Peter D. Turnpenny
Impact in
- Genetics top 1%
- Connective tissue disorders research
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Nephrology top 2%
Papers in
- Genetics 47
- Connective tissue disorders research 14
- Genomics and Rare Diseases 12
- Genomic variations and chromosomal abnormalities 9
- Craniofacial Disorders and Treatments 8
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- Congenital heart defects research 8
- Co-authors
- Sian Ellard (17 shared papers)Kenro Kusumi (11 shared papers)Sally L. Dunwoodie (12 shared papers)Neil V. Whittock (4 shared papers)Judith A. Goodship (3 shared papers)Duncan B. Sparrow (6 shared papers)Paul Warwicker (3 shared papers)Timothy H.J. Goodship (3 shared papers)
- Journals
- European Journal of Human Genetics (11 papers)Journal of Medical Genetics (11 papers)The American Journal of Human Genetics (5 papers)Human Molecular Genetics (3 papers)Kidney International (3 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Peter D. Turnpenny
108 papers receiving 3.8k citations
Peers
Comparison fields: 5 of 120
- Genetics 1.4k
- Nephrology 249
- Genetics 271
- Molecular Biology 1.7k
- Pediatrics, Perinatology and Child Health 486
Countries citing papers authored by Peter D. Turnpenny
This map shows the geographic impact of Peter D. Turnpenny'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 D. Turnpenny with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter D. Turnpenny more than expected).
Fields of papers citing papers by Peter D. Turnpenny
This network shows the impact of papers produced by Peter D. Turnpenny. 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 D. Turnpenny. The network helps show where Peter D. Turnpenny may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter D. Turnpenny, 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 109 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 373 | |
| 2 | 2000 | 297 | |
| 3 | 2011 | 251 | |
| 4 | 2005 | 182 | |
| 5 | 2006 | 158 | |
| 6 | 2004 | 119 | |
| 7 | 2013 | 115 | |
| 8 | 2007 | 109 | |
| 9 | Emery's elements of medical genetics | 1998 | 109 |
| 10 | 2003 | 100 | |
| 11 | 1999 | 88 | |
| 12 | 2010 | 73 | |
| 13 | 2014 | 71 | |
| 14 | 2009 | 62 | |
| 15 | 2018 | 60 | |
| 16 | 1995 | 58 | |
| 17 | 1999 | 57 | |
| 18 | 2008 | 55 | |
| 19 | 2016 | 54 | |
| 20 | 2003 | 53 |
About Peter D. Turnpenny
Peter D. Turnpenny is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 109 papers that have together received 4.0k indexed citations. Recurring topics across this work include Connective tissue disorders research (14 papers), Pediatric Hepatobiliary Diseases and Treatments (13 papers), Genomics and Rare Diseases (12 papers), Congenital Anomalies and Fetal Surgery (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (8 papers), Pharmacological Effects and Toxicity Studies (8 papers) and Craniofacial Disorders and Treatments (8 papers). The work is most often cited by research in Genetics (1.4k citations), Nephrology (249 citations), Genetics (271 citations), Molecular Biology (1.7k citations) and Pediatrics, Perinatology and Child Health (486 citations). Peter D. Turnpenny has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Sian Ellard, Kenro Kusumi, Sally L. Dunwoodie, Neil V. Whittock, Judith A. Goodship, Duncan B. Sparrow, Paul Warwicker, Timothy H.J. Goodship, Rosemary L. Donne and Roy Ward. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, The American Journal of Human Genetics, Human Molecular Genetics and Kidney International.
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.