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
1.
Corson V, Bernhardt B
Am J Med Genet A
. 2021 Jun;
185(11):3230-3235.
PMID: 34061451
In celebration of the 100th birthday of Dr. Victor A. McKusick, we look back at the history of genetic counseling at Johns Hopkins Hospital and at some milestones for the...
2.
Wiisanen Weitzel K, Duong B, Arwood M, Owusu-Obeng A, Abul-Husn N, Bernhardt B, et al.
Pharmacogenomics
. 2019 Oct;
20(15):1103-1112.
PMID: 31588877
Pharmacogenetic testing can help identify primary care patients at increased risk for medication toxicity, poor response or treatment failure and inform drug therapy. While testing availability is increasing, providers are...
3.
Yu J, Appelbaum P, Brothers K, Joffe S, Kauffman T, Koenig B, et al.
Per Med
. 2019 Jul;
16(4):325-333.
PMID: 31313633
Implementing genome and exome sequencing in clinical practice presents challenges, including obtaining meaningful informed consent. Consent may be challenging due to test limitations such as uncertainties associated with test results...
4.
Werner-Lin A, McCoyd J, Bernhardt B
Hastings Cent Rep
. 2019 Jul;
49 Suppl 1:S61-S71.
PMID: 31268568
The development of genomic technologies has seemed almost magical. Excitement about it, both in medicine and among the public, stems from the belief that genomic techniques will illuminate the causes...
5.
Zebrowski A, Ellis D, Barg F, Sperber N, Bernhardt B, Denny J, et al.
Genet Med
. 2018 Nov;
21(7):1534-1540.
PMID: 30467402
Purpose: Research on genomic medicine integration has focused on applications at the individual level, with less attention paid to implementation within clinical settings. Therefore, we conducted a qualitative study using...
6.
Wynn J, Lewis K, Amendola L, Bernhardt B, Biswas S, Joshi M, et al.
BMC Med Genomics
. 2018 May;
11(1):45.
PMID: 29739461
Background: Current medical practice includes the application of genomic sequencing (GS) in clinical and research settings. Despite expanded use of this technology, the process of disclosure of genomic results to...
7.
Amendola L, Robinson J, Hart R, Biswas S, Lee K, Bernhardt B, et al.
J Genet Couns
. 2018 Mar;
27(5):1220-1227.
PMID: 29497922
Clinical and research settings are increasingly incorporating genomic sequencing (GS) technologies. Previous research has explored reasons for declining genetic testing and participation in genetic studies; however, there is a dearth...
8.
Schmidlen T, Sturm A, Hovick S, Scheinfeldt L, Roberts J, Morr L, et al.
J Genet Couns
. 2018 Feb;
27(5):1111-1129.
PMID: 29460110
With the advent of widespread genomic testing for diagnostic indications and disease risk assessment, there is increased need to optimize genetic counseling services to support the scalable delivery of precision...
9.
Werner-Lin A, Zaspel L, Carlson M, Mueller R, Walser S, Desai R, et al.
Am J Med Genet A
. 2018 Feb;
176(3):578-588.
PMID: 29446570
Clinical genome and exome sequencing (CGES) may identify variants leading to targeted management of existing conditions. Yet, CGES often fails to identify pathogenic diagnostic variants and introduces uncertainties by detecting...
10.
Christensen K, Bernhardt B, Jarvik G, Hindorff L, Ou J, Biswas S, et al.
Genet Med
. 2018 Feb;
20(10):1186-1195.
PMID: 29388940
Purpose: Secondary findings from genomic sequencing are becoming more common. We compared how health-care providers with and without specialized genetics training anticipated responding to different types of secondary findings. Methods:...