Barbara A Bernhardt
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Explore the profile of Barbara A Bernhardt including associated specialties, affiliations and a list of published articles.
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75
Citations
1408
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Recent Articles
11.
Walser S, Werner-Lin A, Mueller R, Miller V, Biswas S, Bernhardt B
Per Med
. 2017 Oct;
14(5):409-422.
PMID: 28966657
Aim: This study provides preliminary data on the process and content of returning results from exome sequencing offered to children through one of the Clinical Sequencing Exploratory Research (CSER) projects....
12.
Pennington J, Karavite D, Krause E, Miller J, Bernhardt B, Grundmeier R
J Am Med Inform Assoc
. 2017 Mar;
24(4):851-856.
PMID: 28339689
Clinical genome and exome sequencing can diagnose pediatric patients with complex conditions that often require follow-up care with multiple specialties. The American Academy of Pediatrics emphasizes the role of the...
13.
Reiff M, Bugos E, Giarelli E, Bernhardt B, Spinner N, Sankar P, et al.
J Autism Dev Disord
. 2017 Feb;
47(5):1453-1463.
PMID: 28229350
Despite increasing utilization of chromosomal microarray analysis (CMA) for autism spectrum disorders (ASD), limited information exists about how results influence parents' beliefs about etiology and prognosis. We conducted in-depth interviews...
14.
Miller V, Werner-Lin A, Walser S, Biswas S, Bernhardt B
J Empir Res Hum Res Ethics
. 2017 Feb;
12(1):6-13.
PMID: 28220724
The goal of this study was to examine children's involvement in consent sessions for exome sequencing research and associations of involvement with provider and parent communication. Participants included 44 children...
15.
Han P, Umstead K, Bernhardt B, Green R, Joffe S, Koenig B, et al.
Genet Med
. 2017 Jan;
19(8):918-925.
PMID: 28102863
Purpose: Clinical next-generation sequencing (CNGS) is introducing new opportunities and challenges into the practice of medicine. Simultaneously, these technologies are generating uncertainties of an unprecedented scale that laboratories, clinicians, and...
16.
Werner-Lin A, Walser S, Barg F, Bernhardt B
Am J Med Genet A
. 2017 Jan;
173(2):444-451.
PMID: 28102595
Chromosome microarray (CMA) testing is used widely in prenatal settings. Some copy number variants (CNVs) detected using CMA are associated with variable or uncertain phenotype and/or possible neurocognitive involvement. Little...
17.
Baxter M, Erby L, Roter D, Bernhardt B, Terry P, Guttmacher A
Genet Med
. 2016 Oct;
19(6):659-666.
PMID: 27735923
Purpose: This study aimed to identify factors that influence screening behaviors of adults with hereditary hemorrhagic telangiectasia (HHT). Methods: Participants with a self-reported diagnosis of HHT were recruited from the...
18.
Green R, Goddard K, Jarvik G, Amendola L, Appelbaum P, Berg J, et al.
Am J Hum Genet
. 2016 Jul;
99(1):246.
PMID: 27392080
No abstract available.
19.
Werner-Lin A, McCoyd J, Bernhardt B
J Genet Couns
. 2016 May;
25(5):855-67.
PMID: 27207687
Genetic counselors frequently are called upon to assist patients in understanding the implications of prenatal testing information for their pregnancies and their family's lives. The introduction of highly sensitive testing...
20.
Green R, Goddard K, Jarvik G, Amendola L, Appelbaum P, Berg J, et al.
Am J Hum Genet
. 2016 May;
98(6):1051-1066.
PMID: 27181682
Despite rapid technical progress and demonstrable effectiveness for some types of diagnosis and therapy, much remains to be learned about clinical genome and exome sequencing (CGES) and its role within...