McVean, Gil
Genomics (United Kingdom)
14 papers on CoChatORCID 0000-0002-5012-4162
Most cited papers
- Verified
The UK Biobank resource with deep phenotyping and genomic data
Bycroft, C., Freeman, C., Petkova, D., Band, G., Elliott, L. T., Sharp, K., Motyer, A., Vukcevic, D., Delaneau, O., O’Connell, J., et al. (2018) · Nature
Genetic Associations and EpidemiologyGenetic and phenotypic traits in livestock
Cited by 8,876
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A new multipoint method for genome-wide association studies by imputation of genotypes
Marchini, J., Howie, B., Myers, S., McVean, G., & Donnelly, P. (2007) · Nature Genetics
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 2,609
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Mapping copy number variation by population-scale genome sequencing
1000 Genomes Project, Mills, R. E., Walter, K., Stewart, C., Handsaker, R. E., Chen, K., Alkan, C., Abyzov, A., Yoon, S. C., Ye, K., et al. (2011) · Nature
Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms
Cited by 1,140
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A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome
Myers, S., Bottolo, L., Freeman, C., McVean, G., & Donnelly, P. (2005) · Science
Genetic Associations and EpidemiologyChromosomal and Genetic Variations
Cited by 1,134
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A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC
de Bakker, P. I. W., McVean, G., Sabeti, P. C., Miretti, M. M., Green, T., Marchini, J., Ke, X., Monsuur, A. J., Whittaker, P., Delgado, M., et al. (2006) · Nature Genetics
Genetic Associations and EpidemiologyForensic and Genetic Research
Cited by 766
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A Coalescent-Based Method for Detecting and Estimating Recombination From Gene Sequences
McVean, G., Awadalla, P., & Fearnhead, P. (2002) · Genetics
Evolution and Genetic DynamicsGenetic diversity and population structure
Cited by 708
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Drive Against Hotspot Motifs in Primates Implicates the PRDM9 Gene in Meiotic Recombination
Myers, S., Bowden, R., Tumian, A., Bontrop, R. E., Freeman, C., MacFie, T. S., McVean, G., & Donnelly, P. (2010) · Science
Chromosomal and Genetic VariationsGenomics and Chromatin Dynamics
Cited by 683
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Differential confounding of rare and common variants in spatially structured populations
Mathieson, I., & McVean, G. (2012) · Nature Genetics
Genetic Associations and EpidemiologyForensic and Genetic Research
Cited by 385
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Inferring whole-genome histories in large population datasets
Kelleher, J., Wong, Y., Wohns, A. W., Fadil, C., Albers, P. K., & McVean, G. (2019) · Nature Genetics
Forensic and Genetic ResearchGenetic diversity and population structure
Cited by 313
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UK Biobank release and systematic evaluation of optimised polygenic risk scores for 53 diseases and quantitative traits
Thompson, D. J., Wells, D., Selzam, S., Peneva, I., Moore, R., Sharp, K., Tarran, W. A., Beard, E. J., Riveros-Mckay, F., Giner-Delgado, C., et al. (2022) · medRxiv
Genetic Associations and EpidemiologyGenetic and phenotypic traits in livestock
Cited by 280
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Resolving TYK2 locus genotype-to-phenotype differences in autoimmunity
Dendrou, C. A., Cortes, A., Shipman, L., Evans, H. G., Attfield, K. E., Jostins, L., Barber, T., Kaur, G., Kuttikkatte, S. B., Leach, O. A., et al. (2016) · Science Translational Medicine
Genetic Associations and EpidemiologyRheumatoid Arthritis Research and Therapies
Cited by 264
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A Statistical Method for Predicting Classical HLA Alleles from SNP Data
Leslie, S., Donnelly, P., & McVean, G. (2008) · The American Journal of Human Genetics
Genetic Associations and EpidemiologyForensic and Genetic Research
Cited by 173
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Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants
Panoutsopoulou, K., Hatzikotoulas, K., Xifara, D. K., Colonna, V., Farmaki, A.-E., Ritchie, G. R. S., Southam, L., Gilly, A., Tachmazidou, I., Fatumo, S., et al. (2014) · Nature Communications
Genetic Associations and EpidemiologyForensic and Genetic Research
Cited by 70
- Verified
A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability
Davies, B., Brown, L. A., Cais, O., Watson, J., Clayton, A. J., Chang, V. T., Biggs, D., Preece, C., Hernandez-Pliego, P., Krohn, J., et al. (2017) · Human Molecular Genetics
Sleep and Wakefulness ResearchCircadian rhythm and melatonin
Cited by 48
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