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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 11: 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 |
|---|---|---|---|---|---|
| 1001 | 2 | 4 | 222 1984 LANCET 1(8370):220-220 JANCAR J PREVALENCE OF FRAGILE X-CHROMOSOME | 1 | 3 |
| 1002 | 0 | 0 | 2155 2002 JOURNAL OF MEDICAL GENETICS 39:S76-S76 Jani A; Hodsdon P; Churchley K; Crocker M; Stefanou E; Cranston T; Stewart H; Seller A An atypical week for the Oxford Fragile X service: Two interesting cases | 0 | 0 |
| 1003 | 23 | 49 | 1513 1996 REVISTA MEDICA DE CHILE 124(7):865-872 Jara L; Avendano I; Aspillaga M; Blanco R Molecular and genetic features of fragile X syndrome. A review | 0 | 0 |
| 1004 | 29 | 41 | 1698 1998 REVISTA MEDICA DE CHILE 126(8):911-918 Jara L; Lopez M; Mellado C; Aspillaga M; Avendano I; Blanco R Clinical and metabolic screening for fragile X syndrome in 300 patients with unspecific mental retardation | 0 | 0 |
| 1005 | 5 | 17 | 1072 1993 BIOLOGICAL PSYCHIATRY 33(3):213-216 JEFFRIES FM; REISS AL; BROWN WT; MEYERS DA; GLICKSMAN AC; BANDYOPADHYAY S BIPOLAR SPECTRUM DISORDER AND FRAGILE-X SYNDROME - A FAMILY STUDY | 4 | 13 |
| 1006 | 0 | 3 | 44 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A130-A130 JENKINS E; BROWN T; DUNCAN C; BROOKS J FRAGILE X-CHROMOSOME PRENATAL-DIAGNOSIS | 3 | 4 |
| 1007 | 0 | 0 | 96 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A136-A136 JENKINS E; DUNCAN C; BROOKS J; LELE K; SANZ M; NOLIN S; BROWN T LOW-FREQUENCY FRAGILE X-CHROMOSOMES IN CULTURES FROM NORMAL PEOPLE | 0 | 4 |
| 1008 | 0 | 0 | 766 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):290-290 JENKINS E; GENOVESE M; DUNCAN C; GU H; SCHWARTZRICHSTEIN C; STARKHOUCK S; LELE K; LI SY; KRAWCZUN M COMMON FRAGILE SITE FRA(X)(Q27.2), PRESENT IN ONLY 1 OF 685 CASES SCREENED FOR THE FRAGILE-X SYNDROME | 0 | 0 |
| 1009 | 1 | 8 | 817 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):464-466 JENKINS EC; BROOKS SE; STARKHOUCK SL; DUNCAN CJ; BROOKS SLS; BROWN WT SV40-TRANSFORMED FRAGILE(X) AMNIOCYTES | 1 | 1 |
| 1010 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1011 | 14 | 23 | 383 1986 EXPERIMENTAL CELL BIOLOGY 54(1):40-48 JENKINS EC; BROWN WT; BROOKS J; DUNCAN CJ; SANZ MM; SILVERMAN WP; LELE KP; MASIA A; KATZ E; LUBIN RA; NOLIN SL LOW-FREQUENCIES OF APPARENTLY FRAGILE X-CHROMOSOMES IN NORMAL CONTROL CULTURES - A POSSIBLE EXPLANATION | 16 | 20 |
| 1012 | 0 | 0 | 54 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 |
| 1013 | 1 | 4 | 28 1981 LANCET 2(8258):1292-1292 JENKINS EC; BROWN WT; DUNCAN CJ; BROOKS J; BENYISHAY M; GIORDANO FM; NITOWSKY HM FEASIBILITY OF FRAGILE X-CHROMOSOME PRENATAL-DIAGNOSIS DEMONSTRATED | 56 | 77 |
| 1014 | 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 |
| 1015 | 12 | 19 | 923 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):155-160 JENKINS EC; DUNCAN CJ; GU H; GENOVESE M; KRAWCZUN MS DIALYZED FETAL BOVINE SERUM INCREASES CYTOGENETIC FRAGILE-X EXPRESSION | 1 | 1 |
| 1016 | 3 | 7 | 344 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):531-535 JENKINS EC; DUNCAN CJ; KRAWCZUN MS; BERNS LM; SANZ MM; BROWN WT FREQUENCY OF TRIRADIAL OR MULTIRADIAL CONFIGURATIONS IN FRAGILE-X IDENTIFICATION | 3 | 5 |
| 1017 | 7 | 11 | 725 1990 PATHOBIOLOGY 58(4):236-240 JENKINS EC; DUNCAN CJ; SANZ MM; GENOVESE M; GU H; SCHWARTZRICHSTEIN C; LELE KP; SALANDI ML; KRAWCZUN MS PROGRESS TOWARD AN INTERNAL CONTROL-SYSTEM FOR FRAGILE-X INDUCTION BY 5-FLUORODEOXYURIDINE IN WHOLE-BLOOD CULTURES | 3 | 6 |
