Jonathan S. Berg

21.6k citations

133 papers · 9.3k indexed · 7 hit papers · h-index 38

Impact in

Genetics top 0.2%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Cancer Research top 1%
- Cancer Genomics and Diagnostics

Papers in

Genetics 93
- Genomics and Rare Diseases 74
- BRCA gene mutations in cancer 36
- Genomic variations and chromosomal abnormalities 26
Cancer Research 26
- Cancer Genomics and Diagnostics 26

Co-authors: Richard E. Cheney Heidi L. Rehm Bradford C. Powell Robert L. Nussbaum Christa Lese Martin Michael S. Watson James P. Evans Kelly E. Ormond
Journals: Genetics in Medicine (33 papers)The American Journal of Human Genetics (5 papers)Genome Medicine (5 papers)Human Mutation (4 papers)Nature Cell Biology (3 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

Jonathan S. Berg

124 papers receiving 9.1k citations

Hit Papers

7 papers align trajectories log scale

Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework 2019 · 310 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2019 Genome Medicine
2015 New England Journal of Medicine
2015 The American Journal of Human Genetics
2013 Genetics in Medicine
2013 Genetics in Medicine
2011 Nature Genetics
2001 Molecular Biology of the Cell

Peers

Countries citing papers authored by Jonathan S. Berg

Since Specialization

Citations

This map shows the geographic impact of Jonathan S. Berg'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 Jonathan S. Berg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan S. Berg more than expected).

