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Die folgenden Publikationen sind in der Online-Universitätsbibliographie der Universität Duisburg-Essen verzeichnet. Weitere Informationen finden Sie gegebenenfalls auch auf den persönlichen Webseiten der Person.
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Genetic polymorphisms affecting telomere length and their association with cardiovascular disease in the Heinz-Nixdorf-Recall studyIn: PLoS ONE , Jg. 19 2024, Nr. 5, e0303357DOI (Open Access)
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Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansionsIn: Nature Communications , Jg. 15 2024, Nr. 1, 7665DOI (Open Access)
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Genetic insights into resting heart rate and its role in cardiovascular diseaseIn: Nature Communications , Jg. 14 2023, Nr. 1, 4646DOI (Open Access)
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Klotho KL-VS haplotype does not improve cognition in a population-based sample of adults age 55-87 yearsIn: Scientific Reports , Jg. 11 2021, Nr. 1, 13852DOI, Online Volltext (Open Access)
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Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors : Results of the Heinz Nixdorf Recall StudyIn: Naunyn-Schmiedeberg's Archives of Pharmacology , Jg. 394 2021, Nr. 8, S. 1713 – 1725DOI (Open Access)
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Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcificationIn: BMC Medical Genetics , Jg. 21 2020, Nr. 1, S. 62DOI, Online Volltext (Open Access)
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Genetic risk scores for coronary artery disease and its traditional risk factors : Their role in the progression of coronary artery calcification ; Results of the Heinz Nixdorf Recall studyIn: PLoS ONE , Jg. 15 2020, Nr. 5, S. e0232735DOI, Online Volltext (Open Access)
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Hypoxia-inducible factor-2α is crucial for proper brain developmentIn: Scientific Reports , Jg. 10 2020, Nr. 1, 19146DOI, Online Volltext (Open Access)
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Risk prediction for coronary heart disease by a genetic risk score : results from the Heinz Nixdorf Recall studyIn: BMC Medical Genetics , Jg. 21 2020, S. 178DOI, Online Volltext (Open Access)
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Letter: HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotypeIn: Nature Genetics , Jg. 51 2019, Nr. 11, S. 1580 – 1587DOI (Open Access)
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Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall StudyIn: PLoS ONE , Jg. 14 2019, Nr. 11, 225521DOI, Online Volltext (Open Access)
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Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance : a genome-wide genetic interaction studyIn: Molecular Medicine , Jg. 24 2018, Nr. 1, 30DOI (Open Access)
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An Expanded Genome-Wide Association Study of Type 2 Diabetes in EuropeansIn: Diabetes , Jg. 66 2017, Nr. 11, S. 2888 – 2902DOI (Open Access)
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Defective brain development in mice lacking hypoxia-inducible factor-2a in neural stem cellsIn: Acta Physiologica , Jg. 219 S711 2017, S. 54 – 54
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Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldnessIn: Nature Communications , Jg. 8 2017, S. 14694DOI (Open Access)
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Pharmacogenetic association of blood-lipid related genetic variants with 5-year progression of coronary artery calcification following the treatment with statin in the Heinz Nixdorf Recall studyIn: Atherosclerosis , Jg. 263 2017, S. e278
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Socioeconomic Status Interacts with the Genetic Effect of a Chromosome 9p21.3 Common Variant to Influence Coronary Artery Calcification and Incident Coronary Events in the Heinz Nixdorf Recall Study (Risk Factors, Evaluation of Coronary Calcium, and LifesIn: Circulation: Genomic and Precision Medicine , Jg. 10 2017, Nr. 2DOI (Open Access)
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Socioeconomic Status Interacts with the Genetic Effect of a Chromosome 9p21.3 Common Variant to Influence Coronary Artery Calcification and Incident Coronary Events in the Heinz Nixdorf Recall Study (Risk Factors, Evaluation of Coronary Calcium, and Lifestyle)In: Circulation: Genomic and Precision Medicine , Jg. 10 2017, Nr. 2DOI (Open Access)
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A statistical model for the analysis of beta values in DNA methylation studiesIn: BMC Bioinformatics , Jg. 17 2016, Nr. 1, S. 480DOI (Open Access)
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Anthropometric markers and their association with incident type 2 diabetes mellitus : which marker is best for prediction? Pooled analysis of four German population-based cohort studies and comparison with a nationwide cohort studyIn: BMJ Open , Jg. 6 2016, Nr. 1, S. e009266DOI (Open Access)
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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociIn: Nature Genetics , Jg. 47 2015, Nr. 12, S. 1415 – 1425DOI (Open Access)
