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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 12: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1101 | 6 | 20 | 812 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):429-433 KIMCHISARFATY C; GOITEIN R; KEREM B; WERNER M; MEIDAN B; SCHAAP T ENDOREDUPLICATION AND POLYPLOIDY IN FRAGILE-X CELLS INDUCED BY METHOTREXATE AND FLUORODEOXYURIDINE - IMPLICATIONS FOR DIAGNOSIS | 1 | 3 |
| 1102 | 10 | 22 | 1327 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):223-229 King RA; Hagerman R; Houghton M Ocular findings in fragile X syndrome | 1 | 1 |
| 1103 | 0 | 0 | 78 1982 LANCET 2(8307):1104-1104 KINNELL HG FRAGILE-X DISORDER ASSOCIATED WITH ANTISOCIAL PERSONALITY | 3 | 5 |
| 1104 | 17 | 31 | 431 1987 BRITISH MEDICAL JOURNAL 295(6598):564-565 KINNELL HG FRAGILE X-SYNDROME - AN IMPORTANT PREVENTABLE CAUSE OF MENTAL HANDICAP | 2 | 2 |
| 1105 | 0 | 4 | 151 1983 LANCET 2(8364):1427-1427 KINNELL HG; BANU SP INSTITUTIONAL PREVALENCE OF FRAGILE X-SYNDROME | 5 | 8 |
| 1106 | 13 | 35 | 1375 1995 JOURNAL OF MEDICAL GENETICS 32(12):925-929 KIRCHGESSNER CU; WARREN ST; WILLARD HF X INACTIVATION OF THE FMR1 FRAGILE-X MENTAL-RETARDATION GENE | 5 | 12 |
| 1107 | 4 | 7 | 1985 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):156-161 Kjaer I; Hjalgrim H; Russell BG Cranial and hand skeleton in fragile X syndrome | 0 | 0 |
| 1108 | 12 | 14 | 1506 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 1109 | 0 | 0 | 1348 1995 EPILEPSIA 36:S1-S1 KLUGER G; BOHM I; LAUB MC; WALDENMEIER C; STUHRMANNSPANGENBERG M EEG IN CHILDREN WITH FRAGILE-X PREMUTATION | 0 | 0 |
| 1110 | 16 | 24 | 974 1992 DISEASE MARKERS 10(1):1-5 KNIGHT SJL; HIRST MC; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1111 | 13 | 21 | 934 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):217-223 KNIGHT SJL; HIRST MC; ROCHE A; CHRISTODOULOU Z; HUSON SM; WINTER R; FITCHETT M; MCKINLEY MJ; LINDENBAUM RH; NAKAHORI Y; DAVIES KE MOLECULAR STUDIES OF THE FRAGILE-X SYNDROME | 10 | 19 |
| 1112 | 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 |
| 1113 | 10 | 11 | 1115 1993 JOURNAL OF MEDICAL GENETICS 30(3):193-197 KNOBLOCH O; PELZ F; WICK U; NELSON DL; ZOLL B DIRECT VERSUS INDIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X MENTAL-RETARDATION IN 40 GERMAN FAMILIES AT RISK | 1 | 1 |
| 1114 | 0 | 0 | 45 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A131-A131 KNOLL J; CHUDLEY AE; GERRARD JW EFFICACY OF FUDR IN ENHANCING EXPRESSION OF FRA(X) IN AFFECTED MALES AND CARRIER FEMALES WITH FRAGILE X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 1115 | 0 | 0 | 97 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A139-A139 KNOLL JH; CHUDLEY AE; GERRARD JW FREQUENCY AND REPLICATION PATTERN OF FRAGILE (X) (Q28) IN HETEROZYGOTES | 0 | 0 |
| 1116 | 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 |
| 1117 | 28 | 62 | 2321 2004 BRAIN 127:591-601 Kogan CS; Boutet I; Cornish K; Zangenehpour S; Mullen KT; Holden JJA; Kaloustian VMD; Andermann E; Chaudhuri A Differential impact of the FMR1 gene on visual processing in fragile X syndrome | 0 | 0 |
| 1118 | 15 | 17 | 1173 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):428-435 KOLEHMAINEN K POPULATION-GENETICS OF FRAGILE-X - A MULTIPLE ALLELE MODEL WITH VARIABLE RISK OF CGG REPEAT EXPANSION | 15 | 21 |