Fields of papers citing papers by Jonathan S. Berg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jonathan S. Berg. 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 Jonathan S. Berg. The network helps show where Jonathan S. Berg may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Jonathan S. Berg, 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 Jonathan S. Berg Line = papers co-authored together Jonathan S. Berg links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Group-based medical mistrust in genomic medicine: Associations with patient and provider perceptions of a specialty clinical encounter Genetics in Medicine ·Frank Angelo, Margaret Waltz, Alvina Suryadinata, Jonathan S. Berg, Ann Katherine M. Foreman, Julianne O’Daniel, Christine Rini	2024	1
2	Implementation of a dyadic nomenclature for monogenic diseases The American Journal of Human Genetics ·Courtney Thaxton, Leslie G. Biesecker, Marina T. DiStefano, Melissa Haendel, Ada Hamosh, 憲司川瀬, Sharon E. Plon, Heidi L. Rehm, Jonathan S. Berg	2024	6
3	Question prompt lists and caregiver question asking in pediatric specialty appointments: A randomized controlled trial Patient Education and Counseling ·Margaret Waltz, Alvina Suryadinata, R. Jean Cadigan, Ana Belén Perianes Bermúdez, Nurul Pamisa, Jeannette T. Bensen, Qiyin An, Chad Haldeman‐Englert, Laura Farnan, Ann Katherine M. Foreman, Juan de la Cruz Ferrer, J Dubicka, Feng‐Chang Lin, Lj. Josimović, Julianne O’Daniel, Suzanne C. O’Neill, V Salvi, Bradford C. Powell, Jonathan S. Berg, Christine Rini	2023	6
4	Lumping versus splitting: How to approach defining a disease to enable accurate genomic curation Cell Genomics ·Courtney Thaxton, Jennifer Goldstein, Marina T. DiStefano, Kathleen Wallace, P. Dane Witmer, Melissa Haendel, Ada Hamosh, Heidi L. Rehm, Jonathan S. Berg	2022	17
5	Increased Prevalence of Rare Copy Number Variants in Treatment-Resistant Psychosis Schizophrenia Bulletin ·Martilias S. Farrell, Н.П. Ромашкина, Dae Hwan Kim, Jianmin Zhang, Tazawa Hidekatsu, Rita A. Shaughnessy, 幸雄黒川, 廣田栄子, Gavin Megson, James J. Crowley, Gabriel Lázaro‐Muñoz, Larisa V. Nikankina, Jacob Nielsen, Michael Didriksen, Jonathan S. Berg, Jia Wen, Jin Szatkiewicz, Sophie Wyatt, Patrick F. Sullivan, Richard C. Josiassen	2022	14
6	Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial Trials ·N W Gaggini, Laura V. Milko, Margaret Waltz, Suljo Ljukovac, Maolin Li, Juan de la Cruz Ferrer, Laura Farnan, Myra I. Roche, H. Li, Alexandra F. Lightfoot, Ann Katherine M. Foreman, Julianne O’Daniel, Suzanne C. O’Neill, Feng‐Chang Lin, Tamara S. Roman, Alicia Brandt, Bradford C. Powell, Christine Rini, Jonathan S. Berg, Jeannette T. Bensen	2021	6
7	Engaging Community Stakeholders in Research on Best Practices for Clinical Genomic Sequencing Personalized Medicine ·Suljo Ljukovac, N W Gaggini, Alexandra F. Lightfoot, Nurul Pamisa, Rafi Aharoni, Qiyin An, Juan de la Cruz Ferrer, J Dubicka, Laura V. Milko, Maolin Li, Ravi Kishore Kanamarlapudi, Gerd E. Nysether, V Salvi, Margaret Waltz, Jonathan S. Berg, Christine Rini, Julianne O’Daniel	2020	11
8	Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty Journal of Genetic Counseling ·Margaret Waltz, Anya E. R. Prince, Julianne O’Daniel, Ann Katherine M. Foreman, Bradford C. Powell, Jonathan S. Berg	2020	5
9	Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes Genetics in Medicine ·Christine Rini, Gail E. Henderson, James P. Evans, Jonathan S. Berg, Ann Katherine M. Foreman, Suljo Ljukovac, Margaret Waltz, Julianne O’Daniel, Myra I. Roche	2019	13
10	Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders Genetics in Medicine ·Ryan S. Paquin, Kathleen F. Mittendorf, Megan A. Lewis, Jessica Ezzell Hunter, Kristy Lee, Jonathan S. Berg, Marc S. Williams, Katrina A.B. Goddard	2019	3
11	Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert Panels Genome Medicine ·Dona Kanavy, Shannon McNulty, В.М. Алпатов, Sarah E. Brnich, Chris Bizon, Bradford C. Powell, Jonathan S. Berg	2019	33
12	hCALCRL mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasia The Journal of Experimental Medicine ·J N Fomulu, Fuad Al Mutairi, Reema B. Davis, Daniel O. Kechele, Allan Winterbottom, Joshua C. Snyder, Marc G. Caron, Harvey J. Kliman, Jonathan S. Berg, John Simms, David R. Poyner, Kathleen M. Caron	2018	29
13	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
14	Factors influencing NCGENES research participants- requests for non-medically actionable secondary findings Genetics in Medicine ·Myra I. Roche, Suljo Ljukovac, Cynthia M. Khan, Elizabeth Moore, Feng‐Chang Lin, Julianne O’Daniel, Ann Katherine M. Foreman, Kristy Lee, Bradford C. Powell, Jonathan S. Berg, James P. Evans, Gail E. Henderson, Christine Rini	2018	10
15	Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing Genetics in Medicine ·Deborah Ritter, Лусине Суреновна Полонская, Hannah Cheung, Caleb Davis, Ching C. Lau, Jonathan S. Berg, Chester Brown, Patrick A. Thompson, Richard A. Gibbs, David A. Wheeler, Sharon E. Plon	2015	18
16	The promise and peril of genomic screening in the general population Genetics in Medicine ·Michael C. C. Adams, James P. Evans, Gail E. Henderson, Jonathan S. Berg	2015	39
17	ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing Genetics in Medicine ·Robert C. Green, Jonathan S. Berg, Wayne W. Grody, Sarah S. Kalia, Bruce R. Korf, Christa Lese Martin, Amy L. McGuire, Robert L. Nussbaum, Julianne O’Daniel, Kelly E. Ormond, Heidi L. Rehm, Michael S. Watson, Marc S. Williams, Leslie G. Biesecker Hit paper breakdown →	2013	1643
18	Next-Generation DNA Sequencing, Regulation, and the Limits of Paternalism JAMA ·James P. Evans, Jonathan S. Berg	2011	25
19	Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: Implications for application to clinical testing Genetics in Medicine ·Jonathan S. Berg, James P. Evans, Margaret W. Leigh, Heymut Omran, Chris Bizon, Ketan K. Mane, Michael R. Knowles, Karen E. Weck, Maimoona A. Zariwala	2011	41
20	22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome The American Journal of Human Genetics ·Shay Ben‐Shachar, Zhishuo Ou, Chad A. Shaw, John W. Belmont, Millan S. Patel, Marybeth Hummel, Stephen Amato, Nicole Tartaglia, Jonathan S. Berg, V. Reid Sutton, Seema R. Lalani, A. Craig Chinault, Sau Wai Cheung, James R. Lupski, Ankita Patel	2008	142

About Jonathan S. Berg

Jonathan S. Berg is a scholar working on Genetics, Cancer Research, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Public Health, Environmental and Occupational Health, having authored 133 papers that have together received 9.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (74 papers), BRCA gene mutations in cancer (36 papers), Cancer Genomics and Diagnostics (26 papers), Genomic variations and chromosomal abnormalities (26 papers), Ethics in Clinical Research (18 papers), Genetic factors in colorectal cancer (17 papers), Prenatal Screening and Diagnostics (13 papers) and Cardiomyopathy and Myosin Studies (10 papers). The work is most often cited by research in Genetics (4.5k citations), Cancer Research (1.4k citations), Cell Biology (1.1k citations), Hematology (730 citations) and Molecular Biology (4.0k citations). Jonathan S. Berg has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Richard E. Cheney, Heidi L. Rehm, Bradford C. Powell, Robert L. Nussbaum, Christa Lese Martin, Michael S. Watson, James P. Evans, Kelly E. Ormond, Julianne O’Daniel and Leslie G. Biesecker. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Genome Medicine, Human Mutation and Nature Cell Biology.

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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