Detalhe da pesquisa
1.
Challenges and approaches to calibrating patient phenotype as evidence for cancer gene variant classification under ACMG/AMP guidelines.
Hum Mol Genet
; 33(8): 724-732, 2024 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38271184
2.
Mutation prevalence tables for hereditary cancer derived from multigene panel testing.
Hum Mutat
; 41(8): e1-e6, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32442341
3.
Diagnosing hereditary cancer predisposition in men with prostate cancer.
Genet Med
; 22(9): 1517-1523, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32439974
4.
Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort.
Genet Med
; 22(4): 701-708, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31853058
5.
A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients.
Genet Med
; 22(2): 407-415, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31406321
6.
Family communication and patient distress after germline genetic testing in individuals with pancreatic ductal adenocarcinoma.
Cancer
; 125(14): 2488-2496, 2019 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30980401
7.
Genotype-phenotype associations among panel-based TP53+ subjects.
Genet Med
; 21(11): 2478-2484, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31105275
8.
Somatic TP53 variants frequently confound germ-line testing results.
Genet Med
; 20(8): 809-816, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29189820
9.
Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.
Breast Cancer Res Treat
; 161(3): 575-586, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28008555
10.
Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar.
Genet Med
; 19(10): 1096-1104, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28301460
11.
Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls.
Gynecol Oncol
; 147(2): 375-380, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28888541
12.
Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2.
Gynecol Oncol
; 137(1): 86-92, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25622547
13.
Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients.
Genet Med
; 16(11): 830-7, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24763289
14.
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations.
medRxiv
; 2023 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37609227
15.
Pretest Video Education Versus Genetic Counseling for Patients With Prostate Cancer: ProGen, A Multisite Randomized Controlled Trial.
JCO Oncol Pract
; 19(11): 1069-1079, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37733980
16.
Clinician-Reported Impact of Germline Multigene Panel Testing on Cancer Risk Management Recommendations.
JNCI Cancer Spectr
; 6(2)2022 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35603838
17.
Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer.
J Natl Cancer Inst
; 113(10): 1429-1433, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33146377
18.
Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast.
J Clin Oncol
; 39(35): 3918-3926, 2021 12 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34672684
19.
Risk of Late-Onset Breast Cancer in Genetically Predisposed Women.
J Clin Oncol
; 39(31): 3430-3440, 2021 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34292776
20.
The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort.
J Natl Cancer Inst
; 112(12): 1231-1241, 2020 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32091585