Benjamin M. Helm
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
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- Cardiomyopathy and Myosin Studies
- Cardiac Valve Diseases and Treatments
Papers in
- Genetics 23
- Genomics and Rare Diseases 12
- Genomic variations and chromosomal abnormalities 8
- BRCA gene mutations in cancer 8
- Connective tissue disorders research 3
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- Prenatal Screening and Diagnostics 6
- Co-authors
- Stephanie M. Ware (22 shared papers)Benjamin J. Landis (14 shared papers)Samantha A. Schrier Vergano (8 shared papers)Adam C. Kean (5 shared papers)Andrew Paul Landstrom (1 shared paper)Amy Curry Sturm (1 shared paper)Prince J. Kannankeril (1 shared paper)Jeffrey J. Kim (1 shared paper)
- Journals
- Circulation Genomic and Precision Medicine (3 papers)Genes (2 papers)PEDIATRICS (2 papers)European Journal of Medical Genetics (2 papers)Journal of Genetic Counseling (15 papers)
- Partner nations
- United StatesUnited KingdomAustralia
In The Last Decade
Benjamin M. Helm
45 papers receiving 477 citations
Peers
Comparison fields: 5 of 61
- Genetics 194
- Cardiology and Cardiovascular Medicine 107
- Pediatrics, Perinatology and Child Health 74
- Epidemiology 105
- Molecular Biology 158
Countries citing papers authored by Benjamin M. Helm
This map shows the geographic impact of Benjamin M. Helm'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 Benjamin M. Helm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Benjamin M. Helm more than expected).
Fields of papers citing papers by Benjamin M. Helm
This network shows the impact of papers produced by Benjamin M. Helm. 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 Benjamin M. Helm. The network helps show where Benjamin M. Helm may publish in the future.
Co-authors
The 25 scholars most cited alongside Benjamin M. Helm, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 65 | |
| 2 | 2015 | 51 | |
| 3 | 2016 | 43 | |
| 4 | 2023 | 23 | |
| 5 | 2021 | 22 | |
| 6 | 2017 | 21 | |
| 7 | 2021 | 21 | |
| 8 | 2017 | 20 | |
| 9 | 2017 | 20 | |
| 10 | 2015 | 19 | |
| 11 | 2015 | 17 | |
| 12 | 2017 | 13 | |
| 13 | 2016 | 13 | |
| 14 | 2023 | 12 | |
| 15 | 2022 | 12 | |
| 16 | 2023 | 11 | |
| 17 | 2019 | 10 | |
| 18 | 2023 | 10 | |
| 19 | 2018 | 7 | |
| 20 | 2022 | 7 |
About Benjamin M. Helm
Benjamin M. Helm is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Epidemiology, Cardiology and Cardiovascular Medicine and Molecular Biology, having authored 50 papers that have together received 500 indexed citations. Recurring topics across this work include Congenital heart defects research (14 papers), Congenital Heart Disease Studies (12 papers), Genomics and Rare Diseases (12 papers), Genomic variations and chromosomal abnormalities (8 papers), BRCA gene mutations in cancer (8 papers), Prenatal Screening and Diagnostics (6 papers), Cardiac electrophysiology and arrhythmias (3 papers) and Connective tissue disorders research (3 papers). The work is most often cited by research in Genetics (194 citations), Cardiology and Cardiovascular Medicine (107 citations), Pediatrics, Perinatology and Child Health (74 citations), Epidemiology (105 citations) and Molecular Biology (158 citations). Benjamin M. Helm has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Stephanie M. Ware, Benjamin J. Landis, Samantha A. Schrier Vergano, Adam C. Kean, Andrew Paul Landstrom, Amy Curry Sturm, Prince J. Kannankeril, Jeffrey J. Kim, Christopher Semsarian and Martin Tristani‐Firouzi. Their work appears in journals such as Circulation Genomic and Precision Medicine, Genes, PEDIATRICS, European Journal of Medical Genetics and Journal of Genetic Counseling.
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.