| 1119 | 26 | 42 | 1159 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):328-338 KOLEHMAINEN K; KARANT Y MODELING METHYLATION AND IQ SCORES IN FRAGILE-X FEMALES AND MOSAIC MALES | 4 | 7 |
| 1120 | 4 | 7 | 1314 1995 BRAIN & DEVELOPMENT 17(5):323-323 KONDO I NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN JAPANESE MENTALLY-RETARDED MALES - COMMENT | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1121 | 0 | 0 | 592 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):225-225 KONDO I; ARINAMI T PREVALENCE OF CHROMOSOME-ANOMALIES IN MENTALLY-RETARDED SCHOOL-CHILDREN - STUDY OF POPULATION INCIDENCE OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1122 | 32 | 60 | 2308 2003 TRENDS IN GENETICS 19(3):148-154 Kooy RF Of mice and the fragile X syndrome | 4 | 7 |
| 1123 | 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 |
| 1124 | 18 | 33 | 1784 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(5):526-532 Kooy RF; Reyniers E; Verhoye M; Sijbers J; Bakker CE; Oostra BA; Willems PJ; Van der Linden A Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging | 7 | 20 |
| 1125 | 30 | 45 | 1951 2000 MOLECULAR MEDICINE TODAY 6(5):193-198 Kooy RF; Willemsen R; Oostra BA Fragile X syndrome at the turn of the century | 12 | 18 |
| 1126 | 4 | 28 | 1731 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):298-301 Kotilainen J; Pirinen S Dental maturity is advanced in fragile X syndrome | 2 | 2 |
| 1127 | 0 | 0 | 1563 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):460-460 Koupernik; Doutheau; Rapporteur The fragile X syndrome and its clinical psychotic expression - Discussion | 0 | 0 |
| 1128 | 0 | 0 | 2292 2003 MOVEMENT DISORDERS 18(9):1091-1091 Kraft S; Parboosingh J; Suchowersky O Absence of fragile X premutation alleles in patients referred with spinocerebellar ataxia | 0 | 0 |
| 1129 | 0 | 0 | 1477 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 |
| 1130 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1131 | 19 | 33 | 1697 1998 OPTOMETRY AND VISION SCIENCE 75(12):856-859 Kranjc BS; Brezigar A; Peterlin B Bilateral macular dysplasia in fragile X syndrome | 0 | 0 |
| 1132 | 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 |
| 1133 | 21 | 49 | 534 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):435-442 KRAWCZUN MS; JENKINS EC; BROWN WT; SILVERMAN WP FRAGILE-X EXPRESSION IN SHORT-TERM WHOLE-BLOOD CULTURES IS AFFECTED BY CELL-DENSITY | 2 | 3 |
| 1134 | 2 | 33 | 816 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463 KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; SCHWARTZRICHSTEIN C; HONG G; BROWN WT DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS | 1 | 1 |
| 1135 | 8 | 16 | 340 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):467-473 KRAWCZUN MS; LELE KP; JENKINS EC; BROWN WT FRAGILE-X EXPRESSION INCREASED BY LOW CELL-CULTURE DENSITY | 5 | 8 |
| 1136 | 5 | 13 | 899 1991 SCIENCE 252(5013):1711-1714 KREMER EJ; PRITCHARD M; LYNCH M; YU S; HOLMAN K; BAKER E; WARREN ST; SCHLESSINGER D; SUTHERLAND GR; RICHARDS RI MAPPING OF DNA INSTABILITY AT THE FRAGILE-X TO A TRINUCLEOTIDE REPEAT SEQUENCE P(CCG)N | 200 | 575 |
