Papers by André G. Uitterlinden
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- Use of Selective Serotonin Reuptake Inhibitors and Bone Mineral Density ChangeJournal of Clinical Psychopharmacology · 2017
- Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways2017
- Fifteen Genetic Loci Associated With the Electrocardiographic P WaveCirculation Cardiovascular Genetics · 2017
- Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locusNature Communications · 2017
- Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity2017
- Beta‐blocker use and fall risk in older individuals: Original results from two studies with meta‐analysisBritish Journal of Clinical Pharmacology · 2017
- Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart DiseaseJournal of the American Heart Association · 2017
- Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric TraitsTyöväentutkimus Vuosikirja · 2017
- Characterization of pathogenic SORL1 genetic variants for association with Alzheimer’s disease: a clinical interpretation strategyEuropean Journal of Human Genetics · 2017
- Haplotype reference consortium panel: Practical implications of imputations with large reference panelsHuman Mutation · 2017
- Thyroid Function Tests in the Reference Range and Fracture: Individual Participant Analysis of Prospective CohortsENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) · 2017
- Negative selection in humans and fruit flies involves synergistic epistasisScience · 2017
- A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitisHuman Molecular Genetics · 2017
- Dietary acid load, trabecular bone integrity, and mineral density in an ageing population: the Rotterdam studyOsteoporosis International · 2017
- Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and functionJournal of Clinical Investigation · 2017
- NFAT5 and SLC4A10 Loci Associate with Plasma OsmolalityJournal of the American Society of Nephrology · 2017
- Discovery of novel heart rate-associated loci using the Exome ChipHuman Molecular Genetics · 2017
- Vitamin B12 intake and related biomarkers: Associations in a Dutch elderly populationThe journal of nutrition health & aging · 2017
- A rare missense variant in RCL1 segregates with depression in extended familiesMolecular Psychiatry · 2017
- Genetic correlation between amyotrophic lateral sclerosis and schizophreniaNature Communications · 2017
- Serum Phosphate Is Associated With Fracture Risk: The Rotterdam Study and MrOSJournal of Bone and Mineral Research · 2017
- Epigenome-wide association study (EWAS) on lipids: the Rotterdam StudyClinical Epigenetics · 2017
- Genome-Wide Methylation Analysis Identifies Novel Cpg Loci For Perimembranous Ventricular Septal Defects In HumanEpigenomics · 2017
- Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association StudyPLoS ONE · 2017
- Genome-Wide Association Studies of Multiple Keratinocyte CancersPLoS ONE · 2017
- Meta-GWAS Accuracy and Power (MetaGAP) Calculator Shows that Hiding Heritability Is Partially Due to Imperfect Genetic Correlations across Studies2017
- A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortiumENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) · 2016
- The complex genetics of gait speed: genome-wide meta-analysis approachAging · 2016
- New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.Human Molecular Genetics · 2016
- Genetic susceptibility to multiple sclerosis: Brain structure and cognitive function in the general populationMultiple Sclerosis Journal · 2016
- Heritability of the shape of subcortical brain structures in the general populationNature Communications · 2016
- The Generation R Study: design and cohort update 2017European Journal of Epidemiology · 2016
- DNA methylation signatures of chronic low-grade inflammation are associated with complex diseasesGenome biology · 2016
- Vitamin D and retinal microvascular damageMedicine · 2016
- KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preferenceProceedings of the National Academy of Sciences · 2016
- PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation studyThe Lancet Diabetes & Endocrinology · 2016
- Effects of Two-Year Vitamin B12 and Folic Acid Supplementation on Depressive Symptoms and Quality of Life in Older Adults with Elevated Homocysteine Concentrations: Additional Results from the B-PROOF Study, an RCTNutrients · 2016
- Multiethnic Exome-Wide Association Study of Subclinical AtherosclerosisCirculation Cardiovascular Genetics · 2016
- A DNA methylation biomarker of alcohol consumptionMolecular Psychiatry · 2016
- Gene-gene Interaction Analyses for Atrial FibrillationENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) · 2016
- A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family StudyFrontiers in Genetics · 2016
- Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's DiseasePLoS Genetics · 2016
- Exercise, fasting, and mimetics: toward beneficial combinations?The FASEB Journal · 2016
- Cam Deformity and Acetabular Dysplasia as Risk Factors for Hip OsteoarthritisArthritis & Rheumatology · 2016
- A high-quality human reference panel reveals the complexity and distribution of genomic structural variantsNature Communications · 2016
- Novel Genetic Variants for Cartilage Thickness and Hip OsteoarthritisPLoS Genetics · 2016
- Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE ConsortiumSLEEP · 2016
- DNA methylation-based measures of biological age: meta-analysis predicting time to deathAging · 2016
- Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing geneNature Communications · 2016
- Epigenetic Signatures of Cigarette SmokingCirculation Cardiovascular Genetics · 2016