Florian Oyen
Hamburg, HH, Germany
Last Updated: 09/26/2026
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Found 42 publications
Beyond genotype: challenges in predicting disease risk for carriers of biallelic perforin variants.
Journal: Blood
Published: December 06, 2024
The search for the underlying mutations causing VWD in 13 Venezuelan families.
Journal: Thrombosis research
Published: June 01, 2023
Lack of SMARCB1 expression characterizes a subset of human and murine peripheral T-cell lymphomas.
Journal: Nature communications
Published: May 04, 2023
Natural and cryptic peptides dominate the immunopeptidome of atypical teratoid rhabdoid tumors.
Journal: Journal for immunotherapy of cancer
Published: August 26, 2021
Genetic and Clinical Predictors of Left Atrial Thrombus: A Single Center Case-Control Study.
Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
Published: June 29, 2021
Atypical Teratoid/Rhabdoid Tumor (AT/RT) With Molecular Features of Pleomorphic Xanthoastrocytoma.
Journal: The American journal of surgical pathology
Published: March 19, 2021
Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumor.
Journal: Genes, chromosomes & cancer
Published: February 25, 2021
Evidence for a low-penetrant extended phenotype of rhabdoid tumor predisposition syndrome type 1 from a kindred with gain of SMARCB1 exon 6.
Journal: Pediatric blood & cancer
Published: February 13, 2021
Inhibition of nuclear export restores nuclear localization and residual tumor suppressor function of truncated SMARCB1/INI1 protein in a molecular subset of atypical teratoid/rhabdoid tumors.
Journal: Acta neuropathologica
Published: November 06, 2020
Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS.
Journal: Blood advances
Published: September 14, 2020
Last Updated: 09/26/2026