Detalhe da pesquisa
1.
Clustered mutations in hominid genome evolution are consistent with APOBEC3G enzymatic activity.
Genome Res
; 26(5): 579-87, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27056836
2.
Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations.
Genome Res
; 26(2): 151-62, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26728717
3.
Strong Constraint on Human Genes Escaping X-Inactivation Is Modulated by their Expression Level and Breadth in Both Sexes.
Mol Biol Evol
; 33(2): 384-93, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26494842
4.
Positive Selection on a Regulatory Insertion-Deletion Polymorphism in FADS2 Influences Apparent Endogenous Synthesis of Arachidonic Acid.
Mol Biol Evol
; 33(7): 1726-39, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27188529
5.
Contrasting X-linked and autosomal diversity across 14 human populations.
Am J Hum Genet
; 94(6): 827-44, 2014 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24836452
6.
Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals.
Proc Natl Acad Sci U S A
; 111(29): 10654-9, 2014 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-25002485
7.
Neutral genomic regions refine models of recent rapid human population growth.
Proc Natl Acad Sci U S A
; 111(2): 757-62, 2014 Jan 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-24379384
8.
The genetic history of Cochin Jews from India.
Hum Genet
; 135(10): 1127-43, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27377974
9.
Association of mitochondrial DNA variants with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) symptoms.
J Transl Med
; 14(1): 342, 2016 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27998272
10.
Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome.
J Transl Med
; 14: 19, 2016 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-26791940
11.
Integrating common and rare genetic variation in diverse human populations.
Nature
; 467(7311): 52-8, 2010 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-20811451
12.
Gene-based testing of interactions in association studies of quantitative traits.
PLoS Genet
; 9(2): e1003321, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23468652
13.
X-inactivation informs variance-based testing for X-linked association of a quantitative trait.
BMC Genomics
; 16: 241, 2015 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-25880738
14.
Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation.
Am J Hum Genet
; 91(4): 660-71, 2012 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23040495
15.
The utility of ancient human DNA for improving allele age estimates, with implications for demographic models and tests of natural selection.
J Hum Evol
; 79: 64-72, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25467111
16.
Principal component analysis characterizes shared pathogenetics from genome-wide association studies.
PLoS Comput Biol
; 10(9): e1003820, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25211452
17.
XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome.
J Hered
; 106(5): 666-71, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26268243
18.
Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations.
PLoS Genet
; 8(5): e1002714, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22654671
19.
High burden of private mutations due to explosive human population growth and purifying selection.
BMC Genomics
; 15 Suppl 4: S3, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25056720
20.
The history of African gene flow into Southern Europeans, Levantines, and Jews.
PLoS Genet
; 7(4): e1001373, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21533020