Search details
1.
Conceptualization of utility in translational clinical genomics research.
Am J Hum Genet
; 108(11): 2027-2036, 2021 11 04.
Article
in English
| MEDLINE | ID: mdl-34687653
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.
Article
in English
| MEDLINE | ID: mdl-38676451
3.
Measuring health-related quality of life in children with suspected genetic conditions: validation of the PedsQL proxy-report versions.
Qual Life Res
; 2024 Mar 12.
Article
in English
| MEDLINE | ID: mdl-38472717
4.
Cascade testing after exome sequencing: Retrospective analysis of linked family data at 2 US laboratories.
Genet Med
; 25(5): 100818, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36852743
5.
Access to clinically indicated genetic tests for pediatric patients with Medicaid: Evidence from outpatient genetics clinics in Texas.
Genet Med
; 25(3): 100350, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36547467
6.
Clinically Indicated Genomic Sequencing of Children in Foster Care: Legal and Ethical Issues.
J Pediatr
; 262: 113612, 2023 11.
Article
in English
| MEDLINE | ID: mdl-37468037
7.
US private payers' perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER).
Genet Med
; 24(1): 238-244, 2022 01.
Article
in English
| MEDLINE | ID: mdl-34906461
8.
Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods.
Genet Med
; 24(10): 2014-2027, 2022 10.
Article
in English
| MEDLINE | ID: mdl-35833928
9.
Sex Education on TikTok: A Content Analysis of Themes.
Health Promot Pract
; 23(5): 739-742, 2022 09.
Article
in English
| MEDLINE | ID: mdl-34416842
10.
Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics.
Genet Med
; 23(5): 950-955, 2021 05.
Article
in English
| MEDLINE | ID: mdl-33473204
11.
Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditions.
Genet Med
; 22(8): 1303-1310, 2020 08.
Article
in English
| MEDLINE | ID: mdl-32336750
12.
Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature.
Genet Med
; 21(1): 3-16, 2019 01.
Article
in English
| MEDLINE | ID: mdl-29760485
13.
The Other Side of the Self-Advocacy Coin: How For-Profit Companies Can Divert the Path to Justice in Rare Disease.
Am J Bioeth
; 23(7): 88-91, 2023 07.
Article
in English
| MEDLINE | ID: mdl-37339288
14.
Commentary on the development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE).
Genet Med
; 22(3): 665-666, 2020 03.
Article
in English
| MEDLINE | ID: mdl-31740737
15.
Research Participants' Perspectives on Precision Diagnostics for Alzheimer's Disease.
J Alzheimers Dis
; 97(3): 1261-1274, 2024.
Article
in English
| MEDLINE | ID: mdl-38250770
16.
Framing the Family: A Qualitative Exploration of Factors That Shape Family-Level Experience of Pediatric Genomic Sequencing.
Children (Basel)
; 10(5)2023 Apr 25.
Article
in English
| MEDLINE | ID: mdl-37238322
17.
Lessons learned while starting multi-institutional genetics research in diverse populations: A report from the Clinical Sequencing Evidence-Generating Research (CSER) consortium.
Contemp Clin Trials
; 125: 107063, 2023 Feb.
Article
in English
| MEDLINE | ID: mdl-36567057
18.
Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research.
Eur J Hum Genet
; 31(4): 445-452, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36434257
19.
Parent-Reported Clinical Utility of Pediatric Genomic Sequencing.
Pediatrics
; 152(2)2023 08 01.
Article
in English
| MEDLINE | ID: mdl-37470118
20.
Quality of life, illness perceptions, and parental lived experiences in TANGO2-related metabolic encephalopathy and arrhythmias.
Eur J Hum Genet
; 30(9): 1044-1050, 2022 09.
Article
in English
| MEDLINE | ID: mdl-35691983