| 1018 | 7 | 8 | 1177 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):452-453 JENKINS EC; GENOVESE M; DUNCAN CJ; GU H; STARKHOUCK S; LI SY; HENDERSON J; MORYS I; BROWN WT OCCURRENCE OF ANEUPLOIDY FOR THE X-CHROMOSOME IN OVER 1,300 UNRELATED SPECIMENS SCREENED FOR THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1019 | 10 | 14 | 921 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):136-141 JENKINS EC; GENOVESE MJ; DUNCAN CJ; GU H; STARKHOUCK SL; LELE K; LI SY; KRAWCZUN MS FRA(X)(Q27.2), THE COMMON FRAGILE SITE, OBSERVED IN ONLY ONE OF 760 CASES STUDIED FOR THE FRAGILE-X SYNDROME | 1 | 1 |
| 1020 | 24 | 41 | 1333 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):293-301 Jenkins EC; Houck GE; Ding XH; Li SY; StarkHouck SL; Salerno J; Genovese M; Glicksman A; Nolin SL; Zhong N; Brooks SLS; Dobkin CS; Brown WT An update on fragile X prenatal diagnosis: End of the cytogenetic testing era | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1021 | 5 | 16 | 341 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):475-481 JENKINS EC; KASTIN BR; KRAWCZUN MS; LELE KP; SILVERMAN WP; BROWN WT FRAGILE-X CHROMOSOME FREQUENCY IS CONSISTENT TEMPORALLY AND WITHIN REPLICATE CULTURES | 2 | 3 |
| 1022 | 0 | 0 | 1973 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):431-431 Jenkins EC; Li SY; Yao XL; Lanter S; Sudhalter V; Belser R; Ding XH; Houck GE; Glicksman A; Dobkin CS; Nolin SL; Brown WT Detecting mosaic FMR-1 (fragile X) mutations: Southern blotting versus monoclonal antibody analysis. | 0 | 0 |
| 1023 | 0 | 0 | 1038 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):565-565 JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; LI SY; HOUCK GA; DING XH; STARKHOUCK SL; DOBKIN CA; BROWN WT THE EFFECT OF FRAGILE-X INDUCTION SYSTEMS ON CYTOGENETIC, PCR AND DIREDT DNA ANALYSES OF THE FMR-1 GENE IN CVS CULTURES | 0 | 0 |
| 1024 | 5 | 8 | 1174 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):436-442 JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; LI SY; HOUCK GE; DING XH; STARKHOUCK SL; DOBKIN CS; BROWN WT FRAGILE-X INDUCTION SYSTEMS IN CVS CULTURES - EFFECT ON CYTOGENETIC, PCR, AND GENOMIC SOUTHERN BLOT DNA ANALYSES OF THE FMR-1 GENE | 1 | 1 |
| 1025 | 0 | 0 | 1536 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A128-A128 Jenkins EC; Wen GY; Goldberg EM; Genovese M; Brown WT; Wisniewski HM Fragile X chromosome longitudinal sections studied by transmission electron microscopy. | 0 | 0 |
| 1026 | 7 | 14 | 1741 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):342-346 Jenkins EC; Wen GY; Kim KS; Zhong N; Sapienza VJ; Hong H; Chen J; Li SY; Houck GE; Ding XH; Nolin SL; Dobkin CS; Brown WT Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies | 2 | 2 |
| 1027 | 1 | 7 | 809 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):416-417 JENKINS LS; GRUENERT DC; JENKINS EC; SCHONBERG SA TRANSFORMATION AND ESTABLISHMENT OF FRAGILE-X CELL-LINES FROM AMNIOCYTES | 1 | 1 |
| 1028 | 5 | 8 | 1687 1998 JOURNAL OF MEDICAL GENETICS 35(10):878-878 Jenkins T; Krause A Molecular evidence that fragile X syndrome occurs in the South African black population | 0 | 0 |
| 1029 | 0 | 0 | 2204 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Jiang Y; Wakui K; Liu Q; Kashork CD; Lehoczky J; Shaffer LG; Beaudet AL A fragile X mental retardation protein interacting protein maps to the proximal breakpoint of the Prader-Willi syndrome common deletion region. | 0 | 0 |
