Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment

被引：0
|
作者：
Carayol, J. [1 ]
Philippi, A. [1 ]
Tores, F. [1 ]
机构：
[1] Integragen, Evry, France
来源：
GENETIC EPIDEMIOLOGY | 2007年 / 31卷 / 05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：465 / 465
页数：1
相关论文
共 6 条
  • [1] Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment
    Carayol, J.
    Philippi, A.
    Tores, F.
    GENETIC EPIDEMIOLOGY, 2006, 30 (08) : 666 - 676
  • [2] Estimating haplotype effects on dichotomous outcome for unphased genotype data using a weighted penalized log-likelihood approach
    Souverein, OW
    Zwinderman, AH
    Tanck, MWT
    HUMAN HEREDITY, 2006, 61 (02) : 104 - 110
  • [3] Estimating penetrance from family data using a retrospective likelihood when ascertainment depends on genotype and age of onset
    Carayol, J
    Bonaïti-Pellié, C
    GENETIC EPIDEMIOLOGY, 2004, 27 (02) : 109 - 117
  • [4] Estimating Model-Adjusted Risks, Risk Differences, and Risk Ratios From Complex Survey Data
    Bieler, Gayle S.
    Brown, G. Gordon
    Williams, Rick L.
    Brogan, Donna J.
    AMERICAN JOURNAL OF EPIDEMIOLOGY, 2010, 171 (05) : 618 - 623
  • [5] Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the multiethnic cohort study
    Stram, DO
    Haiman, CA
    Hirschhorn, JN
    Altshuler, D
    Kolonel, LN
    Henderson, BE
    Pike, MC
    HUMAN HEREDITY, 2003, 55 (01) : 27 - 36
  • [6] Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data
    Aldi T Kraja
    Jacek Czajkowski
    Mary F Feitosa
    Ingrid B Borecki
    Michael A Province
    BMC Proceedings, 5 (Suppl 9)
1