S. Hunt

发表

A physical map of 30,000 human genes.

P. Lijnzaad, P. Deloukas, E. Lander, 1998, Science.

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

M. Daly, G. Marth, E. Lander, 2001, Nature.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Simon C. Potter, P. Donnelly, C. Spencer, 2007, Nature.

A second generation human haplotype map of over 3.1 million SNPs

Zhaohui S. Qin, Gudmundur A. Thorisson, L. M. Sung, 2007, Nature.

An SNP map of human chromosome 22

G. D. Wilson, J. Sulston, N. Carter, 2000, Nature.

Genome-Wide Associations of Gene Expression Variation in Humans

S. Hunt, A. Clark, S. Tavaré, 2005, PLoS genetics.

The genome sequence of Schizosaccharomyces pombe

B. Barrell, A. Goffeau, B. Purnelle, 2002, Nature.

The Ensembl Variant Effect Predictor

F. Cunningham, W. McLaren, G. Ritchie, 2016, Genome Biology.

Ensembl 2015

Alessandro Vullo, Daniel R. Zerbino, Laurent Gil, 2014, Nucleic Acids Res..

Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls

Jake K. Byrnes, Tomas W. Fitzgerald, Renwick, 2010 .

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Tanya M. Teslovich, Andrew D. Johnson, Ayellet V. Segrè, 2012, Nature Genetics.

The Fine-Scale Structure of Recombination Rate Variation in the Human Genome

P. Donnelly, P. Deloukas, G. McVean, 2004, Science.

Integrating common and rare genetic variation in diverse human populations

Sharon R Grossman, Pardis C Sabeti, P. Deloukas, 2010, Nature.

Multiple common variants for celiac disease influencing immune gene expression

P. Deloukas, R. Ophoff, L. Peltonen, 2010, Nature Genetics.

The DNA sequence of human chromosome 22

Melanie E. Goward, Antony V. Cox, R. Durbin, 1999, Nature.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Simon C. Potter, David M. Evans, P. Donnelly, 2007, Nature Genetics.

Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia

Simon C. Potter, M. Pirinen, P. Donnelly, 2013, Nature Genetics.

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

Simon C. Potter, Miguel Ángel Martínez, C. Spencer, 2017, Brain : a journal of neurology.

The portability of tagSNPs across populations: a worldwide survey.

P. Deloukas, S. Hunt, H. Cann, 2006, Genome research.

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

Sarah Edkins, Cisca Wijmenga, Lude Franke, 2011, Nature Genetics.

The DNA sequence and analysis of human chromosome 6

I. Dunham, J. L. Ashurst, D. R. Bentley, 2003, Nature.

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Simon C. Potter, Joseph T. Glessner, M. Pirinen, 2011, Nature.

The DNA sequence of the human X chromosome

David L. Steffen, R. Durbin, A. Coulson, 2005, Nature.

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

The impact of SNP density on fine-scale patterns of linkage disequilibrium.

P. Deloukas, A. Morris, S. Hunt, 2004, Human molecular genetics.

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Tanya M. Teslovich, Andrew D. Johnson, Kyle J. Gaulton, 2014, Nature Genetics.

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

P. Donnelly, C. Spencer, C. Freeman, 2010 .

Large-scale association analysis identifies new risk loci for coronary artery disease

J. Danesh, R. Collins, D. Absher, 2013 .

A Genome-wide Survey of the Prevalence and Evolutionary Forces Acting on Human Nonsense Snps

P. Deloukas, C. Tyler-Smith, S. Searle, 2022 .

Ensembl Genomes 2020—enabling non-vertebrate genomic research

James E. Allen, Andrew D. Yates, Mark D. McDowall, 2019, Nucleic Acids Res..

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

M. Pirinen, P. Donnelly, C. Spencer, 2013, Nature Genetics.

Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

Simon C. Potter, Till F. M. Andlauer, M. Pirinen, 2019, Science.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Highly parallel SNP genotyping.

D Bentley, P Deloukas, B G Kermani, 2003, Cold Spring Harbor symposia on quantitative biology.

The nucleotide sequence of Saccharomyces cerevisiae chromosome IX.

N Hamlin, B. Barrell, S. Hunt, 1997, Nature.

Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

M. Pirinen, P. Donnelly, C. Spencer, 2012 .

Ensembl 2020

Astrid Gall, Alessandro Vullo, James E. Allen, 2019, Nucleic Acids Res..

