C McKeown

4.8k total citations
25 papers, 1.3k citations indexed

About

C McKeown is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, C McKeown has authored 25 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in C McKeown's work include Prenatal Screening and Diagnostics (4 papers), Hedgehog Signaling Pathway Studies (3 papers) and Connective tissue disorders research (3 papers). C McKeown is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Hedgehog Signaling Pathway Studies (3 papers) and Connective tissue disorders research (3 papers). C McKeown collaborates with scholars based in United Kingdom, United States and Italy. C McKeown's co-authors include Eric S. Lander, Timothy M. Frayling, Christine Garrett, Kenro Kusumi, Peter D. Turnpenny, Michael Bulman, Robb Krumlauf, Sian Ellard, Andrew T. Hattersley and Dian Donnai and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

C McKeown

23 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
C McKeown United Kingdom 13 735 551 168 139 129 25 1.3k
Luitgard M. Neumann Germany 20 708 1.0× 1.0k 1.8× 207 1.2× 189 1.4× 110 0.9× 46 1.7k
M. Le Merrer France 23 983 1.3× 919 1.7× 227 1.4× 84 0.6× 142 1.1× 93 1.8k
David J. Bunyan United Kingdom 23 991 1.3× 979 1.8× 208 1.2× 108 0.8× 113 0.9× 60 2.0k
Nursel Elçioğlu Türkiye 19 1.2k 1.6× 1.3k 2.4× 169 1.0× 195 1.4× 143 1.1× 70 2.0k
Odyssé Michos United States 15 1.1k 1.5× 242 0.4× 160 1.0× 124 0.9× 171 1.3× 21 1.3k
Carmen V. Pepicelli United States 7 1.2k 1.7× 248 0.5× 273 1.6× 88 0.6× 79 0.6× 8 1.6k
Yves Lacassie United States 18 475 0.6× 425 0.8× 174 1.0× 93 0.7× 92 0.7× 70 952
Jean‐Pierre Fryns Belgium 21 1.2k 1.7× 909 1.6× 206 1.2× 118 0.8× 202 1.6× 25 2.0k
Louise Brueton United Kingdom 24 908 1.2× 604 1.1× 154 0.9× 72 0.5× 205 1.6× 34 1.5k
M.H. Breuning Netherlands 16 1.4k 1.9× 1.7k 3.1× 123 0.7× 81 0.6× 207 1.6× 26 2.1k

Countries citing papers authored by C McKeown

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of C McKeown

This figure shows the co-authorship network connecting the top 25 collaborators of C McKeown. A scholar is included among the top collaborators of C McKeown based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C McKeown. C McKeown is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Brouillard, Pascal, Laurence M. Boon, Nicole Revençu, et al.. (2013). Genotypes and Phenotypes of 162 Families with a <b><i>Glomulin</i></b> Mutation. Molecular Syndromology. 4(4). 157–164. 33 indexed citations
2.
Patel, Chirag, et al.. (2009). Mosaic trisomy 1q: The longest surviving case. American Journal of Medical Genetics Part A. 149A(8). 1795–1800. 11 indexed citations
3.
Clark, Robin D., John M. Graham, Michael J. Friez, et al.. (2009). FG syndrome, an X-linked multiple congenital anomaly syndrome: The clinical phenotype and an algorithm for diagnostic testing. Genetics in Medicine. 11(11). 769–775. 27 indexed citations
4.
Ward, Ken, Celia Moss, & C McKeown. (2006). The cardio-facio-cutaneous syndrome: a manifestation of the Noonan syndrome?. British Journal of Dermatology. 131(2). 270–274. 6 indexed citations
5.
White, Kenneth E., J. M. Segura Cabral, Siobhan I. Davis, et al.. (2005). Mutations that Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation. The American Journal of Human Genetics. 76(2). 361–367. 226 indexed citations
6.
Morgan, Neil V., Shanaz Pasha, Colin A. Johnson, et al.. (2005). A Germline Mutation in BLOC1S3/Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome (HPS8). The American Journal of Human Genetics. 78(1). 160–166. 100 indexed citations
7.
Vatish, Manu, et al.. (2003). Triploid/diploid mosaicism (69XXY/46XX) presenting as severe early onset preeclampsia with a live birth: placental and cytogenetic features. European Journal of Obstetrics & Gynecology and Reproductive Biology. 112(2). 233–235. 3 indexed citations
8.
McKee, Shane, et al.. (2001). Joint and skin laxity with Dandy-Walker malformation and contractures: a distinct recessive syndrome?. Clinical Dysmorphology. 10(3). 177–180. 4 indexed citations
9.
Bulman, Michael, Kenro Kusumi, Timothy M. Frayling, et al.. (2000). Mutations in the human Delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis. Nature Genetics. 24(4). 438–441. 297 indexed citations
10.
Winter, R M, et al.. (1999). Further evidence from two families that craniofrontonasal dysplasia maps to Xp22. Clinical Genetics. 55(6). 473–477. 6 indexed citations
11.
O‘Donnell, Hilary, C McKeown, Clive Gould, Bernice E. Morrow, & Peter Scambler. (1997). Detection of an Atypical 22q11 Deletion That Has No Overlap with the DiGeorge Syndrome Critical Region. The American Journal of Human Genetics. 60(6). 1544–1547. 8 indexed citations
12.
Goodman, Frances R., Stefan Mundlos, Yasuteru Muragaki, et al.. (1997). Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract. Proceedings of the National Academy of Sciences. 94(14). 7458–7463. 170 indexed citations
13.
Gray, R. G. F., A. Green, Sue Hall, & C McKeown. (1995). Prenatal exclusion of the hhh syndrome. Prenatal Diagnosis. 15(5). 474–476. 2 indexed citations
14.
Jouet, Monique, A. Moncla, J. Paterson, et al.. (1995). New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndrome.. PubMed. 56(6). 1304–14. 57 indexed citations
15.
Wilson, David I., et al.. (1993). Noonan's and DiGeorge syndromes with monosomy 22q11.. Archives of Disease in Childhood. 68(2). 187–189. 28 indexed citations
16.
Gray, R. G. F., A. Green, S. C. Chapman, et al.. (1992). Rhizomelic chondrodysplasia punctata — A new clinical variant. Journal of Inherited Metabolic Disease. 15(6). 931–932. 5 indexed citations
17.
Burn, John, et al.. (1992). New dysmorphic syndrome with choanal atresia in siblings. Clinical Dysmorphology. 1(3). 137???144–137???144. 9 indexed citations
18.
Clayton‐Smith, Jill, Peter Farndon, C McKeown, & Dian Donnai. (1990). Examination of fetuses after induced abortion for fetal abnormality.. BMJ. 300(6720). 295–297. 46 indexed citations
19.
McKeown, C. (1988). The Child with Multiple Birth Defects. Journal of Medical Genetics. 25(8). 573.1–573. 3 indexed citations
20.
McHugo, J., et al.. (1987). Ultrasound findings in children with cystic fibrosis. British Journal of Radiology. 60(710). 137–141. 16 indexed citations

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.

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