Manuel Corpas
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 10%
- Congenital heart defects research
- Genetics, Bioinformatics, and Biomedical Research
- Genomics and Phylogenetic Studies
Papers in
-
- Genetics, Bioinformatics, and Biomedical Research 9
- Bioinformatics and Genomic Networks 5
- Gene expression and cancer classification 4
- Genomics and Phylogenetic Studies 4
- Genetics 15
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 5
- Genetic Associations and Epidemiology 5
- Co-authors
- A. Paul Bevan (3 shared papers)Stephen Clayton (2 shared papers)Helen V. Firth (2 shared papers)Nigel P. Carter (1 shared paper)Diana Rajan (1 shared paper)Shola M. Richards (1 shared paper)Steven Van Vooren (1 shared paper)Yves Moreau (1 shared paper)
- Journals
- PLoS Computational Biology (5 papers)Bioinformatics (2 papers)BMC Genomics (2 papers)eLife (2 papers)Frontiers in Genetics (2 papers)
- Partner nations
- United KingdomSpainUnited States
In The Last Decade
Manuel Corpas
38 papers receiving 1.7k citations
Manuel Corpas's Hit Papers
Peers
Comparison fields: 5 of 116
- Genetics 1.0k
- Molecular Biology 822
- Cancer Research 132
- Pediatrics, Perinatology and Child Health 133
- Genetics 73
Countries citing papers authored by Manuel Corpas
This map shows the geographic impact of Manuel Corpas'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 Manuel Corpas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manuel Corpas more than expected).
Fields of papers citing papers by Manuel Corpas
This network shows the impact of papers produced by Manuel Corpas. 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 Manuel Corpas. The network helps show where Manuel Corpas may publish in the future.
Co-authors
The 25 scholars most cited alongside Manuel Corpas, 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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources Hit paper breakdown → | 2009 | 1240 |
| 2 | 2013 | 67 | |
| 3 | 2012 | 50 | |
| 4 | 2022 | 48 | |
| 5 | 2015 | 41 | |
| 6 | 2018 | 39 | |
| 7 | 2014 | 23 | |
| 8 | 2018 | 20 | |
| 9 | 2015 | 19 | |
| 10 | 2015 | 19 | |
| 11 | 2022 | 18 | |
| 12 | 2023 | 17 | |
| 13 | 2015 | 13 | |
| 14 | 2012 | 13 | |
| 15 | 2012 | 12 | |
| 16 | 2015 | 12 | |
| 17 | 2008 | 10 | |
| 18 | 2022 | 9 | |
| 19 | 2024 | 9 | |
| 20 | 2007 | 9 |
About Manuel Corpas
Manuel Corpas is a scholar working on Molecular Biology, Genetics, Information Systems and Management, Clinical Psychology and Infectious Diseases, having authored 44 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetics, Bioinformatics, and Biomedical Research (9 papers), Genomics and Rare Diseases (8 papers), Scientific Computing and Data Management (7 papers), Genomic variations and chromosomal abnormalities (5 papers), Bioinformatics and Genomic Networks (5 papers), Genetic Associations and Epidemiology (5 papers), Gene expression and cancer classification (4 papers) and Genomics and Phylogenetic Studies (4 papers). The work is most often cited by research in Genetics (1.0k citations), Molecular Biology (822 citations), Cancer Research (132 citations), Pediatrics, Perinatology and Child Health (133 citations) and Genetics (73 citations). Manuel Corpas has collaborated with scholars based in United Kingdom, Spain and United States. Frequent co-authors include A. Paul Bevan, Stephen Clayton, Helen V. Firth, Nigel P. Carter, Diana Rajan, Shola M. Richards, Steven Van Vooren, Yves Moreau, Segun Fatumo and Eugene Bragin. Their work appears in journals such as PLoS Computational Biology, Bioinformatics, BMC Genomics, eLife and Frontiers in 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.