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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
Page 3: 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 |
|---|---|---|---|---|---|
| 201 | 13 | 28 | 1663 1998 HUMAN MOLECULAR GENETICS 7(1):109-113 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the FMR1 gene involved in fragile X syndrome | 21 | 47 |
| 202 | 15 | 32 | 335 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):375-380 HAGERMAN RJ; CHUDLEY AE; KNOLL JH; JACKSON AW; KEMPER M; AHMAD R AUTISM IN FRAGILE-X FEMALES | 32 | 46 |
| 203 | 11 | 30 | 618 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(4):513-518 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; HABICHT K LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 34 | 46 |
| 204 | 16 | 19 | 932 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):197-207 ROUSSEAU F; HEITZ D; BIANCALANA V; OBERLE I; MANDEL JL ON SOME TECHNICAL ASPECTS OF DIRECT DNA DIAGNOSIS OF THE FRAGILE-X SYNDROME | 27 | 46 |
| 205 | 25 | 49 | 1357 1995 HUMAN MOLECULAR GENETICS 4(1):45-49 DEGRAAFF E; ROUILLARD P; WILLEMS PJ; SMITS APT; ROUSSEAU F; OOSTRA BA HOTSPOT FOR DELETIONS IN THE CGG REPEAT REGION OF FMR1 IN FRAGILE-X PATIENTS | 27 | 46 |
| 206 | 29 | 49 | 1484 1996 HUMAN MOLECULAR GENETICS 5(3):319-330 Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; Nelson DL Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome | 22 | 46 |
| 207 | 90 | 179 | 2106 2002 ANNUAL REVIEW OF NEUROSCIENCE 25:315-338 O'Donnell WT; Warren ST A decade of molecular studies of fragile X syndrome | 0 | 46 |
| 208 | 4 | 27 | 323 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):195-206 HANSON DM; JACKSON AW; HAGERMAN RJ SPEECH DISTURBANCES (CLUTTERING) IN MILDLY IMPAIRED MALES WITH THE MARTIN-BELL FRAGILE-X SYNDROME | 39 | 45 |
| 209 | 7 | 20 | 458 1987 HUMAN GENETICS 77(1):85-87 KAHKONEN M; ALITALO T; AIRAKSINEN E; MATILAINEN R; LAUNIALA K; AUTIO S; LEISTI J PREVALENCE OF THE FRAGILE-X SYNDROME IN 4 BIRTH COHORTS OF CHILDREN OF SCHOOL AGE | 31 | 45 |
| 210 | 10 | 25 | 888 1991 NUCLEIC ACIDS RESEARCH 19(10):2567-2572 DIETRICH A; KIOSCHIS P; MONACO AP; GROSS B; KORN B; WILLIAMS SV; SHEER D; HEITZ D; OBERLE I; TONIOLO D; WARREN ST; LEHRACH H; POUSTKA A MOLECULAR-CLONING AND ANALYSIS OF THE FRAGILE X-REGION IN MAN | 23 | 45 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 211 | 83 | 119 | 965 1992 BRITISH JOURNAL OF PSYCHIATRY 160:24-35 TURK J THE FRAGILE-X SYNDROME - ON THE WAY TO A BEHAVIORAL-PHENOTYPE | 24 | 45 |
| 212 | 17 | 29 | 1607 1997 JOURNAL OF MEDICAL GENETICS 34(1):1-5 Morton JE; Bundey S; Webb TP; MacDonald F; Rindl PM; Bullock S Fragile X syndrome is less common than previously estimated | 25 | 45 |
| 213 | 22 | 79 | 1877 2000 CEREBRAL CORTEX 10(10):1038-1044 Irwin SA; Galvez R; Greenough WT Dendritic spine structural anomalies in fragile-X mental retardation syndrome | 27 | 45 |
