Simon Hammans
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
-
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Papers in
-
- Mitochondrial Function and Pathology 24
- ATP Synthase and ATPases Research 8
- Muscle Physiology and Disorders 7
-
- Genetic Neurodegenerative Diseases 14
- Hereditary Neurological Disorders 4
- Co-authors
- J A Morgan-Hughes (9 shared papers)A. E. Harding (7 shared papers)Martin Brockington (5 shared papers)M G Sweeney (3 shared papers)Mary G. Sweeney (7 shared papers)Ian Holt (2 shared papers)E M Brett (1 shared paper)T. James Beattie (1 shared paper)
- Journals
- Brain (7 papers)Neuromuscular Disorders (5 papers)Neurology (3 papers)Journal of Neurology Neurosurgery & Psychiatry (3 papers)Journal of Inherited Metabolic Disease (2 papers)
- Partner nations
- United KingdomUnited StatesSpain
In The Last Decade
Simon Hammans
47 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 80
- Clinical Biochemistry 848
- Cellular and Molecular Neuroscience 441
- Molecular Biology 1.5k
- Neurology 203
- Neurology 107
Countries citing papers authored by Simon Hammans
This map shows the geographic impact of Simon Hammans'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 Simon Hammans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simon Hammans more than expected).
Fields of papers citing papers by Simon Hammans
This network shows the impact of papers produced by Simon Hammans. 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 Simon Hammans. The network helps show where Simon Hammans may publish in the future.
Co-authors
The 25 scholars most cited alongside Simon Hammans, 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 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA. | 1991 | 220 |
| 2 | 1991 | 148 | |
| 3 | 1995 | 127 | |
| 4 | 1993 | 120 | |
| 5 | 2005 | 110 | |
| 6 | 2010 | 96 | |
| 7 | 2001 | 72 | |
| 8 | 1995 | 72 | |
| 9 | 1993 | 67 | |
| 10 | 2013 | 62 | |
| 11 | 1997 | 61 | |
| 12 | 2004 | 59 | |
| 13 | 2001 | 59 | |
| 14 | 2009 | 48 | |
| 15 | 1992 | 46 | |
| 16 | 1994 | 44 | |
| 17 | 2005 | 42 | |
| 18 | 2017 | 38 | |
| 19 | 2000 | 36 | |
| 20 | 2013 | 34 |
About Simon Hammans
Simon Hammans is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Clinical Biochemistry, Neurology and Rheumatology, having authored 48 papers that have together received 2.0k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (24 papers), Metabolism and Genetic Disorders (16 papers), Genetic Neurodegenerative Diseases (14 papers), ATP Synthase and ATPases Research (8 papers), Muscle Physiology and Disorders (7 papers), Neurological diseases and metabolism (4 papers), Hereditary Neurological Disorders (4 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). The work is most often cited by research in Clinical Biochemistry (848 citations), Cellular and Molecular Neuroscience (441 citations), Molecular Biology (1.5k citations), Neurology (203 citations) and Neurology (107 citations). Simon Hammans has collaborated with scholars based in United Kingdom, United States and Spain. Frequent co-authors include J A Morgan-Hughes, A. E. Harding, Martin Brockington, M G Sweeney, Mary G. Sweeney, Ian Holt, E M Brett, T. James Beattie, A E Harding and David Robinson. Their work appears in journals such as Brain, Neuromuscular Disorders, Neurology, Journal of Neurology Neurosurgery & Psychiatry and Journal of Inherited Metabolic Disease.
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.