Detalhe da pesquisa
1.
Scaling Genetic Counseling in the Genomics Era.
Annu Rev Genomics Hum Genet
; 22: 339-355, 2021 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-33722076
2.
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.
Am J Hum Genet
; 107(5): 932-941, 2020 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33108757
3.
Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
; 25(10): 100870, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37490054
4.
Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population.
Genet Med
; 25(11): 100923, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37421176
5.
Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.
Am J Hum Genet
; 105(3): 526-533, 2019 09 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31422818
6.
ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial.
Genet Med
; 24(8): 1664-1674, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35522237
7.
An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial.
Genet Med
; 24(11): 2228-2239, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36053287
8.
Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access.
Genet Med
; 24(6): 1196-1205, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35305866
9.
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.
J Genet Couns
; 31(1): 230-241, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34302314
10.
Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory.
Am J Hum Genet
; 102(6): 1078-1089, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29754767
11.
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Am J Hum Genet
; 103(3): 319-327, 2018 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30193136
12.
A review and definition of 'usual care' in genetic counseling trials to standardize use in research.
J Genet Couns
; 30(1): 42-50, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33278053
13.
Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.
Am J Hum Genet
; 98(6): 1067-1076, 2016 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27181684
14.
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
; 98(6): 1051-1066, 2016 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27181682
15.
Response to Stern.
Genet Med
; 26(2): 101030, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38156990
16.
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Genet Med
; 21(5): 1261-1262, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30670880
17.
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Genet Med
; 21(5): 1100-1110, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30287922
18.
Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests.
J Genet Couns
; 28(6): 1208-1213, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31317629
19.
The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
J Genet Couns
; 28(2): 477-490, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30964586
20.
Rare loss of function variants in candidate genes and risk of colorectal cancer.
Hum Genet
; 137(10): 795-806, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30267214