| 214 | 3 | 10 | 2047 2001 NEUROLOGY 57(1):127-130 Hagerman RJ; Leehey M; Heinrichs W; Tassone F; Wilson R; Hills J; Grigsby J; Gage B; Hagerman PJ Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 29 | 45 |
| 215 | 10 | 43 | 176 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):215-239 JENKINS EC; BROWN WT; BROOKS J; DUNCAN CJ; RUDELLI RD; WISNIEWSKI HM EXPERIENCE WITH PRENATAL FRAGILE-X DETECTION | 35 | 44 |
| 216 | 1 | 2 | 224 1984 LANCET 2(8398):349-349 CHOO KH; GEORGE D; FILBY G; HALLIDAY JL; LEVERSHA M; WEBB G; DANKS DM LINKAGE ANALYSIS OF X-LINKED MENTAL-RETARDATION WITH AND WITHOUT FRAGILE-X USING FACTOR-IX GENE PROBE | 22 | 44 |
| 217 | 4 | 12 | 336 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):393-401 REISS AL; FEINSTEIN C; TOOMEY KE; GOLDSMITH B; ROSENBAUM K; CARUSO MA PSYCHIATRIC DISABILITY ASSOCIATED WITH THE FRAGILE-X CHROMOSOME | 29 | 44 |
| 218 | 6 | 18 | 337 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):403-408 WAHLSTROM J; GILLBERG C; GUSTAVSON KH; HOLMGREN G INFANTILE-AUTISM AND THE FRAGILE-X - A SWEDISH MULTICENTER STUDY | 23 | 44 |
| 219 | 4 | 17 | 421 1987 AMERICAN JOURNAL OF MENTAL DEFICIENCY 92(2):234-236 DYKENS EM; HODAPP RM; LECKMAN JF STRENGTHS AND WEAKNESSES IN THE INTELLECTUAL-FUNCTIONING OF MALES WITH FRAGILE-X SYNDROME | 24 | 44 |
| 220 | 6 | 24 | 715 1990 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 29(2):214-219 HODAPP RM; DYKENS EM; HAGERMAN RJ; SCHREINER R; LACHIEWICZ AM; LECKMAN JF DEVELOPMENTAL IMPLICATIONS OF CHANGING TRAJECTORIES OF IQ IN MALES WITH FRAGILE-X SYNDROME | 31 | 44 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 221 | 4 | 23 | 806 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):400-403 JACKY PB; AHUJA YR; ANYANEYEBOA K; BREG WR; CARPENTER NJ; FROSTERISKENIUS UG; FRYNS JP; GLOVER TW; GUSTAVSON KH; HOEGERMAN SF; HOLMGREN G; HOWARDPEEBLES PN; JENKINS EC; KRAWCZUN MS; NERI G; PETTIGREW A; SCHAAP T; SCHONBERG SA; SHAPIRO LR; SPINNER N; STEINBACH P; VIANNAMORGANTE AM; WATSON MS; WILMOT PL GUIDELINES FOR THE PREPARATION AND ANALYSIS OF THE FRAGILE-X CHROMOSOME IN LYMPHOCYTES | 31 | 44 |
| 222 | 15 | 30 | 964 1992 ARCHIVES OF GENERAL PSYCHIATRY 49(1):54-60 FREUND LS; REISS AL; HAGERMAN R; VINOGRADOV S CHROMOSOME FRAGILITY AND PSYCHOPATHOLOGY IN OBLIGATE FEMALE CARRIERS OF THE FRAGILE X-CHROMOSOME | 25 | 44 |
| 223 | 18 | 63 | 1693 1998 NEUROLOGY 50(1):121-130 Mostofsky SH; Mazzocco MMM; Aakalu G; Warsofsky IS; Denckla MB; Reiss AL Decreased cerebellar posterior vermis size in fragile X syndrome - Correlation with neurocognitive performance | 18 | 44 |
| 224 | 17 | 39 | 1791 1999 HUMAN MOLECULAR GENETICS 8(13):2557-2566 Bardoni B; Schenck A; Mandel JL A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein | 26 | 44 |
