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Author Details

Barbara A Bernhardt
Thomas Jefferson University
1980
134
39
PMIDPaper TitleJournal TitlePublished Year
35796432Experiences of genetic testing among individuals with retinitis pigmentosa.Ophthalmic Genet2022
34061451The evolution of genetic counseling at Johns Hopkins Hospital and beyond.Am J Med Genet A2021
30467402Qualitative study of system-level factors related to genomic implementation.Genet Med2019
31588877A stepwise approach to implementing pharmacogenetic testing in the primary care setting.Pharmacogenomics2019
31268568Actions and Uncertainty: How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable.Hastings Cent Rep2019
31313633Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.Per Med2019
29739461Clinical providers' experiences with returning results from genomic sequencing: an interview study.BMC Med Genomics2018
29446570Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results.Am J Med Genet A2018
29388940Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.Genet Med2018
29497922Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.J Genet Couns2018
29460110Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.J Genet Couns2018
27921197Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.J Genet Couns2017
28339689Genomic decision support needs in pediatric primary care.J Am Med Inform Assoc2017
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 Disord2017
28132396Expert Knowledge Influences Decision-Making for Couples Receiving Positive Prenatal Chromosomal Microarray Testing Results.Cult Med Psychiatry2017
28220724An Observational Study of Children's Involvement in Informed Consent for Exome Sequencing Research.J Empir Res Hum Res Ethics2017
28102863A taxonomy of medical uncertainties in clinical genome sequencing.Genet Med2017
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 A2017
28966657How do providers discuss the results of pediatric exome sequencing with families?Per Med2017
27735923Health screening behaviors among adults with hereditary hemorrhagic telangiectasia in North America.Genet Med2017
25911622"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.J Genet Couns2016
26351292Couple's Narratives of Communion and Isolation Following Abnormal Prenatal Microarray Testing Results.Qual Health Res2016
26477867When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority.J Pediatr2016
27207687Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing.J Genet Couns2016
27392080Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Am J Hum Genet2016
27171546Recommendations for the integration of genomics into clinical practice.Genet Med2016
27181682Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Am J Hum Genet2016
26718445Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.Semin Perinatol2016
26940446"Something Extra on Chromosome 5": Parents' Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results.J Genet Couns2016
26729011The IGNITE network: a model for genomic medicine implementation and research.BMC Med Genomics2016
26892110National Society Of Genetic Counselors Natalie Weissberger Paul National Leadership Award Address: "Patients and Research: Paths to Personal and Professional Growth".J Genet Couns2016
25539761Erratum to: How can psychological science inform research about genetic counseling for clinical genomic sequencing?J Genet Couns2015
26478737Illustrative case studies in the return of exome and genome sequencing results.Per Med2015
26198374Experiences with obtaining informed consent for genomic sequencing.Am J Med Genet A2015
26066358Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders.J Autism Dev Disord2015
25995037Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.Prenat Diagn2015
25488723How can psychological science inform research about genetic counseling for clinical genomic sequencing?J Genet Couns2015
23846343Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.J Genet Couns2014
25045402Genetic counselors and the future of clinical genomics.Genome Med2014
24569858An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.J Genet Couns2014
24625446Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group.Genet Med2014
24037030A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice.J Genet Couns2014
22955112Women's experiences receiving abnormal prenatal chromosomal microarray testing results.Genet Med2013
24409195Community pharmacists' attitudes towards clinical utility and ethical implications of pharmacogenetic testing.Per Med2013
23610795Genomic variation: what does it mean?LDI Issue Brief2013
22989118Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.Clin Genet2013
21654153Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.Public Health Genomics2012
23795206Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians.Per Med2012
22711240Factors associated with perceived uncertainty among parents of children with undiagnosed medical conditions.Am J Med Genet A2012
22441809Direct-to-consumer genetic testing: introduction to the special issue.J Genet Couns2012
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Collaborators

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Co-authored papers 29
Abt Associates Inc.
Co-authored papers 12
University of California San Francisco
Co-authored papers 8
The Perelman School of Medicine at the University of Pennsylvania
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Texas Children's Cancer Center, Texas Children's Hospital
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College of Nursing and Health Professionals, Drexel University
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Medical Ethics and Health Policy, University of Pennsylvania
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Children's Hospital of Philadelphia
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Illumina Inc.
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School of Public Health.
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University of North Carolina
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Vagelos College of Physicians and Surgeons, Columbia University
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University of Washington Medical Center
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University of North Carolina-Chapel Hill
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Harvard Medical School, Harvard Pilgrim Health Care Institute
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University of Pennsylvania, Perelman School of Medicine
Co-authored papers 4
University of Washington School of Medicine
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National Human Genome Research Institute, National Institutes of Health
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HudsonAlpha Institute for Biotechnology
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University of California-San Francisco.
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University of Washington School of Medicine.
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University of North Carolina
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National Human Genome Research Institute, National Institutes of Health
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Harvard Medical School, Vanderbilt University, Yale University Yale Law School
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Cincinnati Children's Hospital Medical Center
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Zucker School of Medicine at Hofstra/Northwell, and Lenox Hill Hospital
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Institute for Health Equity Research, Icahn School of Medicine at Mount Sinai
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Coriell Institute for Medical Research
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