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Barbara Bernhardt - Publications

Affiliations: 
Johns Hopkins University, Baltimore, MD 
Area:
Public Health, Genetics, Behavioral Psychology, Oncology, Health Education
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29 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Weitzel KW, Duong BQ, Arwood MJ, Owusu-Obeng A, Abul-Husn NS, Bernhardt BA, Decker B, Denny JC, Dietrich E, Gums J, Madden EB, Pollin TI, Wu RR, Haga SB, Horowitz CR. A stepwise approach to implementing pharmacogenetic testing in the primary care setting. Pharmacogenomics. 20: 1103-1112. PMID 31588877 DOI: 10.2217/Pgs-2019-0053  0.324
2019 Werner-Lin A, Mccoyd JLM, Bernhardt BA. Actions and Uncertainty: How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable. The Hastings Center Report. 49: S61-S71. PMID 31268568 DOI: 10.1002/hast.1018  0.303
2018 Schmidlen T, Sturm AC, Hovick S, Scheinfeldt L, Scott Roberts J, Morr L, McElroy J, Toland AE, Christman M, O'Daniel JM, Gordon ES, Bernhardt BA, Ormond KE, Sweet K. Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing. Journal of Genetic Counseling. PMID 29460110 DOI: 10.1007/S10897-018-0230-Z  0.381
2018 Christensen KD, Bernhardt BA, Jarvik GP, Hindorff LA, Ou J, Biswas S, Powell BC, Grundmeier RW, Machini K, Karavite DJ, Pennington JW, Krantz ID, Berg JS, Goddard KAB. Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29388940 DOI: 10.1038/Gim.2017.243  0.339
2016 Sweet K, Hovick S, Sturm AC, Schmidlen T, Gordon E, Bernhardt B, Wawak L, Wernke K, McElroy J, Scheinfeldt L, Toland AE, Roberts JS, Christman M. Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study. Journal of Genetic Counseling. PMID 27921197 DOI: 10.1007/S10897-016-0044-9  0.348
2016 Werner-Lin A, McCoyd JL, Bernhardt BA. Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing. Journal of Genetic Counseling. PMID 27207687 DOI: 10.1007/s10897-016-9966-5  0.35
2016 Bowdin S, Gilbert A, Bedoukian E, Carew C, Adam MP, Belmont J, Bernhardt B, Biesecker L, Bjornsson HT, Blitzer M, D'Alessandro LC, Deardorff MA, Demmer L, Elliott A, Feldman GL, et al. Recommendations for the integration of genomics into clinical practice. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27171546 DOI: 10.1038/Gim.2016.17  0.347
2016 Fonda Allen J, Stoll K, Bernhardt BA. Pre- and post-test genetic counseling for chromosomal and Mendelian disorders. Seminars in Perinatology. 40: 44-55. PMID 26718445 DOI: 10.1053/j.semperi.2015.11.007  0.361
2015 Amendola LM, Lautenbach D, Scollon S, Bernhardt B, Biswas S, East K, Everett J, Gilmore MJ, Himes P, Raymond VM, Wynn J, Hart R, Jarvik GP. Illustrative case studies in the return of exome and genome sequencing results. Personalized Medicine. 12: 283-295. PMID 26478737 DOI: 10.2217/Pme.14.89  0.382
2015 Walser SA, Kellom KS, Palmer SC, Bernhardt BA. Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing. Prenatal Diagnosis. 35: 870-8. PMID 25995037 DOI: 10.1002/pd.4624  0.325
2014 Bernhardt BA, Kellom K, Barbarese A, Faucett WA, Wapner RJ. An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing. Journal of Genetic Counseling. 23: 938-47. PMID 24569858 DOI: 10.1007/s10897-014-9702-y  0.36
2014 Reiff M, Mueller R, Mulchandani S, Spinner NB, Pyeritz RE, Bernhardt BA. A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice. Journal of Genetic Counseling. 23: 474-88. PMID 24037030 DOI: 10.1007/s10897-013-9653-8  0.399
2013 Tuteja S, Haynes K, Zayac C, Sprague JE, Bernhardt B, Pyeritz R. Community pharmacists' attitudes towards clinical utility and ethical implications of pharmacogenetic testing. Personalized Medicine. 10. PMID 24409195 DOI: 10.2217/Pme.13.85  0.348
2013 Bernhardt BA. A survey of reimbursement for cystic fibrosis carrier testing. Journal of Genetic Counseling. 2: 69-76. PMID 24242318 DOI: 10.1007/BF00962540  0.313
