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Wiss. Mitarbeiterinnen/Mitarbeiter, Institut für Medizinische Informatik, Biometrie und Epidemiologie
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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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High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylationIn: The World Journal of Biological Psychiatry, Jg. 19, 2018, Nr. 3, S. 187 – 199DOI (Open Access)
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Analysis of genes involved in body weight regulation by targeted re-sequencingIn: PLoS ONE, Jg. 11, 2016, Nr. 2, S. e0147904DOI (Open Access)
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Determinants of decreasing major amputation rates in GermanyIn: VASA: European Journal of Vascular Medicine, Jg. 45, 2016, Nr. 4, S. 311 – 315DOI (Open Access)
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Neoadjuvant, anthracycline-free chemotherapy with carboplatin and docetaxel in triple-negative, early-stage breast cancer : a multicentric analysis of rates of pathologic complete response and survivalIn: Chemotherapy, Jg. 28, 2016, Nr. 3, S. 210 – 217DOI (Open Access)
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A structured proteomic approach identifies 14-3-3Sigma as a novel and reliable protein biomarker in panel based differential diagnostics of liver tumorsIn: Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics, Jg. 1854, 2015, Nr. 6, S. 641 – 650
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Differential proteomic and tissue expression analyses identify valuable diagnostic biomarkers of hepatocellular differentiation and hepatoid adenocarcinomasIn: Pathology, Jg. 47, 2015, Nr. 6, S. 543 – 550
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Fine mapping of a GWAS-derived obesity candidate region on chromosome 16p11.2In: PLoS ONE, Jg. 10, 2015, Nr. 5, S. e0125660DOI (Open Access)
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Langzeitergebnisse der Tonsillektomie bei ErwachsenenIn: Deutsches Ärzteblatt, Jg. 112, 2015, Nr. 50, S. 849 – 855
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Long-Term Results From Tonsillectomy in AdultsIn: Deutsches Ärzteblatt International, Jg. 112, 2015, Nr. 50, S. 849 – 855DOI (Open Access)
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Prescription of enoxaparin is associated with decreasing pulmonary embolism mortality rate in GermanyIn: Journal of Thrombosis and Thrombolysis, Jg. 40, 2015, Nr. 4, S. 468 – 473
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Prognostic impact of residual disease after neoadjuvant chemotherapy in 648 patients with triple-negative breast cancerIn: Anticancer Research, Jg. 35, 2015, Nr. 10, S. 5479 – 5484
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Stage-related risk categorization and influence of free margins on survival in triple negative early breast cancer - a population-based study of 2037 TNBC patients with adjuvant chemotherapyIn: Cancer Research, Jg. 75, 2015, Nr. Suppl. 9, P2-13-01
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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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Impact of repetitive exposure to strong static magnetic fields on pregnancy and embryonic development of miceIn: Journal of Magnetic Resonance Imaging, Jg. 39, 2014, Nr. 3, S. 691 – 699
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Repetitive exposure of mice to strong static magnetic fields in utero does not impair fertility in adulthood but may affect placental weight of offspringIn: Journal of Magnetic Resonance Imaging, Jg. 39, 2014, Nr. 3, S. 683 – 690
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Severe Blunt Muscle Trauma in Rats : Only Marginal Hypoxia in the Injured AreaIn: PLoS ONE, Jg. 9, 2014, Nr. 10, S. e111151DOI (Open Access)
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Analyses of Non-Synonymous Obesity Risk Alleles in SH2B1 (rs7498665) and APOB48R (rs180743) in Obese Children and Adolescents Undergoing a 1-year Lifestyle InterventionIn: Experimental and Clinical Endocrinology & Diabetes, Jg. 121, 2013, Nr. 6, S. 334 – 337
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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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Common obesity risk alleles in childhood attention-deficit/hyperactivity disorderIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Jg. 162, 2013, Nr. 4, S. 295 – 305
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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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Genotype-phenotype and genotype-origin correlations in children with familial mediterranean fever in GermanyIn: Zeitschrift für Rheumatologie, Jg. 72, 2013, Nr. Suppl. 2, S. 93
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No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight childrenIn: Journal of Pediatric Endocrinology and Metabolism (JPEM), Jg. 26, 2013, Nr. 11-12, S. 1209 – 1213
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Relationship between carotid intima-media thickness and metabolic syndrome in adolescentsIn: The Journal of Pediatrics, Jg. 163, 2013, Nr. 2, S. 327 – 332.e4
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Do Common Variants Separate between Obese Melanocortin-4 Receptor Gene Mutation Carriers and Non-Carriers? : The Impact of Cryptic RelatednessIn: Hormone Research in Paediatrics, Jg. 77, 2012, Nr. 6, S. 358 – 368
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Does Size Always Matter? : A Simulation Study On The Impact Of Slightly Altered True Genetic ModelsIn: Genetic Epidemiology, Jg. 36, 2012, Nr. 2, S. 168 – 168
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Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma : a long-term follow-up studyIn: British Journal of Cancer (BJC), Jg. 106, 2012, Nr. 6, S. 1171 – 1176
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Significantly Reducing Post-Tonsillectomy Haemorrhage Requiring Surgery by Suturing the Faucial Pillars : A Retrospective AnalysisIn: PLoS ONE, Jg. 7, 2012, Nr. 10, S. e47874DOI (Open Access)
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The fatty acid amide hydrolase (FAAH) gene variant rs324420 AA/AC is not associated with weight loss in a 1-year lifestyle intervention for obese children and adolescentsIn: Hormone and Metabolic Research, Jg. 44, 2012, Nr. 1, S. 75 – 77
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Impact of immunosuppressive therapy on hepatitis C infection after renal transplantationIn: Clinical Nephrology, Jg. 75, 2011, Nr. 1, S. 16 – 25
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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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Oxygen persufflation as adjunct in liver preservation (OPAL) : Study protocol for a randomized controlled trialIn: Trials, Jg. 12, 2011, S. 234DOI (Open Access)
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Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile in head and neck squamous cell carcinomasIn: Journal of Translational Medicine, Jg. 9, 2011, S. 139DOI (Open Access)
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Addressing Genomic Imprinting in a Family-based Genome-wide Association Study
nineteenth annual meeting of the International Genetic Epidemiology Society,In: Genetic Epidemiology. Hoboken: Wiley-Blackwell - STM, Jg. 34, 2010, Nr. 8, S. 943 – 943 -
Impact of immunosupressive therapy on Hepatitis C infection after renal transplantation
19th Annual Congress of the German Transplantation Society, Hamburg, Germany, 7‐9 October 2010,In: Transplant International. Lausanne: Frontiers Media, Jg. 23, 2010, Nr. Suppl. 2, S. 3 -
Molekulargenetische Charakterisierung der Erblichkeit mittels Einzelnukleotidpolymorphismen am Beispiel komplexer anthropometrischer Merkmale unter Variation des Studiendesigns und des genetischen ModellsDuisburg, Essen, 2012