相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Rare, Low-Frequency, and Common Variants in the Protein-Coding Sequence of Biological Candidate Genes from GWASs Contribute to Risk of Rheumatoid Arthritis
Dorothee Diogo et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
Wenqing Fu et al.
NATURE (2013)
Finding the sources of missing heritability in a yeast cross
Joshua S. Bloom et al.
NATURE (2013)
Neutrophil recruitment and function in health and inflammation
Elzbieta Kolaczkowska et al.
NATURE REVIEWS IMMUNOLOGY (2013)
Estimating Genetic Effects and Quantifying Missing Heritability Explained by Identified Rare-Variant Associations
Dajiang J. Liu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis
Catherine T. Jordan et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Seven newly identified loci for autoimmune thyroid disease
Jason D. Cooper et al.
HUMAN MOLECULAR GENETICS (2012)
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Luke Jostins et al.
NATURE (2012)
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
Eli A. Stahl et al.
NATURE GENETICS (2012)
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Lam C. Tsoi et al.
NATURE GENETICS (2012)
Rare and common variants: twenty arguments
Greg Gibson
NATURE REVIEWS GENETICS (2012)
Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase
Chaim O. Jacob et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
Jacob A. Tennessen et al.
SCIENCE (2012)
An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People
Matthew R. Nelson et al.
SCIENCE (2012)
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes
Daniel G. MacArthur et al.
SCIENCE (2012)
Btrim: A fast, lightweight adapter and quality trimming program for next-generation sequencing technologies
Yong Kong
GENOMICS (2011)
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Stephen Sawcer et al.
NATURE (2011)
Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease
Yukihide Momozawa et al.
NATURE GENETICS (2011)
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Gosia Trynka et al.
NATURE GENETICS (2011)
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
Manuel A. Rivas et al.
NATURE GENETICS (2011)
Estimation of effect size distribution from genome-wide association studies and implications for future discoveries
Ju-Hyun Park et al.
NATURE GENETICS (2010)
Common SNPs explain a large proportion of the heritability for human height
Jian Yang et al.
NATURE GENETICS (2010)
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
Amy Strange et al.
NATURE GENETICS (2010)
Deep resequencing reveals excess rare recent variants consistent with explosive population growth
Alex Coventry et al.
NATURE COMMUNICATIONS (2010)
Rare Variants Create Synthetic Genome-Wide Associations
Samuel P. Dickson et al.
PLOS BIOLOGY (2010)
Finding the missing heritability of complex diseases
Teri A. Manolio et al.
NATURE (2009)
Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource
Calliope A. Dendrou et al.
NATURE GENETICS (2009)
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
Jeffrey C. Barrett et al.
NATURE GENETICS (2009)
Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes
Sergey Nejentsev et al.
SCIENCE (2009)
CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease
S Lesage et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
分享论文
