Michael Inouye

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Scott C RitchieSenior Research Associate, University of CambridgeVerified email at medschl.cam.ac.uk
Veikko SalomaaFinnish Institute for Health and WelfareVerified email at thl.fi
Gad AbrahamCSL LimitedVerified email at unimelb.edu.au
Kathryn HoltLSHTM & Monash UniversityVerified email at lshtm.ac.uk
Aki HavulinnaFinnish Institute for Health and WelfareVerified email at thl.fi
Shu Mei TeoBiostatistician/Data scientist Centre for youth mental healthVerified email at unimelb.edu.au
Samuel A. LambertAssistant Professor, University of CambridgeVerified email at medschl.cam.ac.uk
Patrick HoltProfessor, Telethon Kids Institute, University of Western AustraliaVerified email at telethonkids.org.au
Leo LahtiDepartment of Computing, University of Turku, FinlandVerified email at utu.fi
Rob KnightWolfe Family Chair at Rady Children's; Director, Center for Microbiome Innovation; Professor, UCSDVerified email at ucsd.edu
Guillaume MéricBaker Heart & Diabetes Institute, MelbourneVerified email at baker.edu.au
John DaneshUniversity of CambridgeVerified email at medschl.cam.ac.uk
Peter D SlyProfessor, University of QueenslandVerified email at uq.edu.au
Samuli RipattiProfessor of Biometry, University of HelsinkiVerified email at helsinki.fi
Markus Perolaresearch professorVerified email at thl.fi
Adam ButterworthProfessor of Molecular EpidemiologyVerified email at medschl.cam.ac.uk
Justin ZobelComputing and Information Systems, University of MelbourneVerified email at unimelb.edu.au
Emanuele Di AngelantonioUniversity of Cambridge / Human TechnopoleVerified email at medschl.cam.ac.uk
James GernProfessor of Pediatrics and Medicine, University of Wisconsin-MadisonVerified email at medicine.wisc.edu
Dr. Artika NathPostdoctoral Researcher at Baker Heart & Diabetes InstituteVerified email at baker.edu.au

Michael Inouye

Professor of Systems Genomics & Population Health, University of Cambridge; Baker Institute

Verified email at medschl.cam.ac.uk - Homepage

systems genomics computational biology bioinformatics statistical genetics


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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls WTCC Consortium Nature 447 (7145), 661-678, 2007	9537*	2007
Integrating common and rare genetic variation in diverse human populations International HapMap 3 Consortium Nature 467 (7311), 52-58, 2010	3281	2010
Common variants near MC4R are associated with fat mass, weight and risk of obesity RJF Loos, CM Lindgren, S Li, E Wheeler, J Zhao, I Prokopenko, M Inouye, ... Nature genetics 40 (6), 768-775, 2008	1604	2008
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants PR Burton, DG Clayton, LR Cardon, N Craddock, P Deloukas, ... Nature genetics 39 (11), 1329-1337, 2007	1461	2007
The developmental pathway for CD103+ CD8+ tissue-resident memory T cells of skin LK Mackay, A Rahimpour, JZ Ma, N Collins, AT Stock, ML Hafon, ... Nature immunology 14 (12), 1294-1301, 2013	1387	2013
The diploid genome sequence of an Asian individual J Wang, W Wang, R Li, Y Li, G Tian, L Goodman, W Fan, J Zhang, J Li, ... Nature 456 (7218), 60-65, 2008	1164	2008
SRST2: Rapid genomic surveillance for public health and hospital microbiology labs M Inouye, H Dashnow, LA Raven, MB Schultz, BJ Pope, T Tomita, J Zobel, ... Genome Medicine 6 (11), 1-16, 2014	1070*	2014
The infant nasopharyngeal microbiome impacts severity of lower respiratory infection and risk of asthma development SM Teo, D Mok, K Pham, M Kusel, M Serralha, N Troy, BJ Holt, BJ Hales, ... Cell Host & Microbe, 2015	1013	2015
Genome-wide association analysis identifies 20 loci that influence adult height MN Weedon, H Lango, CM Lindgren, C Wallace, DM Evans, M Mangino, ... Nature genetics 40 (5), 575-583, 2008	1012	2008
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource E Sollis, A Mosaku, A Abid, A Buniello, M Cerezo, L Gil, T Groza, O Güneş, ... Nucleic Acids Research, 2022	1001	2022
Variants in MTNR1B influence fasting glucose levels I Prokopenko, C Langenberg, JC Florez, R Saxena, N Soranzo, ... Nature genetics 41 (1), 77-81, 2009	931	2009
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 DA van Heel, L Franke, KA Hunt, R Gwilliam, A Zhernakova, M Inouye, ... Nature genetics 39 (7), 827-829, 2007	858	2007
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study JB Richards, F Rivadeneira, M Inouye*, TM Pastinen, N Soranzo, ... The Lancet 371 (9623), 1505-1512, 2008	817	2008
Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention M Inouye, G Abraham, CP Nelson, AM Wood, MJ Sweeting, F Dudbridge, ... Journal of the American College of Cardiology 72 (16), 1883-1893, 2018	770	2018
Genome-wide association study identifies multiple loci influencing human serum metabolite levels. J Kettunen, T Tukiainen, AP Sarin, A Ortega-Alonso, E Tikkanen, ... Nature genetics, 2012	670	2012
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease SA Fisher, M Tremelling, CA Anderson, R Gwilliam, S Bumpstead, ... Nature genetics 40 (6), 710-712, 2008	560	2008
The polygenic and monogenic basis of blood traits and diseases D Vuckovic, EL Bao, P Akbari, CA Lareau, A Mousas, T Jiang, MH Chen, ... Cell 182 (5), 1214-1231. e11, 2020	557	2020
Towards clinical utility of polygenic risk scores SA Lambert, G Abraham, M Inouye Human molecular genetics 28 (R2), R133-R142, 2019	541	2019
Genetic variants influencing circulating lipid levels and risk of coronary artery disease DM Waterworth, SL Ricketts, K Song, L Chen, JH Zhao, S Ripatti, ... Arteriosclerosis, thrombosis, and vascular biology 30 (11), 2264-2276, 2010	519	2010
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22. 1 V Anttila, H Stefansson, M Kallela, U Todt, GM Terwindt, MS Calafato, ... Nature genetics 42 (10), 869, 2010	502	2010

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