| 225 | 2 | 28 | 108 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(1):113-119 FILIPPI G; RINALDI A; ARCHIDIACONO N; ROCCHI M; BALAZS I; SINISCALCO M LINKAGE BETWEEN G6PD AND FRAGILE-X SYNDROME | 19 | 43 |
| 226 | 2 | 16 | 172 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):159-174 MERYASH DL; CRONK CE; SACHS B; GERALD PS AN ANTHROPOMETRIC STUDY OF MALES WITH THE FRAGILE-X SYNDROME | 26 | 43 |
| 227 | 9 | 47 | 255 1985 ANNALS OF NEUROLOGY 18(6):665-669 WISNIEWSKI KE; FRENCH JH; FERNANDO S; BROWN WT; JENKINS EC; FRIEDMAN E; HILL AL; MIEZEJESKI CM FRAGILE X-SYNDROME - ASSOCIATED NEUROLOGICAL ABNORMALITIES AND DEVELOPMENTAL-DISABILITIES | 27 | 43 |
| 228 | 5 | 17 | 311 1985 TRENDS IN GENETICS 1(4):108-112 SUTHERLAND GR THE ENIGMA OF THE FRAGILE-X CHROMOSOME | 26 | 43 |
| 229 | 7 | 20 | 417 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(2):435-448 MULLEY JC; GEDEON AK; THORN KA; BATES LJ; SUTHERLAND GR LINKAGE AND GENETIC-COUNSELING FOR THE FRAGILE-X USING DNA PROBE-52A, PROBE-F9, PROBE-DX13, AND PROBE-ST14 | 17 | 43 |
| 230 | 5 | 17 | 605 1988 JOURNAL OF MEDICAL GENETICS 25(6):407-414 LOESCH DZ; HAY DA CLINICAL-FEATURES AND REPRODUCTIVE PATTERNS IN FRAGILE-X FEMALE HETEROZYGOTES | 33 | 43 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 231 | 0 | 0 | 639 1989 GENOMICS 4(4):570-578 PATTERSON MN; BELL MV; BLOOMFIELD J; FLINT T; DORKINS H; THIBODEAU SN; SCHAID D; BREN G; SCHWARTZ CE; WIERINGA B; ROPERS HH; CALLEN DF; SUTHERLAND G; FROSTERISKENIUS U; VISSING H; DAVIES KE GENETIC AND PHYSICAL MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 17 | 43 |
| 232 | 5 | 23 | 695 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 | 29 | 43 |
| 233 | 13 | 18 | 981 1992 HUMAN GENETICS 89(1):114-116 WOHRLE D; HIRST MC; KENNERKNECHT I; DAVIES KE; STEINBACH P GENOTYPE MOSAICISM IN FRAGILE-X FETAL TISSUES | 32 | 43 |
| 234 | 0 | 19 | 13 1981 CLINICAL GENETICS 19(2):101-110 GUSTAVSON KH; HOLMGREN G; BLOMQUIST HK; MIKKELSEN M; NORDENSON I; POULSEN H; TOMMERUP N FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 2 SWEDISH FAMILIES | 28 | 42 |
| 235 | 9 | 25 | 889 1991 NUCLEIC ACIDS RESEARCH 19(12):3283-3288 HIRST MC; RACK K; NAKAHORI Y; ROCHE A; BELL MV; FLYNN G; CHRISTADOULOU Z; MACKINNON RN; FRANCIS M; LITTLER AJ; ANAND R; POUSTKA AM; LEHRACH H; SCHLESSINGER D; DURSO M; BUCKLE VJ; DAVIES KE A YAC CONTIG ACROSS THE FRAGILE X SITE DEFINES THE REGION OF FRAGILITY | 16 | 42 |
| 236 | 3 | 7 | 1439 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):370-372 Partington MW; Moore DY; Turner GM Confirmation of early menopause in fragile X carriers | 23 | 42 |
| 237 | 53 | 104 | 1672 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(5):393-405 Feinstein C; Reiss AL Autism: The point of view from fragile X studies | 15 | 42 |
