Paul N. Schofield
Impact in
- Genetics top 1%
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Molecular Biology top 1%
- Biomedical Text Mining and Ontologies
- Epigenetics and DNA Methylation
- Bioinformatics and Genomic Networks
- Renal and related cancers
Papers in
-
- Biomedical Text Mining and Ontologies 78
- Bioinformatics and Genomic Networks 39
- Epigenetics and DNA Methylation 17
- Renal and related cancers 13
- Genetics 60
- Genomics and Rare Diseases 20
- Genetic Syndromes and Imprinting 16
- Co-authors
- Georgios V. Gkoutos (50 shared papers)Robert Hoehndorf (48 shared papers)John P. Sundberg (35 shared papers)Wolf Reik (6 shared papers)Johanna A. Joyce (5 shared papers)Wilhelm Engström (21 shared papers)Eamonn Richard Maher (5 shared papers)Sten Lindham (2 shared papers)
- Journals
- Mammalian Genome (10 papers)International Journal of Radiation Biology (8 papers)Journal of Biomedical Semantics (7 papers)Database (6 papers)Veterinary Pathology (6 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Paul N. Schofield
233 papers receiving 7.4k citations
Paul N. Schofield's Hit Papers
Peers
Comparison fields: 5 of 198
- Genetics 2.5k
- Molecular Biology 4.8k
- Pediatrics, Perinatology and Child Health 812
- Aging 78
- Equine 61
Countries citing papers authored by Paul N. Schofield
This map shows the geographic impact of Paul N. Schofield'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 Paul N. Schofield with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paul N. Schofield more than expected).
Fields of papers citing papers by Paul N. Schofield
This network shows the impact of papers produced by Paul N. Schofield. 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 Paul N. Schofield. The network helps show where Paul N. Schofield may publish in the future.
Co-authors
The 25 scholars most cited alongside Paul N. Schofield, 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 236 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data Hit paper breakdown → | 2013 | 622 |
| 2 | 1999 | 349 | |
| 3 | 1993 | 251 | |
| 4 | 2012 | 247 | |
| 5 | 2005 | 238 | |
| 6 | 2015 | 188 | |
| 7 | 2015 | 181 | |
| 8 | 2011 | 168 | |
| 9 | 1988 | 145 | |
| 10 | 1989 | 133 | |
| 11 | 1999 | 133 | |
| 12 | novH: differential expression in developing kidney and Wilm's tumors. | 1998 | 124 |
| 13 | 2009 | 120 | |
| 14 | 1985 | 106 | |
| 15 | 2014 | 103 | |
| 16 | 1989 | 90 | |
| 17 | 1997 | 81 | |
| 18 | 2012 | 80 | |
| 19 | 2011 | 79 | |
| 20 | 2008 | 77 |
About Paul N. Schofield
Paul N. Schofield is a scholar working on Molecular Biology, Genetics, Biophysics, Endocrinology, Diabetes and Metabolism and Pediatrics, Perinatology and Child Health, having authored 236 papers that have together received 7.7k indexed citations. Recurring topics across this work include Biomedical Text Mining and Ontologies (78 papers), Bioinformatics and Genomic Networks (39 papers), Genomics and Rare Diseases (20 papers), Semantic Web and Ontologies (20 papers), Epigenetics and DNA Methylation (17 papers), Genetic Syndromes and Imprinting (16 papers), Renal and related cancers (13 papers) and Cell Image Analysis Techniques (12 papers). The work is most often cited by research in Genetics (2.5k citations), Molecular Biology (4.8k citations), Pediatrics, Perinatology and Child Health (812 citations), Aging (78 citations) and Equine (61 citations). Paul N. Schofield has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Georgios V. Gkoutos, Robert Hoehndorf, John P. Sundberg, Wolf Reik, Johanna A. Joyce, Wilhelm Engström, Eamonn Richard Maher, Sten Lindham, Brigid L.M. Hogan and John M. Hancock. Their work appears in journals such as Mammalian Genome, International Journal of Radiation Biology, Journal of Biomedical Semantics, Database and Veterinary Pathology.
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.