Detalhe da pesquisa
1.
Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project.
Am J Hum Genet
; 107(4): 596-611, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32853555
2.
Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes.
Genet Med
; 22(1): 60-68, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31312045
3.
Parental Views on Newborn Next Generation Sequencing: Implications for Decision Support.
Matern Child Health J
; 24(7): 856-864, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32424581
4.
Correction: Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes.
Genet Med
; 21(12): 2846, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31341244
5.
Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background.
Genet Med
; 21(3): 727-735, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29976988
6.
Factors influencing NCGENES research participants' requests for non-medically actionable secondary findings.
Genet Med
; 21(5): 1092-1099, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30237575
7.
An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening.
J Pediatr
; 209: 68-76, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30851990
8.
Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment.
Genet Med
; 20(2): 181-189, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28771249
9.
"Possibly positive or certainly uncertain?": participants' responses to uncertain diagnostic results from exome sequencing.
Genet Med
; 20(3): 313-319, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29593351
10.
The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study.
Genet Med
; 20(7): 760-769, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29261173
11.
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
12.
Is "incidental finding" the best term?: a study of patients' preferences.
Genet Med
; 19(2): 176-181, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27490114
13.
A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing.
Genet Med
; 18(5): 467-75, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26270767
14.
"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
J Genet Couns
; 25(1): 62-72, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25911622
15.
Experiences with obtaining informed consent for genomic sequencing.
Am J Med Genet A
; 167A(11): 2635-46, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26198374
16.
The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: report and review.
Am J Med Genet A
; 167A(9): 2176-81, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25920937
17.
Erratum to: How can psychological science inform research about genetic counseling for clinical genomic sequencing?
J Genet Couns
; 24(2): 372, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25539761
18.
How can psychological science inform research about genetic counseling for clinical genomic sequencing?
J Genet Couns
; 24(2): 193-204, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25488723
19.
Genetic information, non-discrimination, and privacy protections in genetic counseling practice.
J Genet Couns
; 23(6): 891-902, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25063358
20.
Can a decision aid enable informed decisions in neonatal nursery recruitment for a fragile X newborn screening study?
Genet Med
; 15(4): 299-306, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23100013