N S Thomas
Impact in
Papers in
-
- dental development and anomalies 6
- Cancer-related gene regulation 4
- Muscle Physiology and Disorders 4
- RNA modifications and cancer 3
- Genetics 16
- Genetics and Neurodevelopmental Disorders 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Neurogenetic and Muscular Disorders Research 3
- Co-authors
- Paul J. Goodfellow (1 shared paper)Peter N. Goodfellow (1 shared paper)S. M. Darling (1 shared paper)Peter S. Harper (11 shared papers)Angus Clarke (10 shared papers)Keith Roberts (5 shared papers)M. Sarfarazi (4 shared papers)J. Zonana (6 shared papers)
- Journals
- Journal of Medical Genetics (10 papers)Human Molecular Genetics (2 papers)The Journal of Pediatrics (1 paper)Human Genetics (1 paper)Cytogenetic and Genome Research (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
N S Thomas
29 papers receiving 726 citations
Peers
Comparison fields: 5 of 73
- Urology 73
- Genetics 241
- Molecular Biology 553
- Rheumatology 76
- Cell Biology 88
Countries citing papers authored by N S Thomas
This map shows the geographic impact of N S 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 N S Thomas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N S Thomas more than expected).
Fields of papers citing papers by N S Thomas
This network shows the impact of papers produced by N S 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 N S Thomas. The network helps show where N S Thomas may publish in the future.
Co-authors
The 25 scholars most cited alongside N S 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1986 | 177 | |
| 2 | 2009 | 58 | |
| 3 | 1992 | 58 | |
| 4 | 1996 | 57 | |
| 5 | 1990 | 51 | |
| 6 | X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis. | 1988 | 46 |
| 7 | 1986 | 36 | |
| 8 | 1998 | 29 | |
| 9 | 1986 | 29 | |
| 10 | 1990 | 27 | |
| 11 | 1987 | 24 | |
| 12 | Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment. | 1993 | 22 |
| 13 | 1994 | 19 | |
| 14 | 1990 | 15 | |
| 15 | 1990 | 14 | |
| 16 | 1984 | 12 | |
| 17 | 1992 | 10 | |
| 18 | 1994 | 10 | |
| 19 | 1993 | 10 | |
| 20 | 1995 | 8 |
About N S Thomas
N S Thomas is a scholar working on Molecular Biology, Genetics, Cell Biology, Genetics and Plant Science, having authored 31 papers that have together received 745 indexed citations. Recurring topics across this work include dental development and anomalies (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Cancer-related gene regulation (4 papers), Muscle Physiology and Disorders (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Chromosomal and Genetic Variations (3 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Urology (73 citations), Genetics (241 citations), Molecular Biology (553 citations), Rheumatology (76 citations) and Cell Biology (88 citations). N S Thomas has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Paul J. Goodfellow, Peter N. Goodfellow, S. M. Darling, Peter S. Harper, Angus Clarke, Keith Roberts, M. Sarfarazi, J. Zonana, Meena Upadhyaya and Hywel Williams. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, The Journal of Pediatrics, Human Genetics and Cytogenetic and Genome Research.
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.