Detalhe da pesquisa
1.
Psychosocial outcomes following germline multigene panel testing in an ethnically and economically diverse cohort of patients.
Cancer
; 127(8): 1275-1285, 2021 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33320347
2.
Multigene assessment of genetic risk for women for two or more breast cancers.
Breast Cancer Res Treat
; 188(3): 759-768, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33826040
3.
Community Practice Implementation of a Self-administered Version of PREMM1,2,6 to Assess Risk for Lynch Syndrome.
Clin Gastroenterol Hepatol
; 16(1): 49-58, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28668538
4.
Impact of a genetic counseling requirement prior to genetic testing.
BMC Health Serv Res
; 18(1): 165, 2018 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29514700
5.
Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing.
JAMA
; 320(12): 1266-1274, 2018 09 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30264118
6.
A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes.
Cancer
; 123(10): 1721-1730, 2017 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28085182
7.
An independent validation of a gene expression signature to differentiate malignant melanoma from benign melanocytic nevi.
Cancer
; 123(4): 617-628, 2017 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27768230
8.
Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory.
Oncologist
; 22(7): 797-803, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28408614
9.
Phase II neoadjuvant clinical trial of carboplatin and eribulin in women with triple negative early-stage breast cancer (NCT01372579).
Breast Cancer Res Treat
; 151(3): 629-38, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26006067
10.
Lynch Syndrome Patients with Limited Family History Identified in a Laboratory Setting: A Descriptive Study.
Oncology
; 89(4): 221-6, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26393997
12.
Interpretation of BRCA2 Splicing Variants: A Case Series of Challenging Variant Interpretations and the Importance of Functional RNA Analysis.
Fam Cancer
; 21(1): 7-19, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33469799
13.
Combinatorial pharmacogenomic algorithm is predictive of sertraline metabolism in patients with major depressive disorder.
Psychiatry Res
; 308: 114354, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34986431
14.
Electrostatic induction of lipid asymmetry.
J Am Chem Soc
; 133(23): 8794-7, 2011 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21595482
15.
Precision medicine and companion diagnostics join the battle against ovarian cancer.
MLO Med Lab Obs
; 48(10): 36-37, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30047653
16.
Age of ovarian cancer diagnosis among BRIP1, RAD51C, and RAD51D mutation carriers identified through multi-gene panel testing.
J Ovarian Res
; 14(1): 61, 2021 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33926482
17.
Association of Family Cancer History With Pathogenic Variants in Specific Breast Cancer Susceptibility Genes.
JCO Precis Oncol
; 52021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34977446
18.
Clinical validation of combinatorial pharmacogenomic testing and single-gene guidelines in predicting psychotropic medication blood levels and clinical outcomes in patients with depression.
Psychiatry Res
; 296: 113649, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33360967
19.
Impact of a Cancer Gene Variant Reclassification Program Over a 20-Year Period.
JCO Precis Oncol
; 42020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32923914
20.
The clinical utility of combinatorial pharmacogenomic testing for patients with depression: a meta-analysis.
Pharmacogenomics
; 21(8): 559-569, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32301649