| 238 | 6 | 35 | 1724 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):248-252 Weiler IJ; Greenough WT Synaptic synthesis of the Fragile X protein: Possible involvement in synapse maturation and elimination | 27 | 42 |
| 239 | 30 | 74 | 1946 2000 MOLECULAR AND CELLULAR BIOLOGY 20(22):8536-8547 Wan LL; Dockendorff TC; Jongens TA; Dreyfuss G Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein | 33 | 42 |
| 240 | 18 | 37 | 672 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):175-180 BROWN WT INVITED EDITORIAL - THE FRAGILE-X - PROGRESS TOWARD SOLVING THE PUZZLE | 28 | 41 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 241 | 6 | 20 | 1096 1993 HUMAN GENETICS 92(5):431-436 ARINAMI T; ASANO M; KOBAYASHI K; YANAGI H; HAMAGUCHI H DATA ON THE CGG REPEAT AT THE FRAGILE X-SITE IN THE NONRETARDED JAPANESE POPULATION AND FAMILY SUGGEST THE PRESENCE OF A SUBGROUP OF NORMAL ALLELES PREDISPOSING TO MUTATE | 21 | 41 |
| 242 | 4 | 11 | 1191 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):522-526 CHONG SS; EICHLER EE; NELSON DL; HUGHES MR ROBUST AMPLIFICATION AND ETHIDIUM-VISIBLE DETECTION OF THE FRAGILE-X-SYNDROME CGG REPEAT USING PFU POLYMERASE | 19 | 41 |
| 243 | 2 | 5 | 1378 1995 LANCET 346(8970):309-310 CONWAY GS; HETTIARACHCHI S; MURRAY A; JACOBS PA FRAGILE-X PREMUTATIONS IN FAMILIAL PREMATURE OVARIAN FAILURE | 19 | 41 |
| 244 | 4 | 21 | 1396 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(5):906-913 Knight SJL; Ritchie RJ; Chakrabarti L; Cross G; Taylor GR; Mueller RF; Hurst J; Paterson J; Yates JRW; Dow DJ; Davies KE A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom | 11 | 41 |
| 245 | 10 | 20 | 1418 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):241-245 Kooy RF; DHooge R; Reyniers E; Bakker CE; Nagels G; DeBoulle K; Storm K; Clincke G; DeDeyn PP; Oostra BA; Willems PJ Transgenic mouse model for the fragile X syndrome | 22 | 41 |
| 246 | 11 | 15 | 1589 1997 HUMAN GENETICS 99(3):308-311 Willemsen R; Smits A; Mohkamsing S; vanBeerendonk H; deHaan A; deVries B; vandenOuweland A; Sistermans E; Galjaard H; Oostra BA Rapid antibody test for diagnosing fragile X syndrome: A validation of the technique | 34 | 41 |
| 247 | 21 | 69 | 1624 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(9):4587-4592 Hansen RS; Canfield TK; Fjeld AD; Mumm S; Laird CD; Gartler SM A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication | 8 | 41 |
| 248 | 56 | 112 | 479 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):463-471 BREGMAN JD; DYKENS E; WATSON M; ORT SI; LECKMAN JF FRAGILE-X SYNDROME - VARIABILITY OF PHENOTYPIC-EXPRESSION | 23 | 40 |
| 249 | 14 | 29 | 612 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(2):304-309 DAHL N; GOONEWARDENA P; MALMGREN H; GUSTAVSON KH; HOLMGREN G; SEEMANOVA E; ANNEREN G; FLOOD A; PETTERSSON U LINKAGE ANALYSIS OF FAMILIES WITH FRAGILE-X MENTAL-RETARDATION, USING A NOVEL RFLP MARKER (DXS 304) | 19 | 40 |
