Evelin Schröck

Career Trajectory

Research Cluster Map

Direct collaborators. Node size = influence, colour = community, dashed = past collaboration.

• Clinically actionable genomic and transcriptomic landscape of advanced neuroendocrine neoplasms

  Med · 2026-05-01 · 1 citations

• Effect of a polygenic risk score in patients with late-onset, early-onset, familial, or hereditary colorectal cancer

  JNCI Cancer Spectrum · 2026-04-10

• Multi-layered molecular profiling informs the diagnosis and targeted therapy of desmoplastic small round cell tumor

  Nature Communications · 2026-04-09 · 2 citations

• Minigene-based characterization and classification of splice-associated variants in succinate dehydrogenase BPreprint

  Research Square · 2026-02-24

• Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study

  European Journal of Human Genetics · 2026-02-13 · 3 citations

• Molecular genotype-phenotype correlation in ACTB- and ACTG1-related non-muscle actinopathies

  The American Journal of Human Genetics · 2026-01-12 · 4 citations

• Effect of a polygenic risk score in patients with late-onset, early-onset, familial, or hereditary colorectal cancer

  JuSER Publikationsportal · 2026-01-01

• Cerebral organoids expressing mutant actin genes reveal cellular mechanism underlying microcephaly

  EMBO Reports · 2025-12-10 · 4 citations

• From genetic risk to clinical action: universal germline testing and surveillance in pancreatic cancer

  Medizinische Genetik · 2025-11-06

• Genetic tumor syndromes – It’s time for action

  Medizinische Genetik · 2025-11-06

• Targeted therapy in patients with genetic tumor syndromes

  Medizinische Genetik · 2025-11-06

• Germany’s national genomDE strategy

  Nature Medicine · 2025-10-15 · 7 citations

• 1715P Clinically actionable genomic and transcriptomic landscape of advanced neuroendocrine neoplasms

  Annals of Oncology · 2025-09-01

• 17.6% of patients in a German cohort with exocrine pancreatic cancer were diagnosed with a genetic tumor syndrome—a case for universal genetic testing?

  ESMO Gastrointestinal Oncology · 2025-08-08

• Identifying Risk Factors for Metachronous Colorectal Cancer in Lynch Syndrome

  Clinical Gastroenterology and Hepatology · 2025-07-30 · 1 citations

• Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

  Nature Genetics · 2025-06-24

• Abstract 6373: From genotype to phenotype: Adding phosphoproteomic analysis to molecularly-guided therapy recommendation in Cancer of Unknown Primary (CUP)

  Cancer Research · 2025-04-21

• Abstract 5039: Machine learning enhances histology-agnostic detection of PTEN deletions in panel sequencing of advanced cancers

  Cancer Research · 2025-04-21

• Long-read genome and RNA sequencing resolve a pathogenic intronic germline LINE-1 insertion in APC

  npj Genomic Medicine · 2025-04-04 · 5 citations

• Comprehensive genomic and transcriptomic analysis enables molecularly guided therapy options in peritoneal and pleural mesothelioma

  ESMO Open · 2025-04-01 · 5 citations