| 1030 | 0 | 0 | 2201 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):162-162 Jin P; Ceman S; Zarnescu DC; Nakamoto M; Mowrey J; Jongens TA; Nelson DL; Moses K; Warren ST Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1031 | 0 | 0 | 1831 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Jin P; Feng Y; Brown V; Warren ST Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays. | 1 | 2 |
| 1032 | 46 | 82 | 1894 2000 HUMAN MOLECULAR GENETICS 9(6):901-908 Jin P; Warren ST Understanding the molecular basis of fragile X syndrome | 36 | 73 |
| 1033 | 35 | 55 | 2307 2003 TRENDS IN BIOCHEMICAL SCIENCES 28(3):152-158 Jin P; Warren ST New insights into fragile X syndrome: from molecules to neurobehaviors | 8 | 16 |
| 1034 | 20 | 39 | 2360 2004 NATURE NEUROSCIENCE 7(2):113-117 Jin P; Zarnescu DC; Ceman S; Nakamoto M; Mowrey J; Jongens TA; Nelson DL; Moses K; Warren ST Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway | 2 | 6 |
| 1035 | 5 | 35 | 2297 2003 NEURON 39(5):739-747 Jin P; Zarnescu DC; Zhang FP; Pearson CE; Lucchesi JC; Moses K; Warren ST RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila | 4 | 9 |
| 1036 | 0 | 0 | 2078 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):175-175 Jin P; Zhang F; Zarnescu DC; Moses K; Lucchesi JC; Nichol K; Pearson CE; Warren ST A Drosophila model of fragile X premutation: CGG repeat instability and dominant-negative effects of premutation riboCGG repeat. | 0 | 0 |
| 1037 | 2 | 17 | 586 1988 HUMAN GENETICS 79(3):231-234 JOHANNISSON R; FROSTERISKENIUS U; SAADALLAH N; HULTEN MA SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .2. 1ST MEIOSIS - LIGHT AND ELECTRON-MICROSCOPY | 1 | 3 |
| 1038 | 7 | 33 | 454 1987 HUMAN GENETICS 76(2):141-147 JOHANNISSON R; REHDER H; WENDT V; SCHWINGER E SPERMATOGENESIS IN 2 PATIENTS WITH THE FRAGILE-X SYNDROME .1. HISTOLOGY - LIGHT AND ELECTRON-MICROSCOPY | 8 | 15 |
| 1039 | 0 | 0 | 1288 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1921-1921 JOHNSON DB; QUAN F; BUCHANNAN JA; POPOVICH BW ALLELIC SIZE LADDERS FCR THE ACCURATE SIZING OF TRINUCLEOTIDE REPEATS IN HUNTINGTON DISEASE AND FRAGILE-X SYNDROME | 0 | 0 |
| 1040 | 0 | 0 | 1282 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1407-1407 JOHNSON JP; CURRY C; MICEK M; LOUIE E; ABRAMS L; DIETZ L TRANSMISSION OF STABLE AND UNSTABLE PREMUTATIONS FROM GREAT-GRANDMOTHER AND GREAT-GRANDFATHER RESPECTIVELY - LESSONS FOR GENETIC-COUNSELING IN FRAGILE-X SYNDROME FAMILIES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1041 | 27 | 39 | 1988 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(4):314-319 Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; Blasey C; Taylor A; Reiss A Neurobehavioral phenotype in carriers of the fragile X premutation | 5 | 5 |
| 1042 | 10 | 57 | 2277 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(4):267-275 Johnston C; Hessl D; Blasey C; Eliez S; Erba H; Dyer-Friedman J; Glaser B; Reiss AL Factors associated with parenting stress in mothers of children with fragile X syndrome | 0 | 0 |
| 1043 | 0 | 0 | 2197 2002 SCIENTIST 16(20):8-8 Johnston N Fragile X, an RNAi connection? | 0 | 0 |
| 1044 | 1 | 2 | 2361 2004 NATURE REVIEWS NEUROSCIENCE 5(1):4-4 Jones R Neurological disorders: Fragile X functions | 0 | 0 |
| 1045 | 9 | 21 | 1391 1995 PSYCHIATRIC GENETICS 5(4):157-160 Jonsson E; Bjorck E; Wahlstrom J; Gustavsson P; Sedvall G Screening for CGG trinucleotide repeat expansion in the fragile X mental retardation 1 gene in schizophrenic patients | 0 | 1 |
| 1046 | 16 | 38 | 835 1991 BIOESSAYS 13(5):243-251 JORDAN BR FRAGILE X-LINKED MENTAL-RETARDATION AND THE DIFFICULTIES OF REVERSE GENETICS | 1 | 1 |