| 250 | 30 | 58 | 621 1989 AMERICAN JOURNAL OF ORTHOPSYCHIATRY 59(1):142-152 HAGERMAN RJ; SOBESKY WE PSYCHOPATHOLOGY IN FRAGILE-X-SYNDROME | 28 | 40 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 251 | 6 | 17 | 737 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(6):1051-1057 RICHARDS RI; SHEN Y; HOLMAN K; KOZMAN H; HYLAND VJ; MULLEY JC; SUTHERLAND GR FRAGILE-X SYNDROME - DIAGNOSIS USING HIGHLY POLYMORPHIC MICROSATELLITE MARKERS | 14 | 40 |
| 252 | 16 | 17 | 1189 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):509-512 NOLIN SL; GLICKSMAN A; HOUCK GE; BROWN WT; DOBKIN CS MOSAICISM IN FRAGILE-X AFFECTED MALES | 36 | 40 |
| 253 | 7 | 34 | 1620 1997 NATURE STRUCTURAL BIOLOGY 4(9):712-716 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; Nilges M; Pastore A The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome | 5 | 40 |
| 254 | 5 | 21 | 470 1987 JOURNAL OF MEDICAL GENETICS 24(1):32-38 VEENEMA H; VEENEMA T; GERAEDTS JPM THE FRAGILE X-SYNDROME IN A LARGE FAMILY .2. PSYCHOLOGICAL INVESTIGATIONS | 28 | 39 |
| 255 | 26 | 44 | 1017 1992 TRENDS IN GENETICS 8(7):249-255 RICHARDS RI; SUTHERLAND GR FRAGILE X-SYNDROME - THE MOLECULAR PICTURE COMES INTO FOCUS | 13 | 39 |
| 256 | 19 | 74 | 1815 1999 MOLECULAR AND CELLULAR BIOLOGY 19(8):5675-5684 White PJ; Borts RH; Hirst MC Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism | 9 | 39 |
| 257 | 0 | 3 | 19 1981 HUMAN GENETICS 59(2):186-186 FONATSCH C A SIMPLE METHOD TO DEMONSTRATE THE FRAGILE X-CHROMOSOME IN FIBROBLASTS | 21 | 38 |
| 258 | 2 | 11 | 116 1983 BRITISH JOURNAL OF PSYCHIATRY 143(SEP):256-260 GILLBERG C IDENTICAL TRIPLETS WITH INFANTILE-AUTISM AND THE FRAGILE-X SYNDROME | 20 | 38 |
| 259 | 13 | 33 | 472 1987 JOURNAL OF MEDICAL GENETICS 24(7):413-421 VEENEMA H; CARPENTER NJ; BAKKER E; HOFKER MH; WARD AM; PEARSON PL THE FRAGILE-X SYNDROME IN A LARGE FAMILY .3. INVESTIGATIONS ON LINKAGE OF FLANKING DNA MARKERS WITH THE FRAGILE SITE-XQ27 | 17 | 38 |
| 260 | 2 | 17 | 552 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(2):407-414 REISS AL; PATEL S; KUMAR AJ; FREUND L PRELIMINARY COMMUNICATION - NEUROANATOMICAL VARIATIONS OF THE POSTERIOR-FOSSA IN MEN WITH THE FRAGILE-X (MARTIN-BELL) SYNDROME | 16 | 38 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 261 | 9 | 28 | 580 1988 EPILEPSIA 29(1):41-47 MUSUMECI SA; COLOGNOLA RM; FERRI R; GIGLI GL; PETRELLA MA; SANFILIPPO S; BERGONZI P; TASSINARI CA FRAGILE-X SYNDROME - A PARTICULAR EPILEPTOGENIC EEG PATTERN | 17 | 38 |
| 262 | 6 | 30 | 594 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(1):41-52 DYKENS E; LECKMAN J; PAUL R; WATSON M COGNITIVE, BEHAVIORAL, AND ADAPTIVE FUNCTIONING IN FRAGILE-X AND NON-FRAGILE-X RETARDED MEN | 32 | 38 |
