Rare variant analyses across multiethnic cohorts identify novel genes for refractive error.
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| Title: | Rare variant analyses across multiethnic cohorts identify novel genes for refractive error. |
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| Authors: | Musolf AM; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA., Haarman AEG; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands., Luben RN; MRC Epidemiology, University of Cambridge School of Clinical Medicine, Cambridge, UK.; NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, UK., Ong JS; Statistical Genetics Laboratory, Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia., Patasova K; Department of Twin Research and Genetic Epidemiology, King's College London, London, UK., Trapero RH; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital, Edinburgh, UK., Marsh J; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital, Edinburgh, UK., Jain I; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA., Jain R; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA., Wang PZ; Institute for Biomedical Sciences, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA., Lewis DD; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA., Tedja MS; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands., Iglesias AI; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands., Li H; Data Science Unit, Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore., Cowan CS; Institute for Molecular and Clinical Ophthalmology Basel, Basel, Switzerland., Biino G; Institute of Molecular Genetics, National Research Council of Italy, Pavia, Italy., Klein AP; Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA., Duggal P; The Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA., Mackey DA; Centre for Ophthalmology and Visual Science, Lions Eye Institute, University of Western Australia, Perth, WA, Australia., Hayward C; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital, Edinburgh, UK., Haller T; Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia., Metspalu A; Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia., Wedenoja J; Department of Ophthalmology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Department of Public Health, University of Helsinki, Helsinki, Finland., Pärssinen O; Department of Ophthalmology, Central Hospital of Central Finland, Jyväskylä, Finland.; Gerontology Research Center, Faculty of Sport and Health Sciences, University of Jyväskylä, Jyväskylä, Finland., Cheng CY; Centre for Quantitative Medicine, DUKE-National University of Singapore, Singapore, Singapore.; Ocular Epidemiology Research Group, Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore., Saw SM; Saw Swee Hock School of Public Health, National University Health Systems, National University of Singapore, Singapore, Singapore.; Myopia Research Group, Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore., Stambolian D; Department of Ophthalmology, University of Pennsylvania, Philadelphia, PA, USA., Hysi PG; Department of Twin Research and Genetic Epidemiology, King's College London, London, UK., Khawaja AP; MRC Epidemiology, University of Cambridge School of Clinical Medicine, Cambridge, UK.; NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, UK., Vitart V; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital, Edinburgh, UK., Hammond CJ; Department of Twin Research and Genetic Epidemiology, King's College London, London, UK., van Duijn CM; Nuffield Department of Population Health, University of Oxford, Oxford, UK., Verhoeven VJM; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands. v.verhoeven@erasmusmc.nl.; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands. v.verhoeven@erasmusmc.nl.; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands. v.verhoeven@erasmusmc.nl., Klaver CCW; Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands. c.c.w.klaver@erasmusmc.nl.; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands. c.c.w.klaver@erasmusmc.nl.; Institute for Molecular and Clinical Ophthalmology Basel, Basel, Switzerland. c.c.w.klaver@erasmusmc.nl.; Department of Ophthalmology, Radboud University Medical Centre, Nijmegen, The Netherlands. c.c.w.klaver@erasmusmc.nl., Bailey-Wilson JE; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA. jebw@mail.nih.gov. |
| Corporate Authors: | Consortium for Refractive Error and Myopia (CREAM) |
| Source: | Communications biology [Commun Biol] 2023 Jan 03; Vol. 6 (1), pp. 6. Date of Electronic Publication: 2023 Jan 03. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Nature Publishing Group UK Country of Publication: England NLM ID: 101719179 Publication Model: Electronic Cited Medium: Internet ISSN: 2399-3642 (Electronic) Linking ISSN: 23993642 NLM ISO Abbreviation: Commun Biol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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