| 1137 | 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 |
| 1138 | 0 | 0 | 55 1982 CLINICAL RESEARCH 30(5):A890-A890 KRUMDIECK CL; HOWARDPEEBLES PN THE ORIGIN OF THE FRAGILE X IN HUMAN-CHROMOSOMES - AN HYPOTHESIS | 0 | 0 |
| 1139 | 0 | 0 | 1005 1992 MONATSSCHRIFT KINDERHEILKUNDE 140(7):404-404 KRUSE K GIRLS WITH FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) | 0 | 0 |
| 1140 | 14 | 29 | 1150 1994 AMERICAN JOURNAL OF HUMAN GENETICS 54(3):437-442 KRUYER H; MILA M; GLOVER G; CARBONELL P; BALLESTA F; ESTIVILL X FRAGILE X SYNDROME AND THE (CGG)(N) MUTATION - 2 FAMILIES WITH DISCORDANT MZ TWINS | 20 | 59 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1141 | 0 | 0 | 1037 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):465-465 KRUYER H; MILA M; GLOVER G; CASTELLVBEL S; CARBONELL P; VOLPINI V; ESTIVILL X MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME (FXS) | 0 | 2 |
| 1142 | 0 | 0 | 743 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 KUHL D; PIERETTI M; REINER O; NELSON D FRAGILE-X SITE - MOLECULAR AND GENETIC-CHARACTERIZATION | 0 | 0 |
| 1143 | 0 | 0 | 751 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):194-194 KUHL DPA; WARREN ST; RIGGINS GJ; NELSON DL; CASKEY CT USE OF CA REPEAT MARKER DXS548 FOR PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME AND THE IDENTIFICATION OF NEW POSSIBLY POLYMORPHIC SITES IN THE FRAGILE-X REGION | 0 | 0 |
| 1144 | 8 | 28 | 2028 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(6):4357-4364 Kumari D; Usdin K Interaction of the transcription factors USF1, USF2, and alpha-Pal/Nrf-1 with the FMR1 promoter - Implications for Fragile X mental retardation syndrome | 12 | 20 |
| 1145 | 20 | 53 | 1207 1994 CELL 77(6):853-861 KUNST CB; WARREN ST CRYPTIC AND POLAR VARIATION OF THE FRAGILE-X REPEAT COULD RESULT IN PREDISPOSING NORMAL ALLELES | 70 | 239 |
| 1146 | 6 | 29 | 2153 2002 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 46:328-339 Kuo AY; Reiss AL; Freund LS; Huffman LC Family environment and cognitive abilities in girls with fragile-X syndrome | 2 | 3 |
| 1147 | 10 | 28 | 813 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):440-444 KUPKE KG; SORENG AL; MULLER U ORIGIN OF THE SUPERNUMERARY X-CHROMOSOME IN A PATIENT WITH FRAGILE-X AND KLINEFELTER SYNDROME | 7 | 9 |
| 1148 | 0 | 0 | 1909 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :146-146 Kwon H; Menon V; Eliez S; Dyer-Friedman J; Glover GH; Reiss AL Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavior and FMR-1 protein expression | 0 | 0 |
| 1149 | 17 | 54 | 1991 2001 AMERICAN JOURNAL OF PSYCHIATRY 158(7):1040-1051 Kwon H; Menon V; Eliez S; Warsofsky IS; White CD; Dyer-Friedman J; Taylor AK; Glover GH; Reiss AL Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavioral and molecular measures | 10 | 21 |
| 1150 | 17 | 24 | 2034 2001 JOURNAL OF KOREAN MEDICAL SCIENCE 16(3):271-275 Kwon SH; Lee KS; Hyun MC; Song KE; Kim JK Molecular screening for Fragile X syndrome in mentally handicapped children in Korea | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1151 | 1 | 1 | 601 1988 JOURNAL OF MEDICAL GENETICS 25(1):64-64 LACA Z; BRANKOVIC S EXPRESSION OF FRAGILE X-CHROMOSOME AND POSSIBLE DELETION IN SUCCESSIVE CELL DIVISIONS | 0 | 0 |
