Detalhe da pesquisa
1.
Airmen and health-care providers' attitudes toward the use of genomic sequencing in the US Air Force: findings from the MilSeq Project.
Genet Med
; 22(12): 2003-2010, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32807975
2.
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
3.
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
4.
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
5.
A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xga.
Transfusion
; 59(3): 908-915, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30592300
6.
Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial.
Genet Med
; 20(12): 1544-1553, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29565423
7.
Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.
J Genet Couns
; 27(5): 1220-1227, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29497922
8.
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Ann Intern Med
; 167(3): 159-169, 2017 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28654958
9.
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
; 99(1): 246, 2016 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27392080
10.
Informed consent for exome sequencing research in families with genetic disease: the emerging issue of incidental findings.
Am J Med Genet A
; 164A(11): 2745-52, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25251809
11.
Newborn screening: education, consent, and the residual blood spot. The position of the national society of genetic counselors.
J Genet Couns
; 23(1): 16-9, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23881473
12.
Mutations in PCYT1A, encoding a key regulator of phosphatidylcholine metabolism, cause spondylometaphyseal dysplasia with cone-rod dystrophy.
Am J Hum Genet
; 94(1): 105-12, 2014 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-24387990
13.
Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.
J Pers Med
; 10(2)2020 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32349224
14.
Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.
J Pers Med
; 10(2)2020 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32413979
15.
A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients.
Circ Cardiovasc Genet
; 10(5)2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29030401