N. Simon Thomas
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 55
- Genomic variations and chromosomal abnormalities 24
- Genetic Syndromes and Imprinting 15
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 14
- Genetics and Neurodevelopmental Disorders 7
-
- Genomics and Chromatin Dynamics 8
- Congenital heart defects research 6
- Co-authors
- Marijcke W. M. Veltman (6 shared papers)Patrick Bolton (6 shared papers)Russell Thompson (5 shared papers)Patricia A. Jacobs (10 shared papers)David J. Bunyan (15 shared papers)C.E. Browne (6 shared papers)John A. Crolla (8 shared papers)Siân E. Roberts (4 shared papers)
- Journals
- Human Genetics (11 papers)European Journal of Human Genetics (6 papers)The American Journal of Human Genetics (6 papers)Human Molecular Genetics (3 papers)European Journal of Medical Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesDenmark
In The Last Decade
N. Simon Thomas
63 papers receiving 2.6k citations
Peers
Comparison fields: 5 of 95
- Genetics 2.0k
- Pediatrics, Perinatology and Child Health 510
- Cognitive Neuroscience 399
- Molecular Biology 1.0k
- Reproductive Medicine 112
Countries citing papers authored by N. Simon Thomas
This map shows the geographic impact of N. Simon 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. Simon 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. Simon Thomas more than expected).
Fields of papers citing papers by N. Simon Thomas
This network shows the impact of papers produced by N. Simon 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. Simon Thomas. The network helps show where N. Simon Thomas may publish in the future.
Co-authors
The 25 scholars most cited alongside N. Simon 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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 181 | |
| 2 | 2004 | 173 | |
| 3 | 2003 | 155 | |
| 4 | 2003 | 149 | |
| 5 | 2008 | 148 | |
| 6 | 2005 | 136 | |
| 7 | 1999 | 133 | |
| 8 | 2020 | 108 | |
| 9 | 2005 | 107 | |
| 10 | 2004 | 100 | |
| 11 | 2004 | 92 | |
| 12 | 2001 | 77 | |
| 13 | 2005 | 70 | |
| 14 | 2009 | 64 | |
| 15 | 2001 | 62 | |
| 16 | 2008 | 61 | |
| 17 | 1998 | 60 | |
| 18 | 2004 | 53 | |
| 19 | 2006 | 50 | |
| 20 | 2006 | 48 |
About N. Simon Thomas
N. Simon Thomas is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Genetics, having authored 67 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (24 papers), Prenatal Screening and Diagnostics (16 papers), Genetic Syndromes and Imprinting (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Chromosomal and Genetic Variations (13 papers), Genomics and Chromatin Dynamics (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Genetics (2.0k citations), Pediatrics, Perinatology and Child Health (510 citations), Cognitive Neuroscience (399 citations), Molecular Biology (1.0k citations) and Reproductive Medicine (112 citations). N. Simon Thomas has collaborated with scholars based in United Kingdom, United States and Denmark. Frequent co-authors include Marijcke W. M. Veltman, Patrick Bolton, Russell Thompson, Patricia A. Jacobs, David J. Bunyan, C.E. Browne, John A. Crolla, Siân E. Roberts, P. A. Jacobs and Nicholas R. Dennis. Their work appears in journals such as Human Genetics, European Journal of Human Genetics, The American Journal of Human Genetics, Human Molecular Genetics and European 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.