Detalhe da pesquisa
1.
Comprehensive evaluation and efficient classification of BRCA1 RING domain missense substitutions.
Am J Hum Genet
; 109(6): 1153-1174, 2022 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35659930
2.
Effectiveness of Contact Precautions to Prevent Transmission of Methicillin-Resistant Staphylococcus aureus and Vancomycin-Resistant Enterococci in Intensive Care Units.
Clin Infect Dis
; 72(Suppl 1): S42-S49, 2021 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33512528
3.
Transmission Dynamics of Clostridioides difficile in 2 High-Acuity Hospital Units.
Clin Infect Dis
; 72(Suppl 1): S1-S7, 2021 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33512524
4.
Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.
PLoS Genet
; 14(2): e1007111, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29389935
5.
Peri-implantation intercourse does not lower fecundability.
Hum Reprod
; 35(9): 2107-2112, 2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32756956
6.
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
7.
Baseline Ability Makes a Larger Contribution to Race Performance in High-School Sprinters Than Race Experience or Training Exposure.
Pediatr Exerc Sci
; 28(4): 565-571, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27362890
8.
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
9.
Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions.
Hum Mutat
; 34(1): 255-65, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22949387
10.
Pathways analysis of differential gene expression induced by engrafting doses of total body irradiation for allogeneic bone marrow transplantation in mice.
Immunogenetics
; 65(8): 597-607, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23703256
11.
Fine mapping of the Bmgr5 quantitative trait locus for allogeneic bone marrow engraftment in mice.
Immunogenetics
; 65(8): 585-96, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23666360
12.
Creation of a national resource with linked genealogy and phenotypic data: the Veterans Genealogy Project.
Genet Med
; 15(7): 541-7, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23328892
13.
Random allelic expression in the adult human body.
Cell Rep
; 42(1): 111945, 2023 01 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36640362
14.
Germline EGFR Mutations and Familial Lung Cancer.
J Clin Oncol
; 41(34): 5274-5284, 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37579253
15.
Effect of linkage disequilibrium on the identification of functional variants.
Genet Epidemiol
; 35 Suppl 1: S115-9, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22128051
16.
Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees.
BMC Genomics
; 13: 676, 2012 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-23190577
17.
Shared genomic segment analysis: the power to find rare disease variants.
Ann Hum Genet
; 76(6): 500-9, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22989048
18.
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.
Hum Genet
; 131(1): 77-85, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21706340
19.
Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer.
Am J Hum Genet
; 85(4): 427-46, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19781682
20.
Automated construction and testing of multi-locus gene-gene associations.
Bioinformatics
; 27(1): 134-6, 2011 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21076150