Mark T. Rogers
Impact in
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- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
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- Neurological diseases and metabolism
- Parkinson's Disease Mechanisms and Treatments
Papers in
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- Muscle Physiology and Disorders 4
- RNA modifications and cancer 2
- Mitochondrial Function and Pathology 2
- Genetics 4
- BRCA gene mutations in cancer 4
- Neurogenetic and Muscular Disorders Research 4
- Co-authors
- Peter S. Harper (3 shared papers)Kate Bushby (1 shared paper)C. Pollitt (1 shared paper)Mary Ann Johnson (1 shared paper)Patrick F. Chinnery (1 shared paper)Evan Reid (1 shared paper)David C. Rubinsztein (1 shared paper)Olivia Osborn (1 shared paper)
- Journals
- Neuromuscular Disorders (4 papers)Gynecologic Oncology (2 papers)The American Journal of Human Genetics (1 paper)European Journal of Human Genetics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesSingapore
In The Last Decade
Mark T. Rogers
11 papers receiving 271 citations
Peers
Comparison fields: 5 of 48
- Cellular and Molecular Neuroscience 143
- Neurology 49
- Genetics 54
- Neurology 57
- Cardiology and Cardiovascular Medicine 64
Countries citing papers authored by Mark T. Rogers
This map shows the geographic impact of Mark T. Rogers'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 Mark T. Rogers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark T. Rogers more than expected).
Fields of papers citing papers by Mark T. Rogers
This network shows the impact of papers produced by Mark T. Rogers. 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 Mark T. Rogers. The network helps show where Mark T. Rogers may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark T. Rogers, 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 | 1998 | 55 | |
| 2 | 2000 | 52 | |
| 3 | 1997 | 51 | |
| 4 | 2004 | 28 | |
| 5 | 1998 | 24 | |
| 6 | 2002 | 18 | |
| 7 | 2014 | 17 | |
| 8 | 2012 | 15 | |
| 9 | 2011 | 12 | |
| 10 | 2014 | 6 | |
| 11 | 2006 | 1 |
About Mark T. Rogers
Mark T. Rogers is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Genetics and Reproductive Medicine, having authored 11 papers that have together received 279 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (4 papers), Muscle Physiology and Disorders (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Ovarian cancer diagnosis and treatment (3 papers), Genetic Neurodegenerative Diseases (3 papers), Family Support in Illness (2 papers), RNA modifications and cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (143 citations), Neurology (49 citations), Genetics (54 citations), Neurology (57 citations) and Cardiology and Cardiovascular Medicine (64 citations). Mark T. Rogers has collaborated with scholars based in United Kingdom, United States and Singapore. Frequent co-authors include Peter S. Harper, Kate Bushby, C. Pollitt, Mary Ann Johnson, Patrick F. Chinnery, Evan Reid, David C. Rubinsztein, Olivia Osborn, Meena Upadhyaya and Andrew Dearlove. Their work appears in journals such as Neuromuscular Disorders, Gynecologic Oncology, The American Journal of Human Genetics, European Journal of Human Genetics and Journal of Medical Genetics.
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.