Detalhe da pesquisa
1.
Novel breast cancer susceptibility loci under linkage peaks identified in African ancestry consortia.
Hum Mol Genet
; 33(8): 687-697, 2024 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38263910
2.
Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibility.
Am J Hum Genet
; 110(7): 1138-1161, 2023 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37339630
3.
An extra X chromosome among adult women in the Million Veteran Program: A more benign perspective of trisomy X.
Am J Med Genet C Semin Med Genet
; : e32083, 2024 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38441278
4.
A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancer.
Int J Cancer
; 153(2): 364-372, 2023 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36916144
5.
Analysis of high-risk pedigrees identifies 11 candidate variants for Alzheimer's disease.
Alzheimers Dement
; 18(2): 307-317, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34151536
6.
A role for the MEGF6 gene in predisposition to osteoporosis.
Ann Hum Genet
; 85(2): 58-72, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33026655
7.
Genetic variants associated with rotator cuff tearing utilizing multiple population-based genetic resources.
J Shoulder Elbow Surg
; 30(3): 520-531, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32663566
8.
Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants.
Neurobiol Dis
; 143: 104972, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32574725
9.
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
10.
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
11.
A genealogical assessment of familial clustering of anorectal malformations.
J Hum Genet
; 63(10): 1029-1034, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29980720
12.
Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies.
Genet Epidemiol
; 40(6): 461-9, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27312771
13.
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
14.
Identification of a genetic variant associated with rotator cuff repair healing.
J Shoulder Elbow Surg
; 25(6): 865-72, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27066960
15.
Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms.
J Shoulder Elbow Surg
; 25(2): 174-9, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26350878
16.
Prostate cancer risk prediction based on complete prostate cancer family history.
Prostate
; 75(4): 390-8, 2015 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25408531
17.
A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis.
Clin Genet
; 97(6): 943-944, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32424863
18.
Significant association of full-thickness rotator cuff tears and estrogen-related receptor-ß (ESRRB).
J Shoulder Elbow Surg
; 24(2): e31-5, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25219474
19.
Identification of specific Y chromosomes associated with increased prostate cancer risk.
Prostate
; 74(9): 991-8, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24796687
20.
Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease.
Hum Genet
; 133(3): 347-56, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24162621