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1.
Improving reporting standards for polygenic scores in risk prediction studies.
Nature
; 591(7849): 211-219, 2021 03.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| MEDLINE | ID: mdl-35294538
8.
Clinical Implementation of Combined Monogenic and Polygenic Risk Disclosure for Coronary Artery Disease.
JACC Adv
; 1(3)2022 Aug.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| 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.
Artículo
en Inglés
| MEDLINE | ID: mdl-33794649
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