| 1047 | 0 | 0 | 655 1989 M S-MEDECINE SCIENCES 5(7):450-458 JORDAN BR; MATTEI JF FRAGILE X-LINKED MENTAL-RETARDATION, 1989 | 2 | 2 |
| 1048 | 5 | 19 | 163 1984 ACTA PSYCHIATRICA SCANDINAVICA 70(5):510-514 JORGENSEN OS; NIELSEN KB; ISAGER T; MOURIDSEN SE FRAGILE X-CHROMOSOME AMONG CHILD PSYCHIATRIC-PATIENTS WITH DISTURBANCES OF LANGUAGE AND SOCIAL RELATIONSHIPS - A PILOT-STUDY | 12 | 21 |
| 1049 | 2 | 13 | 1700 1998 STEROIDS 63(1):2-4 Joseph DR The rat androgen-binding protein (ABP/SHBG) gene contains triplet repeats similar to unstable triplets: Evidence that the ABP/SHBG and the fragile X-related 2 genes overlap | 0 | 8 |
| 1050 | 0 | 0 | 1532 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A33-A33 Ju W; Xu WM; Hwang YW; Brown WT; Zhong N Molecular pathogenetic studies of the fragile X syndrome: Double knockouts of FMR1 and FXR1 affect early development of Xenopus oocytes. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1051 | 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 |
| 1052 | 0 | 0 | 500 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-20 KAHKONEN M; ALITALO T; AIRAKSINEN E; MATILAINER R; LAUNIALA K; AUTIO S; LEISTI J PREVALENCE OF THE FRAGILE-X OR MARTIN-BELL SYNDROME | 0 | 0 |
| 1053 | 2 | 8 | 860 1991 HUMAN GENETICS 87(1):95-96 KAHKONEN M; HAATAJA R; LEISTI J URIDINE ENHANCES EXPRESSION OF THE FRAGILE-X CHROMOSOME IN HUMAN-LYMPHOCYTES | 2 | 2 |
| 1054 | 0 | 0 | 753 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):221-221 KAHKONEN M; VAISANEN ML; WINGVIST R; LEISTI J PRENATAL-DIAGNOSIS OF FRAGILE X SYNDROME | 0 | 0 |
| 1055 | 0 | 0 | 2 1980 AMERICAN JOURNAL OF HUMAN GENETICS 32(6):A114-A114 KAISERMCCAW B; HECHT F THE FRAGILE-X - NO DYSMORPHIC SYNDROME, BUT A MARKER | 2 | 2 |
| 1056 | 0 | 6 | 3 1980 AMERICAN JOURNAL OF MEDICAL GENETICS 7(4):503-505 KAISERMCCAW B; HECHT F; CADIEN JD; MOORE BC FRAGILE X-LINKED MENTAL-RETARDATION | 14 | 22 |
| 1057 | 2 | 12 | 2243 2003 ARCHIVES OF NEUROLOGY 60(9):1197-1200 Kalidas S; Smith DP Functional genomics, fragile X syndrome, and RNA interference | 0 | 0 |
| 1058 | 20 | 33 | 1881 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 |
| 1059 | 11 | 14 | 1875 2000 BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY 107(8):969-972 Kallinen J; Korhonen K; Kortelainen S; Heinonen S; Ryynanen M Pregnancy outcome in carriers of fragile X | 0 | 0 |
| 1060 | 14 | 19 | 1444 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):404-407 Kambouris M; Snow K; Thibodeau S; Bluhm D; Green M; Feldman GL Segregation of the fragile X mutation from a male with a full mutation: Unusual somatic instability in the FMR-1 locus | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1061 | 1 | 5 | 2331 2004 ISRAEL JOURNAL OF PSYCHIATRY AND RELATED SCIENCES 41(1):70-70 Kandil ST; Bilici M; Aksu HB; Celep F; Karaguzel A Early infantile autism and fragile X anomaly | 0 | 0 |
| 1062 | 11 | 13 | 1188 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):501-502 KAPLAN G; KUNG M; MCCLURE M; CRONISTER A DIRECT MUTATION ANALYSIS OF 495 PATIENTS FOR FRAGILE-X CARRIER STATUS PROBAND DIAGNOSIS | 4 | 6 |
| 1063 | 0 | 0 | 757 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):267-267 KARIMINEJAD MH; RAHIMI M; SHIRNESHAN K; VAEZI SA; KARIMINEJAD R FRAGILE-X (BELL,MARTIN) SYNDROME IN AN IRANIAN FAMILY WITH 8 AFFECTED MEMBERS | 0 | 0 |
