Detalhe da pesquisa
1.
Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging.
Proc Natl Acad Sci U S A
; 117(6): 3053-3062, 2020 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31980526
2.
Longitudinal follow-up after telephone disclosure in the randomized COGENT study.
Genet Med
; 22(8): 1401-1406, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32376981
3.
Preferences for in-person disclosure: Patients declining telephone disclosure characteristics and outcomes in the multicenter Communication Of GENetic Test Results by Telephone study.
Clin Genet
; 95(2): 293-301, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30417332
4.
Experience Gained from the Development and Execution of a Multidisciplinary Multi-syndrome Hereditary Colon Cancer Family Conference.
J Cancer Educ
; 34(6): 1204-1212, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30259397
5.
Somatic TP53 variants frequently confound germ-line testing results.
Genet Med
; 20(8): 809-816, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29189820
6.
Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility.
Genet Med
; 17(6): 485-92, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25297947
7.
Direct-to-patient disclosure of results of mismatch repair screening for Lynch syndrome via electronic personal health record: a feasibility study.
Genet Med
; 16(11): 854-61, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24784156
8.
Cost sharing and hereditary cancer risk: predictors of willingness-to-pay for genetic testing.
J Genet Couns
; 23(6): 1002-11, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24794065
9.
Interpretation of genetic testing for lynch syndrome in patients with putative familial colorectal cancer.
J Natl Compr Canc Netw
; 9(11): 1311-20, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22056658
10.
The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.
Fam Cancer
; 17(2): 235-245, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28687971
11.
Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry.
J Natl Cancer Inst
; 110(10): 1059-1066, 2018 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29618041
12.
Use and Patient-Reported Outcomes of Clinical Multigene Panel Testing for Cancer Susceptibility in the Multicenter Communication of Genetic Test Results by Telephone Study.
JCO Precis Oncol
; 22018.
Artigo
em Inglês
| MEDLINE | ID: mdl-31819920
13.
Randomized Noninferiority Trial of Telephone vs In-Person Disclosure of Germline Cancer Genetic Test Results.
J Natl Cancer Inst
; 110(9): 985-993, 2018 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29490071
14.
Genetic Gastric Cancer Susceptibility in the International Clinical Cancer Genomics Community Research Network.
Cancer Genet
; 216-217: 111-119, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29025585
15.
Corrigendum: Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management.
Front Oncol
; 5: 271, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26697406
16.
Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management.
Front Oncol
; 5: 208, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26484312
17.
Bilateral granulosa cell tumors: a novel malignant manifestation of multiple endocrine neoplasia 1 syndrome found in a patient with a rare menin in-frame deletion.
Appl Clin Genet
; 8: 69-73, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25733923
18.
Development of a communication protocol for telephone disclosure of genetic test results for cancer predisposition.
JMIR Res Protoc
; 3(4): e49, 2014 Oct 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-25355401
19.
Implementation and outcomes of telephone disclosure of clinical BRCA1/2 test results.
Patient Educ Couns
; 93(3): 413-9, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24075727
20.
Thirty-nine-year-old with familial colon cancer, and variant of undetermined significance in MSH6.
Semin Oncol
; 39(2): 125-31, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22484182