| 263 | 11 | 24 | 623 1989 AMERICAN JOURNAL ON MENTAL RETARDATION 93(4):406-411 WOLFF PH; GARDNER J; PACCIA J; LAPPEN J THE GREETING BEHAVIOR OF FRAGILE X-MALES | 25 | 38 |
| 264 | 14 | 20 | 991 1992 JOURNAL OF MEDICAL GENETICS 29(6):368-374 MULLEY JC; YU S; GEDEON AK; DONNELLY A; TURNER G; LOESCH D; CHAPMAN CJ; GARDNER RJM; RICHARDS RI; SUTHERLAND GR EXPERIENCE WITH DIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X | 26 | 38 |
| 265 | 6 | 22 | 999 1992 LANCET 339(8803):1210-1213 TURNER G; ROBINSON H; LAING S; VANDENBERK M; COLLEY A; GODDARD A; SHERMAN S; PARTINGTON M POPULATION SCREENING FOR FRAGILE-X | 20 | 38 |
| 266 | 29 | 36 | 1024 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1236-1241 HULL C; HAGERMAN RJ A STUDY OF THE PHYSICAL, BEHAVIORAL, AND MEDICAL PHENOTYPE, INCLUDING ANTHROPOMETRIC MEASURES, OF FEMALES WITH FRAGILE-X SYNDROME | 27 | 38 |
| 267 | 11 | 50 | 1489 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(40):24325-24328 Godde JS; Kass SU; Hirst MC; Wolffe AP Nucleosome assembly on methylated CGG triplet repeats in the Fragile X Mental Retardation gene 1 promoter | 2 | 38 |
| 268 | 13 | 20 | 1493 1996 JOURNAL OF MEDICAL GENETICS 33(12):1007-1010 deVries BBA; Jansen CCAM; Duits AA; Verheij C; Willemsen R; vanHemel JO; vandenOuweland AMW; Niermeijer MF; Oostra BA; Halley DJJ Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family | 31 | 38 |
| 269 | 18 | 36 | 2056 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98(15):8844-8849 Schenck A; Bardoni B; Moro A; Bagni C; Mandel JL A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P | 20 | 38 |
| 270 | 34 | 62 | 2253 2003 CELL 112(3):317-327 Zalfa F; Giorgi M; Primerano B; Moro A; Di Penta A; Reis S; Oostra B; Bagni C The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at Synapses | 16 | 38 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 271 | 9 | 34 | 279 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 |
| 272 | 1 | 15 | 281 1985 HUMAN GENETICS 69(1):44-46 WARREN ST; GLOVER TW; DAVIDSON RL; JAGADEESWARAN P LINKAGE AND RECOMBINATION BETWEEN FRAGILE X-LINKED MENTAL-RETARDATION AND THE FACTOR-IX GENE | 20 | 37 |
| 273 | 10 | 16 | 649 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):417-421 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ THE FRAGILE-X MARKER AND AUTISM IN PERSPECTIVE | 19 | 37 |
| 274 | 6 | 24 | 673 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):181-187 MACKINNON RN; HIRST MC; BELL MV; WATSON JEV; CLAUSSEN U; LUDECKE HJ; SENGER G; HORSTHEMKE B; DAVIES KE MICRODISSECTION OF THE FRAGILE-X REGION | 9 | 37 |
| 275 | 1 | 22 | 958 1992 AMERICAN JOURNAL ON MENTAL RETARDATION 97(1):39-46 HODAPP RM; LECKMAN JF; DYKENS EM; SPARROW SS; ZELINSKY DG; ORT SI K-ABC PROFILES IN CHILDREN WITH FRAGILE-X SYNDROME, DOWN-SYNDROME, AND NONSPECIFIC MENTAL-RETARDATION | 15 | 37 |
