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Author Details
Full Name
Barbara A Bernhardt
Affiliation
Thomas Jefferson University
ORCID
Career Start Year
1980
Papers
134
H Index
39
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35796432
Experiences of genetic testing among individuals with retinitis pigmentosa.
Ophthalmic Genet
2022
34061451
The evolution of genetic counseling at Johns Hopkins Hospital and beyond.
Am J Med Genet A
2021
30467402
Qualitative study of system-level factors related to genomic implementation.
Genet Med
2019
31588877
A stepwise approach to implementing pharmacogenetic testing in the primary care setting.
Pharmacogenomics
2019
31268568
Actions and Uncertainty: How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable.
Hastings Cent Rep
2019
31313633
Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.
Per Med
2019
29739461
Clinical providers' experiences with returning results from genomic sequencing: an interview study.
BMC Med Genomics
2018
29446570
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
2018
29388940
Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.
Genet Med
2018
29497922
Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.
J Genet Couns
2018
29460110
Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.
J Genet Couns
2018
27921197
Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.
J Genet Couns
2017
28339689
Genomic decision support needs in pediatric primary care.
J Am Med Inform Assoc
2017
28229350
"Set in Stone" or "Ray of Hope": Parents' Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASD.
J Autism Dev Disord
2017
28132396
Expert Knowledge Influences Decision-Making for Couples Receiving Positive Prenatal Chromosomal Microarray Testing Results.
Cult Med Psychiatry
2017
28220724
An Observational Study of Children's Involvement in Informed Consent for Exome Sequencing Research.
J Empir Res Hum Res Ethics
2017
28102863
A taxonomy of medical uncertainties in clinical genome sequencing.
Genet Med
2017
28102595
"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
2017
28966657
How do providers discuss the results of pediatric exome sequencing with families?
Per Med
2017
27735923
Health screening behaviors among adults with hereditary hemorrhagic telangiectasia in North America.
Genet Med
2017
25911622
"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
J Genet Couns
2016
26351292
Couple's Narratives of Communion and Isolation Following Abnormal Prenatal Microarray Testing Results.
Qual Health Res
2016
26477867
When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority.
J Pediatr
2016
27207687
Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing.
J Genet Couns
2016
27392080
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
2016
27171546
Recommendations for the integration of genomics into clinical practice.
Genet Med
2016
27181682
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
2016
26718445
Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.
Semin Perinatol
2016
26940446
"Something Extra on Chromosome 5": Parents' Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results.
J Genet Couns
2016
26729011
The IGNITE network: a model for genomic medicine implementation and research.
BMC Med Genomics
2016
26892110
National Society Of Genetic Counselors Natalie Weissberger Paul National Leadership Award Address: "Patients and Research: Paths to Personal and Professional Growth".
J Genet Couns
2016
25539761
Erratum to: How can psychological science inform research about genetic counseling for clinical genomic sequencing?
J Genet Couns
2015
26478737
Illustrative case studies in the return of exome and genome sequencing results.
Per Med
2015
26198374
Experiences with obtaining informed consent for genomic sequencing.
Am J Med Genet A
2015
26066358
Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders.
J Autism Dev Disord
2015
25995037
Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.
Prenat Diagn
2015
25488723
How can psychological science inform research about genetic counseling for clinical genomic sequencing?
J Genet Couns
2015
23846343
Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.
J Genet Couns
2014
25045402
Genetic counselors and the future of clinical genomics.
Genome Med
2014
24569858
An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
J Genet Couns
2014
24625446
Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group.
Genet Med
2014
24037030
A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice.
J Genet Couns
2014
22955112
Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Genet Med
2013
24409195
Community pharmacists' attitudes towards clinical utility and ethical implications of pharmacogenetic testing.
Per Med
2013
23610795
Genomic variation: what does it mean?
LDI Issue Brief
2013
22989118
Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.
Clin Genet
2013
21654153
Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.
Public Health Genomics
2012
23795206
Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians.
Per Med
2012
22711240
Factors associated with perceived uncertainty among parents of children with undiagnosed medical conditions.
Am J Med Genet A
2012
22441809
Direct-to-consumer genetic testing: introduction to the special issue.
J Genet Couns
2012
1 - 50 of 134
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Johns Hopkins McKusick-Nathans Department of Genetic Medicine
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Gail P Jarvik
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Gail E Henderson
University of North Carolina-Chapel Hill
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