Analysis of the genetic architecture of susceptibility to cervical cancer indicates that common SNPs explain a large proportion of the heritability

Pathway analysis of cervical cancer genome-wide association study highlights the MHC region and pathways involved in response to infection

(2014) Dan Chen et al.   HUMAN MOLECULAR GENETICS

Acis-eQTL ofHLA-DRB1and a frameshift mutation ofMICAcontribute to the pattern of association of HLA alleles with cervical cancer

(2014) Dan Chen et al.   Cancer Medicine

Genome-wide Association Study of Susceptibility Loci for Cervical Cancer

(2013) Dan Chen et al.   JNCI-Journal of the National Cancer Institute

A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12

(2013) Yongyong Shi et al.   NATURE GENETICS

Estimating Missing Heritability for Disease from Genome-wide Association Studies

(2011) Sang Hong Lee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Worldwide burden of cervical cancer in 2008

(2011) M. Arbyn et al.   ANNALS OF ONCOLOGY

Genome partitioning of genetic variation for complex traits using common SNPs

(2011) Jian Yang et al.   NATURE GENETICS

GCTA: A Tool for Genome-wide Complex Trait Analysis

(2010) Jian Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Integrating common and rare genetic variation in diverse human populations

(2010)   NATURE

Analysing biological pathways in genome-wide association studies

(2010) Kai Wang et al.   NATURE REVIEWS GENETICS

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

(2008) A. D. Johnson et al.   BIOINFORMATICS

Heritability in the genomics era — concepts and misconceptions

(2008) Peter M. Visscher et al.   NATURE REVIEWS GENETICS