| 1152 | 0 | 0 | 363 1986 ARCHIVOS DE BIOLOGIA Y MEDICINA EXPERIMENTALES 19(1):R133-R133 LACASSIE Y; MORENO R; ALLIENDE MA; DELABARRA F; BARAHONA G; ANRIQUEZ E; COLOMBO M; SEGURE T LACK OF EFFECT OF FOLIC-ACID THERAPY ON MENTAL RETARDED PATIENTS WITH FRAGILE-X OR OTHER AUTOSOMAL FRAGILITIES IN A DOUBLE-BLIND-STUDY | 0 | 0 |
| 1153 | 0 | 1 | 646 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(4):643-643 LACHIEWICZ AM FRAGILE-X SYNDROME - A HANDBOOK FOR FAMILIES AND EDUCATORS - FINUCANE,B | 0 | 0 |
| 1154 | 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 |
| 1155 | 13 | 26 | 1164 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):364-369 LACHIEWICZ AM; DAWSON DV BEHAVIOR PROBLEMS OF YOUNG GIRLS WITH FRAGILE-X-SYNDROME - FACTOR SCORES ON THE CONNERS PARENTS QUESTIONNAIRE | 11 | 18 |
| 1156 | 0 | 0 | 1253 1994 PEDIATRIC RESEARCH 35(4):A23-A23 LACHIEWICZ AM; DAWSON DV AUTISTIC BEHAVIORS OF YOUNG GIRLS WITH FRAGILE X-SYNDROME | 1 | 1 |
| 1157 | 14 | 31 | 1254 1994 PEDIATRICS 93(6):992-995 LACHIEWICZ AM; DAWSON DV DO YOUNG BOYS WITH FRAGILE-X-SYNDROME HAVE MACROORCHIDISM | 13 | 17 |
| 1158 | 27 | 42 | 1851 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(4):229-236 Lachiewicz AM; Dawson DV; Spiridigliozzi GA Physical characteristics of young boys with fragile X syndrome: Reasons for difficulties in making a diagnosis in young males | 9 | 10 |
| 1159 | 0 | 0 | 389 1986 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 7(3):201-202 LACHIEWICZ AM; GULLION CM; SPIRIDIGLIOZZI GA; ALYSWORTH AS DECLINE IN IQ SCORES OF YOUNG FRAGILE X-MALES | 0 | 0 |
| 1160 | 5 | 42 | 422 1987 AMERICAN JOURNAL ON MENTAL RETARDATION 92(3):272-278 LACHIEWICZ AM; GULLION CM; SPIRIDIGLIOZZI GA; AYLSWORTH AS DECLINING IQS OF YOUNG MALES WITH THE FRAGILE X-SYNDROME | 47 | 63 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1161 | 2 | 12 | 830 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):275-278 LACHIEWICZ AM; HOEGERMAN SF; HOLMGREN G; HOLMBERG E; ARINBJARNARSON K ASSOCIATION OF THE ROBIN SEQUENCE WITH THE FRAGILE-X SYNDROME | 5 | 8 |
| 1162 | 0 | 0 | 726 1990 PEDIATRIC RESEARCH 27(4):A12-A12 LACHIEWICZ AM; SPIRIDIGLIOZZI GA; GULLION CA; RANSFORD SK ABERRANT BEHAVIORS OF YOUNG BOYS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1163 | 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 |
| 1164 | 12 | 21 | 1424 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):278-282 Lachiewicz AM; Spiridigliozzi GA; McConkieRosell A; Burgess D; Feng Y; Warren ST; Tarleton J A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene | 9 | 11 |
| 1165 | 19 | 31 | 2023 2001 HUMAN MOLECULAR GENETICS 10(4):329-338 Laggerbauer B; Ostareck D; Keidel EM; Ostareck-Lederer A; Fischer U Evidence that fragile X mental retardation protein is a negative regulator of translation | 55 | 80 |
| 1166 | 0 | 0 | 561 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):91-91 LAING S; LATHAM M; KENNY J; PURVISSMITH S; TURNER G CYTOGENETIC ANOMALIES IN A POPULATION SELECTED FOR FRAGILE-X SCREENING | 0 | 0 |
| 1167 | 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 |
| 1168 | 0 | 0 | 1399 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):1-1 Laing S; Robinson H; Wake S; Wright F; Turner G Normal males and their role in transmission of the fragile x syndrome. | 0 | 0 |
