Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13

被引:0
|
作者
M N Ogdie
S C Bakker
S E Fisher
C Francks
M H Yang
R M Cantor
S K Loo
E van der Meulen
P Pearson
J Buitelaar
A Monaco
S F Nelson
R J Sinke
S L Smalley
机构
[1] UCLA,Department of Human Genetics
[2] University Medical Center,Department of Medical Genetics
[3] Wellcome Trust Centre for Human Genetics,Departments of Psychiatry and Biobehavioral Sciences
[4] Oxford University,Department of Child and Adolescent Psychiatry
[5] Center for Neurobehavioral Genetics,Department of Psychiatry
[6] UCLA,undefined
[7] UCLA,undefined
[8] University Medical Center,undefined
[9] University Medical Center,undefined
来源
Molecular Psychiatry | 2006年 / 11卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:5 / 8
页数:3
相关论文
共 32 条
  • [21] Identification of a Novel Risk Locus for Multiple Sclerosis at 13q31.3 by a Pooled Genome-Wide Scan of 500,000 Single Nucleotide Polymorphisms
    Comabella, Manuel
    Craig, David W.
    Camina-Tato, Montse
    Morcillo, Carlos
    Lopez, Cristina
    Navarro, Arcadi
    Rio, Jordi
    Montalban, Xavier
    Martin, Roland
    PLOS ONE, 2008, 3 (10):
  • [22] Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk
    Moskvina, V.
    Craddock, N.
    Holmans, P.
    Nikolov, I.
    Pahwa, J. S.
    Green, E.
    Owen, M. J.
    O'Donovan, M. C.
    MOLECULAR PSYCHIATRY, 2009, 14 (03) : 252 - 260
  • [23] Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk
    V Moskvina
    N Craddock
    P Holmans
    I Nikolov
    J S Pahwa
    E Green
    M J Owen
    M C O'Donovan
    Molecular Psychiatry, 2009, 14 : 252 - 260
  • [25] Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1
    McMahon, Francis J.
    Akula, Nirmala
    Schulze, Thomas G.
    Muglia, Pierandrea
    Tozzi, Federica
    Detera-Wadleigh, Sevilla D.
    Steele, C. J. M.
    Breuer, Rene
    Strohmaier, Jana
    Wendland, Jens R.
    Mattheisen, Manuel
    Muehleisen, Thomas W.
    Maier, Wolfgang
    Noethen, Markus M.
    Cichon, Sven
    Farmer, Anne
    Vincent, John B.
    Holsboer, Florian
    Preisig, Martin
    Rietschel, Marcella
    NATURE GENETICS, 2010, 42 (02) : 128 - U52
  • [27] Genome-wide copy-number variation analysis identifies common genetic variants at 20p13 associated with aggressiveness of prostate cancer
    Jin, Guangfu
    Sun, Jishan
    Liu, Wennuan
    Zhang, Zheng
    Chu, Lisa W.
    Kim, Seong-Tae
    Sun, Jielin
    Feng, Junjie
    Duggan, David
    Carpten, John D.
    Wiklund, Fredrik
    Gronberg, Henrik
    Isaacs, William B.
    Zheng, S. Lilly
    Xu, Jianfeng
    CARCINOGENESIS, 2011, 32 (07) : 1057 - 1062
  • [28] Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13
    Teltsh, Omri
    Kanyas, Kyra
    Karni, Osnat
    Levi, Adi
    Korner, Mira
    Ben-Asher, Edna
    Lancet, Doron
    Hamdan, Adnan
    Lerer, Bernard
    Kohn, Yoav
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2008, 147B (02) : 209 - 215
  • [29] Genome-wide model-based and model-free linkage analyses co-localize a novel genetic locus on chromosome 9p for familial restless legs syndrome
    Chen, SH
    Ondo, WG
    Rao, SQ
    Li, L
    Wang, Q
    NEUROLOGY, 2004, 62 (07) : A4 - A5
  • [30] Fine-scale mapping at IGAD1 and genome-wide genetic linkage analysis implicate HLA-DQ/DR as a major susceptibility locus in selective IgA deficiency and common variable immunodeficiency
    Kralovicova, J
    Hammarström, L
    Plebani, A
    Webster, ADB
    Vorechovsky, I
    JOURNAL OF IMMUNOLOGY, 2003, 170 (05): : 2765 - 2775