2013 Reiff M, Ross K, Mulchandani S, Propert KJ, Pyeritz RE, Spinner NB, Bernhardt BA. Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families. Clinical Genetics. 83: 23-30. PMID 22989118 DOI: 10.1111/Cge.12004  0.378
2012 Myers MF, Bernhardt BA. Direct-to-consumer genetic testing: introduction to the special issue. Journal of Genetic Counseling. 21: 357-60. PMID 22441809 DOI: 10.1007/s10897-012-9500-3  0.564
2011 Bernhardt BA, Pyeritz RE. When genetic screening is useful, but not used. Ldi Issue Brief. 16: 1-4. PMID 21863606  0.348
2011 Leighton JW, Valverde K, Bernhardt BA. The general public's understanding and perception of direct-to-consumer genetic test results. Public Health Genomics. 15: 11-21. PMID 21720148 DOI: 10.1159/000327159  0.388
2010 Messner DA, Pyeritz RE, Bernhardt BA. Comment on the impact of gene patents and licensing practices on access to genetic testing: lessons from hereditary hemorrhagic telangiectasia. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 12: 746-8. PMID 21068576 DOI: 10.1097/GIM.0b013e3181f872d9  0.345
2008 Giarelli E, Bernhardt BA, Pyeritz RE. Attitudes antecedent to transition to self-management of a chronic genetic disorder. Clinical Genetics. 74: 325-37. PMID 18616734 DOI: 10.1111/J.1399-0004.2008.01052.X  0.317
2006 Myers MF, Chang MH, Jorgensen C, Whitworth W, Kassim S, Litch JA, Armstrong L, Bernhardt B, Faucett WA, Irwin D, Mouchawar J, Bradley LA. Genetic testing for susceptibility to breast and ovarian cancer: evaluating the impact of a direct-to-consumer marketing campaign on physicians' knowledge and practices. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 8: 361-70. PMID 16778598 DOI: 10.1097/01.Gim.0000223544.68475.6C  0.538
2003 Doksum T, Bernhardt BA, Holtzman NA. Does knowledge about the genetics of breast cancer differ between nongeneticist physicians who do or do not discuss or order BRCA testing? Genetics in Medicine : Official Journal of the American College of Medical Genetics. 5: 99-105. PMID 12644779 DOI: 10.1097/01.Gim.0000055198.63593.32  0.357
2002 Geller G, Bernhardt BA, Holtzman NA. The media and public reaction to genetic research. Jama. 287: 773. PMID 11851549 DOI: 10.1001/Jama.287.6.773-Jms0213-3-1  0.331
2001 Doksum T, Bernhardt BA, Holtzman NA. Carrier screening for cystic fibrosis among Maryland obstetricians before and after the 1997 NIH Consensus Conference. Genetic Testing. 5: 111-6. PMID 11551096 DOI: 10.1089/109065701753145565  0.327
2000 Bernhardt BA, Biesecker BB, Mastromarino CL. Goals, benefits, and outcomes of genetic counseling: client and genetic counselor assessment. American Journal of Medical Genetics. 94: 189-97. PMID 10995504 DOI: 10.1002/1096-8628(20000918)94:3<189::AID-AJMG3>3.0.CO;2-E  0.336
1998 James C, Geller G, Bernhardt BA, Docksum T, Holtzman NA. Are practicing and future physicians prepared to obtain informed consent? The case of genetic testing for susceptibility to breast cancer. Community Genetics. 1: 203-12. PMID 11658004 DOI: 10.1159/000016165  0.332
1997 Geller G, Strauss M, Bernhardt BA, Holtzman NA. "Decoding" Informed Consent Insights from Women regarding Breast Cancer Susceptibility Testing The Hastings Center Report. 27: 28. DOI: 10.2307/3527625  0.368
1994 Myers MF, Bernhardt BA, Tambor ES, Holtzman NA. Involving consumers in the development of an educational program for cystic fibrosis carrier screening. American Journal of Human Genetics. 54: 719-26. PMID 8128971  0.537
1992 Bernhardt BA, Pyeritz RE. The organization and delivery of clinical genetics services. Pediatric Clinics of North America. 39: 1-12. PMID 1736250 DOI: 10.1016/S0031-3955(16)38259-1  0.311
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