| 1064 | 0 | 0 | 1918 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:317-317 Karrer JH; Hagerman RJ; Karrer RS; Fitzpatrick D; Vavold J; Gora K; Chaney L Genotypic-specific event-related brain potentials among infants and toddlers with fragile-X syndrome and Down syndrome | 1 | 1 |
| 1065 | 0 | 0 | 465 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):171-171 KASAI R; NARAHARA K; MURAKAMI M; KIKKAWA K; KIMURA S; HIRAMOTO K; KIMOTO H PREVALENCE OF THE FRAGILE(X) SYNDROME IN INSTITUTIONALIZED MENTALLY-RETARDED INDIVIDUALS | 0 | 0 |
| 1066 | 2 | 54 | 1628 1997 PSYCHIATRY RESEARCH-NEUROIMAGING 75(1):31-48 Kates WR; Abrams MT; Kaufmann WE; Breiter SN; Reiss AL Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome | 16 | 53 |
| 1067 | 20 | 42 | 2166 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):159-167 Kates WR; Folley BS; Lanham DC; Capone GT; Kaufmann WE Cerebral growth in fragile X syndrome: Review and comparison with Down syndrome | 2 | 5 |
| 1068 | 25 | 35 | 2168 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):174-178 Kau ASM; Meyer WA; Kaufmann WE Early development in males with fragile X syndrome: A review of the literature | 2 | 3 |
| 1069 | 14 | 37 | 1866 2000 AMERICAN JOURNAL ON MENTAL RETARDATION 105(4):286-299 Kau ASM; Reider EE; Payne L; Meyer WA; Freund L Early behavior signs of psychiatric phenotypes in fragile X syndrome | 2 | 4 |
| 1070 | 21 | 48 | 2316 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 126A(1):9-17 Kau ASM; Tierney E; Bukelis I; Stump MH; Kates WR; Trescher WH; Kaufmann WE Social behavior profile in young males with fragile X syndrome: Characteristics and specificity | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1071 | 0 | 0 | 709 1990 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 12(1):69-69 KAUFMANN PM; LECKMAN JF; ORT SI DELAYED-RESPONSE PERFORMANCE IN MALES WITH FRAGILE-X SYNDROME | 3 | 5 |
| 1072 | 9 | 13 | 2161 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):131-134 Kaufmann WE Neurobiology of fragile X syndrome: From molecular genetics to neurobehavioral phenotype | 0 | 2 |
| 1073 | 0 | 0 | 1540 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A175-A175 Kaufmann WE; Abrams MT; Chen W; Reiss AL Genotype and molecular phenotype in fragile X syndrome. | 0 | 0 |
| 1074 | 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 |
| 1075 | 49 | 82 | 2162 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):135-144 Kaufmann WE; Cohen S; Sun HT; Ho G Molecular phenotype of fragile X syndrome: FMRP, FXRPs, and protein targets | 1 | 1 |
| 1076 | 0 | 0 | 2238 2003 ANNALS OF NEUROLOGY 54:S105-S106 Kaufmann WE; Danko CG; Kau ASM; Thevarajah S; Bukelis I; Tierney E; Neuberger I Increased protein acetylation in lymphocytes predicts autistic behavior in Fragile X syndrome | 0 | 0 |
| 1077 | 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 |
| 1078 | 16 | 17 | 2006 2001 CELL 107(5):555-557 Kaytor MD; Orr HT RNA targets of the fragile X protein | 5 | 13 |
| 1079 | 0 | 0 | 1103 1993 IRISH MEDICAL JOURNAL 86(3):92-& KEENAN E; KEANE V; RAMSEY L FRAGILE-X SYNDROME - A REVIEW | 1 | 1 |
| 1080 | 12 | 17 | 1004 1992 MENTAL RETARDATION 30(6):355-361 KEENAN J; KASTNER T; NATHANSON R; RICHARDSON N; HINTON J; CRESS DA A STATEWIDE PUBLIC AND PROFESSIONAL-EDUCATION PROGRAM ON FRAGILE X SYNDROME | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1081 | 13 | 27 | 519 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):191-200 KEMPER MB; HAGERMAN RJ; ALTSHULSTARK D COGNITIVE PROFILES OF BOYS WITH THE FRAGILE-X SYNDROME | 55 | 73 |
