← André G. Uitterlinden

Papers by André G. Uitterlinden

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51. Multi-ancestry genome-wide association study improves resolution of genes, pathways and pleiotropy for lung function and chronic obstructive pulmonary disease2022
52. Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsHuman Molecular Genetics · 2022
53. Candidate genetic variants and antidepressant-related fall risk in middle-aged and older adultsPLoS ONE · 2022
54. Association between an AMH promoter polymorphism and serum AMH levels in PCOS patientsHuman Reproduction · 2022
55. Development of the ADFICE_IT Models for Predicting Falls and Recurrent Falls in Community-Dwelling Older Adults: Pooled Analyses of European Cohorts With Special Attention to MedicationThe Journals of Gerontology Series A · 2022
56. Elucidating the relationship between migraine risk and brain structure using genetic dataBrain · 2022
57. Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathwaysHuman Molecular Genetics · 2022
58. Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization studyHuman Molecular Genetics · 2022
59. Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathologyNature Communications · 2022
60. Role of the Microbiome in Regulating Bone Metabolism and Susceptibility to OsteoporosisCalcified Tissue International · 2021
61. Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferationHuman Genetics · 2021
62. Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL CholesterolDiabetes Care · 2021
63. Using multivariable Mendelian randomization to estimate the causal effect of bone mineral density on osteoarthritis risk, independently of body mass indexInternational Journal of Epidemiology · 2021
64. CYP11B1 variants influence skeletal maturation via alternative splicingCommunications Biology · 2021
65. Genome Wide Association Metanalysis Of Skull Bone Mineral Density Identifies Loci Relevant For Osteoporosis And Craniosynostosis2021
66. Deciphering osteoarthritis genetics across 826,690 individuals from 9 populationsCell · 2021
67. Impact of SNP microarray analysis of compromised DNA on kinship classification success in the context of investigative genetic genealogyForensic Science International Genetics · 2021
68. Fat metabolism is associated with telomere length in six population-based studiesHuman Molecular Genetics · 2021
69. Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissuesHuman Molecular Genetics · 2021
70. Effect of Genetic Variation in CYP450 on Gonadal Impairment in a European Cohort of Female Childhood Cancer Survivors, Based on a Candidate Gene Approach: Results from the PanCareLIFE StudyCancers · 2021
71. Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansionsTranslational Psychiatry · 2021
72. Skin Autofluorescence, a Noninvasive Biomarker for Advanced Glycation End-products, Is Associated With SarcopeniaThe Journal of Clinical Endocrinology & Metabolism · 2021
73. Continuity of Genetic Risk for Aggressive Behavior Across the Life-CourseBehavior Genetics · 2021
74. Genetic association study of childhood aggression across raters, instruments, and ageTyöväentutkimus Vuosikirja · 2021
75. Association of Insulin Resistance and Type 2 Diabetes With Gut Microbial DiversityJAMA Network Open · 2021
76. Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride ConcentrationsCirculation Genomic and Precision Medicine · 2021
77. TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE studynpj Precision Oncology · 2021
78. Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 DiabetesCirculation Genomic and Precision Medicine · 2021
79. Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of agingGenome biology · 2021
80. A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipidsNature Communications · 2021
81. Prevalence of and risk factors for extended-spectrum beta-lactamase genes carriership in a population-based cohort of middle-aged and elderlyInternational Journal of Antimicrobial Agents · 2021
82. A comparison of genotyping arraysEuropean Journal of Human Genetics · 2021
83. Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2 : A genome‐wide association study in over 12,000 non‐demented participantsAlzheimer s & Dementia · 2021
84. Epigenome-wide association meta-analysis of DNA methylation with coffee and tea consumptionNature Communications · 2021
85. Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymesNature Communications · 2021
86. Vitamin K antagonist anticoagulant usage is associated with increased incidence and progression of osteoarthritisAnnals of the Rheumatic Diseases · 2021
87. Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye colorScience Advances · 2021
88. Age-dependent sex differences in calcium and phosphate homeostasisEndocrine Connections · 2021
89. Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and womenNature Communications · 2021
90. Genetic analysis of mitochondrial DNA copy number and associated traits identifies loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation, and reveals a causal association of mitochondrial function with mortality2021
91. Large-scale association analyses identify host factors influencing human gut microbiome compositionNature Genetics · 2021
92. DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespanMolecular Psychiatry · 2021
93. Possible modification of BRSK1 on the risk of alkylating chemotherapy-related reduced ovarian functionHuman Reproduction · 2020
94. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumPLoS ONE · 2020
95. Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traitsHuman Genetics and Genomics Advances · 2020
96. Smoking-related changes in DNA methylation and gene expression are associated with cardio-metabolic traitsClinical Epigenetics · 2020
97. Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis geneAnnals of the Rheumatic Diseases · 2020
98. Mendelian randomization study on vitamin D levels and osteoarthritis risk: a concise reportLara D. Veeken · 2020
99. Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traitsPLoS Genetics · 2020
100. Genetic basis of falling risk susceptibility in the UK Biobank StudyCommunications Biology · 2020