Detalhe da pesquisa
1.
HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis.
Cell
; 170(6): 1164-1174.e6, 2017 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28886384
2.
Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding.
Am J Hum Genet
; 110(3): 427-441, 2023 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36787739
3.
Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.
Am J Hum Genet
; 106(2): 264-271, 2020 02 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32004448
4.
Association of HPV35 with cervical carcinogenesis among women of African ancestry: Evidence of viral-host interaction with implications for disease intervention.
Int J Cancer
; 147(10): 2677-2686, 2020 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32363580
5.
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.
Hum Mol Genet
; 25(3): 620-9, 2016 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26732429
6.
Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes.
Hum Mol Genet
; 25(8): 1663-76, 2016 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27008888
7.
Combined somatic mutation and copy number analysis in the survival of familial CLL.
Br J Haematol
; 181(5): 604-613, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29687880
8.
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region.
Am J Hum Genet
; 95(4): 462-71, 2014 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25279986
9.
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.
Hum Genet
; 135(11): 1241-1249, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27449771
10.
Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families.
Blood
; 124(1): 24-32, 2014 Jul 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24829207
11.
Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene.
Haematologica
; 101(7): 853-60, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27365461
12.
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.
PLoS Genet
; 9(8): e1003695, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24009516
13.
Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never-smoking women in Asia: a report from the female lung cancer consortium in Asia.
Int J Cancer
; 137(2): 311-9, 2015 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25516442
14.
Dietary iron, iron homeostatic gene polymorphisms and the risk of advanced colorectal adenoma and cancer.
Carcinogenesis
; 35(6): 1276-83, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24536049
15.
Genetic variants in fas signaling pathway genes and risk of gastric cancer.
Int J Cancer
; 134(4): 822-31, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23921907
16.
Evolutionary dynamics of the human NADPH oxidase genes CYBB, CYBA, NCF2, and NCF4: functional implications.
Mol Biol Evol
; 30(9): 2157-67, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23821607
17.
Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer.
Hum Mol Genet
; 21(8): 1918-30, 2012 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22228101
18.
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma.
Hum Mol Genet
; 21(5): 1190-200, 2012 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22113997
19.
Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies.
Hum Mol Genet
; 21(9): 2132-41, 2012 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22323360
20.
Improved detection of low-frequency within-host variants from deep sequencing: A case study with human papillomavirus.
Virus Evol
; 10(1): veae013, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38455683