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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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Leveraging electronic medical records to evaluate a computerized decision support system for staphylococcus bacteremiaIn: npj Digital Medicine, Jg. 8, 2025, Nr. 1, 180DOI (Open Access)
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Youths with Extreme Obesity : A High-Risk Group for Pain and Mental Health ImpairmentsIn: Obesity Facts, Jg. 18, 2025, Nr. 1, S. 21 – 30DOI (Open Access)
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Cytokine Hemoadsorption during Cardiac Surgery Versus Standard Surgical Care for Infective Endocarditis REMOVE : Results from a Multicenter Randomized Controlled TrialIn: Circulation, Jg. 145, 2022, Nr. 13, S. 959 – 968DOI (Open Access)
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Bridging animal and clinical research during SARS-CoV-2 pandemic : A new-old challengeIn: eBioMedicine, Jg. 66, 2021, S. 103291DOI (Open Access)
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Safety and efficacy of prednisone versus placebo in short-term prevention of episodic cluster headache : A multicentre, double-blind, randomised controlled trialIn: The Lancet Neurology, Jg. 20, 2021, Nr. 1, S. 29 – 37
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Air Pollution and Progression of Atherosclerosis in Different Vessel Beds : Results from a Prospective Cohort Study in the Ruhr Area, GermanyIn: Environmental Health Perspectives, Jg. 128, 2020, Nr. 10, S. 107003DOI (Open Access)
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Health related quality of life associated with extreme obesity in adolescents : Results from the baseline evaluation of the YES-studyIn: Health and Quality of Life Outcomes, Jg. 18, 2020, S. 58DOI (Open Access)
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Hospital-wide ELectronic medical record evaluated computerised decision support system to improve outcomes of Patients with staphylococcal bloodstream infection (HELP) : study protocol for a multicentre stepped-wedge cluster randomised trialIn: BMJ Open, Jg. 10, 2020, Nr. 2, S. e033391DOI (Open Access)
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Air pollution, traffic noise and development of subclinical atherosclerosis in the thoracic aortaIn: Circulation, Jg. 139, 2019, Nr. Suppl. 1, S. P102
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Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders : A Swedish Nationwide Population Study Using Multiple Genetically Informative ApproachesIn: Biological Psychiatry, Jg. 86, 2019, Nr. 8, S. 577 – 586DOI (Open Access)
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Comment on 'Naked mole-rat mortality rates defy Gompertzian laws by not increasing with age'In: eLife, Jg. 8, 2019, e45415DOI (Open Access)
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Current gaps in sepsis immunology: new opportunities for translational researchIn: The Lancet Infectious Diseases, Jg. 19, 2019, Nr. 12, S. e422 – e436DOI (Open Access)
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Do adolescents with extreme obesity differ according to previous treatment seeking behavior? : The Youth with Extreme obesity Study (YES) cohortIn: International Journal of Obesity, Jg. 43, 2019, S. 103 – 115
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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms Across Eight Psychiatric DisordersIn: Cell, Jg. 179, 2019, Nr. 7, S. 1469 – 1482.e11.DOI (Open Access)
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Psychosoziale Charakterisierung und Integrative Versorgung arbeitsloser Jugendlicher mit extremer Adipositas : ein ModellprojektIn: Psychotherapie, Psychosomatik, Medizinische Psychologie (PPmP), Jg. 69, 2019, Nr. 12, S. 490 – 498
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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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Positron Emission Tomography-Guided Therapy of Aggressive Non-Hodgkin Lymphomas (PETAL) : A Multicenter, Randomized Phase III TrialIn: Journal of Clinical Oncology (JCO), Jg. 36, 2018, Nr. 20, S. 2024 – 2034DOI (Open Access)
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Smart Medical Information Technology for Healthcare (SMITH) : Data Integration based on Interoperability StandardsIn: Methods of Information in Medicine = Methodik der Information in der Medizin, Jg. 57, 2018, Nr. S 01, S. e92 – e105DOI (Open Access)
