Search details
1.
The Human Tumor Atlas Network: Charting Tumor Transitions across Space and Time at Single-Cell Resolution.
Cell
; 181(2): 236-249, 2020 04 16.
Article
in English
| MEDLINE | ID: mdl-32302568
2.
Organization of the human intestine at single-cell resolution.
Nature
; 619(7970): 572-584, 2023 Jul.
Article
in English
| MEDLINE | ID: mdl-37468586
3.
Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network.
Am J Hum Genet
; 111(6): 999-1005, 2024 Jun 06.
Article
in English
| MEDLINE | ID: mdl-38688278
4.
Addressing underrepresentation in genomics research through community engagement.
Am J Hum Genet
; 109(9): 1563-1571, 2022 09 01.
Article
in English
| MEDLINE | ID: mdl-36055208
5.
Universal Germline-Genetic Testing for Breast Cancer: Implementation in a Rural Practice and Impact on Shared Decision-Making.
Ann Surg Oncol
; 31(1): 325-334, 2024 Jan.
Article
in English
| MEDLINE | ID: mdl-37814187
6.
Germline cancer susceptibility in individuals with melanoma.
J Am Acad Dermatol
; 2024 Mar 20.
Article
in English
| MEDLINE | ID: mdl-38513832
7.
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
; 25(4): 100006, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36621880
8.
Racial disparities in cascade testing for cancer predisposition genes.
Prev Med
; 172: 107539, 2023 07.
Article
in English
| MEDLINE | ID: mdl-37156429
9.
Germline Genetic Testing After Cancer Diagnosis.
JAMA
; 330(1): 43-51, 2023 07 03.
Article
in English
| MEDLINE | ID: mdl-37276540
10.
Fumarate hydratase variant prevalence and manifestations among individuals receiving germline testing.
Cancer
; 128(4): 675-684, 2022 02 15.
Article
in English
| MEDLINE | ID: mdl-34724198
11.
CDH1 germline variants are enriched in patients with colorectal cancer, gastric cancer, and breast cancer.
Br J Cancer
; 126(5): 797-803, 2022 03.
Article
in English
| MEDLINE | ID: mdl-34949788
12.
Cancer risks associated with heterozygous ATM loss of function and missense pathogenic variants based on multigene panel analysis.
Breast Cancer Res Treat
; 196(2): 355-361, 2022 Nov.
Article
in English
| MEDLINE | ID: mdl-36094610
13.
Unexpected actionable genetic variants revealed by multigene panel testing of patients with uterine cancer.
Gynecol Oncol
; 166(2): 344-350, 2022 08.
Article
in English
| MEDLINE | ID: mdl-35691755
14.
Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
J Genet Couns
; 31(4): 949-955, 2022 08.
Article
in English
| MEDLINE | ID: mdl-35218578
15.
Comprehensive Genetic Testing for Pediatric Hypertrophic Cardiomyopathy Reveals Clinical Management Opportunities and Syndromic Conditions.
Pediatr Cardiol
; 43(3): 616-623, 2022 Mar.
Article
in English
| MEDLINE | ID: mdl-34714385
16.
Democratizing genomics: Leveraging software to make genetics an integral part of routine care.
Am J Med Genet C Semin Med Genet
; 187(1): 14-27, 2021 03.
Article
in English
| MEDLINE | ID: mdl-33296144
17.
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
BMC Med
; 19(1): 199, 2021 08 18.
Article
in English
| MEDLINE | ID: mdl-34404389
18.
Prevalence of pathogenic germline cancer risk variants in high-risk urothelial carcinoma.
Genet Med
; 22(4): 709-718, 2020 04.
Article
in English
| MEDLINE | ID: mdl-31844177
19.
Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization.
Genet Med
; 21(4): 861-866, 2019 04.
Article
in English
| MEDLINE | ID: mdl-30214068
20.
ASO Visual Abstract: Universal Germline Genetic Testing for Breast Cancer: Implementation in a Rural Practice and Impact on Shared Decision Making.
Ann Surg Oncol
; 31(2): 1020, 2024 02.
Article
in English
| MEDLINE | ID: mdl-37978112