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Author Details

Alan F Wright
1977
343
97
PMIDPaper TitleJournal TitlePublished Year
3651358410q26 - The enigma in age-related macular degeneration.Prog Retin Eye Res2023
38046619measurement of mitochondrial ROS production in mouse models of photoreceptor degeneration.2023
33402679Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
33884923Choroidal neovascularisation in a predicted female choroideraemia carrier treated with intravitreal anti-vascular endothelial growth factor.European Journal of Ophthalmology2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
32989287Genome-wide association study identifies 48 common genetic variants associated with handedness.Nat Hum Behav2021
31306056Lipidomics, Atrial Conduction, and Body Mass Index.Circ Genom Precis Med2019
30496607Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study.International Journal of Cancer2019
30285110Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.Hum Mol Genet2019
29545425Unilateral retinitis pigmentosa occurring in an individual with a mutation in the gene.BMJ Case Reports2018
29935669Genome-Wide Association Studies Identify Disease Mechanisms in Age-Related Macular Degeneration.Ophthalmology2018
29971438Cone Vision Changes in the Enhanced S-Cone Syndrome Caused by NR2E3 Gene Mutations.Invest Ophthalmol Vis Sci2018
30429575Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30224653Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
29437585MR-PheWAS: exploring the causal effect of SUA level on multiple disease outcomes by using genetic instruments in UK Biobank.Ann Rheum Dis2018
28270201Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.Genome Med2017
28509723Determinants of retinal microvascular features and their relationships in two European populations.Journal of Hypertension2017
28814713Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models.Nat Commun2017
28939808Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration.Sci Rep2017
28448500Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.PLoS Genet2017
28443625Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.Nat Commun2017
28832619Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.PLoS Genet2017
28739976Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.Hypertension2017
27876822A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.Nat Commun2016
25869804GWAS for executive function and processing speed suggests involvement of the CADM2 gene.Mol Psychiatry2016
27020472Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.Nat Commun2016
27142678Genetic variants in RBFOX3 are associated with sleep latency.Eur J Hum Genet2016
26833246New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.Nat Commun2016
27049301Whole-exome sequencing in an isolated population from the Dalmatian island of Vis.Eur J Hum Genet2016
26831199Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Nat Commun2016
27225129Genome-wide association study identifies 74 loci associated with educational attainment.Nature2016
27355579Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.PLoS Genet2016
26561523A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.Hum Mol Genet2016
26348595Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa.Gene Therapy2016
26696135Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.Heredity2016
2765946652 Genetic Loci Influencing Myocardial Mass.J Am Coll Cardiol2016
27798627Genome-wide analysis identifies 12 loci influencing human reproductive behavior.Nat Genet2016
27798110Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.Hum Mol Genet2016
26105150Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.Blood2015
28721259Fine mapping the <i>CETP</i> region reveals a common intronic insertion associated to HDL-C.NPJ Aging Mech Dis2015
25673413Genetic studies of body mass index yield new insights for obesity biology.Nature2015
25751400Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels.Nat Commun2015
25918167Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models.Human Molecular Genetics2015
25367360Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.Hum Genet2015
25744449Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.Twin Res Hum Genet2015
25823570Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia.Nat Commun2015
25648963Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium.Biol Psychiatry2015
25811787Modulation of genetic associations with serum urate levels by body-mass-index in humans.PLoS One2015
25644384Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).Mol Psychiatry2015
25938534Long-term effects of retinal gene therapy in childhood blindness.New England Journal of Medicine2015
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University of Oxford
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Erasmus University Medical Center
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Harvard T.H. Chan School of Public Health
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German Research Center for Cardiovascular Disease (DZHK)
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King's College London
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Institute for Biomedicine, Affiliated institute of the University of Lubeck
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University of Michigan School of Public Health ann arbor
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University Medical Center Rotterdam
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National Institute on Aging
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Baylor College of Medicine
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University Medicine Greifswald
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