Peter Beighton
Impact in
- Developmental Biology top 0.2%
- Congenital limb and hand anomalies
- Genetics top 0.2%
- Connective tissue disorders research
- Dermatological and Skeletal Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 278
- Connective tissue disorders research 199
- Dermatological and Skeletal Disorders 51
- Genomics and Rare Diseases 32
- Craniofacial Disorders and Treatments 25
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- Congenital limb and hand anomalies 44
- Co-authors
- Greta Beighton (24 shared papers)Louis P. Solomon (13 shared papers)Colin Lionel Soskolne (6 shared papers)Frank Horan (15 shared papers)Petros Tsipouras (7 shared papers)Herman A. Hamersma (22 shared papers)Anne De Paepe (2 shared papers)Beat Steinmann (2 shared papers)
- Journals
- Clinical Genetics (41 papers)Journal of Medical Genetics (23 papers)Annals of the Rheumatic Diseases (13 papers)The American Journal of Human Genetics (6 papers)Human Molecular Genetics (5 papers)
- Partner nations
- South AfricaUnited KingdomUnited States
In The Last Decade
Peter Beighton
421 papers receiving 18.3k citations
Peter Beighton's Hit Papers
Peers
Comparison fields: 5 of 161
- Developmental Biology 741
- Genetics 7.7k
- Orthopedics and Sports Medicine 2.3k
- Rheumatology 1.3k
- Sensory Systems 429
Countries citing papers authored by Peter Beighton
This map shows the geographic impact of Peter Beighton'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 Beighton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Beighton more than expected).
Fields of papers citing papers by Peter Beighton
This network shows the impact of papers produced by Peter Beighton. 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 Beighton. The network helps show where Peter Beighton may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Beighton, 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 441 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | de la Chapelle, A. Hit paper breakdown → | 1997 | 2730 |
| 2 | LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development Hit paper breakdown → | 2001 | 1892 |
| 3 | Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997 Hit paper breakdown → | 1998 | 1412 |
| 4 | Articular mobility in an African population. Hit paper breakdown → | 1973 | 1304 |
| 5 | Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein Hit paper breakdown → | 2001 | 834 |
| 6 | International nosology of heritable disorders of connective tissue, Berlin, 1986 Hit paper breakdown → | 1988 | 575 |
| 7 | ORTHOPAEDIC ASPECTS OF THE EHLERS. DANLOS SYNDROME Hit paper breakdown → | 1969 | 496 |
| 8 | 2002 | 254 | |
| 9 | 2000 | 249 | |
| 10 | 2000 | 241 | |
| 11 | Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13. | 1996 | 222 |
| 12 | McKusick's heritable disorders of connective tissue | 1993 | 212 |
| 13 | 1970 | 198 | |
| 14 | 2002 | 183 | |
| 15 | 2003 | 181 | |
| 16 | 2010 | 158 | |
| 17 | 2001 | 156 | |
| 18 | Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium. | 1992 | 153 |
| 19 | 2005 | 148 | |
| 20 | 1992 | 147 |
About Peter Beighton
Peter Beighton is a scholar working on Genetics, Developmental Biology, Rheumatology, Sensory Systems and Molecular Biology, having authored 441 papers that have together received 19.9k indexed citations. Recurring topics across this work include Connective tissue disorders research (199 papers), Dermatological and Skeletal Disorders (51 papers), Congenital limb and hand anomalies (44 papers), Genomics and Rare Diseases (32 papers), Craniofacial Disorders and Treatments (25 papers), Hearing, Cochlea, Tinnitus, Genetics (21 papers), Bone Tumor Diagnosis and Treatments (21 papers) and dental development and anomalies (20 papers). The work is most often cited by research in Developmental Biology (741 citations), Genetics (7.7k citations), Orthopedics and Sports Medicine (2.3k citations), Rheumatology (1.3k citations) and Sensory Systems (429 citations). Peter Beighton has collaborated with scholars based in South Africa, United Kingdom and United States. Frequent co-authors include Greta Beighton, Louis P. Solomon, Colin Lionel Soskolne, Frank Horan, Petros Tsipouras, Herman A. Hamersma, Anne De Paepe, Beat Steinmann, RICHARD J. WENSTRUP and B. J. Cremin. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Annals of the Rheumatic Diseases, The American Journal of Human Genetics 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.