Estimating founder contributions in an isolated population.

被引:0
|
作者
Nolan, DK
Cox, N
Ober, C
机构
[1] Univ Chicago, Comm Genet, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Med, Chicago, IL 60637 USA
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
257
引用
收藏
页码:227 / 227
页数:1
相关论文
共 50 条
  • [21] Gene finding for Parkinson's disease in a genetically isolated population.
    Heutink, P
    Dekker, MCJ
    Bonifati, V
    Houwing-Duistermaat, JJ
    Sandkuijl, LA
    van Swieten, JC
    Oostra, BA
    van Duijn, CM
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 199 - 199
  • [22] Recurring pathogenic variants in the BRCA2 gene in the Ethiopian Jewish population. Founder mutations?
    Ludman, Mark D.
    Philipsborn, Shira Litz
    Hartmajer, Shulamit
    Shwartzman, Nitzan Sharon
    Reinstein, Eyal
    FAMILIAL CANCER, 2022, 21 (02) : 121 - 123
  • [23] Population.
    不详
    LANCET, 1925, 1 : 1090 - 1090
  • [24] Recurring pathogenic variants in the BRCA2 gene in the Ethiopian Jewish population. Founder mutations?
    Mark D. Ludman
    Shira Litz Philipsborn
    Shulamit Hartmajer
    Nitzan Sharon Shwartzman
    Eyal Reinstein
    Familial Cancer, 2022, 21 : 121 - 123
  • [25] Founder effect, ancestral haplotype, and predisposing chromosome of spinocerebellar ataxia type 6 in the Japanese population.
    Yabe, I
    Sasaki, H
    Yamashita, I
    Takada, A
    Hamada, T
    Tashiro, K
    Suzuki, Y
    Kida, H
    Takiyama, Y
    Nishizawa, M
    Hokezu, Y
    Nagamatsu, K
    Oda, T
    Ohnishi, A
    Inoue, I
    Hata, A
    ANNALS OF NEUROLOGY, 1999, 46 (03) : 480 - 480
  • [26] Genotype and phenotype studies in autosomal dominant retinitis pigmentosa (adRP) of the French Canadian founder population.
    Coussa, Razek Georges
    Chakarova, Christina
    Ajlan, Radwan
    Kavalec, Conrad
    Khan, Aysha
    Lopez, Irma
    Ren, Huanan
    Waseem, Naushin
    Bhattacharya, Shomi S.
    Koenekoop, Robert K.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2014, 55 (13)
  • [27] Estimating the divergence of founder mutations in cancer susceptibility variants found in the Japanese population
    Nakamura, Wataru
    Hirata, Makoto
    Oda, Satoyo
    Sugawa, Masahiro
    Mateos, Raul N.
    Chiba, Kenichi
    Okada, Ai
    Sakamoto, Yoshitaka
    Sakamoto, Hiromi
    Shiraishi, Kouya
    Kohno, Takashi
    Yoshida, Teruhiko
    Shiraishi, Yuichi
    CANCER SCIENCE, 2025, 116 : 218 - 218
  • [28] Heritability and common genetic variants in electrocardiographic traits in an isolated founder population
    Smith, J. G.
    Lowe, J. K.
    Kovvali, S.
    Maller, J.
    Daly, M. J.
    Stoffel, M.
    Altshuler, D. M.
    Friedman, J. M.
    Breslow, J. L.
    Newton-Cheh, C.
    EUROPEAN HEART JOURNAL, 2008, 29 : 161 - 162
  • [29] Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia
    Marrosu, MG
    Murru, R
    Murru, MR
    Costa, G
    Zavattari, P
    Whalen, M
    Cocco, E
    Mancosu, C
    Schirru, L
    Solla, E
    Fadda, E
    Melis, C
    Porru, I
    Rolesu, M
    Cucca, F
    HUMAN MOLECULAR GENETICS, 2001, 10 (25) : 2907 - 2916
  • [30] Genome-wide screen for quantitative trait loci (QTLs) influencing lipid levels in a founder population.
    Newman, DL
    McPeek, MS
    Abney, M
    Dytch, H
    Scanu, AM
    Parry, R
    Ober, C
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 324 - 324