Detalhe da pesquisa
1.
Improving reporting standards for polygenic scores in risk prediction studies.
Nature
; 591(7849): 211-219, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33692554
2.
Models of communication for polygenic scores and associated psychosocial and behavioral effects on recipients: A systematic review.
Genet Med
; 25(1): 1-11, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36322150
3.
Clinical genetic counseling and translation considerations for polygenic scores in personalized risk assessments: A Practice Resource from the National Society of Genetic Counselors.
J Genet Couns
; 32(3): 558-575, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36617640
4.
Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test.
Genet Med
; 23(9): 1689-1696, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33976420
5.
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders.
NPJ Genom Med
; 9(1): 15, 2024 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38409289
6.
Evaluating the impact of a new educational tool on understanding of polygenic risk scores for alcohol use disorder.
Front Psychiatry
; 13: 1025483, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36506445
7.
Association of the Interaction Between Familial Hypercholesterolemia Variants and Adherence to a Healthy Lifestyle With Risk of Coronary Artery Disease.
JAMA Netw Open
; 5(3): e222687, 2022 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35294538
8.
Clinical Implementation of Combined Monogenic and Polygenic Risk Disclosure for Coronary Artery Disease.
JACC Adv
; 1(3)2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-36147540
9.
Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilization.
Genome Med
; 14(1): 114, 2022 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36207733
10.
Design and user experience testing of a polygenic score report: a qualitative study of prospective users.
BMC Med Genomics
; 14(1): 238, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34598685
11.
Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History.
JAMA Netw Open
; 3(4): e203959, 2020 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32347951
12.
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.
Nat Commun
; 11(1): 3635, 2020 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32820175
13.
Rare Genetic Variants Associated With Sudden Cardiac Death in Adults.
J Am Coll Cardiol
; 74(21): 2623-2634, 2019 11 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31727422
14.
Concordance of a High Polygenic Score Among Relatives: Implications for Genetic Counseling and Cascade Screening.
Circ Genom Precis Med
; 14(2): e003262, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33794649