Area of research
Pathology and Forensic Medicine · Genetics
Research interest
Research interests include Lymphoma Diagnosis and Treatment, Chronic Lymphocytic Leukemia Research, Glioma Diagnosis and Treatment, and Genetic Associations and Epidemiology.
Use of Potentially Inappropriate Medication and Association with Falls During Hospitalisation: An Analysis Based on Electronic Health Records (POLAR_MI project).
The utility of explainable AI for MRI analysis: Relating model predictions to neuroimaging features of the aging brain
The utility of explainable AI for MRI analysis: Relating model predictions to neuroimaging features of the aging brain.
The Relationship Between Anxiety and Employment Status in a German Working-Age Population: Findings on Sex-Specific Prevalence Rates and Associated Factors of Anxiety From the LIFE-Adult-Study.
European Nuclear Medicine Guide - update 2026
Erratum zu: Messung der körperlichen Fitness in der NAKO Gesundheitsstudie – Methoden, Qualitätssicherung und erste deskriptive Ergebnisse
Genetic risk factors underlying white matter hyperintensities and cortical atrophy
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Gesundheitskompetenz, Anlaufstellen, ungedeckte subjektive Bedarfe und Behandlungszufriedenheit von Long-COVID-Betroffenen mit langanhaltender neuropsychiatrischer Symptomatik
The utility of explainable A.I. for MRI analysis: Relating model predictions to neuroimaging features of the aging brain
Effect of Hyperthermic Intraperitoneal Chemotherapy on Cytoreductive Surgery in Gastric Cancer With Synchronous Peritoneal Metastases: The Phase III GASTRIPEC-I Trial
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database
Global distributions of age- and sex-related arterial stiffness: systematic review and meta-analysis of 167 studies with 509,743 participants
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
OTTERS: a powerful TWAS framework leveraging summary-level reference data
Radiation and Dose-densification of R-CHOP in Primary Mediastinal B-cell Lymphoma: Subgroup Analysis of the UNFOLDER Trial
Radiation and Dose-densification of R-CHOP in Aggressive B-cell Lymphoma With Intermediate Prognosis: The UNFOLDER Study
Announcement of the German Medical Text Corpus Project (GeMTeX)
Framework and baseline examination of the German National Cohort (NAKO)
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
Towards the interpretability of deep learning models for multi-modal neuroimaging: Finding structural changes of the ageing brain
Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour
Theranostic AGuIX nanoparticles as radiosensitizer: A phase I, dose-escalation study in patients with multiple brain metastases (NANO-RAD trial)
Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomas
Renal function and lipid metabolism are major predictors of circumpapillary retinal nerve fiber layer thickness—the LIFE-Adult Study
SPARC-positive macrophages are the superior prognostic factor in the microenvironment of diffuse large B-cell lymphoma and independent of MYC rearrangement and double-/triple-hit status
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report