PANOGA: a web server for identification of SNP-targeted pathways from genome-wide association study data

Identifying SNP targeted pathways in partial epilepsies with genome-wide association study data

(2013) B. Bakir-Gungor et al.   EPILEPSY RESEARCH

The Identification of Pathway Markers in Intracranial Aneurysm Using Genome-Wide Association Data from Two Different Populations

(2013) Burcu Bakir-Gungor et al.   PLoS One

Five Years of GWAS Discovery

(2012) Peter M. Visscher et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Network biology methods integrating biological data for translational science

(2012) G. Bebek et al.   BRIEFINGS IN BIOINFORMATICS

NEW: Network-Enabled Wisdom in Biology, Medicine, and Health Care

(2012) E. E. Schadt et al.   Science Translational Medicine

Experimental Designs for Robust Detection of Effects in Genome-Wide Case–Control Studies

(2011) Roderick D. Ball   GENETICS

A New Methodology to Associate SNPs with Human Diseases According to Their Pathway Related Context

(2011) Burcu Bakir-Gungor et al.   PLoS One

Uncovering the roles of rare variants in common disease through whole-genome sequencing

(2010) Elizabeth T. Cirulli et al.   NATURE REVIEWS GENETICS

SPOT: a web-based tool for using biological databases to prioritize SNPs after a genome-wide association study

(2010) S. F. Saccone et al.   NUCLEIC ACIDS RESEARCH

Gene and pathway-based second-wave analysis of genome-wide association studies

(2009) Gang Peng et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Functional annotations improve the predictive score of human disease-related mutations in proteins

(2009) Remo Calabrese et al.   HUMAN MUTATION