Detalhe da pesquisa
1.
Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.
Am J Hum Genet
; 110(11): 1950-1958, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37883979
2.
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups.
Am J Hum Genet
; 106(5): 707-716, 2020 05 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32386537
3.
Conducting inclusive research in genetics for transgender, gender-diverse, and sex-diverse individuals: Case analyses and recommendations from a clinical genomics study.
J Genet Couns
; 2023 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37667436
4.
Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network.
Genet Med
; 24(6): 1297-1305, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35341654
5.
Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results.
Genet Med
; 24(10): 2123-2133, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35943490
6.
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.
Genet Med
; 24(5): 1130-1138, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35216901
7.
Do research participants share genomic screening results with family members?
J Genet Couns
; 31(2): 447-458, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34665896
8.
Framework for Implementing and Tracking a Molecular Tumor Board at a National Cancer Institute-Designated Comprehensive Cancer Center.
Oncologist
; 26(11): e1962-e1970, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34390291
9.
Neptune: an environment for the delivery of genomic medicine.
Genet Med
; 23(10): 1838-1846, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34257418
10.
NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 1.2021.
J Natl Compr Canc Netw
; 19(10): 1122-1132, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34666312
11.
Breast cancer screening implications of risk modeling among female relatives of ATM and CHEK2 carriers.
Cancer
; 126(8): 1651-1655, 2020 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31967672
12.
A Web-Based Tool to Automate Portions of Pretest Genetic Counseling for Inherited Cancer.
J Natl Compr Canc Netw
; 18(7): 841-847, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32634774
13.
Patients' willingness to reconsider cancer genetic testing after initially declining: Mention it again.
J Genet Couns
; 29(1): 18-24, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31553110
14.
The impact of variant classification on the clinical management of hereditary cancer syndromes.
Genet Med
; 21(2): 426-430, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29875428
15.
Physicians' perspectives on receiving unsolicited genomic results.
Genet Med
; 21(2): 311-318, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29904163
16.
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study.
Hered Cancer Clin Pract
; 17: 31, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31890059
17.
Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews.
Hered Cancer Clin Pract
; 16: 11, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29760830
18.
Subsequent breast and high grade serous carcinomas after risk-reducing salpingo-oophorectomy in BRCA mutation carriers and patients with history of breast cancer.
Ann Diagn Pathol
; 36: 28-30, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30055521
19.
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
20.
Identification and Management of TP53 Gene Carriers Detected Through Multigene Panel Testing.
South Med J
; 110(10): 643-648, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28973705