Peter Holmans
Impact in
- Biological Psychiatry top 1%
- Genetics top 0.2%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 110
- Genetic Associations and Epidemiology 84
- Genomic variations and chromosomal abnormalities 32
- Genetics and Neurodevelopmental Disorders 26
- Genetic Mapping and Diversity in Plants and Animals 18
- Genomics and Rare Diseases 17
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- Bioinformatics and Genomic Networks 18
- Mitochondrial Function and Pathology 13
- Co-authors
- Michael O‘Donovan (76 shared papers)Michael J. Owen (70 shared papers)Nick Craddock (18 shared papers)Valentina Moskvina (19 shared papers)George Kirov (21 shared papers)Peter McGuffin (18 shared papers)Nigel Williams (23 shared papers)Lesley Jones (25 shared papers)
- Journals
- Human Molecular Genetics (16 papers)Molecular Psychiatry (15 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (15 papers)Genetic Epidemiology (8 papers)The American Journal of Human Genetics (8 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Peter Holmans
201 papers receiving 9.3k citations
Peers
Comparison fields: 5 of 153
- Biological Psychiatry 349
- Genetics 3.8k
- Psychiatry and Mental health 1.6k
- Cellular and Molecular Neuroscience 1.8k
- Cognitive Neuroscience 1.0k
Countries citing papers authored by Peter Holmans
This map shows the geographic impact of Peter Holmans'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 Peter Holmans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Holmans more than expected).
Fields of papers citing papers by Peter Holmans
This network shows the impact of papers produced by Peter Holmans. 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 Peter Holmans. The network helps show where Peter Holmans may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Holmans, 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 211 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 383 | |
| 2 | 2010 | 353 | |
| 3 | Asymptotic properties of affected-sib-pair linkage analysis. | 1993 | 294 |
| 4 | 2009 | 284 | |
| 5 | 2009 | 283 | |
| 6 | 2008 | 269 | |
| 7 | 2005 | 241 | |
| 8 | 1998 | 202 | |
| 9 | 2009 | 199 | |
| 10 | 2007 | 175 | |
| 11 | 2016 | 169 | |
| 12 | 2000 | 148 | |
| 13 | 2011 | 144 | |
| 14 | 2005 | 139 | |
| 15 | 1997 | 133 | |
| 16 | 2010 | 132 | |
| 17 | 2020 | 128 | |
| 18 | 2015 | 126 | |
| 19 | 2011 | 121 | |
| 20 | 2019 | 110 |
About Peter Holmans
Peter Holmans is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Psychiatry and Mental health and Physiology, having authored 211 papers that have together received 9.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (84 papers), Genomic variations and chromosomal abnormalities (32 papers), Genetic Neurodegenerative Diseases (30 papers), Genetics and Neurodevelopmental Disorders (26 papers), Genetic Mapping and Diversity in Plants and Animals (18 papers), Bioinformatics and Genomic Networks (18 papers), Genomics and Rare Diseases (17 papers) and Mitochondrial Function and Pathology (13 papers). The work is most often cited by research in Biological Psychiatry (349 citations), Genetics (3.8k citations), Psychiatry and Mental health (1.6k citations), Cellular and Molecular Neuroscience (1.8k citations) and Cognitive Neuroscience (1.0k citations). Peter Holmans has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Michael O‘Donovan, Michael J. Owen, Nick Craddock, Valentina Moskvina, George Kirov, Peter McGuffin, Nigel Williams, Lesley Jones, Lisa Jones and Anita Thapar. Their work appears in journals such as Human Molecular Genetics, Molecular Psychiatry, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Genetic Epidemiology and The American Journal of 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.