Search details
1.
Novel breast cancer susceptibility loci under linkage peaks identified in African ancestry consortia.
Hum Mol Genet
; 33(8): 687-697, 2024 Apr 08.
Article
in English
| 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.
Article
in English
| 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.
Article
in English
| 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.
Article
in English
| 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.
Article
in English
| MEDLINE | ID: mdl-34151536
6.
A role for the MEGF6 gene in predisposition to osteoporosis.
Ann Hum Genet
; 85(2): 58-72, 2021 03.
Article
in English
| 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.
Article
in English
| MEDLINE | ID: mdl-32663566
8.
Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants.
Neurobiol Dis
; 143: 104972, 2020 09.
Article
in English
| 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.
Article
in English
| MEDLINE | ID: mdl-27666373
10.
A genealogical assessment of familial clustering of anorectal malformations.
J Hum Genet
; 63(10): 1029-1034, 2018 Oct.
Article
in English
| MEDLINE | ID: mdl-29980720
11.
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.
Article
in English
| MEDLINE | ID: mdl-27262462
12.
Identification of a genetic variant associated with rotator cuff repair healing.
J Shoulder Elbow Surg
; 25(6): 865-72, 2016 Jun.
Article
in English
| MEDLINE | ID: mdl-27066960
13.
Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms.
J Shoulder Elbow Surg
; 25(2): 174-9, 2016 Feb.
Article
in English
| MEDLINE | ID: mdl-26350878
14.
Prostate cancer risk prediction based on complete prostate cancer family history.
Prostate
; 75(4): 390-8, 2015 Mar 01.
Article
in English
| MEDLINE | ID: mdl-25408531
15.
A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis.
Clin Genet
; 97(6): 943-944, 2020 06.
Article
in English
| MEDLINE | ID: mdl-32424863
16.
Significant association of full-thickness rotator cuff tears and estrogen-related receptor-ß (ESRRB).
J Shoulder Elbow Surg
; 24(2): e31-5, 2015 Feb.
Article
in English
| MEDLINE | ID: mdl-25219474
17.
Identification of specific Y chromosomes associated with increased prostate cancer risk.
Prostate
; 74(9): 991-8, 2014 Jun.
Article
in English
| MEDLINE | ID: mdl-24796687
18.
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.
Article
in English
| MEDLINE | ID: mdl-24162621
19.
Genetic risk and likelihood of prostate cancer detection on first biopsy by ancestry.
J Natl Cancer Inst
; 116(5): 753-757, 2024 May 08.
Article
in English
| MEDLINE | ID: mdl-38212986
20.
Adrenal-Permissive Germline HSD3B1 Allele and Prostate Cancer Outcomes.
JAMA Netw Open
; 7(3): e242976, 2024 Mar 04.
Article
in English
| MEDLINE | ID: mdl-38506808