Arne Jahn

University Hospital Carl Gustav Carus — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

13h-index986citations60works1.92yr avg
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Research Topics

Cancer Genomics and Diagnostics(22), Genomics and Rare Diseases(10), Pancreatic and Hepatic Oncology Research(8), BRCA gene mutations in cancer(7), Genetic factors in colorectal cancer(6)

Publications60 total

Minigene-based characterization and classification of splice-associated variants in succinate dehydrogenase B
2026Open Access
Targeted therapy in patients with genetic tumor syndromes
Medizinische Genetik·2025Open Access
Jugendliche mit familiärer adenomatöser Polyposis coli – Karzinomentstehung und Kolektomie vor dem 18. Lebensjahr
Zeitschrift für Gastroenterologie·2025
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·2025Open Access
Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)—a European cohort study
BJC Reports·2025· 1 citedOpen Access
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)
Genetics in Medicine·2025· 2 citedOpen Access
Long-read genome and RNA sequencing resolve a pathogenic intronic germline LINE-1 insertion in APC
npj Genomic Medicine·2025· 2 citedOpen Access
Comprehensive genomic and transcriptomic analysis enables molecularly guided therapy options in peritoneal and pleural mesothelioma
ESMO Open·2025· 3 citedOpen Access
Multi-Layered Molecular Profiling Informs the Diagnosis and Targeted Therapy of Desmoplastic Small Round Cell Tumor
2025Open Access
Genomic landscape and molecularly informed therapy in thymic carcinoma and other advanced thymic epithelial tumors
Med·2025· 5 citedOpen Access
ZBTB48 is a priming factor regulating B-cell-specific CIITA expression
The EMBO Journal·2024· 4 citedOpen Access
Identification of Succinate Dehydrogenase Gene Variant Carriers by Blood Biomarkers
Journal of the Endocrine Society·2024· 7 citedOpen Access
Mismatch repair deficiency and microsatellite instability in adrenocortical carcinoma: Diagnosis, prevalence, and clinical impact
Endocrine Abstracts·2024
Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS)
Cancers·2024· 2 citedOpen Access
NCT/DKFZ MASTER handbook of interpreting whole-genome, transcriptome, and methylome data for precision oncology
npj Precision Oncology·2023· 29 citedOpen Access
De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias
Genetics in Medicine·2023· 4 citedOpen Access
Beitrag der Humangenetik zur Präzisionsonkologie
Die Onkologie·2023Open Access
ZBTB48 is a pioneer factor regulating B-cell-specific CIITA expression
2023Open Access
De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias
Genetics in Medicine·2023· 6 citedOpen Access
A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children
Genetics in Medicine·2023· 5 citedOpen Access
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Frequent Co-authors

Evelin Schröck(26), Hanno Glimm(19), Christoph Heining(18), Stefan Fröhling(18), Barbara Hutter(17), Albrecht Stenzinger(17), Daniel Hübschmann(16), Andreas Möck(15), Martina Fröhlich(15), Sebastian Uhrig(15), Laura Gieldon(15), Christoph E. Heilig(15), Peter Horak(14), Simon Kreutzfeldt(14), Lino Möhrmann(14), Dorothea Hanf(14), Daniel B. Lipka(14), Melanie Boerries(13), Anna Lena Illert(13), Jennifer Hüllein(12)