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
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 5
- Neurogenetic and Muscular Disorders Research 3
- Co-authors
- S. M. Darling (1 shared paper)Paul J. Goodfellow (1 shared paper)Peter N. Goodfellow (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)Cytogenetic and Genome Research (2 papers)The Journal of Pediatrics (1 paper)Human Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
N S Thomas
30 papers receiving 748 citations
Peers
Comparison fields: 5 of 75
- Urology 76
- Genetics 257
- Molecular Biology 580
- Cell Biology 95
- Rheumatology 80
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 | 176 | |
| 2 | 1992 | 58 | |
| 3 | 2009 | 58 | |
| 4 | 1996 | 57 | |
| 5 | 1990 | 50 | |
| 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 | 28 | |
| 10 | 1990 | 27 | |
| 11 | 1986 | 26 | |
| 12 | 1987 | 24 | |
| 13 | 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 |
| 14 | 1994 | 19 | |
| 15 | 1990 | 15 | |
| 16 | 1990 | 14 | |
| 17 | 1984 | 12 | |
| 18 | 1993 | 10 | |
| 19 | 1992 | 10 | |
| 20 | 1994 | 10 |
About N S Thomas
N S Thomas is a scholar working on Molecular Biology, Genetics, Cell Biology, Surgery and Genetics, having authored 31 papers that have together received 768 indexed citations. Recurring topics across this work include dental development and anomalies (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Cancer-related gene regulation (4 papers), Muscle Physiology and Disorders (4 papers), Chromosomal and Genetic Variations (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Urology (76 citations), Genetics (257 citations), Molecular Biology (580 citations), Cell Biology (95 citations) and Rheumatology (80 citations). N S Thomas has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include S. M. Darling, Paul J. Goodfellow, Peter N. Goodfellow, Peter S. Harper, Angus Clarke, Keith Roberts, M. Sarfarazi, J. Zonana, Hywel Williams and Meena Upadhyaya. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Cytogenetic and Genome Research, The Journal of Pediatrics and Human 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.