Common variants near MC4R are associated with fat mass, weight and risk of obesity

Subhajyoti De, Inês Barroso, Philippe Froguel, 2008, Nature Genetics.

Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21

Matti Pirinen, Peter Donnelly, Robert Plomin, 2010, Human molecular genetics.

A first-generation linkage disequilibrium map of human chromosome 22

Lon R. Cardon, Andres Metspalu, David Beare, 2002, Nature.

Genome-wide and fine-resolution association analysis of malaria in West Africa

Peter Donnelly, Michael Inouye, Giorgio Sirugo, 2009, Nature Genetics.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Christian Gieger, Jianxin Shi, Inês Barroso, 2013, Nature Genetics.

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1

Matti Pirinen, Peter Donnelly, Robert Plomin, 2010, Nature Genetics.

Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes.

Andrew P Morris, Panos Deloukas, Sarah Hunt, 2004, American journal of human genetics.

High density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

Eli Stahl, Christopher I. Amos, Sarah Edkins, 2012, Nature Genetics.

The Influence of Recombination on Human Genetic Diversity

Peter Donnelly, Gil McVean, Simon Myers, 2006, PLoS genetics.

Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants.

Jiannis Ragoussis, Andrew P Morris, Xiayi Ke, 2005, Genome research.

A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence.

P Sham, S Minoshima, B. Roe, 2001, Genome research.

Edinburgh Research Explorer Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

Peter Donnelly, Robert Plomin, Elvira Bramon, 2022 .

Clustered Coding Variants in the Glutamate Receptor Complexes of Individuals with Schizophrenia and Bipolar Disorder

P. Visscher, A. McRae, I. Deary, 2011, PloS one.

The DNA sequence and biological annotation of human chromosome 1

I. Dunham, C. Clee, D. R. Bentley, 2006, Nature.

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

Simon C. Potter, M. Pirinen, P. Donnelly, 2017, Translational Psychiatry.

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes 1 2 Primary

John P. Rice, Melissa J. Green, Robert C. Thompson, 2018 .

A linkage disequilibrium map of chromosome 22

R. Mägi, P. Deloukas, G. Abecasis, 2002 .

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

The GA4GH Variation Representation Specification (VRS): a Computational Framework for the Precise Representation and Federated Identification of Molecular Variation

Alex H. Wagner, Matthew H. Brush, Andrew D. Yates, 2021, bioRxiv.

High-resolution landmark framework for the sequence-ready mapping of Xq23-q26.1.

C. Soderlund, S. Hunt, D. Bentley, 1999, Genome research.

The Ensembl COVID-19 resource: ongoing integration of public SARS-CoV-2 data

Andrew D. Yates, Carla A. Cummins, Denye N. Ogeh, 2020, bioRxiv.

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

Jean-François Dartigues, Günther Deuschl, Yoav Ben-Shlomo, 2017, Genome Biology.

Population-Specific Risk of Type 2 Diabetes Conferred by HNF4A P2 Promoter Variants

Inês Barroso, Mark I. McCarthy, Mark Walker, 2008, Diabetes.

Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

M. Pirinen, P. Donnelly, C. Spencer, 2019, Nature Communications.

corrigendum: The genome sequence of Schizosaccharomyces pombe

B. Barrell, A. Goffeau, B. Purnelle, 2003, Nature.

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Matti Pirinen, Christian Gieger, Peter Donnelly, 2012 .

Corrigendum: Multiple common variants for celiac disease influencing immune gene expression

P. Deloukas, R. Ophoff, L. Peltonen, 2010, Nature Genetics.

The DNA sequence and biological annotation of human chromosome 1 (vol 441, pg 315, 2006)

R. Durbin, G. McVean, A. Coulson, 2006 .

The Chromosome 6 database at the Sanger Centre.

S. Hunt, C. Rice, I. Dunham, 1997, DNA sequence : the journal of DNA sequencing and mapping.

Database update Ensembl variation resources

Irina M. Armean, F. Cunningham, W. McLaren, 2018 .

Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease

Simon C. Potter, Thomas W. Mühleisen, Benjamin J. Wright, 2011, PLoS genetics.

