C McKeown
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 5%
- Connective tissue disorders research
- Genetic Syndromes and Imprinting
- Craniofacial Disorders and Treatments
Papers in
- Genetics 11
- Connective tissue disorders research 3
- Craniofacial Disorders and Treatments 3
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- Congenital heart defects research 2
- Hedgehog Signaling Pathway Studies 2
- Peroxisome Proliferator-Activated Receptors 2
- Protein Tyrosine Phosphatases 2
- Co-authors
- Kenro Kusumi (1 shared paper)Christine Garrett (1 shared paper)Michael Bulman (1 shared paper)Eric S. Lander (1 shared paper)Timothy M. Frayling (1 shared paper)Andrew T. Hattersley (1 shared paper)Peter D. Turnpenny (1 shared paper)Robb Krumlauf (1 shared paper)
- Journals
- Journal of Medical Genetics (3 papers)The American Journal of Human Genetics (3 papers)British Journal of Dermatology (1 paper)Prenatal Diagnosis (1 paper)British Journal of Radiology (1 paper)
- Partner nations
- United KingdomUnited StatesPoland
In The Last Decade
C McKeown
23 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 76
- Developmental Biology 79
- Genetics 512
- Nephrology 120
- Molecular Biology 668
- Cell Biology 133
Countries citing papers authored by C McKeown
This map shows the geographic impact of C McKeown'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 C McKeown with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C McKeown more than expected).
Fields of papers citing papers by C McKeown
This network shows the impact of papers produced by C McKeown. 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 C McKeown. The network helps show where C McKeown may publish in the future.
Co-authors
The 25 scholars most cited alongside C McKeown, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 298 | |
| 2 | 2005 | 227 | |
| 3 | 1997 | 170 | |
| 4 | 2005 | 101 | |
| 5 | Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations. | 2000 | 97 |
| 6 | 1988 | 77 | |
| 7 | New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndrome. | 1995 | 57 |
| 8 | 1990 | 46 | |
| 9 | 1996 | 36 | |
| 10 | 2013 | 33 | |
| 11 | 1993 | 29 | |
| 12 | 2009 | 27 | |
| 13 | 1987 | 16 | |
| 14 | 2009 | 11 | |
| 15 | 1992 | 9 | |
| 16 | 1997 | 8 | |
| 17 | 1999 | 6 | |
| 18 | 2006 | 6 | |
| 19 | 1992 | 5 | |
| 20 | 2001 | 4 |
About C McKeown
C McKeown is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Epidemiology, having authored 25 papers that have together received 1.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Connective tissue disorders research (3 papers), Craniofacial Disorders and Treatments (3 papers), Congenital heart defects research (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Pediatric Hepatobiliary Diseases and Treatments (2 papers), Peroxisome Proliferator-Activated Receptors (2 papers) and Protein Tyrosine Phosphatases (2 papers). The work is most often cited by research in Developmental Biology (79 citations), Genetics (512 citations), Nephrology (120 citations), Molecular Biology (668 citations) and Cell Biology (133 citations). C McKeown has collaborated with scholars based in United Kingdom, United States and Poland. Frequent co-authors include Kenro Kusumi, Christine Garrett, Michael Bulman, Eric S. Lander, Timothy M. Frayling, Andrew T. Hattersley, Peter D. Turnpenny, Robb Krumlauf, Sian Ellard and Dian Donnai. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, British Journal of Dermatology, Prenatal Diagnosis and British Journal of Radiology.
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.