Duncan C; Dobkin C; Jenkins E Prenatal diagnosis and carrier screening for fragile X by PCR | 16 | 25 |
| 398 | 15 | 25 | 1446 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):428-433 Meadows KL; Pettay D; Newman J; Hersey J; Ashley AE; Sherman SL Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population | 9 | 25 |
| 399 | 4 | 13 | 1952 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 73(1):87-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation | 20 | 25 |
| 400 | 13 | 54 | 2148 2002 JOURNAL OF BIOLOGICAL CHEMISTRY 277(40):37804-37810 Ohashi S; Koike K; Omori A; Ichinose S; Ohara S; Kobayashi S; Sato TA; Anzai K Identification of mRNA/protein (mRNP) complexes containing Pur alpha, mStaufen, Fragile X Protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor | 8 | 25 |
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