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← André G. Uitterlinden

Papers by André G. Uitterlinden

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  1. Vitamin D status and metabolic syndrome in the elderly: the Rotterdam StudyEuropean Journal of Endocrinology · 2014
  2. Genetic diversity is a predictor of mortality in humansBMC Genetics · 2014
  3. Results of 2-year vitamin B treatment on cognitive performanceNeurology · 2014
  4. Determinants of maternal pregnancy one-carbon metabolism and newborn human DNA methylation profilesReproduction · 2014
  5. Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortiumTyöväentutkimus Vuosikirja · 2014
  6. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statinsNature Communications · 2014
  7. A novel common variant in DCST2 is associated with length in early life and height in adulthoodHuman Molecular Genetics · 2014
  8. A Genetic Variant in the Seed Region of miR-4513 Shows Pleiotropic Effects on Lipid and Glucose Homeostasis, Blood Pressure, and Coronary Artery DiseaseHuman Mutation · 2014
  9. Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous processNature Communications · 2014
  10. Genome-Wide Meta-Analysis of Myopia and Hyperopia Provides Evidence for Replication of 11 LociPLoS ONE · 2014
  11. Common genetic variants associated with cognitive performance identified using the proxy-phenotype methodProceedings of the National Academy of Sciences · 2014
  12. GWAS of Longevity in CHARGE Consortium Confirms APOE and FOXO3 CandidacyThe Journals of Gerontology Series A · 2014
  13. Methylation of Bone SOST , Its mRNA, and Serum Sclerostin Levels Correlate Strongly With Fracture Risk in Postmenopausal WomenJournal of Bone and Mineral Research · 2014
  14. Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial FibrillationCirculation · 2014
  15. Inhibin Alpha-Subunit (INHA) Expression in Adrenocortical Cancer Is Linked to Genetic and Epigenetic INHA Promoter VariationPLoS ONE · 2014
  16. Thiazides and the risk of hypokalemia in the general populationJournal of Hypertension · 2014
  17. FTO genetic variants, dietary intake and body mass index: insights from 177 330 individualsHuman Molecular Genetics · 2014
  18. Genome-wide association study of height-adjusted BMI in childhood identifies functional variant inADCY3Obesity · 2014
  19. Non-linear associations between serum 25-OH vitamin D and indices of arterial stiffness and arteriosclerosis in an older populationAge and Ageing · 2014
  20. Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant dataBMJ · 2014
  21. Genome Wide Association Identifies Common Variants at the SERPINA6/SERPINA1 Locus Influencing Plasma Cortisol and Corticosteroid Binding GlobulinPLoS Genetics · 2014
  22. Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung FunctionPLoS ONE · 2014
  23. Expression and Gene Variation Studies Deny Association of Human HSD3B1 Gene With Aldosterone Production or Blood PressureAmerican Journal of Hypertension · 2014
  24. Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass AttainmentPLoS Genetics · 2014
  25. C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome‐wide meta‐analysisAnnals of Neurology · 2014
  26. Intrinsic and Extrinsic Risk Factors for Sagging EyelidsJAMA Dermatology · 2014
  27. Effect of Genetic Variants Associated With Plasma Homocysteine Levels on Stroke RiskStroke · 2014
  28. Pleiotropic genes for metabolic syndrome and inflammationMolecular Genetics and Metabolism · 2014
  29. Analysis of Rare Variants in the C3 Gene in Patients with Age-Related Macular DegenerationPLoS ONE · 2014
  30. Sex‐specific effects of naturally occurring variants in the dopamine receptor D2 locus on insulin secretion and Type 2 diabetes susceptibilityDiabetic Medicine · 2014
  31. Susceptibility to Chronic Mucus Hypersecretion, a Genome Wide Association StudyPLoS ONE · 2014
  32. Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of ageHuman Molecular Genetics · 2014
  33. Bone Mineral Density and Chronic Lung Disease Mortality: The Rotterdam StudyThe Journal of Clinical Endocrinology & Metabolism · 2014
  34. Methylation of Migraine-Related Genes in Different Tissues of the RatPLoS ONE · 2014
  35. Genome-Wide Association Study for Circulating Tissue Plasminogen Activator Levels and Functional Follow-Up Implicates Endothelial STXBP5 and STX2Arteriosclerosis Thrombosis and Vascular Biology · 2014
  36. A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any AgeCancer Epidemiology Biomarkers & Prevention · 2014
  37. BMI-Associated Alleles Do Not Constitute Risk Alleles for Polycystic Ovary Syndrome Independently of BMI: A Case-Control StudyPLoS ONE · 2014
  38. Predicting Stroke Through Genetic Risk FunctionsStroke · 2014
  39. Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markersInternational Journal of Epidemiology · 2014
  40. A Genetic Deconstruction of Neurocognitive Traits in Schizophrenia and Bipolar DisorderPLoS ONE · 2013
  41. Assessment of Osteoarthritis Candidate Genes in a Meta‐Analysis of Nine Genome‐Wide Association StudiesArthritis & Rheumatology · 2013
  42. The SLCO1B1 c.521T>C polymorphism is associated with dose decrease or switching during statin therapy in the Rotterdam StudyPharmacogenetics and Genomics · 2013
  43. Epigenetic Profiles in Children with a Neural Tube Defect; A Case-Control Study in Two PopulationsPLoS ONE · 2013
  44. Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation–differentiation balance early in life and optic nerve degeneration at old ageHuman Molecular Genetics · 2013
  45. Education influences the role of genetics in myopiaEuropean Journal of Epidemiology · 2013
  46. Cross-Ethnic Meta-Analysis of Genetic Variants for Polycystic Ovary SyndromeThe Journal of Clinical Endocrinology & Metabolism · 2013
  47. PLS3 Mutations in X-Linked Osteoporosis with FracturesNew England Journal of Medicine · 2013
  48. An Activating Mutation in the Kinase Homology Domain of the Natriuretic Peptide Receptor-2 Causes Extremely Tall Stature Without Skeletal DeformitiesThe Journal of Clinical Endocrinology & Metabolism · 2013
  49. Meta-Analysis of Genome-Wide Association Studies Identifies Six New Loci for Serum Calcium ConcentrationsPLoS Genetics · 2013
  50. Systematic identification of trans eQTLs as putative drivers of known disease associationsNature Genetics · 2013