| 1169 | 15 | 42 | 447 1987 GENETICS 117(3):587-599 LAIRD CD PROPOSED MECHANISM OF INHERITANCE AND EXPRESSION OF THE HUMAN FRAGILE-X SYNDROME OF MENTAL-RETARDATION | 92 | 167 |
| 1170 | 2 | 5 | 550 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):693-696 LAIRD CD FRAGILE-X MUTATION PROPOSED TO BLOCK COMPLETE REACTIVATION IN FEMALES OF AN INACTIVE X-CHROMOSOME | 7 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1171 | 4 | 53 | 624 1989 AMERICAN ZOOLOGIST 29(2):569-591 LAIRD CD FROM POLYTENE CHROMOSOMES TO HUMAN EMBRYOLOGY - CONNECTIONS VIA THE HUMAN FRAGILE-X SYNDROME | 1 | 3 |
| 1172 | 11 | 25 | 804 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):391-395 LAIRD CD POSSIBLE ERASURE OF THE IMPRINT ON A FRAGILE-X CHROMOSOME WHEN TRANSMITTED BY A MALE | 8 | 15 |
| 1173 | 12 | 15 | 1063 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 46(6):687-688 LAIRD CD IMPRINTING AND IMPRINT ERASURE AS VIEWED THROUGH THE FRAGILE-X SYNDROME | 2 | 5 |
| 1174 | 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 |
| 1175 | 8 | 26 | 1649 1998 EPIGENETICS 214:280-290 Laird; Pillus; Hirst; Bestor; Jaenisch; Wilkins; Gasser; Wolffe; Francke; Bird; Riggs; Horz Rules of DNA methylation in humans inferred from the fragile X gene, FMR1 - Final general discussion | 0 | 0 |
| 1176 | 0 | 0 | 1769 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-768 Lanham DC; Mazzocco MM; Denckla MB Depression and anxiety in girls with Fragile X or Turner Syndrome. | 1 | 1 |
| 1177 | 0 | 32 | 52 1982 CANADIAN MEDICAL ASSOCIATION JOURNAL 127(2):123-126 LARBRISSEAU A; JEAN P; MESSIER B; RICHER CL FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 6 | 9 |
| 1178 | 0 | 0 | 200 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 |
| 1179 | 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 |
| 1180 | 0 | 0 | 1715 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A279-A279 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson J; Brondum-Nielsen K; Hasholt L; Norgarrd-Pedersen B; Vuust J Haplotype and AGG-interspersion analysis of FMR1(CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1181 | 21 | 33 | 1853 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 93(2):99-106 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson JN; Brondum-Nielsen K; Hasholt L; Norgaard-Pedersen B; Vuust J Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles | 2 | 6 |
| 1182 | 14 | 19 | 1591 1997 HUMAN GENETICS 100(5-6):564-568 Larsen LA; Gronskov K; NorgaardPedersen B; BrondumNielsen K; Hasholt L; Vuust J High-throughput analysis of fragile X (CGG)(n) alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis | 5 | 23 |
| 1183 | 0 | 0 | 1452 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G5-G5 Larsen LA; NorgaardPedersen B; Vuust J Analysis of fragile X CGG repeats in the normal range by PCR amplification and automated capillary electrophoresis. | 0 | 0 |
| 1184 | 4 | 9 | 1019 1992 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 92(4):28-31 LASTOCHKINA NA; KUPRIYANOVA TA; PUCHINSKAYA LM; MARINCHEVA GS; GORKOVA SA THE CLINICOELECTROPHYSIOLOGICAL CHARACTERIZATION OF WOMEN, HETEROZYGOUS CARRIERS OF FRAGILE X-CHROMOSOME | 1 | 1 |
