Evidence of linkage disequilibrium between schizophrenia and the SCA1 CAG repeat on chromosome 6p23

被引：0
|
作者：
Wang, SB
DeteraWadleigh, SD
Coon, H
Sun, CE
Goldin, LR
Duffy, DL
Byerley, WF
Gershon, ES
Diehl, SR
机构：
[1] NIDR,MOL EPIDEMIOL & DIS INDICATORS BRANCH,DEODP,NIH,BETHESDA,MD 20892
[2] NIMH,CLIN NEUROGENET BRANCH,NIH,BETHESDA,MD 20892
[3] UNIV UTAH,SCH MED,DEPT PSYCHIAT,SALT LAKE CITY,UT 84112
[4] JOHNS HOPKINS UNIV,SCH HYG & PUBL HLTH,BALTIMORE,MD
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1996年 / 59卷 / 03期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：731 / 736
页数：6
相关论文
共 50 条
  • [31] Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval
    Levi, A
    Kohn, Y
    Kanyas, K
    Amann, D
    Pae, CU
    Hamdan, A
    Segman, RH
    Avidan, N
    Karni, O
    Korner, M
    Jun, TY
    Beckmann, JS
    Macciardi, F
    Lerer, B
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2005, 13 (06) : 763 - 771
  • [32] Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval
    Adi Levi
    Yoav Kohn
    Kyra Kanyas
    Daniela Amann
    Chi-Un Pae
    Adnan Hamdan
    Ronnen H Segman
    Nili Avidan
    Osnat Karni
    Mira Korner
    Tae-Yun Jun
    Jacques S Beckmann
    Fabio Macciardi
    Bernard Lerer
    European Journal of Human Genetics, 2005, 13 : 763 - 771
  • [33] Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22
    Turic, D
    Robinson, L
    Duke, M
    Morris, DW
    Webb, V
    Hamshere, M
    Milham, C
    Hopkin, E
    Pound, K
    Fernando, S
    Grierson, A
    Easton, M
    Williams, N
    Van Den Bree, M
    Chowdhury, R
    Gruen, J
    Stevenson, J
    Krawczak, M
    Owen, MJ
    O'Donovan, MC
    Williams, J
    MOLECULAR PSYCHIATRY, 2003, 8 (02) : 176 - 185
  • [34] Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3–22
    D Turic
    L Robinson
    M Duke
    D W Morris
    V Webb
    M Hamshere
    C Milham
    E Hopkin
    K Pound
    S Fernando
    A Grierson
    M Easton
    N Williams
    M Van Den Bree
    R Chowdhury
    J Gruen
    J Stevenson
    M Krawczak
    M J Owen
    M C O'Donovan
    J Williams
    Molecular Psychiatry, 2003, 8 : 176 - 185
  • [35] Linkage disequilibrium mapping provides further evidence for a gene for reading disability on chromosome 6p21.3-22
    Williams, J
    Turic, D
    Robinson, L
    Duke, M
    Morris, DW
    Webb, V
    Hamshere, M
    Grierson, A
    Williams, N
    Van Den Bree, M
    Chowdhury, R
    McGuffin, P
    Stevenson, J
    Krawczak, M
    Owen, MJ
    O'Donovan, MC
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (07): : 725 - 725
  • [36] Linkage disequilibrium mapping provides further evidence for a gene for reading disability on chromosome 6P21.3-22.
    O'Donovan, MC
    Turic, D
    Robinson, L
    Duke, M
    Morris, DW
    Webb, V
    Hamshere, M
    Grierson, A
    Williams, N
    Van den Bree, M
    Chowdhury, R
    McGuffin, R
    Stevenson, J
    Krawczak, M
    Owen, MJ
    Williams, J
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 497 - 497
  • [37] Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22
    van den Bree, M
    Robinson, L
    Turic, D
    Duke, M
    Morris, DW
    Hamshere, M
    Grierson, A
    Easton, M
    Raha-Chowdhury, R
    Gruen, J
    Stevenson, J
    Krawczak, M
    Owen, MJ
    O'Donovan, MC
    Williams, J
    BEHAVIOR GENETICS, 2003, 33 (06) : 722 - 722
  • [38] Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: Tentative association between B37 and schizophrenia
    MorrisRosendahl, DJ
    Burgert, E
    Uyanik, G
    Mayerova, A
    Duval, F
    Macher, JP
    Crocq, MA
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 74 (03): : 324 - 330
  • [39] No evidence for linkage of chromosome 6p markers to schizophrenia in Southern African Bantu-speaking families
    Riley, BP
    Rajagopalan, S
    MogudiCarter, M
    Jenkins, T
    Williamson, R
    PSYCHIATRIC GENETICS, 1996, 6 (02) : 41 - 49
  • [40] Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p
    Jodice, C
    Mantuano, E
    Veneziano, L
    Trettel, F
    Sabbadini, G
    Calandriello, L
    Francia, A
    Spadaro, M
    Pierelli, F
    Salvi, F
    Ophoff, RA
    Frants, RR
    Frontali, M
    HUMAN MOLECULAR GENETICS, 1997, 6 (11) : 1973 - 1978
12345