Sumit Parikh
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
- Molecular Biology top 5%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA regulation and disease
Papers in
-
- Mitochondrial Function and Pathology 32
- ATP Synthase and ATPases Research 9
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- Metabolism and Genetic Disorders 29
- 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)Nicole I. Wolf (2 shared papers)Niklas Darín (2 shared papers)Irina Anselm (2 shared papers)Andrea Gropman (3 shared papers)
- Journals
- Molecular Genetics and Metabolism (7 papers)Mitochondrion (4 papers)Pediatric Neurology (4 papers)Ophthalmic Genetics (3 papers)Haemophilia (3 papers)
- Partner nations
- United StatesAustraliaCanada
In The Last Decade
Sumit Parikh
63 papers receiving 2.4k citations
Sumit Parikh's Hit Papers
Peers
Comparison fields: 5 of 123
- Clinical Biochemistry 811
- Molecular Biology 1.5k
- Genetics 453
- Aging 26
- Psychiatry and Mental health 223
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 70 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society Hit paper breakdown → | 2014 | 372 |
| 2 | 2008 | 269 | |
| 3 | 2009 | 252 | |
| 4 | 2007 | 190 | |
| 5 | 2014 | 123 | |
| 6 | 2019 | 98 | |
| 7 | 2016 | 84 | |
| 8 | 2015 | 81 | |
| 9 | 2016 | 72 | |
| 10 | 2014 | 69 | |
| 11 | 2015 | 63 | |
| 12 | 2016 | 53 | |
| 13 | 2016 | 46 | |
| 14 | 2018 | 45 | |
| 15 | 2015 | 43 | |
| 16 | 2011 | 41 | |
| 17 | 2013 | 30 | |
| 18 | 2014 | 28 | |
| 19 | 2016 | 26 | |
| 20 | 2020 | 26 |
About Sumit Parikh
Sumit Parikh is a scholar working on Molecular Biology, Clinical Biochemistry, Genetics, Cellular and Molecular Neuroscience and Psychiatry and Mental health, having authored 70 papers that have together received 2.4k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (32 papers), Metabolism and Genetic Disorders (29 papers), ATP Synthase and ATPases Research (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (7 papers), Genetic Neurodegenerative Diseases (6 papers), Migraine and Headache Studies (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Clinical Biochemistry (811 citations), Molecular Biology (1.5k citations), Genetics (453 citations), Aging (26 citations) and Psychiatry and Mental health (223 citations). Sumit Parikh has collaborated with scholars based in United States, Australia and Canada. Frequent co-authors include Richard Haas, Russell P. Saneto, Bruce H. Cohen, Marni J. Falk, Nicole I. Wolf, Niklas Darín, Irina Anselm, Andrea Gropman, Mary Kay Koenig and Amy Goldstein. Their work appears in journals such as Molecular Genetics and Metabolism, Mitochondrion, Pediatric Neurology, Ophthalmic Genetics and Haemophilia.
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.