Detalhe da pesquisa
1.
Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations.
Am J Hum Genet
; 110(10): 1690-1703, 2023 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37673066
2.
Thirteen cancers associated with HIV infection in a Black South African cancer patient population (1995-2016).
Int J Cancer
; 152(2): 183-194, 2023 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36054877
3.
Kaposi sarcoma-associated herpesvirus, HIV-1 and Kaposi sarcoma risk in black South Africans diagnosed with cancer during antiretroviral treatment rollout.
Int J Cancer
; 152(10): 2081-2089, 2023 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36727526
4.
Usefulness of high-risk HPV early oncoprotein (E6 and E7) serological markers in the detection of cervical cancer: A systematic review and meta-analysis.
J Med Virol
; 95(1): e27900, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35641882
5.
Fine-mapping inflammatory bowel disease loci to single-variant resolution.
Nature
; 547(7662): 173-178, 2017 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-28658209
6.
The Health and Economic Burdens of Lymphatic Filariasis Prior to Mass Drug Administration Programs.
Clin Infect Dis
; 70(12): 2561-2567, 2020 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31343064
7.
Genetic and Inflammatory Biomarkers Classify Small Intestine Inflammation in Asymptomatic First-degree Relatives of Patients With Crohn's Disease.
Clin Gastroenterol Hepatol
; 18(4): 908-916.e13, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31202982
8.
Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population.
Carcinogenesis
; 40(4): 513-520, 2019 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30753320
9.
Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.
Am J Hum Genet
; 98(6): 1092-1100, 2016 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27236921
10.
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.
Nature
; 498(7453): 232-5, 2013 Jun 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-23698362
11.
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
PLoS Genet
; 11(2): e1004955, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25671699
12.
Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
BMC Med Genet
; 17: 26, 2016 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27037036
13.
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
Nat Genet
; 39(2): 207-11, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17200669
14.
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
Nat Genet
; 39(2): 162-4, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17200671
15.
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
Nat Genet
; 39(7): 830-2, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17554261
16.
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.
Am J Hum Genet
; 90(4): 636-47, 2012 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22482804
17.
Lamina propria macrophage phenotypes in relation to Escherichia coli in Crohn's disease.
BMC Gastroenterol
; 15: 75, 2015 Jul 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26137941
18.
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.
Gastroenterology
; 145(2): 339-47, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23624108
19.
Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4.
Hepatology
; 58(3): 1074-83, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22821403
20.
New links to the pathogenesis of Crohn disease provided by genome-wide association scans.
Nat Rev Genet
; 9(1): 9-14, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17968351