Detalhe da pesquisa
1.
Risk SNP-Mediated Promoter-Enhancer Switching Drives Prostate Cancer through lncRNA PCAT19.
Cell
; 174(3): 564-575.e18, 2018 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30033362
2.
Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry.
Am J Hum Genet
; 110(7): 1200-1206, 2023 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37311464
3.
Molecular Characteristics of Early-Onset Colorectal Cancer According to Detailed Anatomical Locations: Comparison With Later-Onset Cases.
Am J Gastroenterol
; 118(4): 712-726, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36707929
4.
Antibodies to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in All of Us Research Program Participants, 2 January to 18 March 2020.
Clin Infect Dis
; 74(4): 584-590, 2022 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34128970
5.
Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases.
Int J Cancer
; 151(3): 348-360, 2022 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35383926
6.
Familial recurrence risk with varying amount of family history.
Genet Epidemiol
; 43(4): 440-448, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30740785
7.
Potential impact of family history-based screening guidelines on the detection of early-onset colorectal cancer.
Cancer
; 126(13): 3013-3020, 2020 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32307706
8.
Returning genomic results in a Federally Qualified Health Center: the intersection of precision medicine and social determinants of health.
Genet Med
; 22(9): 1552-1559, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32371921
9.
Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome.
Br J Cancer
; 121(10): 869-876, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31551580
10.
Biallelic BRCA2 Mutations Shape the Somatic Mutational Landscape of Aggressive Prostate Tumors.
Am J Hum Genet
; 98(5): 818-829, 2016 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27087322
11.
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Am J Hum Genet
; 99(4): 877-885, 2016 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27666373
12.
AA9int: SNP interaction pattern search using non-hierarchical additive model set.
Bioinformatics
; 34(24): 4141-4150, 2018 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29878078
13.
Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer.
PLoS Genet
; 12(10): e1006296, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27723779
14.
gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels.
Genet Epidemiol
; 41(4): 297-308, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28211093
15.
Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array.
Br J Cancer
; 118(6): e9, 2018 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29438362
16.
Comprehensively evaluating cis-regulatory variation in the human prostate transcriptome by using gene-level allele-specific expression.
Am J Hum Genet
; 96(6): 869-82, 2015 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25983244
17.
DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome.
Mod Pathol
; 31(10): 1608-1618, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29884888
18.
FIRE: functional inference of genetic variants that regulate gene expression.
Bioinformatics
; 33(24): 3895-3901, 2017 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28961785
19.
SNP interaction pattern identifier (SIPI): an intensive search for SNP-SNP interaction patterns.
Bioinformatics
; 33(6): 822-833, 2017 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28039167
20.
Germline miRNA DNA variants and the risk of colorectal cancer by subtype.
Genes Chromosomes Cancer
; 56(3): 177-184, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27636879