Barbara A. Bernhardt

7.1k citations

115 papers · 4.0k indexed · h-index 39

Impact in

Genetics top 0.5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
Pediatrics, Perinatology and Child Health top 0.5%
- Prenatal Screening and Diagnostics
- Ethics and Legal Issues in Pediatric Healthcare

Papers in

Genetics 73
- BRCA gene mutations in cancer 57
- Genomics and Rare Diseases 26
- Genomic variations and chromosomal abnormalities 18
Pediatrics, Perinatology and Child Health 31
- Prenatal Screening and Diagnostics 19
- Ethics and Legal Issues in Pediatric Healthcare 12
- Childhood Cancer Survivors' Quality of Life 7

Co-authors: Reed E. Pyeritz Gail Geller Neil A. Holtzman Ellen Tambor Teresa Doksum Allison Werner‐Lin Kathleen Valverde Ronald J. Wapner
Journals: Genetics in Medicine (18 papers)Public Health Genomics (4 papers)Cancer (2 papers)Prenatal Diagnosis (2 papers)Qualitative Health Research (2 papers)
Partner nations: United States Australia Switzerland

In The Last Decade

Barbara A. Bernhardt

114 papers receiving 3.8k citations

Peers

Countries citing papers authored by Barbara A. Bernhardt

Since Specialization

Citations

This map shows the geographic impact of Barbara A. Bernhardt's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Barbara A. Bernhardt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara A. Bernhardt more than expected).

