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← André G. Uitterlinden

Papers by André G. Uitterlinden

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  1. Vitamin D receptor: a new risk marker for clinical restenosis after percutaneous coronary interventionExpert Opinion on Therapeutic Targets · 2010
  2. A genome‐wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22Arthritis & Rheumatism · 2010
  3. Genome-Wide Association Studies of MRI-Defined Brain InfarctsStroke · 2010
  4. PROP1, HESX1, POU1F1, LHX3 and LHX4 Mutation and Deletion Screening and GH1 P89L and IVS3+1/+2 Mutation Screening in a Dutch Nationwide Cohort of Patients with Combined Pituitary Hormone DeficiencyHormone Research in Paediatrics · 2010
  5. Genetic Polymorphisms in the Locus Control Region and Promoter of GH1 Are Related to Serum IGF-I Levels and Height in Patients with Isolated Growth Hormone Deficiency and Healthy ControlsHormone Research in Paediatrics · 2010
  6. Associations of polymorphisms of eight muscle- or metabolism-related genes with performance in Mount Olympus marathon runnersJournal of Applied Physiology · 2010
  7. Pharmacogenetic risk factors for altered bone mineral density and body composition in pediatric acute lymphoblastic leukemiaHaematologica · 2009
  8. Interaction between polymorphisms in the OCT1 and MATE1 transporter and metformin responsePharmacogenetics and Genomics · 2009
  9. Hedgehog-interacting protein is a COPD susceptibility gene: the Rotterdam StudyEuropean Respiratory Journal · 2009
  10. The association of serum testosterone levels and ventricular repolarizationEuropean Journal of Epidemiology · 2009
  11. The Role of Body Mass Index, Insulin, and Adiponectin in the Relation Between Fat Distribution and Bone Mineral DensityCalcified Tissue International · 2009
  12. Influence of genetic variation inCYP3A4andABCB1on dose decrease or switching during simvastatin and atorvastatin therapyPharmacoepidemiology and Drug Safety · 2009
  13. Association of the Exon 3 Deleted/Full-LengthGHRPolymorphism with Recombinant Growth Hormone Dose in Growth Hormone-Deficient AdultsPharmacogenomics · 2009
  14. SIRT1 Genetic Variation Is Related to BMI and Risk of ObesityDiabetes · 2009
  15. The Rotterdam Study: 2010 objectives and design updateEuropean Journal of Epidemiology · 2009
  16. Tissue Effect on Genetic Control of Transcript Isoform VariationPLoS Genetics · 2009
  17. Population genomics in a disease targeted primary cell modelGenome Research · 2009
  18. Vitamin D Status, Bone Mineral Density, and the Development of Radiographic Osteoarthritis of the KneeJCR Journal of Clinical Rheumatology · 2009
  19. Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam StudyHuman Molecular Genetics · 2009
  20. Genetic Variants Associated With Cardiac Structure and FunctionJAMA · 2009
  21. A genome-wide association study of acenocoumarol maintenance dosageHuman Molecular Genetics · 2009
  22. A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variationHuman Molecular Genetics · 2009
  23. Variation at the ANP32A gene is associated with risk of hip osteoarthritis in womenArthritis & Rheumatism · 2009
  24. NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE ConsortiumPLoS Genetics · 2009
  25. A genome-wide association study suggests that a locus within the ataxin 2 binding protein 1 gene is associated with hand osteoarthritis: the Treat-OA consortiumJournal of Medical Genetics · 2009
  26. Vitamin D Binding Protein Genotype and OsteoporosisCalcified Tissue International · 2009
  27. Large‐scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and handArthritis & Rheumatism · 2009
  28. Genome-wide association meta-analysis for total serum bilirubin levelsHuman Molecular Genetics · 2009
  29. Genetic polymorphisms of GnRH and gonadotrophic hormone receptors affect the phenotype of polycystic ovary syndromeHuman Reproduction · 2009
  30. Genomewide Association Studies of StrokeNew England Journal of Medicine · 2009
  31. Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame SizePLoS Genetics · 2009
  32. Association of Novel Genetic Loci With Circulating Fibrinogen LevelsCirculation Cardiovascular Genetics · 2009
  33. Genetic Variation in the Multidrug and Toxin Extrusion 1 Transporter Protein Influences the Glucose-Lowering Effect of Metformin in Patients With Diabetes: A Preliminary StudyDiabetes · 2009
  34. Genotypes Associated With Reduced Activity of VKORC1 and CYP2C9 and Their Modification of Acenocoumarol Anticoagulation During the Initial Treatment PeriodClinical Pharmacology & Therapeutics · 2009
  35. Breast-Feeding Modifies the Association of PPARγ2 Polymorphism Pro12Ala With Growth in Early LifeDiabetes · 2009
  36. Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumCirculation Cardiovascular Genetics · 2009
  37. Growth Hormone Dose in Growth Hormone-Deficient Adults is Not Associated with IGF-1 Gene PolymorphismsPharmacogenomics · 2009
  38. Haplotypes of theNR4A2/NURR1gene and cardiovascular disease: The Rotterdam StudyHuman Mutation · 2009
  39. The −G1245A IGF1 polymorphism is related with small head size and less brain sparing in small for gestational age born childrenEuropean Journal of Endocrinology · 2009
  40. Birth Size, Postnatal Growth and Growth during Growth Hormone Treatment in Small-for-Gestational-Age Children: Associations with IGF1 Gene Polymorphisms and Haplotypes?Hormone Research in Paediatrics · 2009
  41. Genetic Variation in the Renin-Angiotensin System and Arterial Stiffness. The Rotterdam StudyClinical and Experimental Hypertension · 2009
  42. Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillationEuropean Heart Journal · 2008
  43. The effect of catechol-O-methyltransferase Met/Val functional polymorphism on smoking cessation: retrospective and prospective analyses in a cohort studyPharmacogenetics and Genomics · 2008
  44. The Rationale and Design of the Perindopril Genetic Association Study (PERGENE): A Pharmacogenetic Analysis of Angiotensin-Converting Enzyme Inhibitor Therapy in Patients with Stable Coronary Artery DiseaseCardiovascular Drugs and Therapy · 2008
  45. Glucocorticoid receptor gene polymorphisms and childhood adversity are associated with depression: New evidence for a gene–environment interactionAmerican Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2008
  46. Cataract Surgery and the Risk of Aging Macula Disorder: The Rotterdam StudyInvestigative Ophthalmology & Visual Science · 2008
  47. Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysisView · 2008
  48. Genetic Testing in Clinical PracticeAnnual Review of Medicine · 2008
  49. Identification of a common variant at the NOS1AP locus strongly associated to QT-interval durationHuman Molecular Genetics · 2008
  50. Impact of thyroid function and polymorphisms in the type 2 deiodinase on blood pressure: the Rotterdam Study and the Rotterdam Scan StudyClinical Endocrinology · 2008