Simon Potter
Impact in
- Genetics top 0.05%
- Genetic Associations and Epidemiology
- Inflammatory Bowel Disease
- Molecular Biology top 0.2%
- Genomics and Phylogenetic Studies
Papers in
- Genetics 18
- Genetic Associations and Epidemiology 17
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- Genomics and Phylogenetic Studies 9
- Epigenetics and DNA Methylation 5
- Co-authors
- ROBERT FINN (7 shared papers)Sean R. Eddy (3 shared papers)Young Mi Park (2 shared papers)Rodrigo López (2 shared papers)Gustavo A Salazar (3 shared papers)Matloob Qureshi (3 shared papers)Jaina Mistry (2 shared papers)Alex G. Bateman (2 shared papers)
- Journals
- Nature Genetics (14 papers)Nucleic Acids Research (10 papers)Nature Communications (6 papers)The American Journal of Human Genetics (5 papers)Nature (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Simon Potter
80 papers receiving 46.2k citations
Simon Potter's Hit Papers
Peers
Comparison fields: 5 of 164
- Genetics 9.4k
- Molecular Biology 7.2k
- Rheumatology 1.7k
- Pathology and Forensic Medicine 1.6k
- Plant Science 3.2k
Countries citing papers authored by Simon Potter
This map shows the geographic impact of Simon Potter'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 Simon Potter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simon Potter more than expected).
Fields of papers citing papers by Simon Potter
This network shows the impact of papers produced by Simon Potter. 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 Simon Potter. The network helps show where Simon Potter may publish in the future.
Co-authors
The 25 scholars most cited alongside Simon Potter, 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 80 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls Hit paper breakdown → | 2007 | 7887 |
| 2 | Initial sequencing and comparative analysis of the mouse genome Hit paper breakdown → | 2002 | 5353 |
| 3 | The Pfam protein families database: towards a more sustainable future Hit paper breakdown → | 2015 | 4573 |
| 4 | The Pfam protein families database in 2019 Hit paper breakdown → | 2018 | 3431 |
| 5 | The EMBL-EBI search and sequence analysis tools APIs in 2019 Hit paper breakdown → | 2019 | 3286 |
| 6 | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Hit paper breakdown → | 2011 | 2243 |
| 7 | New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk Hit paper breakdown → | 2010 | 1857 |
| 8 | HMMER web server: 2018 update Hit paper breakdown → | 2018 | 1812 |
| 9 | Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes Hit paper breakdown → | 2012 | 1589 |
| 10 | Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants Hit paper breakdown → | 2007 | 1189 |
| 11 | InterPro in 2019: improving coverage, classification and access to protein sequence annotations Hit paper breakdown → | 2018 | 1143 |
| 12 | InterPro in 2017—beyond protein family and domain annotations Hit paper breakdown → | 2016 | 1101 |
| 13 | A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 Hit paper breakdown → | 2010 | 884 |
| 14 | Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility Hit paper breakdown → | 2011 | 755 |
| 15 | Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease Hit paper breakdown → | 2011 | 656 |
| 16 | Variants in MTNR1B influence fasting glucose levels Hit paper breakdown → | 2008 | 634 |
| 17 | A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease Hit paper breakdown → | 2011 | 583 |
| 18 | Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes Hit paper breakdown → | 2018 | 551 |
| 19 | 2009 | 460 | |
| 20 | 2009 | 450 |
About Simon Potter
Simon Potter is a scholar working on Genetics, Molecular Biology, Neurology, Ophthalmology and Rheumatology, having authored 80 papers that have together received 47.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (17 papers), Genomics and Phylogenetic Studies (9 papers), Epigenetics and DNA Methylation (5 papers), Parkinson's Disease Mechanisms and Treatments (5 papers), Aortic aneurysm repair treatments (3 papers), Multiple Sclerosis Research Studies (3 papers), Eating Disorders and Behaviors (2 papers) and Schizophrenia research and treatment (2 papers). The work is most often cited by research in Genetics (9.4k citations), Molecular Biology (7.2k citations), Rheumatology (1.7k citations), Pathology and Forensic Medicine (1.6k citations) and Plant Science (3.2k citations). Simon Potter has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include ROBERT FINN, Sean R. Eddy, Young Mi Park, Rodrigo López, Gustavo A Salazar, Matloob Qureshi, Jaina Mistry, Alex G. Bateman, Aurélien Luciani and Alex Mitchell. Their work appears in journals such as Nature Genetics, Nucleic Acids Research, Nature Communications, The American Journal of Human Genetics and Nature.
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.