All Publications
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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
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
Demographic history and rare allele sharing among human populations.. Proceedings of the National Academy of Sciences of the United States of America. .
108(29):11983-8 (2011) Abstract
Dietary adaptation of FADS genes in Europe varied across time and geography.. Nature ecology & evolution. .
1:167 (2017) Abstract
The genetic history of Cochin Jews from India.. Human genetics. .
(2016) Abstract
The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry.. PloS one. .
11(3):e0152056 (2016) Abstract
The history of African gene flow into Southern Europeans, Levantines, and Jews. PLoS Genet.. .
7:e1001373 (2011) Abstract
Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations.. Genome research. .
26(2):151-62 (2016) 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
A map of human genome variation from population-scale sequencing.. Nature. .
467(7319):1061-73 (2010) Abstract
Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome.. Journal of translational medicine. .
14(1):19 (2016) 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 genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation. Am. J. Hum. Genet.. .
91:660–671 (2012) Abstract
Population Genomic Analysis of 962 Whole Genome Sequences of Humans Reveals Natural Selection in Non-Coding Regions. PLoS ONE. .
10:e0121644 (2015) Abstract
Positive Selection on a Regulatory Insertion-Deletion Polymorphism in FADS2 Influences Apparent Endogenous Synthesis of Arachidonic Acid.. Molecular Biology and Evolution. .
33(7):1726-39 (2016) Abstract
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
The variant call format and VCFtools.. Bioinformatics (Oxford, England). .
27(15):2156-8 (2011) Abstract
XWAS: a toolset for genetic data analysis and association studies of the X chromosome. Journal of Heredity. .
106(5):6 (2015)