John R.W. Yates - Concepedia

Author

John R.W. Yates

Also Known As

Derlet, Robert W, J R W Yates, J R Yates, J Yates, J. R W Yates, J. R. W. YATES, J. R. W. Yates, J. R.W. Yates, J. Yates, J.R.W Yates

108

Publications

8.9K

Citations

H-Index

137

Concepts

All Affiliations

University of Cambridge Addenbrooke's Hospital University College London University of Edinburgh Moorfields Eye Hospital

About

John R.W. Yates is an author at University of Cambridge specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	31	47	5.2K
2	Public Health	16	17	2K
3	Natural Sciences	4	4	134
4	Education	2	2	48
5	Health Sciences	2	2	193

John R.W. Yates

Publications

8.5K

Citations

H-Index

Page 1

	Year	Citations
Clinical Features and Natural History of von Hippel-Lindau Disease Eamonn R. Maher, John R.W. Yates, R W J Harries, QJM	1990	947
Complement C3 Variant and the Risk of Age-Related Macular Degeneration John R.W. Yates, Tiina Sepp, Baljinder K. Matharu, New England Journal of Medicine	2007	823
Seven new loci associated with age-related macular degeneration Lars G. Fritsche, Wei Chen, Matthew Schu, Nature Genetics Ocular DiseaseOphthalmologyAge-related DiseasesPathologyNew Loci	2013	790
Von Hippel-Lindau disease: a genetic study. Eamonn R. Maher, L Iselius, John R.W. Yates, Journal of Medical Genetics GeneticsReproductive HealthGenetic EpidemiologyPathologyVon Hippel-lindau	1991	602
EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9 Alan Fryer, J. M. Connor, S. Povey, The Lancet CytogeneticsGenetic DisorderGeneticsPathologyTuberous Sclerosis	1987	514
Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocenteses M.A. Ferguson‐Smith, John R.W. Yates Prenatal Diagnosis FertilityGeneticsReproductive HealthMajor Chromosome AberrationsGynecology	1984	391
p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation Hans van Bokhoven, Ben C.J. Hamel, Mike Bamshad, The American Journal of Human Genetics Eec SyndromeDevelopmental BiologyGenetic DisorderGeneticsPathology	2001	376
Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome) Esther Meyer, Derek Lim, Shanaz Pasha, PLoS Genetics GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	2009	318
Complement Factor H Variant Y402H Is a Major Risk Determinant for Geographic Atrophy and Choroidal Neovascularization in Smokers and Nonsmokers Tiina Sepp, Jane C. Khan, Deborah A. Thurlby, Investigative Ophthalmology & Visual Science	2006	185
Elastin: mutational spectrum in supravalvular aortic stenosis Kay Metcalfe, Agnes K Rucka, Leslie Smoot, European Journal of Human Genetics Cardiovascular DiseaseValve DiseaseVascular BiologyMutational SpectrumValvular Heart Disease	2000	174

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