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A Structured, Manual-Based Low-Level Intervention vs. Treatment as Usual Evaluated in a Randomized Controlled Trial for Adolescents with Extreme Obesity - the STEREO TrialIn: Obesity Facts, Jg. 10, 2017, Nr. 4, S. 341 – 352DOI (Open Access)
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A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingIn: Scientific Reports, Jg. 7, 2017, Nr. 1DOI (Open Access)
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Comparison of coronary artery calcification, carotid intima-media thickness and ankle-brachial index for predicting 10-year incident cardiovascular events in the general populationIn: European Heart Journal, Jg. 38, 2017, Nr. 23, S. 1815 – 1822
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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass indexIn: Molecular Psychiatry, Jg. 22, 2017, S. 192 – 201DOI, Online Volltext (Open Access)
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Medical and Psychosocial Implications of Adolescent extreme Obesity : Acceptance and Effects of Structured Care Program - Yes Study. A Consortium of the BMBFIn: Hormone Research in Paediatrics, Jg. 88, 2017, Nr. Suppl. 1, 10th Individual Abstracts for International Meeting of Pediatric Endocrinology: Free Communication and Poster Sessions, Abstracts, S. 161
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Phase II dose–response trials : A simulation study to compare analysis method performance under design considerationsIn: Journal of Biopharmaceutical Statistics, Jg. 27, 2017, Nr. 5, S. 885 – 901
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Safety of Simultaneous Coronary Artery Bypass Grafting and Carotid Endarterectomy Versus Isolated Coronary Artery Bypass Grafting : A Randomized Clinical TrialIn: Stroke, Jg. 48, 2017, Nr. 10, S. 2769 – 2775DOI (Open Access)
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A Genome-Wide Study of Gene-Fine Particulate Air Pollution Interaction Effects on Carotid Intima-Media Thickness - the Heinz Nixdorf Recall StudyIn: Genetic Epidemiology, Jg. 40, 2016, Nr. 7, S. 659 – 660
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AQP5-1364A/C polymorphism and the AQP5 expression influence sepsis survival and immune cell migration : a prospective laboratory and patient studyIn: Journal of Translational Medicine, Jg. 14, 2016, Nr. 1, 321DOI (Open Access)
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Association of common variants identified by recent genome-wide association studies with obesity in Chinese children : A case-control studyIn: BMC Medical Genetics, Jg. 17, 2016, S. 7DOI (Open Access)
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Linkage and Association Analysis Identifies TRAF1 Influencing Common Carotid Intima-Media ThicknessIn: Stroke, Jg. 47, 2016, Nr. 12, S. 2904 – 2909DOI (Open Access)
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Mitochondrial DNA : an endogenous trigger for immune paralysisIn: Anesthesiology, Jg. 124, 2016, Nr. 4, S. 923 – 933
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Update of the effect estimates for common variants associated with carotid intima media thickness within four independent samples : The Bonn IMT Family Study, the Heinz Nixdorf Recall Study, the SAPHIR Study and the Bruneck StudyIn: Atherosclerosis, Jg. 249, 2016, S. 83 – 87
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CEACAM1-3S drives melanoma cells into NK cell-mediated cytolysis and enhances patient survivalIn: Cancer Research, Jg. 75, 2015, Nr. 9, S. 1897 – 1907DOI (Open Access)
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Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity : a systematic review and meta-analysis with evidence from up to 331 175 individualsIn: Human Molecular Genetics, Jg. 24, 2015, Nr. 12, S. 3582 – 3594DOI (Open Access)
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Engineered liposomes sequester bacterial exotoxins and protect from severe invasive infections in miceIn: Nature Biotechnology, Jg. 33, 2015, Nr. 1, S. 81 – 88
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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, Online Volltext (Open Access)
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Indications for potential parent-of-origin effects within the FTO geneIn: PLoS ONE, Jg. 10, 2015, Nr. 3, S. e0119206DOI (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, Online Volltext (Open Access)
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Replication effort for common variants associated with carotid intima media thickness within four independent samplesIn: Genetic Epidemiology, Jg. 39, 2015, Nr. 7, S. 550 – 551
