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. |
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| 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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| ISSN: | 1460-2083 |
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| DOI: | 10.1093/hmg/ddac004 |
