C McKeown
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 5%
- Connective tissue disorders research
- Genetic Syndromes and Imprinting
Papers in
-
- Hedgehog Signaling Pathway Studies 3
- Protein Tyrosine Phosphatases 2
- Peroxisome Proliferator-Activated Receptors 2
- Genetics 11
- Connective tissue disorders research 3
- Craniofacial Disorders and Treatments 3
- Co-authors
- Kenro Kusumi (1 shared paper)Christine Garrett (1 shared paper)Robb Krumlauf (1 shared paper)Sian Ellard (1 shared paper)Michael Bulman (1 shared paper)Eric S. Lander (1 shared paper)Timothy M. Frayling (1 shared paper)Peter D. Turnpenny (1 shared paper)
- Journals
- Journal of Medical Genetics (3 papers)The American Journal of Human Genetics (3 papers)Nature Genetics (1 paper)Journal of Inherited Metabolic Disease (1 paper)Genetics in Medicine (1 paper)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
C McKeown
23 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 83
- Developmental Biology 86
- Genetics 551
- Nephrology 122
- Molecular Biology 735
- Cell Biology 139
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 | 297 | |
| 2 | 2005 | 226 | |
| 3 | 1997 | 170 | |
| 4 | 2005 | 100 | |
| 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 | 28 | |
| 12 | 2009 | 27 | |
| 13 | 1987 | 16 | |
| 14 | 2009 | 11 | |
| 15 | 1992 | 9 | |
| 16 | 1997 | 8 | |
| 17 | 2006 | 6 | |
| 18 | 1999 | 6 | |
| 19 | 1992 | 5 | |
| 20 | 2001 | 4 |
About C McKeown
C McKeown is a scholar working on Molecular Biology, Genetics, 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), Hedgehog Signaling Pathway Studies (3 papers), Protein Tyrosine Phosphatases (2 papers), Gestational Trophoblastic Disease Studies (2 papers), Congenital Anomalies and Fetal Surgery (2 papers) and Peroxisome Proliferator-Activated Receptors (2 papers). The work is most often cited by research in Developmental Biology (86 citations), Genetics (551 citations), Nephrology (122 citations), Molecular Biology (735 citations) and Cell Biology (139 citations). C McKeown has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Kenro Kusumi, Christine Garrett, Robb Krumlauf, Sian Ellard, Michael Bulman, Eric S. Lander, Timothy M. Frayling, Peter D. Turnpenny, Andrew T. Hattersley and Dian Donnai. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, Nature Genetics, Journal of Inherited Metabolic Disease and Genetics in Medicine.
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.