Erratum: The genome sequence of Schizosaccharomyces pombe (Nature (2002) 415 (871-880))

G. Volckaert, J. Sgouros, S. Hunt, 2003 .

Common VKORC1 and GGCX polymorphisms associated with warfarin dose

S. Hunt, D. Bentley, K. Downes, 2005, The Pharmacogenomics Journal.

Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children

Anne W. Ndungu, M. Pirinen, P. Donnelly, 2016, American journal of human genetics.

2002genome sequence of Schizosaccharomyces pombe. V. Wood, R. Gwilliam, M -A.

B. Barrell, A. Goffeau, B. Purnelle, 2002 .

The Ensembl Variant Effect Predictor

F. Cunningham, W. McLaren, G. Ritchie, 2016, bioRxiv.

Ensembl 2018

Astrid Gall, Alessandro Vullo, Jane Loveland, 2017, Nucleic Acids Res..

A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease

Simon C. Potter, M. Pirinen, D. Hernandez, 2011, PLoS genetics.

Ensembl variation resources

Laurent Gil, Paul Flicek, Fiona Cunningham, 2018, Database J. Biol. Databases Curation.

Ensembl 2014

Daniel R. Zerbino, Laurent Gil, Ewan Birney, 2013, Nucleic Acids Res..

Common variants in the HLA-DRB1-HLA-DQA1 Class II region are associated with susceptibility to visceral leishmaniasis

M. Pirinen, P. Donnelly, C. Spencer, 2013, Nature Genetics.

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Paul Weston, Robert Plomin, Elvira Bramon, 2011, Nature Genetics.

A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

Mark I. McCarthy, Philippe Froguel, Paul Elliott, 2011, Nature Genetics.

Ensembl 2017

Alessandro Vullo, Matthew R. Laird, Daniel R. Zerbino, 2016, Nucleic Acids Res..

Ensembl 2021

Astrid Gall, James E. Allen, Daniel R. Zerbino, 2020, Nucleic Acids Res..

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation

M. Pirinen, P. Donnelly, C. Spencer, 2014, Biological Psychiatry.

The DNA sequence and comparative analysis of human chromosome 20

D R Bentley, J E Sulston, C Carder, 2004, Nature.

A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.

Stephan Beck, Xiayi Ke, Panos Deloukas, 2005, American journal of human genetics.

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X

P. Deloukas, R. Durbin, J. Sulston, 2001, Nature.

A re-examination of proximodistal patterning during vertebrate limb development

Lon R. Cardon, Andres Metspalu, Jaak Vilo, 2022 .

Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.

S. Hunt, F. Collins, M. Boehnke, 2004, Diabetes.

Complete MHC haplotype sequencing for common disease gene mapping.

Sophie Palmer, Stephan Beck, Ian Dunham, 2004, Genome research.

Variants in MTNR1B influence fasting glucose levels

Inês Barroso, Paul Scheet, Nicole Soranzo, 2009, Nature Genetics.

Ensembl 2019

Astrid Gall, Alessandro Vullo, Jane Loveland, 2018, Nucleic Acids Res..

A polygenic resilience score moderates the genetic risk for schizophrenia

M. Pirinen, P. Donnelly, C. Spencer, 2019, Molecular Psychiatry.

Ensembl 2016

Daniel R. Zerbino, Laurent Gil, Ewan Birney, 2015, Nucleic Acids Res..

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

M. Pirinen, P. Donnelly, C. Spencer, 2012, Nature Genetics.

Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis

Sampath Prahalad, Carl D. Langefeld, Wei-Min Chen, 2013, Nature Genetics.

Genetic evidence of assortative mating in humans

Tanya M. Teslovich, Ross M. Fraser, Brendan P. Zietsch, 2017, Nature Human Behaviour.

Ensembl 2013

Laurent Gil, Paul Flicek, Fiona Cunningham, 2012, Nucleic Acids Res..

DNA sequence and analysis of human chromosome 9

I. Dunham, J. L. Ashurst, D. R. Bentley, 2003, Nature.

The DNA sequence and analysis of human chromosome 13

I. Dunham, J. L. Ashurst, D. R. Bentley, 2004, Nature.

Genetic Determinants of Major Blood Lipids in Pakistanis Compared With Europeans

Simon C. Potter, J. Danesh, P. Deloukas, 2010, Circulation. Cardiovascular genetics.

Genetic Determinants of Major Blood Lipids in Pakistan Is Compared with Europeans Running title: Saleheen et al.; Genetic loci for major lipids in Pakistan

Willem, Simon C. Potter, Saleem, 2010 .

