Detalhe da pesquisa
1.
Mapping copy number variation by population-scale genome sequencing.
Nature
; 470(7332): 59-65, 2011 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-21293372
2.
Genotype copy number variations using Gaussian mixture models: theory and algorithms.
Stat Appl Genet Mol Biol
; 11(5): 5, 2012 Oct 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-23079517
3.
Mild Plasmodium falciparum malaria following an episode of severe malaria is associated with induction of the interferon pathway in Malawian children.
Infect Immun
; 80(3): 1150-5, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22232187
4.
Blindly using Wald's test can miss rare disease-causal variants in case-control association studies.
Ann Hum Genet
; 76(2): 168-77, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22256951
5.
A comparison of approaches to control for confounding factors by regression models.
Hum Hered
; 72(3): 194-205, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22086357
6.
Resequencing of pooled DNA for detecting disease associations with rare variants.
Genet Epidemiol
; 34(5): 492-501, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20578089
7.
Enhancing the power to detect low-frequency variants in genome-wide screens.
Genetics
; 196(4): 1293-302, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24496013
8.
The effect of menu labeling with calories and exercise equivalents on food selection and consumption.
BMC Obes
; 1: 21, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-26217508
9.
The clinical significance of inflammatory cytokines in primary cell culture in endometrial carcinoma.
Mol Oncol
; 7(1): 41-54, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22944067