Iain Mathieson - Google Scholar Citations

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Gil McVeanProfessor of Statistical Genetics, University of OxfordVerified email at well.ox.ac.uk
Andy RimmerWellcome Trues Centre For Human Genetics, OxfordVerified email at well.ox.ac.uk
Gerton LunterAssociate Professor, University of OxfordVerified email at well.ox.ac.uk
Zamin IqbalEuropean Bioinformatics Institute - EMBLVerified email at ebi.ac.uk
Jonathan FlintUniversity of California, Los AngelesVerified email at well.ox.ac.uk
Marcus MunafoUniversity of BristolVerified email at bristol.ac.uk
Isaac TurnerPhD Student, University of Oxford, UKVerified email at dtc.ox.ac.uk
Stefano LiseCentre for Evolution and Cancer, Institute of Cancer Research, LondonVerified email at icr.ac.uk
David KeaysGroup Leader, Institute of Molecular PathologyVerified email at imp.ac.at
Nick PattersonStaff scientist, Broad InstituteVerified email at broadinstitute.org
Joshua C. RandallWellcome Trust Sanger InstituteVerified email at sanger.ac.uk
Iosif LazaridisResearch Associate, Department of Genetics, Harvard Medical SchoolVerified email at genetics.med.harvard.edu
Wolfgang HaakMax Planck Institute for the Science of Human HistoryVerified email at shh.mpg.de
Alan CooperDirector, Australian Centre for Ancient DNA, University of AdelaideVerified email at adelaide.edu.au
David W AnthonyProfessor of Anthropology, Hartwick CollegeVerified email at hartwick.edu
Joseph PickrellNew York Genome CenterVerified email at nygenome.org
Bastien LlamasAustralian Centre for Ancient DNA - University of AdelaideVerified email at adelaide.edu.au
Carles Lalueza-FoxInstitut de Biologia EvolutivaVerified email at upf.edu
Johannes KrauseProfessor Archaeogenetics and PaleogeneticsVerified email at shh.mpg.de
Nadin RohlandVerified email at genetics.med.harvard.edu

Iain Mathieson

University of Pennsylvania

Verified email at mail.med.upenn.edu - Homepage

Genetics


Title	Cited by	Year
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	5429	2012
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	2797	2015
Genome-wide patterns of selection in 230 ancient Eurasians I Mathieson, I Lazaridis, N Rohland, S Mallick, N Patterson, ... Nature 528 (7583), 499, 2015	383	2015
Integrating mapping-, assembly-and haplotype-based approaches for calling variants in clinical sequencing applications A Rimmer, H Phan, I Mathieson, Z Iqbal, SRF Twigg, AOM Wilkie, ... Nature genetics 46 (8), 912, 2014	344*	2014
Differential confounding of rare and common variants in spatially structured populations I Mathieson, G McVean Nature genetics 44 (3), 243, 2012	249	2012
The genetic history of ice age Europe Q Fu, C Posth, M Hajdinjak, M Petr, S Mallick, D Fernandes, ... Nature 534 (7606), 200, 2016	240	2016
The Simons genome diversity project: 300 genomes from 142 diverse populations S Mallick, H Li, M Lipson, I Mathieson, M Gymrek, F Racimo, M Zhao, ... Nature 538 (7624), 201, 2016	227	2016
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits JC Randall, TW Winkler, Z Kutalik, SI Berndt, AU Jackson, KL Monda, ... PLoS genetics 9 (6), e1003500, 2013	212	2013
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome FR Day, DA Hinds, JY Tung, L Stolk, U Styrkarsdottir, R Saxena, ... Nature communications 6, 8464, 2015	93	2015
Meta-analysis indicates that common variants at the DISC1 locus are not associated with schizophrenia I Mathieson, MR Munafò, J Flint Molecular psychiatry 17 (6), 634, 2012	80	2012
Strong male bias drives germline mutation in chimpanzees O Venn, I Turner, I Mathieson, N de Groot, R Bontrop, G McVean Science 344 (6189), 1272-1275, 2014	79	2014
Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development S Lise, Y Clarkson, E Perkins, A Kwasniewska, ES Akha, ... PLoS genetics 8 (12), e1003074, 2012	56	2012
Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies AT Pagnamenta, S Lise, V Harrison, H Stewart, S Jayawant, ... Journal of human genetics 57 (1), 70, 2012	55	2012
Estimating selection coefficients in spatially structured populations from time series data of allele frequencies I Mathieson, G McVean Genetics, genetics. 112.147611, 2013	48	2013
Demography and the age of rare variants I Mathieson, G McVean PLoS genetics 10 (8), e1004528, 2014	47	2014
The genomic history of southeastern Europe I Mathieson, S Alpaslan-Roodenberg, C Posth, A Szécsényi-Nagy, ... Nature 555 (7695), 197, 2018	41	2018
Differences in the rare variant spectrum among human populations I Mathieson, D Reich PLoS genetics 13 (2), e1006581, 2017	13*	2017
Ancient Human Genomics: The First Decade P Skoglund, I Mathieson Annual review of genomics and human genetics, 2018	1	2018
Signals of polygenic adaptation on height have been overestimated due to uncorrected population structure in genome-wide association studies M Sohail, RM Maier, A Ganna, A Bloemendal, AR Martin, MC Turchin, ... bioRxiv, 355057, 2018	1	2018
The evolution of CHC22 clathrin influences its role in human glucose metabolism M Fumagalli, Y Diekmann, SM Camus, A Burke, MD Camus, PJ Norman, ... bioRxiv, 307264, 2018		2018

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