Detalhe da pesquisa
1.
The evolution of genetic counseling at Johns Hopkins Hospital and beyond.
Am J Med Genet A
; 185(11): 3230-3235, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34061451
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.
Qualitative study of system-level factors related to genomic implementation.
Genet Med
; 21(7): 1534-1540, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30467402
4.
Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.
Genet Med
; 20(10): 1186-1195, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29388940
5.
Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results.
Am J Med Genet A
; 176(3): 578-588, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29446570
6.
Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.
J Genet Couns
; 27(5): 1111-1129, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29460110
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.
Health screening behaviors among adults with hereditary hemorrhagic telangiectasia in North America.
Genet Med
; 19(6): 659-666, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27735923
9.
A taxonomy of medical uncertainties in clinical genome sequencing.
Genet Med
; 19(8): 918-925, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28102863
10.
"They Can't Find Anything Wrong with Him, Yet": Mothers' experiences of parenting an infant with a prenatally diagnosed copy number variant (CNV).
Am J Med Genet A
; 173(2): 444-451, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28102595
11.
Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing.
J Genet Couns
; 25(5): 855-67, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27207687
12.
"Something Extra on Chromosome 5": Parents' Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results.
J Genet Couns
; 25(5): 1116-26, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26940446
13.
"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
14.
Couple's Narratives of Communion and Isolation Following Abnormal Prenatal Microarray Testing Results.
Qual Health Res
; 26(14): 1975-1987, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26351292
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.
Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.
Prenat Diagn
; 35(9): 870-8, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25995037
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.
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
20.
Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group.
Genet Med
; 16(10): 727-35, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24625446