Papers by André G. Uitterlinden
Page 8 · newest first
- Risk of Frailty in Elderly With COPD: A Population-Based StudyThe Journals of Gerontology Series A · 2015
- Development of a Food Group-Based Diet Score and Its Association with Bone Mineral Density in the Elderly: The Rotterdam StudyNutrients · 2015
- Prenatal parental tobacco smoking, gene specific DNA methylation, and newborns size: the Generation R studyClinical Epigenetics · 2015
- Identification of IDUA and WNT16 Phosphorylation-Related Non-Synonymous Polymorphisms for Bone Mineral Density in Meta-Analyses of Genome-Wide Association StudiesJournal of Bone and Mineral Research · 2015
- The Rotterdam Study: 2016 objectives and design updateEuropean Journal of Epidemiology · 2015
- BMD Loci Contribute to Ethnic and Developmental Differences in Skeletal Fragility across Populations: Assessment of Evolutionary Selection PressuresMolecular Biology and Evolution · 2015
- Determinants for Quantitative Sensory Testing and the Association with Chronic Musculoskeletal Pain in the General Elderly PopulationPain Practice · 2015
- Low vitamin D status is associated with more depressive symptoms in Dutch older adultsEuropean Journal of Nutrition · 2015
- Effects of 2-year vitamin B12 and folic acid supplementation in hyperhomocysteinemic elderly on arterial stiffness and cardiovascular outcomes within the B-PROOF trialJournal of Hypertension · 2015
- Improving Phenotypic Prediction by Combining Genetic and Epigenetic AssociationsThe American Journal of Human Genetics · 2015
- Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFBlood · 2015
- The Association between Metabolic Syndrome, Bone Mineral Density, Hip Bone Geometry and Fracture Risk: The Rotterdam StudyPLoS ONE · 2015
- WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thicknessHuman Molecular Genetics · 2015
- Use of statins is associated with lower serum total and non-sex hormone-binding globulin-bound testosterone levels in male participants of the Rotterdam StudyEuropean Journal of Endocrinology · 2015
- Subclinical Thyroid Dysfunction and Fracture RiskJAMA · 2015
- Gene × dietary pattern interactions in obesity: analysis of up to 68 317 adults of European ancestryHuman Molecular Genetics · 2015
- Tobacco smoking is associated with methylation of genes related to coronary artery diseaseClinical Epigenetics · 2015
- Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-upHuman Genetics · 2015
- Cell Specific eQTL Analysis without Sorting CellsPLoS Genetics · 2015
- Identification of a novelFGFRL1MicroRNA target site polymorphism for bone mineral density in meta-analyses of genome-wide association studiesHuman Molecular Genetics · 2015
- Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activityBlood · 2015
- Association of polymorphisms in the beta-2 adrenergic receptor gene with fracture risk and bone mineral densityOsteoporosis International · 2015
- Genetic risk of neurodegenerative diseases is associated with mild cognitive impairment and conversion to dementiaAlzheimer s & Dementia · 2015
- Characteristics of de novo structural changes in the human genomeGenome Research · 2015
- GWAS for executive function and processing speed suggests involvement of the CADM2 geneENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) · 2015
- Physical fitness, activity and hand-grip strength are not associated with arterial stiffness in older individualsThe journal of nutrition health & aging · 2015
- Adiposity as a cause of cardiovascular disease: a Mendelian randomization studyInternational Journal of Epidemiology · 2015
- Incremental predictive value of 152 single nucleotide polymorphisms in the 10-year risk prediction of incident coronary heart disease: the Rotterdam StudyInternational Journal of Epidemiology · 2015
- Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in HumansView · 2015
- Genome-Wide Association Study in an Admixed Case Series Reveals IL12A as a New Candidate in Behçet DiseasePLoS ONE · 2015
- A Meta-analysis of Gene Expression Signatures of Blood Pressure and HypertensionPLoS Genetics · 2015
- A novel variant of FGFR3 causes proportionate short statureEuropean Journal of Endocrinology · 2015
- Pleiotropy among Common Genetic Loci Identified for Cardiometabolic Disorders and C-Reactive ProteinPLoS ONE · 2015
- Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R StudyEuropean Journal of Epidemiology · 2015
- Pioglitazone and bladder cancer risk: a multipopulation pooled, cumulative exposure analysis.WOS · 2015
- IRF4, MC1R and TYR genes are risk factors for actinic keratosis independent of skin colorHuman Molecular Genetics · 2015
- Rare variants in γ‐aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromesAnnals of Neurology · 2015
- A Genetic Risk Score for Thyroid Peroxidase Antibodies Associates With Clinical Thyroid Disease in Community-Based PopulationsThe Journal of Clinical Endocrinology & Metabolism · 2015
- Effect of Vitamin B12 and Folic Acid Supplementation on Bone Mineral Density and Quantitative Ultrasound Parameters in Older People with an Elevated Plasma Homocysteine Level: B-PROOF, a Randomized Controlled TrialCalcified Tissue International · 2015
- Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk FactorsDiabetes · 2015
- Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRICirculation Cardiovascular Genetics · 2015
- Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)Molecular Psychiatry · 2015
- ARHGEF12 influences the risk of glaucoma by increasing intraocular pressureHuman Molecular Genetics · 2015
- Meta‐analysis of Genome‐Wide Association Studies Identifies Novel Loci Associated With Optic Disc MorphologyGenetic Epidemiology · 2015
- The rs13064411 polymorphism in the WDR52 gene, associated with PCSK9 levels, modifies statin-induced changes in serum total and LDL cholesterol levelsPharmacogenetics and Genomics · 2015
- PAPSS2 Deficiency Causes Androgen Excess via Impaired DHEA Sulfation—In Vitro and in Vivo Studies in a Family Harboring Two Novel PAPSS2 MutationsThe Journal of Clinical Endocrinology & Metabolism · 2015
- Association of Rare Loss-Of-Function Alleles in HAL , Serum HistidineCirculation Cardiovascular Genetics · 2015
- Single nucleotide polymorphisms in CRTC1 and BARX1 are associated with esophageal adenocarcinomaSHILAP Revista de lepidopterología · 2015
- Vitamin D Receptor Polymorphisms Are Associated with Reduced Esophageal Vitamin D Receptor Expression and Reduced Esophageal Adenocarcinoma RiskMolecular Medicine · 2015
- No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index: Results from Meta-Analyses of 80,607 SubjectsPLoS ONE · 2014