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Gil McVean

University of Oxford · GB
Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, Genomics and Phylogenetic Studies, Evolution and Genetic Dynamics, and Genetic Mapping and Diversity in Plants and Animals.
h-index
105
citations
133,785
works
311
NIH funding
primary concept
email

Recent publications

A disease-specific convergence of host and Epstein–Barr virus genetics in multiple sclerosis
Proceedings of the National Academy of Sciences 2025cited by 22position: middledoi
Genetic mapping across autoimmune diseases reveals shared associations and mechanisms
Nature Genetics 2024cited by 32position: middledoi
High-resolution African HLA resource uncovers HLA-DRB1 expression effects underlying vaccine response
Nature Medicine 2024cited by 19position: middledoi
A common NFKB1 variant detected through antibody analysis in UK Biobank predicts risk of infection and allergy
The American Journal of Human Genetics 2024cited by 2position: middledoi
A unified genealogy of modern and ancient genomes
Science 2022cited by 197position: lastdoi
Recommendations for improving statistical inference in population genomics
PLoS Biology 2022cited by 157position: middledoi
Identification of host–pathogen-disease relationships using a scalable multiplex serology platform in UK Biobank
Nature Communications 2022cited by 106position: middledoi
Mouse fetal growth restriction through parental and fetal immune gene variation and intercellular communications cascade
Nature Communications 2022cited by 22position: middledoi
Insights into malaria susceptibility using genome-wide data on 17,000 individuals from Africa, Asia and Oceania
Nature Communications 2019cited by 217position: middledoi
Identification of host-pathogen-disease relationships using a scalable Multiplex Serology platform in UK Biobank
medRxiv 2019cited by 26position: middledoi
The UK Biobank resource with deep phenotyping and genomic data
Nature 2018cited by 9,617position: middledoi
High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs
PLoS Computational Biology 2016cited by 107position: lastdoi
Class II HLA interactions modulate genetic risk for multiple sclerosis
Nature Genetics 2015cited by 415position: middledoi
Stable recombination hotspots in birds
Science 2015cited by 391position: middledoi
The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease
PLoS Genetics 2015cited by 136position: middledoi
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Nature Communications 2014cited by 455position: middledoi
Rare variants in <i>PPARG</i> with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
Proceedings of the National Academy of Sciences 2014cited by 177position: middledoi
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Nature Genetics 2013cited by 1,435position: middledoi
Multiple populations of artemisinin-resistant Plasmodium falciparum in Cambodia
Nature Genetics 2013cited by 488position: middledoi
Multiple Instances of Ancient Balancing Selection Shared Between Humans and Chimpanzees
Science 2013cited by 361position: middledoi
Hypervariable antigen genes in malaria have ancient roots
BMC Evolutionary Biology 2013cited by 55position: lastdoi
An integrated map of genetic variation from 1,092 human genomes
Nature 2012cited by 8,206position: middledoi
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
Nature Genetics 2012cited by 1,000position: middledoi
Bayesian refinement of association signals for 14 loci in 3 common diseases
Nature Genetics 2012cited by 552position: middledoi
A Fine-Scale Chimpanzee Genetic Map from Population Sequencing
Science 2012cited by 322position: lastdoi
Psoriasis Patients Are Enriched for Genetic Variants That Protect against HIV-1 Disease
PLoS Genetics 2012cited by 75position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Molly Przeworski · Columbia University3 papers (2012–2015)Ellen M. Leffler · University of Utah3 papers (2012–2015)Alexander J. Mentzer · Centre for Human Genetics3 papers (2016–2024)Oliver Venn · Illumina (United States)3 papers (2012–2015)Adrián Cortés · Institute of Human Genetics3 papers (2018–2024)Susanne P. Pfeifer · Centre for Human Genetics3 papers (2012–2022)Peter Donnelly · Genomics (United Kingdom)3 papers (2012–2018)Ronald E. Bontrop · Utrecht University2 papers (2012–2013)Mary Carrington · Cancer Institute (WIA)2 papers (2012–2022)Laure Ségurel · Éco-Anthropologie2 papers (2012–2013)Nicole Brenner · German Cancer Research Center2 papers (2019–2024)Adrian V. S. Hill · Centre for Human Genetics2 papers (2019–2024)Adam Auton · Albert Einstein College of Medicine2 papers (2012–2013)Alexander Dilthey · Düsseldorf University Hospital2 papers (2012–2016)Rory Bowden · Parks Victoria2 papers (2012–2013)Amanda Y. Chong · Centre for Human Genetics2 papers (2019–2024)Naomi E. Allen · University of Oxford2 papers (2018–2019)Thomas J. Littlejohns · University of Oxford2 papers (2019–2024)Zamin Iqbal · University of Cape Town2 papers (2012–2016)Tim Waterboer · German Cancer Research Center2 papers (2019–2024)