Seth Dobrin
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in ⓘ
-
- Gene expression and cancer classification 3
- Advanced biosensing and bioanalysis techniques 1
- Genetics 6
- Genetic Associations and Epidemiology 4
- Genetic Mapping and Diversity in Plants and Animals 2
- Genomic variations and chromosomal abnormalities 2
- Connective tissue disorders research 1
- Co-authors
- D. Holmes Morton (2 shared papers)Kevin A. Strauss (2 shared papers)Erik G. Puffenberger (2 shared papers)Dietrich A. Stephan (2 shared papers)Matthew J. Huentelman (1 shared paper)David Page (1 shared paper)Jan Struyf (1 shared paper)E. Claffey (2 shared papers)
- Journals
- Expert Review of Molecular Diagnostics (2 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2 papers)Pharmacogenomics (1 paper)BMC Genomics (1 paper)Journal of Orthopaedic Research® (1 paper)
- Partner nations
- United StatesIrelandUnited Kingdom
In The Last Decade
Seth Dobrin
14 papers receiving 774 citations
Peers
Comparison fields: 5 of 83
- Genetics 441
- Cognitive Neuroscience 239
- Developmental Neuroscience 27
- Molecular Biology 372
- Psychiatry and Mental health 80
Countries citing papers authored by Seth Dobrin
This map shows the geographic impact of Seth Dobrin'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 Seth Dobrin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Seth Dobrin more than expected).
Fields of papers citing papers by Seth Dobrin
This network shows the impact of papers produced by Seth Dobrin. 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 Seth Dobrin. The network helps show where Seth Dobrin may publish in the future.
Co-authors
The 25 scholars most cited alongside Seth Dobrin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 479 | |
| 2 | 2004 | 108 | |
| 3 | 2007 | 50 | |
| 4 | 2009 | 40 | |
| 5 | 2008 | 33 | |
| 6 | 2007 | 31 | |
| 7 | 2007 | 20 | |
| 8 | 2006 | 10 | |
| 9 | 2003 | 7 | |
| 10 | 2004 | 5 | |
| 11 | 2024 | 2 | |
| 12 | 2007 | 2 | |
| 13 | 2023 | 1 | |
| 14 | 2006 | 1 | |
| 15 | 2024 | 0 |
About Seth Dobrin
Seth Dobrin is a scholar working on Molecular Biology, Genetics, Surgery, Health Informatics and Physiology, having authored 15 papers that have together received 789 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (4 papers), Gene expression and cancer classification (3 papers), Artificial Intelligence in Healthcare and Education (2 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Advanced biosensing and bioanalysis techniques (1 paper), Connective tissue disorders research (1 paper) and Bipolar Disorder and Treatment (1 paper). The work is most often cited by research in Genetics (441 citations), Cognitive Neuroscience (239 citations), Developmental Neuroscience (27 citations), Molecular Biology (372 citations) and Psychiatry and Mental health (80 citations). Seth Dobrin has collaborated with scholars based in United States, Ireland and United Kingdom. Frequent co-authors include D. Holmes Morton, Kevin A. Strauss, Erik G. Puffenberger, Dietrich A. Stephan, Matthew J. Huentelman, David Page, Jan Struyf, E. Claffey, Patrick O. McKeon and S. Roche. Their work appears in journals such as Expert Review of Molecular Diagnostics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Pharmacogenomics, BMC Genomics and Journal of Orthopaedic Research®.
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.