Detalhe da pesquisa
1.
Association of rare, recurrent nonsynonymous variants in the germline of prostate cancer patients of African ancestry.
Prostate
; 83(5): 454-461, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36567534
2.
Association of sickle cell trait with adverse pregnancy outcomes in a population-based cohort.
Acta Obstet Gynecol Scand
; 102(8): 1100-1105, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37358249
3.
Calibration of polygenic risk scores is required prior to clinical implementation: results of three common cancers in UKB.
J Med Genet
; 59(3): 243-247, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33443076
4.
Cystic fibrosis F508del carriers and cancer risk: Results from the UK Biobank.
Int J Cancer
; 148(7): 1658-1664, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33300603
5.
Observed evidence for guideline-recommended genes in predicting prostate cancer risk from a large population-based cohort.
Prostate
; 81(13): 1002-1008, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34254341
6.
Association of prostate cancer polygenic risk score with number and laterality of tumor cores in active surveillance patients.
Prostate
; 81(10): 703-709, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33956350
7.
Somatic DNA copy number alterations in non-dysplastic Barrett's esophagus.
Surg Endosc
; 35(7): 3961-3970, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32749611
8.
Feasibility and performance of a novel probe panel to detect somatic DNA copy number alterations in clinical specimens for predicting prostate cancer progression.
Prostate
; 80(14): 1253-1262, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32803894
9.
Germline HOXB13 G84E mutation carriers and risk to twenty common types of cancer: results from the UK Biobank.
Br J Cancer
; 123(9): 1356-1359, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32830201
10.
Knowledge-based analyses reveal new candidate genes associated with risk of hepatitis B virus related hepatocellular carcinoma.
BMC Cancer
; 20(1): 403, 2020 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32393195
11.
Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility.
Int J Cancer
; 145(9): 2372-2382, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30714141
12.
A comprehensive evaluation of CHEK2 germline mutations in men with prostate cancer.
Prostate
; 78(8): 607-615, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29520813
13.
Reclassification of prostate cancer risk using sequentially identified SNPs: Results from the REDUCE trial.
Prostate
; 77(11): 1179-1186, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28670847
14.
Association between variants in genes involved in the immune response and prostate cancer risk in men randomized to the finasteride arm in the Prostate Cancer Prevention Trial.
Prostate
; 77(8): 908-919, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28317149
15.
Genetic variation in STAT4 predicts response to interferon-α therapy for hepatitis B e antigen-positive chronic hepatitis B.
Hepatology
; 63(4): 1102-11, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26704347
16.
Preimplantation genetic haplotyping for six Chinese pedigrees with thalassemia using a single nucleotide polymorphism microarray.
Prenat Diagn
; 37(5): 460-468, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28258706
17.
Adding genetic risk score to family history identifies twice as many high-risk men for prostate cancer: Results from the prostate cancer prevention trial.
Prostate
; 76(12): 1120-9, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27197965
18.
Key genes involved in the immune response are generally not associated with intraprostatic inflammation in men without a prostate cancer diagnosis: Results from the prostate cancer prevention trial.
Prostate
; 76(6): 565-74, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26771888
19.
Randomized trial finds that prostate cancer genetic risk score feedback targets prostate-specific antigen screening among at-risk men.
Cancer
; 122(22): 3564-3575, 2016 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27433786
20.
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
Hum Genet
; 135(8): 923-38, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27262462