Barbara Bernhardt
Affiliations: | Johns Hopkins University, Baltimore, MD |
Area:
Public Health, Genetics, Behavioral Psychology, Oncology, Health EducationGoogle:
"Barbara Bernhardt"Mean distance: 53433
Cross-listing: PHTree
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Weitzel KW, Duong BQ, Arwood MJ, et al. (2019) A stepwise approach to implementing pharmacogenetic testing in the primary care setting. Pharmacogenomics. 20: 1103-1112 |
| Werner-Lin A, Mccoyd JLM, Bernhardt BA. (2019) Actions and Uncertainty: How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable. The Hastings Center Report. 49: S61-S71 |
| Schmidlen T, Sturm AC, Hovick S, et al. (2018) Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing. Journal of Genetic Counseling |
| Christensen KD, Bernhardt BA, Jarvik GP, et al. (2018) 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 |
| Sweet K, Hovick S, Sturm AC, et al. (2016) Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study. Journal of Genetic Counseling |
| Werner-Lin A, McCoyd JL, Bernhardt BA. (2016) Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing. Journal of Genetic Counseling |
| Bowdin S, Gilbert A, Bedoukian E, et al. (2016) Recommendations for the integration of genomics into clinical practice. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Fonda Allen J, Stoll K, Bernhardt BA. (2016) Pre- and post-test genetic counseling for chromosomal and Mendelian disorders. Seminars in Perinatology. 40: 44-55 |
| Amendola LM, Lautenbach D, Scollon S, et al. (2015) Illustrative case studies in the return of exome and genome sequencing results. Personalized Medicine. 12: 283-295 |
| Walser SA, Kellom KS, Palmer SC, et al. (2015) Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing. Prenatal Diagnosis. 35: 870-8 |