Search Results - "Teumer, Alexander"
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1
Common Methods for Performing Mendelian Randomization
Published in Frontiers in cardiovascular medicine (28-05-2018)“…Mendelian randomization (MR) is a framework for assessing causal inference using cross-sectional data in combination with genetic information. This paper…”
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2
Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome
Published in Nature communications (24-09-2021)“…Comparing transcript levels between healthy and diseased individuals allows the identification of differentially expressed genes, which may be causes,…”
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3
Copy Number Variations and Cognitive Phenotypes in Unselected Populations
Published in JAMA : the journal of the American Medical Association (26-05-2015)“…IMPORTANCE: The association of copy number variations (CNVs), differing numbers of copies of genetic sequence at locations in the genome, with phenotypes such…”
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4
Genome-wide association study of chronic periodontitis in a general German population
Published in Journal of clinical periodontology (01-11-2013)“…Aim To identify loci associated with chronic periodontitis through a genome‐wide association study (GWAS). Materials and Methods A GWAS was performed in 4032…”
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5
Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank
Published in Nature communications (09-03-2023)“…Genome-wide association studies have discovered hundreds of associations between common genotypes and kidney function but cannot comprehensively investigate…”
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6
Moderation of Adult Depression by a Polymorphism in the FKBP5 Gene and Childhood Physical Abuse in the General Population
Published in Neuropsychopharmacology (01-09-2011)“…Childhood maltreatment and depressive disorders have both been associated with a dysregulation of the hypothalamic-pituitary-adrenal axis. The FKBP5 gene codes…”
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7
Correction: Analysis of epidemiological association patterns of serum thyrotropin by combining random forests and Bayesian networks
Published in PloS one (10-11-2023)“…[This corrects the article DOI: 10.1371/journal.pone.0271610.]…”
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Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities
Published in Nature communications (03-08-2022)“…Aortic dimensions and distensibility are key risk factors for aortic aneurysms and dissections, as well as for other cardiovascular and cerebrovascular…”
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9
Analysis of epidemiological association patterns of serum thyrotropin by combining random forests and Bayesian networks
Published in PloS one (21-07-2022)“…Background Approaching epidemiological data with flexible machine learning algorithms is of great value for understanding disease-specific association…”
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10
A genome-wide association study of metabolic traits in human urine
Published in Nature genetics (01-06-2011)“…Karsten Suhre and colleagues report a genome-wide association study of metabolic traits in human urine, using NMR spectrometry to measure 59 metabolites in…”
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11
Discovery of novel eGFR-associated multiple independent signals using a quasi-adaptive method
Published in Frontiers in genetics (31-10-2022)“…A decreased estimated glomerular filtration rate (eGFR) leading to chronic kidney disease is a significant public health problem. Kidney function is a…”
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12
Mendelian randomization indicates causal effects of estradiol levels on kidney function in males
Published in Frontiers in endocrinology (Lausanne) (19-12-2023)“…Chronic kidney disease (CKD) is a public health burden worldwide. Epidemiological studies observed an association between sex hormones, including estradiol,…”
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13
Methylation Patterns of the FKBP5 Gene in Association with Childhood Maltreatment and Depressive Disorders
Published in International journal of molecular sciences (01-02-2024)“…Childhood maltreatment is an important risk factor for adult depression and has been associated with changes in the hypothalamic pituitary adrenal (HPA) axis,…”
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14
TREML2 Gene Expression and Its Missense Variant rs3747742 Associate with White Matter Hyperintensity Volume and Alzheimer's Disease-Related Brain Atrophy in the General Population
Published in International journal of molecular sciences (09-11-2022)“…Although the common pathology of Alzheimer's disease (AD) and white matter hyperintensities (WMH) is disputed, the gene has been implicated in both conditions:…”
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15
Effects of Thyroid Function on Hemostasis, Coagulation, and Fibrinolysis: A Mendelian Randomization Study
Published in Thyroid (New York, N.Y.) (01-09-2021)“…Untreated hypothyroidism is associated with acquired von Willebrand syndrome, and hyperthyroidism is associated with increased thrombosis risk. However, the…”
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16
Limited evidence for blood eQTLs in human sexual dimorphism
Published in Genome medicine (11-08-2022)“…The genetic underpinning of sexual dimorphism is very poorly understood. The prevalence of many diseases differs between men and women, which could be in part…”
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17
Effects of Apolipoprotein E polymorphism on carotid intima-media thickness, incident myocardial infarction and incident stroke
Published in Scientific reports (24-03-2022)“…The Apolipoprotein E (APOE) gene polymorphism (rs429358 and rs7412) shows a well-established association with lipid profiles, but its effect on cardiovascular…”
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18
Polygenic Architecture of Human Neuroanatomical Diversity
Published in Cerebral cortex (New York, N.Y. 1991) (14-04-2020)“…Abstract We analyzed the genomic architecture of neuroanatomical diversity using magnetic resonance imaging and single nucleotide polymorphism (SNP) data from…”
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Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism
Published in Scientific reports (06-06-2017)“…1,5-anhydroglucitol (1,5-AG) is a biomarker of hyperglycemic excursions associated with diabetic complications. Because of its structural similarity to…”
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Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity
Published in Cortex (01-01-2015)“…The genetic determinants of cerebral asymmetries are unknown. Sex differences in asymmetry of the planum temporale (PT), that overlaps Wernicke's classical…”
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