| 1082 | 0 | 0 | 1529 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Kenneson A; Cramer DW; Warren ST The fragile X premutation is not a major risk for early menopause. | 0 | 0 |
| 1083 | 30 | 43 | 1552 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(6):1362-1369 Kenneson A; Cramer DW; Warren ST Fragile X premutations are not a major cause of early menopause | 11 | 22 |
| 1084 | 0 | 0 | 1708 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A105-A105 Kenneson A; Hagedorn CH; Warren ST Quantitative studies of the fragile X mental retardation 1 (FMR1) gene product, FMRP. | 0 | 0 |
| 1085 | 68 | 102 | 2076 2001 SEMINARS IN REPRODUCTIVE MEDICINE 19(2):159-165 Kenneson A; Warren ST The female and the fragile X reviewed | 1 | 3 |
| 1086 | 0 | 0 | 1836 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Kenneson A; Zhang F; Warren ST Fragile X premutation alleles are associated with reduced FMRP levels due to a reduction of message translatability. | 0 | 0 |
| 1087 | 2 | 11 | 219 1984 JOURNAL OF NERVOUS AND MENTAL DISEASE 172(9):549-551 KERBESHIAN J; BURD L; MARTSOLF J A FAMILY WITH FRAGILE-X SYNDROME | 7 | 20 |
| 1088 | 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 |
| 1089 | 2 | 2 | 295 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 KERBESHIAN J; BURD L; MARTSOLF JT THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 1 | 1 |
| 1090 | 16 | 33 | 1199 1994 AMERICAN JOURNAL ON MENTAL RETARDATION 98(4):455-462 KERBY DS; DAWSON BL AUTISTIC FEATURES, PERSONALITY, AND ADAPTIVE-BEHAVIOR IN MALES WITH THE FRAGILE-X SYNDROME AND NO AUTISM | 12 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1091 | 0 | 0 | 501 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-21 KEREM B; GOITEIN R; SCHAAP T THE DISTRIBUTION OF FRAGILE-X CHROMOSOMES IN AMNIOTIC CELLS CULTURED BY THE INSITU TECHNIQUE | 1 | 1 |
| 1092 | 2 | 29 | 569 1988 CHROMOSOMA 97(1):6-10 KEREM B; GOITEIN R; SCHAAP T CYTOLOGICAL EVIDENCE OF DEFECTIVE TEMPLATE IN THE FRAGILE X-CHROMOSOME | 2 | 5 |
| 1093 | 11 | 67 | 1376 1995 JOURNAL OF MOLECULAR BIOLOGY 254(4):638-656 KETTANI A; KUMAR RA; PATEL DJ SOLUTION STRUCTURE OF A DNA QUADRUPLEX CONTAINING THE FRAGILE-X SYNDROME TRIPLET REPEAT | 12 | 95 |
| 1094 | 33 | 52 | 2169 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):179-186 Keysor CS; Mazzocco MMM A developmental approach to understanding fragile X syndrome in females | 5 | 5 |
| 1095 | 14 | 57 | 2121 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 | 1 |
| 1096 | 0 | 0 | 1838 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):130-130 Khalifa M; Struthers J High frequency of Klinefelter syndrome among a large population of patients referred for Fragile X syndrome testing due to undiagnosed mental retardation. | 0 | 0 |
| 1097 | 11 | 44 | 671 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):744-753 KHALIFA MM; REISS AL; MIGEON BR METHYLATION STATUS OF GENES FLANKING THE FRAGILE SITE IN MALES WITH THE FRAGILE-X SYNDROME - A TEST OF THE IMPRINTING HYPOTHESIS | 4 | 7 |
| 1098 | 46 | 98 | 1772 1999 BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE 77(4):331-342 Khandjian EW Biology of the fragile X mental retardation protein, an RNA-binding protein | 12 | 22 |
| 1099 | 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 |
| 1100 | 10 | 31 | 1503 1996 NATURE GENETICS 12(1):91-93 Khandjian EW; Corbin F; Woerly S; Rousseau F The fragile X mental retardation protein is associated with ribosomes | 58 | 93 |
Page 11: 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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