Arne E. Jahn
Dresden, SN, Germany
Last Updated: 09/26/2026
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Found 43 publications
Beyond in silico prediction: multi-omics to identify a pathogenic deep intronic HNRNPK variant in Au-Kline syndrome.
Journal: Journal of human genetics
Published: April 30, 2026
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?
Journal: ESMO gastrointestinal oncology
Published: February 06, 2026
Targeted therapy in patients with genetic tumor syndromes.
Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V
Published: November 10, 2025
Mismatch repair deficiency and microsatellite instability in adrenocortical carcinoma.
Journal: ESMO open
Published: July 22, 2025
Multi-layered molecular profiling informs the diagnosis and targeted therapy of desmoplastic small round cell tumor.
Journal: Nature communications
Published: February 25, 2025
Long-read genome and RNA sequencing resolve a pathogenic intronic germline LINE-1 insertion in APC.
Journal: NPJ genomic medicine
Published: September 17, 2024
Genomic landscape and molecularly informed therapy in thymic carcinoma and other advanced thymic epithelial tumors.
Journal: Med (New York, N.Y.)
Published: September 04, 2024
Comprehensive genomic and transcriptomic analysis enables molecularly guided therapy options in peritoneal and pleural mesothelioma.
Journal: ESMO open
Published: August 16, 2024
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS).
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 12, 2024
Identification of Succinate Dehydrogenase Gene Variant Carriers by Blood Biomarkers.
Journal: Journal of the Endocrine Society
Published: May 24, 2024
Last Updated: 09/26/2026