Detalhe da pesquisa
1.
Family secrets: Experiences and outcomes of participating in direct-to-consumer genetic relative-finder services.
Am J Hum Genet;
109(3): 486-497, 2022 03 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35216680
2.
Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for pediatric diagnostic testing.
Genet Med;
: 101146, 2024 Apr 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38676451
3.
Compassion and equity-focused clinical genomics training for health professional learners.
J Genet Couns;
2024 Feb 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38363012
4.
A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants.
Am J Hum Genet;
107(5): 953-962, 2020 11 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33157008
5.
An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm.
Am J Hum Genet;
107(5): 942-952, 2020 11 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33157007
6.
Optimal Integration of Behavioral Medicine into Clinical Genetics and Genomics.
Am J Hum Genet;
104(2): 193-196, 2019 02 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30735659
7.
Physician preparedness for big genomic data: a review of genomic medicine education initiatives in the United States.
Hum Mol Genet;
27(R2): R250-R258, 2018 08 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29750248
8.
Interdisciplinary development of a standardized introduction to gene drives for lay audiences.
BMC Med Res Methodol;
20(1): 273, 2020 11 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33153449
9.
Social Media Surveillance in Schools: Rethinking Public Health Interventions in the Digital Age.
J Med Internet Res;
22(11): e22612, 2020 11 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33179599
10.
Using Participatory Design to Inform the Connected and Open Research Ethics (CORE) Commons.
Sci Eng Ethics;
26(1): 183-203, 2020 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30725245
11.
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
Hum Mol Genet;
25(15): 3383-3394, 2016 08 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27329760
12.
PRINCESS: Privacy-protecting Rare disease International Network Collaboration via Encryption through Software guard extensionS.
Bioinformatics;
33(6): 871-878, 2017 03 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28065902
13.
Differences in Neurocognitive Impairment Among HIV-Infected Latinos in the United States.
J Int Neuropsychol Soc;
24(2): 163-175, 2018 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28874213
14.
Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.
Am J Med Genet B Neuropsychiatr Genet;
174(4): 413-426, 2017 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28447399
15.
The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository.
Neuroimage;
124(Pt B): 1149-1154, 2016 Jan 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25937488
16.
Reimagining Human Research Protections for 21st Century Science.
J Med Internet Res;
18(12): e329, 2016 12 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28007687
17.
Commentary on the development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE).
Genet Med;
22(3): 665-666, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31740737
18.
A genome sequencing program for novel undiagnosed diseases.
Genet Med;
17(12): 995-1001, 2015 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25790160
19.
De novo KCNB1 mutations in epileptic encephalopathy.
Ann Neurol;
76(4): 529-540, 2014 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25164438
20.
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia.
Ann Neurol;
75(4): 542-9, 2014 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24700542