Michael Oldridge
Impact in
- Developmental Biology top 1%
- Congenital limb and hand anomalies
- Genetics top 0.5%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Connective tissue disorders research
Papers in
- Genetics 20
- Craniofacial Disorders and Treatments 14
- Cleft Lip and Palate Research 12
- Connective tissue disorders research 8
- Genomic variations and chromosomal abnormalities 4
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- Wnt/β-catenin signaling in development and cancer 5
- Developmental Biology and Gene Regulation 4
- Co-authors
- Andrew O.M. Wilkie (20 shared papers)Sarah F. Slaney (3 shared papers)Richard Hayward (2 shared papers)William Reardon (2 shared papers)Michael D. Poole (2 shared papers)Robin M. Winter (2 shared papers)Louise J. Pulleyn (2 shared papers)Paul Rutland (2 shared papers)
- Journals
- The American Journal of Human Genetics (9 papers)Nature Genetics (5 papers)European Journal of Human Genetics (3 papers)Human Molecular Genetics (2 papers)The Lancet (1 paper)
- Partner nations
- United KingdomIndiaUnited States
In The Last Decade
Michael Oldridge
28 papers receiving 2.9k citations
Michael Oldridge's Hit Papers
Peers
Comparison fields: 5 of 98
- Developmental Biology 207
- Genetics 2.0k
- Molecular Biology 1.7k
- Genetics 129
- Aging 16
Countries citing papers authored by Michael Oldridge
This map shows the geographic impact of Michael Oldridge'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 Michael Oldridge with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael Oldridge more than expected).
Fields of papers citing papers by Michael Oldridge
This network shows the impact of papers produced by Michael Oldridge. 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 Michael Oldridge. The network helps show where Michael Oldridge may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael Oldridge, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome Hit paper breakdown → | 1995 | 671 |
| 2 | 1995 | 343 | |
| 3 | 2000 | 232 | |
| 4 | 1996 | 215 | |
| 5 | 1999 | 179 | |
| 6 | Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome. | 1996 | 175 |
| 7 | 2000 | 163 | |
| 8 | 1998 | 143 | |
| 9 | 2000 | 134 | |
| 10 | 2000 | 126 | |
| 11 | 1997 | 108 | |
| 12 | 1997 | 102 | |
| 13 | 2000 | 90 | |
| 14 | 2003 | 76 | |
| 15 | 2012 | 50 | |
| 16 | 2012 | 40 | |
| 17 | 1997 | 35 | |
| 18 | 2001 | 34 | |
| 19 | 1999 | 20 | |
| 20 | 2001 | 18 |
About Michael Oldridge
Michael Oldridge is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Developmental Biology and Surgery, having authored 29 papers that have together received 3.0k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (14 papers), Cleft Lip and Palate Research (12 papers), Connective tissue disorders research (8 papers), Wnt/β-catenin signaling in development and cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Developmental Biology and Gene Regulation (4 papers), Prenatal Screening and Diagnostics (3 papers) and Congenital limb and hand anomalies (3 papers). The work is most often cited by research in Developmental Biology (207 citations), Genetics (2.0k citations), Molecular Biology (1.7k citations), Genetics (129 citations) and Aging (16 citations). Michael Oldridge has collaborated with scholars based in United Kingdom, India and United States. Frequent co-authors include Andrew O.M. Wilkie, Sarah F. Slaney, Richard Hayward, William Reardon, Michael D. Poole, Robin M. Winter, Louise J. Pulleyn, Paul Rutland, Steven A. Wall and Anthony D. Hockley. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, European Journal of Human Genetics, Human Molecular Genetics and The Lancet.
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.