| 276 | 7 | 26 | 1106 1993 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 23(1):135-145 DYKENS EM; HODAPP RM; ORT SI; LECKMAN JF TRAJECTORY OF ADAPTIVE-BEHAVIOR IN MALES WITH FRAGILE X-SYNDROME | 27 | 37 |
| 277 | 17 | 53 | 1820 1999 NEUROSCIENCE 94(1):185-192 Paradee W; Melikian HE; Rasmussen DL; Kenneson A; Conn PJ; Warren ST Fragile X mouse: Strain effects of knockout phenotype and evidence suggesting deficient amygdala function | 19 | 37 |
| 278 | 0 | 15 | 70 1982 JOURNAL OF MEDICAL GENETICS 19(1):44-48 WEBB GC; HALLIDAY JL; PITT DB; JUDGE CG; LEVERSHA M FRAGILE (X)(Q27) SITES IN A PEDIGREE WITH FEMALE CARRIERS SHOWING MILD TO SEVERE MENTAL-RETARDATION | 19 | 36 |
| 279 | 3 | 15 | 296 1985 JOURNAL OF MEDICAL GENETICS 22(2):85-91 TUCKERMAN E; WEBB T; BUNDEY SE FREQUENCY AND REPLICATION STATUS OF THE FRAGILE-X, FRA(X)(Q27-28), IN A PAIR OF MONOZYGOTIC TWINS OF MARKEDLY DIFFERING INTELLIGENCE | 21 | 36 |
| 280 | 9 | 45 | 381 1986 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 51:195-203 MANDEL JL; ARVEILER B; CAMERINO G; HANAUER A; HEILIG R; KOENIG M; OBERLE I 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 281 | 16 | 49 | 515 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):123-142 PROUTY LA; ROGERS RC; STEVENSON RE; DEAN JH; PALMER KK; SIMENSEN RJ; COSTON GN; SCHWARTZ CE FRAGILE-X SYNDROME - GROWTH, DEVELOPMENT, AND INTELLECTUAL FUNCTION | 28 | 36 |
| 282 | 3 | 31 | 609 1988 SCHIZOPHRENIA RESEARCH 1(4):277-281 DELISI LE; REISS AL; WHITE BJ; GERSHON ES CYTOGENETIC STUDIES OF MALES WITH SCHIZOPHRENIA - SCREENING FOR THE FRAGILE X-CHROMOSOME AND OTHER CHROMOSOMAL-ABNORMALITIES | 1 | 36 |
| 283 | 3 | 10 | 825 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):511-513 MUSUMECI SA; FERRI R; ELIA M; COLOGNOLA RM; BERGONZI P; TASSINARI CA EPILEPSY AND FRAGILE-X SYNDROME - A FOLLOW-UP-STUDY | 21 | 36 |
| 284 | 11 | 17 | 872 1991 JOURNAL OF MEDICAL GENETICS 28(12):824-829 HIRST MC; NAKAHORI Y; KNIGHT SJL; SCHWARTZ C; THIBODEAU SN; ROCHE A; FLINT TJ; CONNOR JM; FRYNS JP; DAVIES KE GENOTYPE PREDICTION IN THE FRAGILE-X SYNDROME | 27 | 36 |
| 285 | 30 | 56 | 909 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):47-55 FISCH GS IS AUTISM ASSOCIATED WITH THE FRAGILE-X SYNDROME | 19 | 36 |
| 286 | 27 | 37 | 1183 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):474-481 HAGERMAN RJ; WILSON P; STALEY LW; LANG KA; FAN T; UHLHORN C; JEWELLSMART S; HULL C; DRISKO J; FLOM K; TAYLOR AK EVALUATION OF SCHOOL-CHILDREN AT HIGH-RISK FOR FRAGILE-X-SYNDROME UTILIZING BUCCAL CELL FMR-1 TESTING | 17 | 36 |
| 287 | 18 | 64 | 1596 1997 HUMAN MOLECULAR GENETICS 6(11):1791-1801 Stoger R; Kajimura TM; Brown WT; Laird CD Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1 | 12 | 36 |
