Jonathan S Berg

ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 13

Top Venues

Genetics in medicine : official journal of the American College of Medical Genetics

Journal of personalized medicine

Human mutation

Genome medicine

University of North Carolina at Chapel Hill School of Medicine

University of North Carolina at Chapel Hill (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of North Carolina at Chapel Hill School of Medicine

United States

Associate Professor :: Genetics

Education History

University of North Carolina at Chapel Hill

United States

PHD

Publications

Kimberly S Foss, Julianne M O'Daniel, Jonathan S Berg, Sabrina N Powell, Rosemary Jean Cadigan, Kristine J Kuczynski, Laura V Milko, Katherine W Saylor, Megan Roberts, Karen Weck, Gail E Henderson
Correction: Foss et al. The Rise of Population Genomic Screening: Characteristics of Current Programs and the Need for Evidence Regarding Optimal Implementation. J. Pers. Med. 2022, 12 , 692. Journal of personalized medicine 14 (3) (2024)
Kimberly S Foss, Julianne M O'Daniel, Jonathan S Berg, Sabrina N Powell, Rosemary Jean Cadigan, Kristine J Kuczynski, Laura V Milko, Katherine W Saylor, Megan Roberts, Karen Weck, Gail E Henderson
Correction: Foss et al. The Rise of Population Genomic Screening: Characteristics of Current Programs and the Need for Evidence Regarding Optimal Implementation. J. Pers. Med. 2022, 12 , 692. Journal of personalized medicine 14 (3) (2024)
Laura V Milko, Jonathan S Berg
Age-Based Genomic Screening during Childhood: Ethical and Practical Considerations in Public Health Genomics Implementation. International journal of neonatal screening 9 (3) (2023)
Kimberly S Foss, Julianne M O'Daniel, Jonathan S Berg, Sabrina N Powell, Rosemary Jean Cadigan, Kristine J Kuczynski, Laura V Milko, Katherine W Saylor, Megan Roberts, Karen Weck, Gail E Henderson
The Rise of Population Genomic Screening: Characteristics of Current Programs and the Need for Evidence Regarding Optimal Implementation. Journal of personalized medicine 12 (5) (2022)
Daniela M DeCristo, Laura V Milko, Julianne M O'Daniel, Ann Katherine M Foreman, Lonna F Mollison, Bradford C Powell, Cynthia M Powell, Jonathan S Berg
Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making. Genome medicine 13 (1) (2021)
Ida Griesemer, Brooke S Staley, Alexandra F Lightfoot, Lizzy Bain, Derrick Byrd, Carol Conway, Tracey L Grant, Barbara Leach, Laura V Milko, Lonna Mollison, Nadiah Porter, Sharron Reid, Gerri Smith, Margaret Waltz, Jonathan S Berg, Christine Rini, Julianne M O'Daniel
Engaging community stakeholders in research on best practices for clinical genomic sequencing. Personalized medicine 17 (6) (2020)
Ryan S Paquin, Kathleen F Mittendorf, Megan A Lewis, Jessica Ezzell Hunter, Kristy Lee, Jonathan S Berg, Marc S Williams, Katrina A B Goddard
Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
E Andres Rivera-Munoz, Laura V Milko, Steven M Harrison, Danielle R Azzariti, C Lisa Kurtz, Kristy Lee, Jessica L Mester, Meredith A Weaver, Erin Currey, William Craigen, Charis Eng, Birgit Funke, Madhuri Hegde, Ray E Hershberger, Rong Mao, Robert D Steiner, Lisa M Vincent, Christa L Martin, Sharon E Plon, Erin Ramos, Michael J Bamshad, Michael Watson, Jonathan S Berg
ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation. Human mutation 39 (11) (2019)
Sarah E Brnich, E Andres Rivera-Munoz, Jonathan S Berg
Quantifying the potential of functional evidence to reclassify variants of uncertain significance in the categorical and Bayesian interpretation frameworks. Human mutation 39 (11) (2018)
Patricia Himes, Tia L Kauffman, Kristin R Muessig, Laura M Amendola, Jonathan S Berg, Michael O Dorschner, Marian Gilmore, Deborah A Nickerson, Jacob A Reiss, Carolyn Sue Richards, Alan F Rope, Dana K Simpson, Benjamin S Wilfond, David L Veenstra, Katrina A B Goddard
Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing. Genetics in medicine : official journal of the American College of Medical Genetics 19 (7) (2017)
Jessica Ezzell Hunter, Stephanie A Irving, Leslie G Biesecker, Adam H Buchanan, Brian Jensen, Kristy Lee, Christa Lese Martin, Laura Milko, Kristin R Muessig, Annie D Niehaus, Julianne M O'Daniel, Margaret A Piper, Erin M Ramos, Sheri D Schully, Alan F Scott, Anne Slavotinek, Nara Sobreira, Natasha Strande, Meredith Weaver, Elizabeth M Webber, Marc S Williams, Jonathan S Berg, James P Evans, Katrina A B Goddard
A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation. Genetics in medicine : official journal of the American College of Medical Genetics 18 (12) (2016)
Jonathan S Berg
Exploring the importance of case-level clinical information for variant interpretation. Genetics in medicine : official journal of the American College of Medical Genetics 19 (1) (2016)
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin, Gregory M Cooper, Soma Das, Joshua L Deignan, Michael O Dorschner, James P Evans, Arezou A Ghazani, Katrina A B Goddard, Michele C Gornick, Kelly D F Hagman, Tina Hambuch, Madhuri Hegde, Lucia A Hindorff, Ingrid A Holm, Gail P Jarvik, Amy Knight Johnson, Lindsey Mighion, Massimo Morra, Sharon E Plon, Sumit Punj, Carolyn Sue Richards, Avni Santani, Brian H Shirts, Nancy B Spinner, Sha Tang, Karen E Weck, Susan M Wolf, Yaping Yang, Michael J Bamshad
A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories. Genetics in medicine : official journal of the American College of Medical Genetics 19 (5) (2016)
Michael C Adams, James P Evans, Gail E Henderson, Jonathan S Berg
The promise and peril of genomic screening in the general population. Genetics in medicine : official journal of the American College of Medical Genetics 18 (6) (2015)
Jonathan S Berg, Ann Katherine M Foreman, Julianne M O'Daniel, Jessica K Booker, Lacey Boshe, Timothy Carey, Kristy R Crooks, Brian C Jensen, Eric T Juengst, Kristy Lee, Daniel K Nelson, Bradford C Powell, Cynthia M Powell, Myra I Roche, Cecile Skrzynia, Natasha T Strande, Karen E Weck, Kirk C Wilhelmsen, James P Evans
A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing. Genetics in medicine : official journal of the American College of Medical Genetics 18 (5) (2015)

Jonathan S Berg.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Jonathan S Berg