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A genome-wide association study of anorexia nervosaIn: Molecular Psychiatry, Jg. 19, 2014, Nr. 10, S. 1085 – 1094DOI, Online Volltext (Open Access)
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Correction: Hydrocortisone Fails to Abolish NF-κB1 Protein Nuclear Translocation in Deletion Allele Carriers of the NFKB1 Promoter Polymorphism (-94ins/delATTG) and Is Associated with Increased 30-Day Mortality in Septic ShockIn: PLoS ONE, Jg. 9, 2014, Nr. 10, S. 0112369DOI (Open Access)
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Day-patient treatment after short inpatient care versus continued inpatient treatment in adolescents with anorexia nervosa (ANDI) : A multicentre, randomised, open-label, non-inferiority trialIn: Lancet, Jg. 383, 2014, Nr. 9924, S. 1222 – 1229
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Defining the role of common variation in the genomic and biological architecture of adult human heightIn: Nature Genetics, Jg. 46, 2014, Nr. 11, S. 1173 – 1186DOI, Online Volltext (Open Access)
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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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Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesityIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Jg. 165, 2014, Nr. 4, S. 283 – 293
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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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Hydrocortisone Fails to Abolish NF-κB1 Protein Nuclear Translocation in Deletion Allele Carriers of the NFKB1 Promoter Polymorphism (-94ins/delATTG) and Is Associated with Increased 30-Day Mortality in Septic ShockIn: PLoS ONE, Jg. 9, 2014, Nr. 8, e104953DOI (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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Isoform-specific function of CEACAM1 during tumorigenesis : CEACAM1-3S, a novel prognostic biomarker in malignant melanomaIn: Experimental Dermatology, Jg. 23, 2014, Nr. 3, S. E45
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Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass IndexIn: PLoS Genetics, Jg. 10, 2014, Nr. 7, S. e1004508DOI (Open Access)
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Positron Emission Tomography (PET) Guided Therapy of Aggressive Lymphomas - a Randomized Controlled Trial Comparing Different Treatment Approaches Based on Interim PET Results (PETAL Trial)In: Blood, Jg. 124, 2014, Nr. 21, S. 391
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Quality control and conduct of genome-wide association meta-analysesIn: Nature Protocols, Jg. 9, 2014, Nr. 5, S. 1192 – 1212DOI, Online Volltext (Open Access)
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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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TERT promoter mutation status as an independent prognostic factor in cutaneous melanomaIn: Journal of the National Cancer Institute (JNCI), Jg. 106, 2014, Nr. 9
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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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Die Coronary Artery Bypass graft surgery in patients with Asymptomatic Carotid Stenosis (CABACS) RCT Studie : Rationale, Stand und PerspektivenIn: Gefäßchirurgie, Jg. 18, 2013, Nr. 7, S. 638 – 643
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Gene Set of Nuclear-Encoded Mitochondrial Regulators Is Enriched for Common Inherited Variation in ObesityIn: PLoS ONE, Jg. 8, 2013, Nr. 2, S. e55884DOI, Online Volltext (Open Access)
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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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Medical and psychosocial implications of adolescent extreme obesity - Acceptance and effects of structured care, short : Youth with Extreme Obesity Study (YES)In: BMC Public Health, Jg. 13, 2013, Nr. 1, S. 789DOI (Open Access)
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Meta-analysis of Genetic Associations in up to 339,224 Individuals Identify 66 New Loci for Bmi, Confirming a Neuronal Contribution to Body Weight Regulation and Implicating Several Novel PathwaysIn: Circulation, Jg. 127, 2013, Nr. Suppl.12
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Molecular Genetic Aspects of Weight RegulationIn: Deutsches Ärzteblatt International, Jg. 110, 2013, Nr. 19, S. 338 – 344
