Mark S. Bateman
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Congenital Ear and Nasal Anomalies
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 10
- Congenital Ear and Nasal Anomalies 5
- Genetics and Neurodevelopmental Disorders 2
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
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- Congenital heart defects research 5
- Genomics and Chromatin Dynamics 2
- Co-authors
- John Barber (10 shared papers)Lionel Willatt (2 shared papers)Morag N. Collinson (4 shared papers)John R.W. Yates (1 shared paper)James C. Nicholson (1 shared paper)Andrew Green (1 shared paper)N R Dennis (1 shared paper)Viv Maloney (3 shared papers)
- Journals
- Cytogenetic and Genome Research (3 papers)Clinical Endocrinology (1 paper)European Journal of Human Genetics (1 paper)Atherosclerosis (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesPortugal
In The Last Decade
Mark S. Bateman
12 papers receiving 175 citations
Peers
Comparison fields: 5 of 38
- Genetics 170
- Pediatrics, Perinatology and Child Health 54
- Genetics 18
- Developmental Biology 4
- Plant Science 55
Countries citing papers authored by Mark S. Bateman
This map shows the geographic impact of Mark S. Bateman'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 Mark S. Bateman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark S. Bateman more than expected).
Fields of papers citing papers by Mark S. Bateman
This network shows the impact of papers produced by Mark S. Bateman. 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 Mark S. Bateman. The network helps show where Mark S. Bateman may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark S. Bateman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 73 | |
| 2 | 2013 | 38 | |
| 3 | 2012 | 38 | |
| 4 | 2015 | 31 | |
| 5 | 2010 | 26 | |
| 6 | 2011 | 7 | |
| 7 | 2017 | 5 | |
| 8 | 2012 | 3 | |
| 9 | 2013 | 3 | |
| 10 | 2020 | 2 | |
| 11 | 2020 | 1 | |
| 12 | 1994 | 1 |
About Mark S. Bateman
Mark S. Bateman is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Surgery, having authored 12 papers that have together received 228 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Congenital heart defects research (5 papers), Congenital Ear and Nasal Anomalies (5 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genomics and Chromatin Dynamics (2 papers), Genomics and Rare Diseases (1 paper), Genetic Syndromes and Imprinting (1 paper) and Immunodeficiency and Autoimmune Disorders (1 paper). The work is most often cited by research in Genetics (170 citations), Pediatrics, Perinatology and Child Health (54 citations), Genetics (18 citations), Developmental Biology (4 citations) and Plant Science (55 citations). Mark S. Bateman has collaborated with scholars based in United Kingdom, United States and Portugal. Frequent co-authors include John Barber, Lionel Willatt, Morag N. Collinson, John R.W. Yates, James C. Nicholson, Andrew Green, N R Dennis, Viv Maloney, Shuwen Huang and Jill A. Rosenfeld. Their work appears in journals such as Cytogenetic and Genome Research, Clinical Endocrinology, European Journal of Human Genetics, Atherosclerosis and 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.