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Genetic studies of body mass index yield new insights for obesity biologyIn: Nature , Jg. 518 2015, Nr. 7538, S. 197 – 206DOI (Open Access)
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New genetic loci link adipose and insulin biology to body fat distributionIn: Nature , Jg. 518 2015, Nr. 7538, S. 187 – 196DOI (Open Access)
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Serum lipid levels, body mass index, and their role in coronary artery calcification : a polygenic analysisIn: Circulation , Jg. 8 2015, Nr. 2, S. 327 – 333
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Exploring genetic variants predisposing to diabetes mellitus and their association with indicators of socioeconomic statusIn: BMC Public Health , Jg. 14 2014, Nr. 1, S. 609DOI (Open Access)
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Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorderIn: Molecular Psychiatry , Jg. 19 2014, Nr. 1, S. 115 – 121DOI (Open Access)
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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityIn: Nature Genetics , Jg. 46 2014, Nr. 3, S. 234 – 244DOI (Open Access)
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Bipolar disorder risk alleles in children with ADHDIn: Journal of Neural Transmission , Jg. 120 2013, Nr. 11, S. 1611 – 1617
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Diabetes incidence does not differ between subjects with and without high depressive symptoms - 5-year follow-up results of the Heinz Nixdorf Recall StudyIn: Diabetic medicine , Jg. 30 2013, Nr. 1, S. 65 – 69
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Genetic associations with valvular calcification and aortic stenosisIn: The New England Journal of Medicine , Jg. 368 2013, Nr. 6, S. 503 – 512
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureIn: Nature Genetics , Jg. 45 2013, Nr. 5, S. 501 – 512
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Microsomal triglyceride transfer protein -164 T > C gene polymorphism and risk of cardiovascular disease : results from the EPIC-Potsdam case-cohort studyIn: BMC Medical Genetics , Jg. 14 2013, Nr. 1, S. 19DOI (Open Access)
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Risk for High depressive symptoms in diagnosed and previously undetected diabetes : 5-year follow-up results of the Heinz Nixdorf recall studyIn: PLoS ONE , Jg. 8 2013, Nr. 2, S. e56300DOI (Open Access)
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Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall StudyIn: BMC Medical Genetics , Jg. 14 2013, Nr. 1, S. 23DOI (Open Access)
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Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric TraitsIn: PLoS Genetics , Jg. 9 2013, Nr. 6, e1003500DOI (Open Access)
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Addendum: Genome-wide association study in German patients with attention deficit/hyperactivity disorderIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics , Jg. 159B 2012, Nr. 4, S. 476
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Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesIn: Nature Genetics , Jg. 44 2012, Nr. 9, S. 981 – 990
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PHH3 immunostaining improves interobserver agreement of mitotic index in thin melanomasIn: American Journal of Dermatopathology , Jg. 34 2012, Nr. 3, S. 266 – 269
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Tumor Suppressive MicroRNAs miR-34a/c Control Cancer Cell Expression of ULBP2, a Stress-Induced Ligand of the Natural Killer Cell Receptor NKG2DIn: Cancer Research , Jg. 72 2012, Nr. 2, S. 460 – 471
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Coronary artery calcification and diabetes mellitus : sex-specific impact on incidence of cardiovascular disease – results of the Heinz Nixdorf Recall-StudyIn: Atherosclerosis Supplements , Jg. 12 2011, Nr. 1, S. 63
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Genome-wide association study in German patients with attention deficit/hyperactivity disorderIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics , Jg. 156B 2011, Nr. 8, S. 888 – 897
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Missing Heritability in the Tails of Quantitative Traits? : A Simulation Study on the Impact of Slightly Altered True Genetic ModelsIn: Human Heredity , Jg. 72 2011, Nr. 3, S. 173 – 181
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Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the heinz nixdorf recall cohortIn: Arteriosclerosis, Thrombosis, and Vascular Biology , Jg. 30 2010, Nr. 9, S. 1867 – 1872DOI (Open Access)
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GWAS meta-analysis yields novel insights into the biology of male-pattern baldnessIn: European Journal of Human Genetics , Jg. 26 2019, Nr. Suppl., S. 761 – 762DOI (Open Access)
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Male-pattern baldness and its association with coronary heart diseaseIn: Journal of Investigative Dermatology , Jg. 137 2017, Nr. 10 Suppl. 2, S. S239DOI (Open Access)
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Association of Diabetes-Mellitus-Related genetic variants with coronary artery calcificationIn: Atherosclerosis Supplements , Jg. 12 2011, Nr. 1, S. 128