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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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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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SPECT/CT for Sentinel Lymph Node Detection in Patients With Melanoma - ReplyIn: JAMA: Journal of the American Medical Association, Jg. 309, 2013, Nr. 3, S. 232 – 233
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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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Study protocol of Prednisone in episodic Cluster Headache (PredCH) : a randomized, double-blind, placebo-controlled parallel group trial to evaluate the efficacy and safety of oral prednisone as an add-on therapy in the prophylactic treatment of episodic cluster headache with verapamilIn: BMC Neurology, Jg. 13, 2013, S. 99DOI (Open Access)
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A genome-wide association meta-analysis identifies new childhood obesity lociIn: Nature Genetics, Jg. 44, 2012, Nr. 5, S. 526 – 531
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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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Atypical Melanocytic Proliferations and New Primary Melanomas in Patients With Advanced Melanoma Undergoing Selective BRAF InhibitionIn: Journal of Clinical Oncology (JCO), Jg. 30, 2012, Nr. 19, S. 2375 – 2383
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Common variants at 12q15 and 12q24 are associated with infant head circumferenceIn: Nature Genetics, Jg. 44, 2012, Nr. 5, S. 532 – 538
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Common variants at 6q22 and 17q21 are associated with intracranial volumeIn: Nature Genetics, Jg. 44, 2012, Nr. 5, S. 539 – 544
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DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorderIn: PLoS ONE, Jg. 7, 2012, Nr. 4, Art. Nr. e35424DOI (Open Access)
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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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Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and humanIn: Nature, Jg. 483, 2012, Nr. 7389, S. 350 – 354
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Fat mass and obesity-associated gene (FTO) in eating disorders : Evidence for association of the rs9939609 obesity risk allele with Bulimia nervosa and anorexia nervosaIn: Obesity Facts, Jg. 5, 2012, Nr. 3, S. 408 – 419
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Low adiponectin, high levels of apoptosis and increased peripheral blood neutrophil activity in healthy obese subjectsIn: Obesity Facts, Jg. 5, 2012, Nr. 3, S. 305 – 318
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Multiscale assessment of treatment efficacy in adults with ADHD : a randomized placebo-controlled, multi-centre study with extended-release methylphenidateIn: The World Journal of Biological Psychiatry, Jg. 13, 2012, Nr. 1, S. 48 – 59
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Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variantsIn: BMC Medical Genomics, Jg. 5, 2012, S. 65DOI, Online Volltext (Open Access)
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Randomized comparison of synchronous CABG and carotid endarterectomy vs. isolated CABG in patients with asymptomatic carotid stenosis : the CABACS trialIn: International Journal of Stroke, Jg. 7, 2012, Nr. 4, S. 354 – 360
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SDCCAG8 obesity alleles and reduced weight loss after a lifestyle intervention in overweight children and adolescentsIn: Obesity, Jg. 20, 2012, Nr. 2, S. 466 – 470
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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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βhCG and PAPP-A in First Trimester : Predictive Factors for Preeclampsia?In: Hypertension in Pregnancy, Jg. 31, 2012, Nr. 2, S. 261 – 267
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Aquaporin 5 gene promoter -1364A/C polymorphism associated with 30-day survival in severe sepsisIn: Anesthesiology, Jg. 114, 2011, Nr. 4, S. 912 – 917DOI (Open Access)
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Assessment of a chloride-poor versus a chloride-containing version of a modified histidine-tryptophan-ketoglutarate solution in a rat liver transplantation modelIn: Liver Transplantation, Jg. 17, 2011, Nr. 6, S. 650 – 660
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Common Variants Near MC4R : Exploring Gender Effects in Overweight and Obese Children and Adolescents Participating in a Lifestyle InterventionIn: Obesity Facts, Jg. 4, 2011, Nr. 1, S. 67 – 75