Genetic loci for major lipids in Pakistan

Fazal-ur-Rehman, Simon C. Potter, J. Danesh, 2010 .

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease

Alastair Forbes, Carlo Berzuini, Lon Cardon, 2008, Nature Genetics.

A haplotype map of the human genome The International HapMap Consortium

Li, Yi, Jun, 2005 .

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.

Andrew P Morris, Xiayi Ke, Panos Deloukas, 2004, Human molecular genetics.

The DNA sequence and comparative analysis of human chromosome 10

A. Taylor, J. L. Ashurst, M. C. Jones, 2004, Nature.

Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.

Simon C. Potter, Benjamin J. Wright, T. Assimes, 2011, American journal of human genetics.

University of Dundee Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children Rautanen,

Anne W. Ndungu, M. Pirinen, P. Donnelly, 2017 .

Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus

M. Pirinen, P. Donnelly, C. Spencer, 2013, Human molecular genetics.

Complement genes contribute sex-biased vulnerability in diverse illnesses

Simon C. Potter, Christopher W. Whelan, M. Pirinen, 2020, Nature.

Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.

P. Deloukas, D. Strachan, S. Hunt, 2009, Gastroenterology.

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

Cue Hyunkyu Lee, Gao T. Wang, Benjamin J. Wright, 2016, Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease.

Ensembl variation resources

Laurent Gil, Paul Flicek, Fiona Cunningham, 2010, BMC Genomics.

Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study

Andres Metspalu, Michael Doherty, Nigel Arden, 2012, The Lancet.

The European Variation Archive: a FAIR resource of genomic variation for all species

Thomas M. Keane, S. Hunt, H. Parkinson, 2021, Nucleic Acids Res..

The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identification

Matthew H. Brush, Andrew D. Yates, David A. Kreda, 2021, Cell genomics.

Overview of the MHC fine mapping data

P. Deloukas, S. Hunt, K. Lohman, 2009, Diabetes, obesity & metabolism.

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett’s esophagus

Simon C. Potter, M. Pirinen, P. Donnelly, 2012, Nature Genetics.

Genome-Wide Association Study Implicates HLA-C * 01 : 02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia Irish Schizophrenia Genomics

Kelleher, P. Deloukas, E. Bramon, 2012 .

Population-specific risk of type 2 diabetes ( T 2 D ) conferred by HNF 4 A P 2 promoter variants : a lesson for replication studies

Inês Barroso, Mark Walker, Panagiotis Deloukas, 2008 .

Variation Within the Gene Encoding the Upstream Stimulatory Factor 1 Does Not Influence Susceptibility to Type 2 Diabetes in Samples From Populations With Replicated Evidence of Linkage to Chromosome 1q

Philippe Froguel, Mark Walker, Mark I McCarthy, 2006, Diabetes.

A Variant in LDLR Is Associated With Abdominal Aortic Aneurysm

Simon C. Potter, Benjamin J. Wright, P. Deloukas, 2013, Circulation. Cardiovascular genetics.

Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP

Fiona Cunningham, Archie Campbell, David R. FitzPatrick, 2019, Nature Communications.

VEP-G2P: A Tool for Efficient, Flexible and Scalable Diagnostic Filtering of Genomic Variants

M. Hurles, W. McLaren, S. Hunt, 2018, bioRxiv.

A plugin for the Ensembl Variant Effect Predictor that uses MaxEntScan to predict variant spliceogenicity

Amanda B. Spurdle, Michael T. Parsons, Sarah E. Hunt, 2018, Bioinform..

Using genome-wide complex trait analysis to quantify ‘ missing heritability ’ in Parkinson ’ s disease

Simon C. Potter, M. Pirinen, P. Deloukas, 2012 .

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

Matti Pirinen, David M. Herrington, Alex Doney, 2014, Nature Communications.

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

Adriana I. Iglesias, M. Pirinen, P. Donnelly, 2014, Nature Communications.

Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium maps

Andrew Collins, Panos Deloukas, William J Tapper, 2004, Proceedings of the National Academy of Sciences of the United States of America.

The DNA sequence and biological annotation of human chromosome 1

I. Dunham, C. Clee, D. R. Bentley, 2006, Nature.

A comparison of tagging methods and their tagging space.

