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Precision Oncology in Northern Germany – Integrating Multi-Omics and AI to Support Evidence-Based Molecular Tumor Boards

Spatial Mapping of Gonad Development in DSD

PD-L1–linked spatial decoupling of tumour–immune interactions in EBV-positive DLBCL

Characterisation of leydig cells in individuals with genetic defects of androgen signalling

A new variant in the 3’-UTR of the SRD5A2 gene leads to highly efficient exonisation of an Alu element and contributes to 5α-steroid reductase type 2 deficiency

Exploring gonadal development in differences of sex development using spatial transcriptomics

Characterization of testicular developmental defects in MYRF-associated DSD

Exonisation of an Alu element in the 3’-UTR contributes to SRD5A2 deficiency

Cutaneous dysbiosis in inherited ichthyoses/epidermal differentiation disorders: a prospective case-control study

A liquid biopsy-centered, pan-cancer, open next generation sequencing panel to support clinical decision-making (LION panel)

C70-02 Targetable Cytokines Promote Dysmorphic Mucosa via Cell-Cell Interactions Revealed by Single-Cell RNA-Sequencing in Post-Covid Syndrome

Genetic Profiling of Autoimmune Diseases and Exploring Clusters Through Polygenic Risk Score Analysis Using Cohort Data from the UK Biobank

Mitochondrial toxins cause widespread downregulation of pathways in X-linked dystonia-parkinsonism patient-derived neurons

Biomarker Identification of Myocardial Infarction Subtypes

Organoids serve as viable in vitro model for functional precision medicine for mesonephric-like adenocarcinoma of the ovary

P102 Beyond hinge motifs: the molecular basis of transporter-mediated kinase inhibitor resistance

Method development for pancreatic and ovarian cancer baseline ctDNA detection and measurable residual disease monitoring

IGH::FENDRR and specific KRAS mutations define a novel B-ALL molecular subtype with poor chemotherapy response

Adenosine Pathway Activation Defines Genetically Linked Immunosuppressive Subtypes in Solid Tumor Brain Metastases

Multi-Omics Characterization of a KIF1C Structural Variant in a Patient with a Complex Movement Disorder Partially Responsive to Deep Brain Stimulation