| 288 | 17 | 28 | 1673 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):499-508 Bailey DB; Mesibov GB; Hatton DD; Clark RD; Roberts JE; Mayhew L Autistic behavior in young boys with fragile X syndrome | 29 | 36 |
| 289 | 16 | 54 | 1727 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):268-279 Miller LJ; McIntosh DN; McGrath J; Shyu V; Lampe M; Taylor AK; Tassone F; Neitzel K; Stackhouse T; Hagerman RJ Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report | 29 | 36 |
| 290 | 17 | 50 | 1790 1999 HUMAN MOLECULAR GENETICS 8(5):863-869 Tamanini F; Bontekoe C; Bakker CE; van Unen L; Anar B; Willemsen R; Yoshida M; Galjaard H; Oostra BA; Hoogeveen AT Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations | 26 | 36 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 291 | 0 | 0 | 47 1982 AMERICAN JOURNAL OF MEDICAL GENETICS 11(4):489-495 HECHT F; JACKY PB; SUTHERLAND GR THE FRAGILE X-CHROMOSOME - CURRENT METHODS | 16 | 35 |
| 292 | 2 | 3 | 64 1982 HUMAN GENETICS 61(3):262-263 FRYNS JP; VANDENBERGHE H TRANSMISSION OF FRAGILE (X)(Q27) FROM NORMAL MALE(S) | 25 | 35 |
| 293 | 6 | 26 | 136 1983 HUMAN GENETICS 64(3):240-245 NIELSEN KB; TOMMERUP N; POULSEN H; JACOBSEN P; BECK B; MIKKELSEN M CARRIER DETECTION AND X-INACTIVATION STUDIES IN THE FRAGILE-X SYNDROME - CYTOGENETIC STUDIES IN 63 OBLIGATE AND POTENTIAL CARRIERS OF THE FRAGILE-X | 23 | 35 |
| 294 | 4 | 16 | 170 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):111-121 HAGERMAN RJ; VANHOUSEN K; SMITH ACM; MCGAVRAN L CONSIDERATION OF CONNECTIVE-TISSUE DYSFUNCTION IN THE FRAGILE-X SYNDROME | 25 | 35 |
| 295 | 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 |
| 296 | 10 | 36 | 521 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):213-225 WOLFF PH; GARDNER J; LAPPEN J; PACCIA J; MERYASH D VARIABLE EXPRESSION OF THE FRAGILE-X SYNDROME IN HETEROZYGOUS FEMALES OF NORMAL INTELLIGENCE | 28 | 35 |
| 297 | 5 | 9 | 878 1991 LANCET 338(8772):956-957 HIRST M; KNIGHT S; DAVIES K; CROSS G; OCRAFT K; RAEBURN S; HEEGER S; EUNPU D; JENKINS EC; LINDENBAUM R PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 29 | 35 |
| 298 | 18 | 29 | 1434 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):340-345 Sobesky WE; Taylor AK; Pennington BF; Bennetto L; Porter D; Riddle J; Hagerman RJ Molecular/clinical correlations in females with fragile X | 26 | 35 |
| 299 | 24 | 29 | 1508 1996 PEDIATRICS 97(1):122-126 Hagerman RJ; Staley LW; OConner R; Lugenbeel K; Nelson D; McLean SD; Taylor A Learning-disabled males with a fragile X CGG expansion in the upper premutation size range | 25 | 35 |
| 300 | 19 | 66 | 669 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):696-719 LAIRD CD; LAMB MM; THORNE JL 2 PROGENITOR CELLS FOR HUMAN OOGONIA INFERRED FROM PEDIGREE DATA AND THE X-INACTIVATION IMPRINTING MODEL OF THE FRAGILE-X SYNDROME | 28 | 34 |
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