Detalhe da pesquisa
1.
Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations.
medRxiv;
2023 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37333246
2.
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med;
25(4): 100006, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36621880
3.
The evolution of drug resistance in clinical isolates of Candida albicans.
Elife;
4: e00662, 2015 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25646566
4.
The influence of rare genetic variation in SLC30A8 on diabetes incidence and ß-cell function.
J Clin Endocrinol Metab;
99(5): E926-30, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24471563
5.
Punctuated evolution of prostate cancer genomes.
Cell;
153(3): 666-77, 2013 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-23622249
6.
Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity.
Nat Genet;
45(5): 478-86, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23525077
7.
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis.
Am J Hum Genet;
92(1): 15-27, 2013 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23261300
8.
Personalized genetic risk counseling to motivate diabetes prevention: a randomized trial.
Diabetes Care;
36(1): 13-9, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22933432
9.
New susceptibility loci associated with kidney disease in type 1 diabetes.
PLoS Genet;
8(9): e1002921, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23028342
10.
Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathy.
Diabetes;
61(8): 2187-94, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22721967
11.
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.
Nat Genet;
44(6): 685-9, 2012 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-22610119
12.
The mutational landscape of head and neck squamous cell carcinoma.
Science;
333(6046): 1157-60, 2011 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-21798893
13.
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.
Nat Genet;
43(8): 801-5, 2011 Jul 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21775993
14.
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.
Nat Genet;
43(8): 753-60, 2011 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-21706003
15.
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.
Hum Genet;
130(5): 685-99, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21597964
16.
The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA.
Hum Genet;
130(5): 607-21, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21424828
17.
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.
PLoS Genet;
6(10): e1001183, 2010 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-21060860
18.
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.
Science;
330(6010): 1551-7, 2010 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21051598
19.
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses.
Lancet;
376(9750): 1393-400, 2010 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-20971364
20.
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia.
N Engl J Med;
363(23): 2220-7, 2010 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-20942659