Jonathan P. Tyrer
Impact in
- Genetics top 0.05%
- Genetic Associations and Epidemiology
- BRCA gene mutations in cancer
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Reproductive Medicine top 0.2%
- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 77
- Genetic Associations and Epidemiology 43
- BRCA gene mutations in cancer 37
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- Ovarian cancer diagnosis and treatment 32
- Co-authors
- Jack M. Cuzick (2 shared papers)Stephen William Duffy (2 shared papers)Paul D.P. Pharoah (24 shared papers)Douglas F. Easton (18 shared papers)Alison Margaret Dunning (10 shared papers)Peter J Tyrer (4 shared papers)Kristy E. Driver (5 shared papers)Bruce A.J. Ponder (3 shared papers)
- Journals
- Nature Genetics (19 papers)Cancer Epidemiology Biomarkers & Prevention (13 papers)Cancer Research (8 papers)Nature Communications (8 papers)Human Molecular Genetics (7 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Jonathan P. Tyrer
170 papers receiving 26.7k citations
Jonathan P. Tyrer's Hit Papers
Peers
Comparison fields: 5 of 210
- Genetics 11.9k
- Reproductive Medicine 2.1k
- Cancer Research 3.3k
- Endocrine and Autonomic Systems 756
- Molecular Biology 7.7k
Countries citing papers authored by Jonathan P. Tyrer
This map shows the geographic impact of Jonathan P. Tyrer'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 Jonathan P. Tyrer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan P. Tyrer more than expected).
Fields of papers citing papers by Jonathan P. Tyrer
This network shows the impact of papers produced by Jonathan P. Tyrer. 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 Jonathan P. Tyrer. The network helps show where Jonathan P. Tyrer may publish in the future.
Co-authors
The 25 scholars most cited alongside Jonathan P. Tyrer, 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 172 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic studies of body mass index yield new insights for obesity biology Hit paper breakdown → | 2015 | 3477 |
| 2 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index Hit paper breakdown → | 2010 | 2419 |
| 3 | Hundreds of variants clustered in genomic loci and biological pathways affect human height Hit paper breakdown → | 2010 | 1546 |
| 4 | Defining the role of common variation in the genomic and biological architecture of adult human height Hit paper breakdown → | 2014 | 1377 |
| 5 | Association analysis identifies 65 new breast cancer risk loci Hit paper breakdown → | 2017 | 1013 |
| 6 | A breast cancer prediction model incorporating familial and personal risk factors Hit paper breakdown → | 2004 | 1013 |
| 7 | Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk Hit paper breakdown → | 2015 | 859 |
| 8 | Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes Hit paper breakdown → | 2018 | 765 |
| 9 | Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci Hit paper breakdown → | 2018 | 623 |
| 10 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study Hit paper breakdown → | 2015 | 542 |
| 11 | Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture Hit paper breakdown → | 2013 | 512 |
| 12 | Rare and low-frequency coding variants alter human adult height Hit paper breakdown → | 2017 | 476 |
| 13 | 2013 | 463 | |
| 14 | Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche Hit paper breakdown → | 2014 | 458 |
| 15 | Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants Hit paper breakdown → | 2015 | 446 |
| 16 | Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk Hit paper breakdown → | 2017 | 415 |
| 17 | 2014 | 365 | |
| 18 | Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer Hit paper breakdown → | 2017 | 355 |
| 19 | Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer Hit paper breakdown → | 2015 | 345 |
| 20 | 2012 | 342 |
About Jonathan P. Tyrer
Jonathan P. Tyrer is a scholar working on Genetics, Reproductive Medicine, Cancer Research, Molecular Biology and Pathology and Forensic Medicine, having authored 172 papers that have together received 27.3k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (43 papers), BRCA gene mutations in cancer (37 papers), Ovarian cancer diagnosis and treatment (32 papers), Cancer-related molecular mechanisms research (30 papers), RNA modifications and cancer (19 papers), Epigenetics and DNA Methylation (16 papers), Genetic factors in colorectal cancer (15 papers) and Cancer Genomics and Diagnostics (10 papers). The work is most often cited by research in Genetics (11.9k citations), Reproductive Medicine (2.1k citations), Cancer Research (3.3k citations), Endocrine and Autonomic Systems (756 citations) and Molecular Biology (7.7k citations). Jonathan P. Tyrer has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Jack M. Cuzick, Stephen William Duffy, Paul D.P. Pharoah, Douglas F. Easton, Alison Margaret Dunning, Peter J Tyrer, Kristy E. Driver, Bruce A.J. Ponder, Bruce A.J. Ponder and Nicholas Seivewright. Their work appears in journals such as Nature Genetics, Cancer Epidemiology Biomarkers & Prevention, Cancer Research, Nature Communications and Human Molecular 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.