All Publications
A map of human genome variation from population-scale sequencing.. Nature. .
467(7319):1061-73 (2010) Abstract
An integrated map of genetic variation from 1,092 human genomes.. Nature. .
491(7422):56-65 (2012) Abstract
Integrating common and rare genetic variation in diverse human populations. Nature. .
467:52–58 (2010) Abstract
NRE: a tool for exploring neutral loci in the human genome. BMC Bioinformatics. .
13(1):301 (2012) Abstract
Genome-wide inference of natural selection on human transcription factor binding sites. Nat. Genet.. .
45:723–729 (2013) Abstract
Contrasting X-linked and autosomal diversity across 14 human populations.. American journal of human genetics. .
94(6):827-44 (2014) Abstract
Combining evidence of natural selection with association analysis increases power to detect malaria-resistance variants. Am. J. Hum. Genet.. .
81:234–242 (2007) Abstract
Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome.. Journal of translational medicine. .
14(1):19 (2016) Abstract
Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation. PLoS Comput. Biol.. .
8:e1002600 (2012) Abstract
Accounting for eXentricities: Analysis of the X Chromosome in GWAS Reveals X-Linked Genes Implicated in Autoimmune Diseases.. PloS one. .
9(12):e113684 (2014) Abstract
Principal component analysis characterizes shared pathogenetics from genome-wide association studies.. PLoS computational biology. .
10(9):e1003820 (2014) Abstract
Association between rs2294020 in X-linked CCDC22 and susceptibility to autoimmune diseases with focus on systemic lupus erythematosus.. Immunology letters. .
181:58-62 (2017) Abstract
The variant call format and VCFtools.. Bioinformatics (Oxford, England). .
27(15):2156-8 (2011) Abstract
Neurocontroller analysis via evolutionary network minimization. Artif. Life. .
12:435–448 (2006) Abstract
Evolutionary network minimization: Adaptive implicit pruning of successful agents. Advances in Artificial Life. .
:319–327 (2003) Abstract
Explosive genetic evidence for explosive human population growth.. Current opinion in genetics & development. .
41:130-139 (2016) Abstract
High burden of private mutations due to explosive human population growth and purifying selection. BMC Genomics. .
15(Suppl 4)(S3) (2014) Abstract
XWAS: a toolset for genetic data analysis and association studies of the X chromosome. Journal of Heredity. .
106(5):6 (2015)
Rare LPL gene variants attenuate triglyceride reduction and HDL cholesterol increase in response to fenofibric acid therapy in individuals with mixed dyslipidemia.. Atherosclerosis. .
234(2):249-253 (2014) Abstract
Neutral genomic regions refine models of recent rapid human population growth.. Proceedings of the National Academy of Sciences of the United States of America. .
111(2):757-62 (2014) Abstract
Population growth inflates the per-individual number of deleterious mutations and reduces their mean effect.. Genetics. .
195(3):969-78 (2013) Abstract
Analyses of X-linked and autosomal genetic variation in population-scale whole genome sequencing. Nat. Genet.. .
43:741–743 (2011) Abstract