Natural and orthogonal model for estimating gene–gene interactions applied to cutaneous melanoma

A Unified Framework Integrating Parent-of-Origin Effects for Association Study

(2013) Feifei Xiao et al.   PLoS One

Cancer statistics, 2012

(2012) Rebecca Siegel et al.   CA-A CANCER JOURNAL FOR CLINICIANS

Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility

(2012) Mario Capasso et al.   CARCINOGENESIS

Multivariate Detection of Gene-Gene Interactions

(2012) Indika Rajapakse et al.   GENETIC EPIDEMIOLOGY

HERC2 rs12913832 modulates human pigmentation by attenuating chromatin-loop formation between a long-range enhancer and the OCA2 promoter

(2012) M. Visser et al.   GENOME RESEARCH

Natural and Orthogonal Interaction Framework for Modeling Gene-Environment Interactions with Application to Lung Cancer

(2012) Jianzhong Ma et al.   HUMAN HEREDITY

Genome-wide association study identifies novel loci predisposing to cutaneous melanoma†

(2011) Christopher I. Amos et al.   HUMAN MOLECULAR GENETICS

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

(2011) Georg B. Ehret et al.   NATURE

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

(2010)   NATURE

Genome-wide association study identifies three loci associated with melanoma risk

(2009) D Timothy Bishop et al.   NATURE GENETICS

Detecting gene–gene interactions that underlie human diseases

(2009) Heather J Cordell   NATURE REVIEWS GENETICS

A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color

(2008) Richard A. Sturm et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A method for detecting epistasis in genome-wide studies using case-control multi-locus association analysis

(2008) Javier Gayán et al.   BMC GENOMICS

How To Perform Meaningful Estimates of Genetic Effects

(2008) José M. Álvarez-Castro et al.   PLoS Genetics