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Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia.

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Title: Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia.
Authors: Guggenheim JA; School of Optometry & Vision Sciences, Cardiff University, Cardiff, CF24 4HQ, UK., Clark R; School of Optometry & Vision Sciences, Cardiff University, Cardiff, CF24 4HQ, UK., Cui J; School of Optometry & Vision Sciences, Cardiff University, Cardiff, CF24 4HQ, UK., Terry L; School of Optometry & Vision Sciences, Cardiff University, Cardiff, CF24 4HQ, UK., Patasova K; Section of Ophthalmology, School of Life Course Sciences, King's College London, WC2R 2LS, UK.; Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, WC2R 2LS, UK., Haarman AEG; Department of Ophthalmology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.; Department of Epidemiology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands., Musolf AM; Statistical Genetics Section, Computational and Statistical Genomics Branch, Nation Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21224, USA., Verhoeven VJM; Department of Ophthalmology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.; Department of Clinical Genetics, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands., Klaver CCW; Department of Ophthalmology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.; Department of Epidemiology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.; Department of Ophthalmology, Radboud University Medical Center, 6525EX Nijmegen, The Netherlands.; Institute of Molecular and Clinical Ophthalmology Basel, CH-4031 Basel, Switzerland., Bailey-Wilson JE; Statistical Genetics Section, Computational and Statistical Genomics Branch, Nation Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21224, USA., Hysi PG; Section of Ophthalmology, School of Life Course Sciences, King's College London, WC2R 2LS, UK.; Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, WC2R 2LS, UK., Williams C; Centre for Academic Child Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, BS8 1NU, UK.
Corporate Authors: CREAM Consortium, UK Biobank Eye Vision Consortium
Source: Human molecular genetics [Hum Mol Genet] 2022 Jun 04; Vol. 31 (11), pp. 1909-1919.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia.
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  Data: <searchLink fieldCode="AU" term="%22Guggenheim+JA%22">Guggenheim JA</searchLink>; School of Optometry & Vision Sciences, Cardiff University, Cardiff, CF24 4HQ, UK.<br /><searchLink fieldCode="AU" term="%22Clark+R%22">Clark R</searchLink>; School of Optometry & Vision Sciences, Cardiff University, Cardiff, CF24 4HQ, UK.<br /><searchLink fieldCode="AU" term="%22Cui+J%22">Cui J</searchLink>; School of Optometry & Vision Sciences, Cardiff University, Cardiff, CF24 4HQ, UK.<br /><searchLink fieldCode="AU" term="%22Terry+L%22">Terry L</searchLink>; School of Optometry & Vision Sciences, Cardiff University, Cardiff, CF24 4HQ, UK.<br /><searchLink fieldCode="AU" term="%22Patasova+K%22">Patasova K</searchLink>; Section of Ophthalmology, School of Life Course Sciences, King's College London, WC2R 2LS, UK.; Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, WC2R 2LS, UK.<br /><searchLink fieldCode="AU" term="%22Haarman+AEG%22">Haarman AEG</searchLink>; Department of Ophthalmology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.; Department of Epidemiology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Musolf+AM%22">Musolf AM</searchLink>; Statistical Genetics Section, Computational and Statistical Genomics Branch, Nation Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21224, USA.<br /><searchLink fieldCode="AU" term="%22Verhoeven+VJM%22">Verhoeven VJM</searchLink>; Department of Ophthalmology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.; Department of Clinical Genetics, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Klaver+CCW%22">Klaver CCW</searchLink>; Department of Ophthalmology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.; Department of Epidemiology, Erasmus Medical Center GD, 3015GD Rotterdam, The Netherlands.; Department of Ophthalmology, Radboud University Medical Center, 6525EX Nijmegen, The Netherlands.; Institute of Molecular and Clinical Ophthalmology Basel, CH-4031 Basel, Switzerland.<br /><searchLink fieldCode="AU" term="%22Bailey-Wilson+JE%22">Bailey-Wilson JE</searchLink>; Statistical Genetics Section, Computational and Statistical Genomics Branch, Nation Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21224, USA.<br /><searchLink fieldCode="AU" term="%22Hysi+PG%22">Hysi PG</searchLink>; Section of Ophthalmology, School of Life Course Sciences, King's College London, WC2R 2LS, UK.; Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, WC2R 2LS, UK.<br /><searchLink fieldCode="AU" term="%22Williams+C%22">Williams C</searchLink>; Centre for Academic Child Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, BS8 1NU, UK.
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  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2022 Jun 04; Vol. 31 (11), pp. 1909-1919.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE
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              Text: 2022 Jun 04
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