Fields of papers citing papers by Barbara A. Bernhardt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara A. Bernhardt. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Barbara A. Bernhardt. The network helps show where Barbara A. Bernhardt may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Barbara A. Bernhardt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Barbara A. Bernhardt Line = papers co-authored together Barbara A. Bernhardt links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Actions and Uncertainty: How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable The Hastings Center Report ·Allison Werner‐Lin, Judith L. M. McCoyd, Barbara A. Bernhardt	2019	17
2	Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing Journal of Genetic Counseling ·Tara Schmidlen, Amy C. Sturm, Shelly R. Hovick, Laura Scheinfeldt, J. Scott Roberts, 鶉子山草, Joseph P. McElroy, Amanda E. Toland, Michael F. Christman, Julianne O’Daniel, Erynn S. Gordon, Barbara A. Bernhardt, Kelly E. Ormond, Kevin Sweet	2018	22
3	Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results American Journal of Medical Genetics Part A ·Allison Werner‐Lin, Nurul Wahida Amalin Abdul Aziz, Shiyi Jin, Rebecca Mueller, Sarah A. Walser, Pornwalee Porapakkham, Barbara A. Bernhardt	2018	21
4	Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings Genetics in Medicine ·Kurt D. Christensen, Barbara A. Bernhardt, Gail P. Jarvik, Lucia A. Hindorff, Jeffrey Ou, Sawona Biswas, Bradford C. Powell, Robert W. Grundmeier, Kalotina Machini, Dean Karavite, Jeffrey W. Pennington, Ian D. Krantz, Jonathan S. Berg, Katrina A.B. Goddard	2018	5
5	Qualitative study of system-level factors related to genomic implementation Genetics in Medicine ·Alexis Zebrowski, Daoqiu Yang, Frances K. Barg, Nina Sperber, Barbara A. Bernhardt, Joshua C. Denny, Paul Dexter, Geoffrey S. Ginsburg, Carol R. Horowitz, Julie A. Johnson, Mia Levy, Lori A. Orlando, Toni I. Pollin, Todd C. Skaar, Stephen E. Kimmel	2018	32
6	Counselees’ Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study Journal of Genetic Counseling ·Kevin Sweet, Shelly R. Hovick, Amy C. Sturm, Tara Schmidlen, Erynn S. Gordon, Barbara A. Bernhardt, Xiaodan Mu, Ngeow Wei Cheong, Joseph P. McElroy, Laura Scheinfeldt, Amanda E. Toland, J. Scott Roberts, Michael F. Christman	2016	16
7	Health screening behaviors among adults with hereditary hemorrhagic telangiectasia in North America Genetics in Medicine ·Susheela Yadav, Lori H. Erby, Debra Roter, Barbara A. Bernhardt, Peter B. Terry, Alan E. Guttmacher	2016	2
8	“They Can't Find Anything Wrong with Him, Yet”: Mothers’ experiences of parenting an infant with a prenatally diagnosed copy number variant (CNV) American Journal of Medical Genetics Part A ·Allison Werner‐Lin, Sarah A. Walser, Frances K. Barg, Barbara A. Bernhardt	2016	40
9	Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group Genetics in Medicine ·Stacy W. Gray, Yolanda Martins, Lindsay Z. Feuerman, Barbara A. Bernhardt, Barbara B. Biesecker, Kurt D. Christensen, Steven Joffe, Christine Rini, David L. Veenstra, Amy L. McGuire	2014	51
10	Genetic counselors and the future of clinical genomics Genome Medicine ·Barbara A. Bernhardt	2014	11
11	“What does it mean?”: Uncertainties in understanding results of chromosomal microarray testing Genetics in Medicine ·Marian Reiff, Barbara A. Bernhardt, Surabhi Mulchandani, Томшинская Ирина Николаевна, Yanlang Zhong, Reed E. Pyeritz, Nancy B. Spinner	2012	90
12	When genetic screening is useful, but not used. PubMed ·Barbara A. Bernhardt, Reed E. Pyeritz	2011	0
13	Pregnancy as a proclamation of faith: Ultra‐Orthodox Jewish women navigating the uncertainty of pregnancy and prenatal diagnosis American Journal of Medical Genetics Part A ·Elly Teman, أحمد لعروسى, Barbara A. Bernhardt	2010	28
14	Transillumination of the fingers for vascular anomalies: a novel method for evaluating hereditary hemorrhagic telangiectasia Genetics in Medicine ·Emile R. Mohler, Vijay Doraiswamy, 한백진, Barbara A. Bernhardt, Reed E. Pyeritz	2009	2
15	Scientists' and science writers' experiences reporting genetic discoveries: Toward an ethic of trust in science journalism Genetics in Medicine ·Gail Geller, Barbara A. Bernhardt, Moch. Gandung Satriya, Patrícia Oliveira Carmo, Neil A. Holtzman	2005	25
16	Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patients Genetics in Medicine ·Kira Apse, Barbara B. Biesecker, Francis M. Giardiello, С.Х. Йигиталиев, Barbara A. Bernhardt	2004	47
17	Utilization of BRCA1/2 genetic testing in the clinical setting Cancer ·Soo Chin Lee, Barbara A. Bernhardt, Kathy J. Helzlsouer	2002	49
18	Carrier Screening for Cystic Fibrosis among Maryland Obstetricians before and after the 1997 NIH Consensus Conference Genetic Testing ·Teresa Doksum, Barbara A. Bernhardt, Neil A. Holtzman	2001	8
19	Are Practicing and Future Physicians Prepared to Obtain Informed Consent? The Case of Genetic Testing forSusceptibility to Breast Cancer Public Health Genomics ·Cynthia A. James, Gail Geller, Barbara A. Bernhardt, Teresa Doksum, Neil A. Holtzman	1998	19
20	Population-Based Carrier Screening for Cystic Fibrosis Clinical Obstetrics & Gynecology ·Teresa Doksum, Barbara A. Bernhardt	1996	7

About Barbara A. Bernhardt

Barbara A. Bernhardt is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, General Health Professions and Health, having authored 115 papers that have together received 4.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (57 papers), Genomics and Rare Diseases (26 papers), Ethics in Clinical Research (23 papers), Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (18 papers), Ethics and Legal Issues in Pediatric Healthcare (12 papers), Climate Change Communication and Perception (9 papers) and Childhood Cancer Survivors' Quality of Life (7 papers). The work is most often cited by research in Genetics (2.4k citations), Pediatrics, Perinatology and Child Health (1.2k citations), Public Health, Environmental and Occupational Health (884 citations), Pharmacology (166 citations) and General Health Professions (470 citations). Barbara A. Bernhardt has collaborated with scholars based in United States, Australia and Switzerland. Frequent co-authors include Reed E. Pyeritz, Gail Geller, Neil A. Holtzman, Ellen Tambor, Teresa Doksum, Allison Werner‐Lin, Kathleen Valverde, Ronald J. Wapner, Barbara B. Biesecker and S S Siegelman. Their work appears in journals such as Genetics in Medicine, Public Health Genomics, Cancer, Prenatal Diagnosis and Qualitative Health Research.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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