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Comparison of the Efficacy of Two Different Modified Release Methylphenidate Preparations for Children and Adolescents with Attention-Deficit/Hyperactivity Disorder in a Natural Setting : Comparison of the Efficacy of Medikinet®Retard and Concerta®—a Randomized, Controlled, Double-Blind Multicenter Clinical Crossover TrialIn: Journal of Child and Adolescent Psychopharmacology, Jg. 21, 2011, Nr. 5, S. 445 – 454
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Elevated serum matrix metalloproteinase 7 levels predict poor prognosis after radical prostatectomyIn: International Journal of Cancer, Jg. 128, 2011, Nr. 6, S. 1486 – 1492
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Evaluation of the obesity genes FTO and MC4R and the type 2 diabetes mellitus gene TCF7L2 for contribution to stroke risk : The Mannheim-Heidelberg Stroke StudyIn: Obesity Facts, Jg. 4, 2011, Nr. 4, S. 290 – 296
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Expander-Implant-Reconstruction – Aesthetic Outcome and Patients' Satisfaction in a 10-Year-PeriodIn: Cancer Research, Jg. 71, 2011, Nr. 24
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Extended longevity of reproductives appears to be common in Fukomys mole-rats (Rodentia, Bathyergidae).In: PLoS ONE, Jg. 6, 2011, Nr. 4, e18757DOI, Online Volltext (Open Access)
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Genetic variation of the ghrelin activator gene ghrelin O-acyltransferase (GOAT) is associated with anorexia nervosa.In: Journal of Psychiatric Research, Jg. 45, 2011, Nr. 5, S. 706 – 711
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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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Genotyp des GNB3-C825T-Polymorphismus : Risikofaktor für die Entwicklung und den Verlauf eines Prostatakarzinoms?In: Der Urologe, Jg. 50, 2011, Nr. 9, S. 1137 – 1142
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Ghrelin, leptin and adiponectin as possible predictors of the hedonic value of odorsIn: Regulatory Peptides, Jg. 167, 2011, Nr. 1, S. 112 – 117
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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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Is there an association between hospital accreditation and patient satisfaction with hospital care? : A survey of 37,000 patients treated by 73 hospitalsIn: International Journal for Quality in Health Care, Jg. 23, 2011, Nr. 3, S. 278 – 283
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Lack of Association of the Genotype in the GNAS Fok I Polymorphism and Prostate CancerIn: Urologia Internationalis, Jg. 87, 2011, Nr. 1, S. 80 – 86
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Lack of association of cd36 snps with early onset obesity : A meta-analysis in 9,973 european subjectsIn: Obesity, Jg. 19, 2011, Nr. 4, S. 833 – 839
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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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Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysisIn: Human Molecular Genetics, Jg. 20, 2011, Nr. 4, S. 840 – 852
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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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Polymorphonuclear granulocytes in human head and neck cancer: Enhanced inflammatory activity, modulation by cancer cells and expansion in advanced diseaseIn: International Journal of Cancer, Jg. 129, 2011, Nr. 9, S. 2183 – 2193
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Relationship between MTNR1B (melatonin receptor 1B gene) polymorphism rs10830963 and glucose levels in overweight children and adolescentsIn: Pediatric Diabetes, Jg. 12, 2011, Nr. 4 Part 2, S. 435 – 441
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The CoMeCo-Trial : comparison of the efficacy of two methylphenidate preparations for children and adolescents with ADHD in a natural settingIn: European Child and Adolescent Psychiatry, Jg. 20, 2011, Nr. Suppl. 1, S. 116
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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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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass indexIn: Nature Genetics, Jg. 42, 2010, Nr. 11, S. 937 – 948DOI (Open Access)
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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass indexIn: Nature Genetics, Jg. 42, 2010, Nr. 11, S. 937 – 948
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Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from BerlinIn: European Journal of Endocrinology (EJE), Jg. 163, 2010, Nr. 2, S. 259 – 264
