All Publications
Filters: Author is Keinan, Alon [Clear All Filters]
Crowdsourced genealogies and genomes.. Science (New York, N.Y.). .
360(6385):153-154 (2018)
Dietary adaptation of FADS genes in Europe varied across time and geography.. Nature ecology & evolution. .
1:167 (2017) 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
Explosive genetic evidence for explosive human population growth.. Current opinion in genetics & development. .
41:130-139 (2016) Abstract
The genetic history of Cochin Jews from India.. Human genetics. .
(2016) 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
Clustered mutations in hominid genome evolution are consistent with APOBEC3G enzymatic activity. Genome Research. .
(2016)
The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry.. PloS one. .
11(3):e0152056 (2016) Abstract
Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations.. Genome research. .
26(2):151-62 (2016) Abstract
Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome.. Journal of translational medicine. .
14(1):19 (2016) Abstract
X-inactivation informs variance-based testing for X-linked association of a quantitative trait. BMC Genomics. .
16:241 (2015)
Strong Constraint on Human Genes Escaping X-Inactivation Is Modulated by their Expression Level and Breadth in Both Sexes. Molecular Biology and Evolution. .
33(2):384-393 (2015) Abstract
XWAS: a toolset for genetic data analysis and association studies of the X chromosome. Journal of Heredity. .
106(5):6 (2015)
Biological Knowledge-Driven Analysis of Epistasis in Human GWAS with Application to Lipid Traits. Epistasis. .
1253:35-45 (2015) Abstract
Population Genomic Analysis of 962 Whole Genome Sequences of Humans Reveals Natural Selection in Non-Coding Regions. PLoS ONE. .
10:e0121644 (2015) Abstract
Principal component analysis characterizes shared pathogenetics from genome-wide association studies.. PLoS computational biology. .
10(9):e1003820 (2014) Abstract
Reply to Just et al.: Mitochondrial DNA heteroplasmy could be reliably detected with massively parallel sequencing technologies.. Proceedings of the National Academy of Sciences of the United States of America. .
111(43):E4548-50 (2014)
The utility of ancient human DNA for improving allele age estimates, with implications for demographic models and tests of natural selection.. Journal of human evolution. .
(2014) 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
Contrasting X-linked and autosomal diversity across 14 human populations.. American journal of human genetics. .
94(6):827-44 (2014) Abstract
Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals.. Proceedings of the National Academy of Sciences of the United States of America. .
(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
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