Detalhe da pesquisa
1.
Monkeypox in Montréal: Epidemiology, Phylogenomics, and Public Health Response to a Large North American Outbreak.
Ann Intern Med
; 176(1): 67-76, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36508736
2.
Noncatalytic PTEN missense mutation predisposes to organ-selective cancer development in vivo.
Genes Dev
; 29(16): 1707-20, 2015 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26302789
3.
Clinical Considerations in the Selection of Preexposure Prophylaxis for HIV Prevention in Canada.
Can J Infect Dis Med Microbiol
; 2022: 3913439, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36081603
4.
Concurrent germline BRCA1, BRCA2, and CHEK2 pathogenic variants in hereditary breast cancer: a case series.
Breast Cancer Res Treat
; 186(2): 569-575, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33507482
5.
How Have Multigene Panels Changed the Clinical Practice of Genetic Counseling and Testing.
J Natl Compr Canc Netw
; 19(1): 103-108, 2021 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33406496
6.
Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma.
Ophthalmology
; 127(5): 668-678, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32081490
7.
Metastatic breast cancer patient perceptions of somatic tumor genomic testing.
BMC Cancer
; 20(1): 389, 2020 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32375690
8.
NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 1.2020.
J Natl Compr Canc Netw
; 18(4): 380-391, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32259785
9.
Germline large deletion of BAP1 and decreased expression in non-tumor choroid in uveal melanoma patients with high risk for inherited cancer.
Genes Chromosomes Cancer
; 58(9): 650-656, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30883995
10.
Current prostate cancer genetic testing capabilities and considerations.
Can J Urol
; 26(5 Suppl 2): 38-39, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31629427
11.
Analysis of the exome aggregation consortium (ExAC) database suggests that the BAP1-tumor predisposition syndrome is underreported in cancer patients.
Genes Chromosomes Cancer
; 57(9): 478-481, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29761599
12.
"Second-Class Status?" Insight into Communication Patterns and Common Concerns Among Men with Hereditary Breast and Ovarian Cancer Syndrome.
J Genet Couns
; 27(4): 885-893, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29404823
13.
Germline BAP1 alterations in familial uveal melanoma.
Genes Chromosomes Cancer
; 56(2): 168-174, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27718540
14.
NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.
J Natl Compr Canc Netw
; 15(1): 9-20, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28040716
15.
PTEN is a negative regulator of NK cell cytolytic function.
J Immunol
; 194(4): 1832-40, 2015 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25595786
16.
Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
J Natl Compr Canc Netw
; 14(2): 153-62, 2016 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26850485
17.
Risk factors for anthracycline-associated cardiotoxicity.
Support Care Cancer
; 24(5): 2173-2180, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26563179
18.
Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases.
Genes Chromosomes Cancer
; 53(2): 177-82, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24243779
19.
MIF promoter polymorphisms are associated with epiretinal membrane but not retinal detachment with PVR in an american population.
Exp Eye Res
; 185: 107667, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31108057
20.
Gene panel testing for inherited cancer risk.
J Natl Compr Canc Netw
; 12(9): 1339-46, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25190699