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Associations between BMI and the FTO gene are age dependent: Results from the GINI and LISA birth cohort studies up to age 6 yearsIn: Obesity Facts, Jg. 3, 2010, Nr. 3, S. 173 – 180
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Child and adolescent psychiatric geneticsIn: European Child and Adolescent Psychiatry, Jg. 19, 2010, Nr. 3, S. 259 – 279
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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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Evaluating Strategies for Marker Ranking in Genome-wide Association Studies of Complex TraitsIn: Methods of Information in Medicine = Methodik der Information in der Medizin, Jg. 49, 2010, Nr. 6, S. 632 – 640
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Investigation of a Genome Wide Association Signal for Obesity : Synthetic Association and Haplotype Analyses at the Melanocortin 4 Receptor Gene LocusIn: PLoS ONE, Jg. 5, 2010, Nr. 11, S. e13967DOI, Online Volltext (Open Access)
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Large effects on body mass index and insulin resistance of fat mass and obesity associated gene (FTO) variants in patients with polycystic ovary syndrome (PCOS)In: BMC Medical Genetics, Jg. 11, 2010, 12DOI (Open Access)
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Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesityIn: BMC Medical Genetics, Jg. 11, 2010, S. 2DOI (Open Access)
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Radioembolization with yttrium-90 glass microspheres in hepatocellular carcinoma : European experience on safety and long-term survivalIn: Hepatology, Jg. 52, 2010, Nr. 5, S. 1741 – 1749DOI (Open Access)
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The Cathepsin D (224C/T) polymorphism confers an increased risk to develop alzheimer's disease in menIn: Journals of Gerontology Series A: Biological Sciences and Medical Sciences, Jg. 65 A, 2010, Nr. 3, S. 219 – 224
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Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study GroupsIn: PLoS Genetics, Jg. 6, 2010, Nr. 4DOI (Open Access)
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Biodistribution of 10B for boron neutron capture therapy (BNCT) in a mouse model after injection of sodium mercaptoundecahydro-closo- dodecaborate and l-para-boronophenylalanineIn: Radiation research, Jg. 172, 2009, Nr. 4, S. 493 – 499
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Flexible designs for genomewide association studiesIn: Biometrics, Jg. 65, 2009, Nr. 3, S. 815 – 821
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Gastric inhibitory polypeptide receptor : Association analyses for obesity of several polymorphisms in large study groupsIn: BMC Medical Genetics, Jg. 10, 2009DOI (Open Access)
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Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestryIn: BMC Medical Genetics, Jg. 10, 2009DOI (Open Access)
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Procolipase gene : no association with early-onset obesity or fat intakeIn: Obesity Facts, Jg. 2, 2009, Nr. 1, S. 40 – 44DOI (Open Access)
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'Fat mass and obesity associated' gene (FTO): No significant association of variant rs9939609 with weight loss in a lifestyle intervention and lipid metabolism markers in German obese children and adolescentsIn: BMC Medical Genetics, Jg. 9, 2008, S. 85DOI (Open Access)
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Common variants near MC4R are associated with fat mass, weight and risk of obesityIn: Nature Genetics, Jg. 40, 2008, Nr. 6, S. 768 – 775
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Gene-environment interactions for complex traits : Definitions, methodological requirements and challengesIn: European Journal of Human Genetics, Jg. 16, 2008, Nr. 10, S. 1164 – 1172DOI, Online Volltext (Open Access)
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Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosaIn: Child and Adolescent Psychiatry and Mental Health, Jg. 2, 2008DOI, Online Volltext (Open Access)
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Plasma Chromogranin A as Marker for Survival in Patients With Metastatic Endocrine Gastroenteropancreatic TumorsIn: Clinical Gastroenterology and Hepatology, Jg. 6, 2008, Nr. 7, S. 820 – 827
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Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children : First evidence of polar overdominance in humansIn: European Journal of Human Genetics, Jg. 16, 2008, Nr. 9, S. 1126 – 1134DOI (Open Access)
