World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
83
Citations
49840
World Ranking
3415
National Ranking
77

Overview

Michael Inouye is affiliated with the Baker IDI Heart and Diabetes Institute in Australia. Their research spans multiple disciplines within the life sciences, with a primary focus on Biochemistry, Genetics, and Molecular Biology, demonstrated by their publication record of 258 works in this field. Medicine is another prominent area, with 147 publications attributed to this domain.

The scientist's work covers several subfields of study, including Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine, Epidemiology, and Physiology. Their research topics address a range of biomedical concerns, such as Genetic Associations and Epidemiology, Gut Microbiota and Health, Bioinformatics and Genomic Networks, Liver Disease Diagnosis and Treatment, Metabolomics and Mass Spectrometry Studies, Epigenetics and DNA Methylation, and Genomics and Rare Diseases.

Michael Inouye has contributed frequently to various academic journals and venues. The most common platforms for their work include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature Communications
  • Nature Genetics
  • Journal of the American College of Cardiology
  • Nature

Recent publications by Michael Inouye highlight several topics and collaborations. Significant papers include:

  • "The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource" (2022, Nucleic Acids Research)
  • "The Polygenic Score Catalog as an open database for reproducibility and systematic evaluation" (2021, Nature Genetics)
  • "Stroke genetics informs drug discovery and risk prediction across ancestries" (2022, Nature)
  • "Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort" (2022, Nature Genetics)
  • "Greengenes2 unifies microbial data in a single reference tree" (2023, Nature Biotechnology)

The scientist has collaborated extensively with a group of co-authors who frequently appear on their publications. Notable frequent collaborators include:

  • Aki S. Havulinna
  • Teemu Niiranen
  • Veikko Salomaa
  • Scott C. Ritchie
  • Leo Lahti

Best Publications

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

    Paul R. Burton;David G. Clayton;Lon R. Cardon;Nick Craddock

  • Integrating common and rare genetic variation in diverse human populations

    D M Altshuler;R A Gibbs;L Peltonen

  • Genome-wide association study identifies eight loci associated with blood pressure

    Christopher Newton-Cheh;Christopher Newton-Cheh;Toby Johnson;Toby Johnson;Vesela Gateva;Martin D. Tobin

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

    Paul R Burton;David G Clayton;Lon R Cardon;Nick Craddock

  • The developmental pathway for CD103(+)CD8+ tissue-resident memory T cells of skin.

    Laura K Mackay;Azad Rahimpour;Joel Z Ma;Nicholas Collins

  • The diploid genome sequence of an Asian individual.

    Jun Wang;Wei Wang;Ruiqiang Li;Ruiqiang Li;Yingrui Li;Yingrui Li;Yingrui Li

  • SRST2: Rapid genomic surveillance for public health and hospital microbiology labs

    Michael Inouye;Harriet Dashnow;Harriet Dashnow;Lesley Ann Raven;Mark B. Schultz

  • The infant nasopharyngeal microbiome impacts severity of lower respiratory infection and risk of asthma development

    Shu Mei Teo;Danny Mok;Kym Pham;Merci Kusel

  • Genome-wide association analysis identifies 20 loci that influence adult height

    M N Weedon;H Lango;C M Lindgren;C M Lindgren;C Wallace

  • Variants in MTNR1B influence fasting glucose levels

    Inga Prokopenko;Claudia Langenberg;Jose C. Florez;Jose C. Florez;Richa Saxena;Richa Saxena

  • A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

    David A. van Heel;Lude Franke;Karen A. Hunt;Rhian Gwilliam

  • Bone mineral density, osteoporosis, and osteoporotic fractures : a genome-wide association study

    J.B. Richards;F. Rivadeneira;M. Inouye;T.M. Pastinen

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

    Sergey Nejentsev;Joanna M. M. Howson;Neil M. Walker;Jeffrey Szeszko

  • The polygenic and monogenic basis of blood traits and diseases

    Dragana Vuckovic;Erik L. Bao;Parsa Akbari;Caleb A. Lareau

  • Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention.

    Michael Inouye;Gad Abraham;Christopher P. Nelson;Angela M. Wood

  • Genome-wide association study identifies multiple loci influencing human serum metabolite levels

    Johannes Kettunen;Johannes Kettunen;Taru Tukiainen;Antti-Pekka Sarin;Antti-Pekka Sarin;Alfredo Ortega-Alonso

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

    Sheila A Fisher;Mark Tremelling;Carl A Anderson;Rhian Gwilliam

  • Genetic variants influencing circulating lipid levels and risk of coronary artery disease.

    Dawn M. Waterworth;Sally L. Ricketts;Kijoung Song;Li Chen

  • Towards clinical utility of polygenic risk scores.

    Samuel A Lambert;Gad Abraham;Gad Abraham;Gad Abraham;Michael Inouye

  • Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

    Anttila;Stefansson H;Kallela M;Todt U

Frequent Co-Authors

Kathryn E. Holt
Kathryn E. Holt London School of Hygiene & Tropical Medicine
Markus Perola
Markus Perola Finnish Institute for Health and Welfare
Aki S. Havulinna
Aki S. Havulinna Finnish Institute for Health and Welfare
Samuli Ripatti
Samuli Ripatti University of Helsinki
Johannes Kettunen
Johannes Kettunen University of Oulu
Veikko Salomaa
Veikko Salomaa Finnish Institute for Health and Welfare
Patrick G. Holt
Patrick G. Holt University of Western Australia
Olli T. Raitakari
Olli T. Raitakari Turku University Hospital
Aarno Palotie
Aarno Palotie University of Helsinki
John Danesh
John Danesh University of Cambridge

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