John Broxholme, Xiayi Ke, Panos Deloukas, 2005, Human molecular genetics.

Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study

Simon C. Potter, Bjarni V. Halldórsson, A. Hofman, 2010, Annals of the rheumatic diseases.

Haplotype‐based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1–DQA1–DQB1 haplotype

P. Deloukas, W. McLaren, S. Hunt, 2009, Diabetes, obesity & metabolism.

Complement genes contribute sex-biased vulnerability in diverse disorders

Christopher W. Whelan, M. Pirinen, C. Spencer, 2020, Nature.

Using ancestry-informative markers to identify fine structure across 15 populations of European origin

Graham M Lord, Günter P. Wagner, I. Ntalla, 2014, European Journal of Human Genetics.

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

Tariq Ahmad, Sarah Edkins, Christopher G Mathew, 2011, Nature Genetics.

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

Matti Pirinen, Peter Donnelly, Robert Plomin, 2014, Nature Communications.

Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease

Simon C. Potter, M. Pirinen, C. Spencer, 2016, npj Genomic Medicine.

Annotation and curation of human genomic variations: an ELIXIR Implementation Study

Marcella Attimonelli, Fiona Cunningham, Roberto Preste, 2020, F1000Research.

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

Simon C. Potter, Miguel Ángel Martínez, C. Spencer, 2017, Genome Biology.

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Tanya M. Teslovich, Andrew D. Johnson, Kyle J. Gaulton, 2014 .

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Tanya M. Teslovich, Andrew D. Johnson, Simon C. Potter, 2012, Nature Genetics.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

P. Donnelly, C. Spencer, A. Silman, 2007, Nature genetics.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.

John P. Rice, Simon C. Potter, Melissa J. Green, 2018, Cell.

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

Simon C. Potter, Miguel Ángel Martínez, C. Spencer, 2016, American journal of human genetics.

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

Simon C. Potter, C. Spencer, A. Silman, 2007, Nature.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Thomas W. Mühleisen, David M. Evans, M. Jarvelin, 2013, Nature Genetics.

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

C. Gieger, S. Hunt, S. Ripatti, 2016 .

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

M. Pirinen, P. Donnelly, C. Spencer, 2013, Nature Genetics.

Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations

Vincent H. Everett, Annette Lee, P. Gregersen, 2018, Genome Medicine.

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

Simon C. Potter, P. Donnelly, C. Spencer, 2009, Nature Genetics.

Genome-wide and fine-resolution association analysis of malaria in West Africa

P. Donnelly, P. Deloukas, J. Marchini, 2009, Nature Genetics.

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

C. Spencer, C. Freeman, P. Deloukas, 2012 .

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Simon C. Potter, Adriana I. Iglesias, M. Pirinen, 2018, Nature Communications.

Large-scale association analysis identifies new risk loci for coronary artery disease

J. Danesh, R. Collins, D. Absher, 2012, Nature Genetics.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

P. Donnelly, C. Spencer, A. Silman, 2007, Nature Genetics.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Thomas W. Mühleisen, M. Jarvelin, M. Peters, 2013, Nature Genetics.

A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility

Simon C. Potter, M. Pirinen, P. Donnelly, 2014, Genes and Immunity.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Thomas W. Mühleisen, M. Jarvelin, M. Peters, 2013, Nature Genetics.

A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation

Simon C. Potter, M. Pirinen, P. Donnelly, 2014, Biological Psychiatry.

Integrating common and rare genetic variation in diverse human populations

Joshua M. Korn, Pardis C Sabeti, P. Deloukas, 2010, Nature.

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Tanya M. Teslovich, Andrew D. Johnson, Ross M. Fraser, 2012, Nature Genetics.

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

C. Freeman, P. Deloukas, E. Bramon, 2010, Nature Genetics.

From long range mapping to sequence-ready contigs on human chromosome 6.

C. Soderlund, A. Butler, C. Clee, 1997, DNA Sequence.

Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes.

P. Deloukas, S. Hunt, L. Cardon, 2004, American journal of human genetics.

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

M. Pirinen, C. Freeman, P. Deloukas, 2020 .

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

Madeline, Melissa J. Green, Janice M. Fullerton, 2017 .

Overview of the MHC fine mapping data

S. Hunt, K. Lohman, P. Deloukas, 2009, Diabetes, obesity & metabolism.