Nick Thomas
Impact in
- Genetics top 1%
- Genomics and Rare Diseases
- Neurogenetic and Muscular Disorders Research
- Molecular Biology top 2%
- Muscle Physiology and Disorders
- dental development and anomalies
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
Papers in
-
- RNA modifications and cancer 12
- Muscle Physiology and Disorders 10
- RNA Research and Splicing 9
- Ubiquitin and proteasome pathways 6
- Neurology 10
- Neurofibromatosis and Schwannoma Cases 10
- Co-authors
- D.N. Cooper (13 shared papers)Matthew Mort (4 shared papers)Peter D. Stenson (4 shared papers)Edward V. Ball (4 shared papers)Andrew D. Phillips (2 shared papers)Michael Krawczak (7 shared papers)Shaun S. Abeysinghe (2 shared papers)Peter S. Harper (12 shared papers)
- Journals
- Human Mutation (9 papers)Human Genetics (6 papers)Journal of Medical Genetics (5 papers)Neuromuscular Disorders (3 papers)Human Genomics (2 papers)
- Partner nations
- United KingdomGermanyUnited States
In The Last Decade
Nick Thomas
41 papers receiving 4.6k citations
Nick Thomas's Hit Papers
Peers
Comparison fields: 5 of 125
- Genetics 1.2k
- Molecular Biology 2.9k
- Neurology 461
- Genetics 307
- Cell Biology 376
Countries citing papers authored by Nick Thomas
This map shows the geographic impact of Nick Thomas'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 Nick Thomas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nick Thomas more than expected).
Fields of papers citing papers by Nick Thomas
This network shows the impact of papers produced by Nick Thomas. 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 Nick Thomas. The network helps show where Nick Thomas may publish in the future.
Co-authors
The 25 scholars most cited alongside Nick Thomas, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Human Gene Mutation Database (HGMD®): 2003 update Hit paper breakdown → | 2003 | 1367 |
| 2 | The Human Gene Mutation Database: 2008 update Hit paper breakdown → | 2009 | 635 |
| 3 | X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein Hit paper breakdown → | 1996 | 557 |
| 4 | 2006 | 273 | |
| 5 | 1988 | 239 | |
| 6 | 2000 | 212 | |
| 7 | 2002 | 106 | |
| 8 | 2011 | 101 | |
| 9 | 2003 | 99 | |
| 10 | 1984 | 95 | |
| 11 | 2007 | 88 | |
| 12 | 2004 | 72 | |
| 13 | 1983 | 65 | |
| 14 | 2011 | 57 | |
| 15 | Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. | 1990 | 55 |
| 16 | 1989 | 46 | |
| 17 | 2010 | 43 | |
| 18 | 2009 | 43 | |
| 19 | 1985 | 43 | |
| 20 | 2008 | 42 |
About Nick Thomas
Nick Thomas is a scholar working on Molecular Biology, Neurology, Genetics, Rheumatology and Genetics, having authored 41 papers that have together received 4.7k indexed citations. Recurring topics across this work include RNA modifications and cancer (12 papers), Neurofibromatosis and Schwannoma Cases (10 papers), Muscle Physiology and Disorders (10 papers), RNA Research and Splicing (9 papers), Ubiquitin and proteasome pathways (6 papers), Genetics and Neurodevelopmental Disorders (4 papers), Bone Tumor Diagnosis and Treatments (4 papers) and Cellular transport and secretion (4 papers). The work is most often cited by research in Genetics (1.2k citations), Molecular Biology (2.9k citations), Neurology (461 citations), Genetics (307 citations) and Cell Biology (376 citations). Nick Thomas has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include D.N. Cooper, Matthew Mort, Peter D. Stenson, Edward V. Ball, Andrew D. Phillips, Michael Krawczak, Shaun S. Abeysinghe, Peter S. Harper, Meena Upadhyaya and Angus Clarke. Their work appears in journals such as Human Mutation, Human Genetics, Journal of Medical Genetics, Neuromuscular Disorders and Human Genomics.
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.