| 1185 | 6 | 25 | 979 1992 GENOMICS 12(4):818-821 LAVAL SH; BLAIR HJ; HIRST MC; DAVIES KE; BOYD Y MAPPING OF FMR1, THE GENE IMPLICATED IN FRAGILE X-LINKED MENTAL-RETARDATION, ON THE MOUSE X-CHROMOSOME | 0 | 9 |
| 1186 | 15 | 64 | 1590 1997 HUMAN GENETICS 100(3-4):407-414 Lavedan CN; Garrett L; Nussbaum RL Trinucleotide repeats (CGG)(22)TGG(CGG)(43)TGG(CGG)(21) from the fragile X gene remain stable in transgenic mice | 9 | 19 |
| 1187 | 0 | 3 | 294 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 LAWRENCE RJ THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 0 | 0 |
| 1188 | 2 | 5 | 1295 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 57(3):508-509 LAXOVA R FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 2 | 3 |
| 1189 | 0 | 0 | 1545 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A313-A313 Layman LC; Moffitt DV; McDonough PG; Song M; Shamoun D; Ledbetter DH; Das S Correlation and vertical transmission of fragile X syndrome and ovarian failure within a single family. | 0 | 0 |
| 1190 | 0 | 0 | 1803 1999 JOURNAL OF MEDICAL GENETICS 36:S64-S64 Lazarau L; Warburton SA; Roberts CE; Hughes HE; Bartlett S; Meredith AL; Ravine D Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1191 | 0 | 0 | 1931 2000 JOURNAL OF MEDICAL GENETICS 37:S66-S66 Lazarou LP; Myring J; Knight SJL; Gardner AP; Clarke A Fragile X (E) syndrome. How common is it? | 0 | 0 |
| 1192 | 0 | 0 | 1718 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A474-A474 Lazarou LP; Warburton S; Roberts CE; Lindley VH; Bartlett S; Hughes HE; Meredith L; Ravine D Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male. | 0 | 0 |
| 1193 | 0 | 1 | 2255 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 |
| 1194 | 2 | 6 | 598 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-460 LECOUTEUR A; RUTTER M; SUMMERS D; BUTLER L FRAGILE-X IN FEMALE AUTISTIC TWINS | 8 | 14 |
| 1195 | 7 | 13 | 338 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):429-443 LEDBETTER DH; AIRHART SD; NUSSBAUM RL SOMATIC-CELL HYBRID STUDIES OF FRAGILE-(X) EXPRESSION IN A CARRIER FEMALE AND TRANSMITTING MALE | 10 | 18 |
| 1196 | 1 | 14 | 339 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):445-455 LEDBETTER DH; AIRHART SD; NUSSBAUM RL CAFFEINE ENHANCES FRAGILE-(X) EXPRESSION IN SOMATIC-CELL HYBRIDS | 5 | 18 |
| 1197 | 0 | 0 | 502 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):21-21 LEDBETTER DH; LEDBETTER SA HIGH-LEVELS OF FRAGILE-X EXPRESSION IN NORMAL MALES INDUCED BY APHIDICOLIN | 0 | 0 |
| 1198 | 12 | 23 | 402 1986 NATURE 324(6093):161-163 LEDBETTER DH; LEDBETTER SA; NUSSBAUM RL IMPLICATIONS OF FRAGILE-X EXPRESSION IN NORMAL MALES FOR THE NATURE OF THE MUTATION | 31 | 56 |
| 1199 | 4 | 16 | 810 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):418-420 LEDBETTER SA; SCHWARTZ CE; DAVIES KE; LEDBETTER DH NEW SOMATIC-CELL HYBRIDS FOR PHYSICAL MAPPING IN DISTAL XQ AND THE FRAGILE-X REGION | 0 | 14 |
| 1200 | 22 | 62 | 2261 2003 DEVELOPMENT 130(22):5543-5552 Lee A; Li WJ; Xu KY; Bogert BA; Su K; Gao FB Control of dendritic development by the Drosophila fragile X-related gene involves the small GTPase Rac1 | 2 | 3 |
Page 12: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
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