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Transmission disequilibrium studies in early onset of obsessive-compulsive disorder for polymorphisms in genes of the dopaminergic systemIn: Journal of Neural Transmission, Jg. 115, 2008, Nr. 7, S. 1071 – 1078
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Val103Ile polymorphism of the melanocortin-4 receptor gene (MC4R) in cancer cachexiaIn: BMC Cancer, Jg. 8, 2008, 85DOI (Open Access)
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Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescentsIn: BMC Medical Genetics, Jg. 8, 2007DOI (Open Access)
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Association and linkage of allelic variants of the dopamine transporter gene in ADHDIn: Molecular Psychiatry, Jg. 12, 2007, Nr. 10, S. 923 – 933DOI (Open Access)
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Genome Wide Association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variantsIn: PLoS ONE, Jg. 2, 2007, Nr. 12DOI (Open Access)
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Mutation screen and association studies in the Diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13In: BMC Genetics, Jg. 8, 2007DOI (Open Access)
-
No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in GermansIn: Hormone and Metabolic Research, Jg. 39, 2007, Nr. 11, S. 840 – 844
-
The V103I polymorphism of the MC4R gene and obesity: Population based studies and meta-analysis of 29 563 individualsIn: International Journal of Obesity, Jg. 31, 2007, Nr. 9, S. 1437 – 1441DOI (Open Access)
-
The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohortsIn: PLoS Genetics, Jg. 3, 2007, Nr. 4, S. 0627 – 0633DOI (Open Access)
-
Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studiesIn: Human Molecular Genetics, Jg. 15, 2006, Nr. 18, S. 2772 – 2783
-
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from GermanyIn: The Journal of Clinical Endocrinology & Metabolism (JCEM), Jg. 91, 2006, Nr. 5, S. 1761 – 1769DOI (Open Access)
-
Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorderIn: The International Journal of Neuropsychopharmacology, Jg. 9, 2006, Nr. 4, S. 437 – 442DOI (Open Access)
-
Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesityIn: Journal of Nutrition, Jg. 135, 2005, Nr. 6, S. 1387 – 1392DOI (Open Access)
-
Lack of support for the association between GAD2 polymorphisms and severe human obesityIn: PLoS Biology, Jg. 3, 2005, Nr. 9, e315DOI (Open Access)
-
Positron-emission tomography-guided therapy of aggressive non-Hodgkin lymphomas -final results of the PETAL trial
Jahrestagung der Deutschen, Österreichischen und Schweizerischen Gesellschaften für Hämatologie und Medizinische Onkologie, 29. September-3. Oktober 2017, Stuttgart, Germany,In: Oncology Research and Treatment. Basel: Karger, Jg. 40, 2017, Nr. Suppl. 3, S. 202 – 203 -
Genetic variation at three genetic loci involved in anorexia nervosa are associated with body weight regulation
16th International Congress of ESCAP European Society for Child and Adolescent Psychiatry 20–24 June 2015, Madrid, Spain,In: European Child and Adolescent Psychiatry. Berlin: Springer Nature, Jg. 24, 2015, Nr. Suppl. 1, S. 64 -
Treatment Results of Large Choroidal Melanoma with the Ru-106/I-125-Bi-Nuclide Applicator
19. Jahreskongress der Deutschen Gesellschaft für Radioonkologie Berlin, 9. bis 12. Mai 2013,In: Strahlentherapie und Onkologie: Journal of Radiation Oncology, Biology, Physics. Heidelberg: Springer, Jg. 189, 2013, Nr. Suppl. 1, S. 92 -
Risk-reducing surgery by skin-sparing mastectomy (SSM) and immediate implant-based reconstruction with and without titanized meshes and quality of lifeIn: Journal of Clinical Oncology (JCO). Alexandria: American Society of Clinical Oncology (ASCO), Jg. 30, 2012, Nr. 27_suppl, S. 48 – 48
-
Association of Diabetes-Mellitus-Related genetic variants with coronary artery calcificationIn: Atherosclerosis Supplements: Elsevier, Jg. 12, 2011, Nr. 1, S. 128
-
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 -
Genetics of obesityIn: European Neuropsychopharmacology. Amsterdam: Elsevier, Jg. 20, 2010, Nr. Suppl. 3, S. S190
-
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 -
Linkage genome scan and subsequent association studies show involvement of the vitamin D receptor gene in idiopathic short statureIn: Genetic Epidemiology. Hoboken: Wiley-Blackwell - STM, Jg. 31, 2007, Nr. 5, S. 450 – 513
-
Methodische Strategien zur statistischen Modellierung genetischer Varianten für komplexe Phänotypen im Rahmen genomweiter AnalysenDuisburg, Essen, 2012