Sumit Parikh
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
- Molecular Biology top 5%
- Mitochondrial Function and Pathology
Papers in
-
- Metabolism and Genetic Disorders 29
-
- Epilepsy research and treatment 11
- Migraine and Headache Studies 5
- Co-authors
- Richard Haas (7 shared papers)Russell P. Saneto (6 shared papers)Bruce H. Cohen (7 shared papers)Marni J. Falk (6 shared papers)Niklas Darín (2 shared papers)Nicole Ingeborg Wolf (2 shared papers)Irina A. Anselm (2 shared papers)Mary Kay Koenig (4 shared papers)
- Journals
- Molecular Genetics and Metabolism (9 papers)Neurology (6 papers)Pediatric Neurology (6 papers)Mitochondrion (6 papers)Genetics in Medicine (4 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Sumit Parikh
89 papers receiving 3.9k citations
Sumit Parikh's Hit Papers
Peers
Comparison fields: 5 of 122
- Clinical Biochemistry 732
- Molecular Biology 1.8k
- Genetics 796
- Psychiatry and Mental health 433
- Cognitive Neuroscience 328
Countries citing papers authored by Sumit Parikh
This map shows the geographic impact of Sumit Parikh'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 Sumit Parikh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sumit Parikh more than expected).
Fields of papers citing papers by Sumit Parikh
This network shows the impact of papers produced by Sumit Parikh. 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 Sumit Parikh. The network helps show where Sumit Parikh may publish in the future.
Co-authors
The 25 scholars most cited alongside Sumit Parikh, 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 96 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants Hit paper breakdown → | 2012 | 462 |
| 2 | Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society Hit paper breakdown → | 2014 | 450 |
| 3 | 2008 | 300 | |
| 4 | 2009 | 284 | |
| 5 | 2017 | 229 | |
| 6 | 2007 | 215 | |
| 7 | 2014 | 154 | |
| 8 | 2019 | 123 | |
| 9 | 2016 | 100 | |
| 10 | 2015 | 90 | |
| 11 | 2016 | 87 | |
| 12 | 2015 | 79 | |
| 13 | 2014 | 78 | |
| 14 | 2022 | 68 | |
| 15 | 2016 | 67 | |
| 16 | 2015 | 66 | |
| 17 | 2016 | 62 | |
| 18 | 2019 | 59 | |
| 19 | 2018 | 58 | |
| 20 | 2023 | 58 |
About Sumit Parikh
Sumit Parikh is a scholar working on Clinical Biochemistry, Psychiatry and Mental health, Molecular Biology, Genetics and Gastroenterology, having authored 96 papers that have together received 4.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (42 papers), Metabolism and Genetic Disorders (29 papers), Epilepsy research and treatment (11 papers), Genetics and Neurodevelopmental Disorders (10 papers), Migraine and Headache Studies (5 papers), Genomics and Rare Diseases (5 papers), Hereditary Neurological Disorders (3 papers) and Gastrointestinal motility and disorders (3 papers). The work is most often cited by research in Clinical Biochemistry (732 citations), Molecular Biology (1.8k citations), Genetics (796 citations), Psychiatry and Mental health (433 citations) and Cognitive Neuroscience (328 citations). Sumit Parikh has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Richard Haas, Russell P. Saneto, Bruce H. Cohen, Marni J. Falk, Niklas Darín, Nicole Ingeborg Wolf, Irina A. Anselm, Mary Kay Koenig, Andrea Lynne Gropman and Amy C. Goldstein. Their work appears in journals such as Molecular Genetics and Metabolism, Neurology, Pediatric Neurology, Mitochondrion and Genetics in Medicine.
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.