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Genetics

D-Index
66
Citations
17430
World Ranking
2604
National Ranking
332

Research.com Recognitions

  • 1934 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

John R.W. Yates is affiliated with the University of Cambridge in the United Kingdom. Their research spans several fields with a particular focus on Biochemistry, Genetics and Molecular Biology, as well as Agricultural and Biological Sciences. Within these broader domains, they have contributed extensively to Genetics, Animal Science and Zoology, and Plant Science. Other relevant subfields in their work include Cancer Research and Ophthalmology.

Their scholarly output covers a range of topics related to genetic and phenotypic traits in livestock, genetic mapping and diversity in plants and animals, genetics and plant breeding, cancer-related molecular mechanisms research, retinal diseases and treatments, the complement system in diseases, and retinal imaging and analysis.

Frequent coauthors collaborating with John R.W. Yates include:

  • Karolina Kaseja
  • E. J. Smith
  • J. Conington
  • Georgios Banos
  • Sebastian Mucha

John R.W. Yates has published in various scientific venues, notably:

  • Animal - science proceedings
  • Meat Science
  • animal
  • Nature Communications
  • Journal of Animal Breeding and Genetics

Some recent papers include:

  • "Increased circulating levels of Factor H-Related Protein 4 are strongly associated with age-related macular degeneration," 2020, Nature Communications
  • "Prediction of intramuscular fat in lamb by visible and near-infrared spectroscopy in an abattoir environment," 2020, Meat Science
  • "Including genotypic information in genetic evaluations increases the accuracy of sheep breeding values," 2023, Journal of Animal Breeding and Genetics
  • "Discovery of hidden pedigree errors combining genomic information with the genomic relationship matrix in Texel sheep," 2022, animal
  • "Genome-wide association study of health and production traits in meat sheep," 2023, animal

In recognition of their contributions, John R.W. Yates was named a Fellow of the American Association for the Advancement of Science (AAAS) in 1934.

Best Publications

  • Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34

    Marjon van Slegtenhorst;Ronald de Hoogt;Caroline Hermans;Mark Nellist

  • Complement C3 Variant and the Risk of Age-Related Macular Degeneration

    John R W Yates;Tiina Sepp;Baljinder K Matharu;Jane C Khan

  • Clinical Features and Natural History of von Hippel-Lindau Disease

    E R Maher;J R Yates;R Harries;Caroline Benjamin

  • Seven new loci associated with age-related macular degeneration

    Lars G. Fritsche;Lars G. Fritsche;Wei Chen;Wei Chen;Matthew Schu;Brian L. Yaspan

  • Von Hippel-Lindau disease: a genetic study.

    E R Maher;L Iselius;J R Yates;M Littler

  • Clinical and molecular genetics of Stickler syndrome

    Martin P Snead;John R W Yates

  • Smoking and age related macular degeneration: the number of pack years of cigarette smoking is a major determinant of risk for both geographic atrophy and choroidal neovascularisation

    J C Khan;D A Thurlby;H Shahid;D G Clayton

  • Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients

    Andrew J. Green;Moyra Smith;John R.W. Yates

  • 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;Eugenio Sangiorgi

  • A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagen

    Allan J. Richards;John R. W. Yates;Rebecca Williams;Stewart J. Payne

  • Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).

    Esther Meyer;Derek Lim;Shanaz Pasha;Louise J. Tee

  • X-Linked Retinoschisis

    N. D. L. George;J. R. W. Yates;A. T. Moore;A. T. Moore

  • Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)

    J.T. Dendunnen;T. Kraayenbrink;T. Kraayenbrink;M. van Schooneveld;M. van Schooneveld;E. van de Vosse

  • The tuberous sclerosis gene on chromosome 9q34 acts as a growth suppressor

    Andrew J. Green;Philip H. Johnson;John R.W. Yates

  • Loss of heterozygosity in tuberous sclerosis hamartomas.

    T. Sepp;J. R. W. Yates;A. J. Green

  • Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma.

    E. R. Maher;J. R. W. Yates;M. A. Ferguson-Smith

  • Age-related macular degeneration and the complement system.

    S. Khandhadia;V. Cipriani;V. Cipriani;J.R.W. Yates;J.R.W. Yates;Andrew J. Lotery

  • Elastin: mutational spectrum in supravalvular aortic stenosis.

    Kay Metcalfe;Agnes K Rucka;Leslie Smoot;Guenter Hofstadler

  • Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the Emery-Dreifuss muscular dystrophy phenotype

    Juliet A. Ellis;Molly Craxton;John R. W. Yates;John Kendrick-Jones

  • Human Gene Mapping 10

    John R W Yates

Frequent Co-Authors

Anthony T. Moore
Anthony T. Moore University of California, San Francisco
Malcolm A. Ferguson-Smith
Malcolm A. Ferguson-Smith University of Cambridge
Andrew R. Webster
Andrew R. Webster University College London
Andrew Green
Andrew Green Boston Children's Hospital
David G. Clayton
David G. Clayton University of Cambridge
Caroline Hayward
Caroline Hayward University of Edinburgh
Alan F. Wright
Alan F. Wright University of Edinburgh
Eamonn R. Maher
Eamonn R. Maher University of Cambridge
David E. Barton
David E. Barton University College Dublin
Anand Swaroop
Anand Swaroop National Institutes of Health

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