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Stuart MacGregor

Researcher Next ID · RN-022557

Researcher · Medicine

Queensland Health

Brisbane, Mexico

Not currently recruitingFunding unknown
Works count
574
Citation count
34,182
H-index
92
i10-index
304

Research interests

Medicine
Biochemistry, Genetics and Molecular Biology
Glaucoma and retinal disorders
Genetic Associations and Epidemiology
Retinal Diseases and Treatments
Ophthalmology and Visual Impairment Studies
Corneal surgery and disorders

Publications

  • The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

    Nature Genetics · 2023 · 10.1038/s41588-023-01323-z

  • Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia

    Nature Genetics · 2020 · 10.1038/s41588-020-0599-0

  • Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

    Nature Genetics · 2020 · 10.1038/s41588-019-0556-y

  • Implementing MR‐PRESSO and GCTA‐GSMR for pleiotropy assessment in Mendelian randomization studies from a practitioner's perspective

    Genetic Epidemiology · 2019 · 10.1002/gepi.22207

  • GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability

    Nature Neuroscience · 2018 · 10.1038/s41593-018-0206-1

  • Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

    Nature Genetics · 2018 · 10.1038/s41588-018-0127-7

  • Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism

    Nature Communications · 2017 · 10.1038/ncomms15539

  • Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma

    Nature Genetics · 2016 · 10.1038/ng.3482

  • Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

    Nature Genetics · 2015 · 10.1038/ng.3373

  • VEGAS2: Software for More Flexible Gene-Based Testing

    Twin Research and Human Genetics · 2014 · 10.1017/thg.2014.79

  • Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

    Nature Genetics · 2014 · 10.1038/ng.3087

  • Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

    Nature Genetics · 2013 · 10.1038/ng.2554

  • Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

    Nature Genetics · 2013 · 10.1038/ng.2506

  • Genome-wide association meta-analysis identifies new endometriosis risk loci

    Nature Genetics · 2012 · 10.1038/ng.2445

  • Genome-wide association study identifies three new melanoma susceptibility loci

    Nature Genetics · 2011 · 10.1038/ng.959

  • A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

    Nature · 2011 · 10.1038/nature10630

  • Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1

    Nature Genetics · 2011 · 10.1038/ng.824

  • Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

    Nature Genetics · 2010 · 10.1038/ng.661

  • Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

    Nature Genetics · 2010 · 10.1038/ng.731

  • Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned

    Molecular Psychiatry · 2010 · 10.1038/mp.2010.109

  • A Versatile Gene-Based Test for Genome-wide Association Studies

    The American Journal of Human Genetics · 2010 · https://doi.org/10.1016/j.ajhg.2010.06.009

  • Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans

    The American Journal of Human Genetics · 2009 · 10.1016/j.ajhg.2009.10.009

  • Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

    Nature · 2009 · https://doi.org/10.1038/nature08185

  • Rare chromosomal deletions and duplications increase risk of schizophrenia

    Nature · 2008 · https://doi.org/10.1038/nature07239

  • Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder

    The American Journal of Human Genetics · 2003 · https://doi.org/10.1086/376547

Current projects

    No projects listed.