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F. Oyen · SciRah

Researcher profile · Semantic Scholar

F. Oyen

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F. Oyen — researcher profile on SciRah

h-index: 26
Works: 76
Citations: 3,060

Most-cited papers

Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes.
P. Johann, S. Erkek, M. Zapatka, K. Kerl +54 more
2016Cancer Cell504 citations Open access
Semantic Scholar
Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.
R. Schneppenheim, M. Frühwald, S. Gesk, M. Hasselblatt +9 more
2010American Journal of Human Genetics317 citations Open access
Semantic Scholar
Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression.
M. Hasselblatt, S. Gesk, F. Oyen, S. Rossi +9 more
2011American Journal of Surgical Pathology230 citations
Semantic Scholar
von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP.
R. Schneppenheim, U. Budde, F. Oyen, Dorothea Angerhaus +11 more
2003Blood230 citations Open access
Semantic Scholar
SMARCA4-mutated atypical teratoid/rhabdoid tumors are associated with inherited germline alterations and poor prognosis
M. Hasselblatt, I. Nagel, F. Oyen, K. Bartelheim +18 more
2014Acta Neuropathologica171 citations Open access
Semantic Scholar
High‐resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors
M. Hasselblatt, Sarah Isken, Anna Linge, K. Eikmeier +10 more
2013Genes, Chromosomes and Cancer149 citations
Semantic Scholar
Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis
M. Hasselblatt, C. Thomas, V. Hovestadt, D. Schrimpf +26 more
2016Acta Neuropathologica137 citations
Semantic Scholar
Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor
U. Kordes, S. Gesk, M. Frühwald, N. Graf +8 more
2010Genes, Chromosomes and Cancer104 citations
Semantic Scholar
Cribriform Neuroepithelial Tumor (CRINET): A Nonrhabdoid Ventricular Tumor With INI1 Loss and Relatively Favorable Prognosis
M. Hasselblatt, F. Oyen, S. Gesk, U. Kordes +7 more
2009Journal of Neuropathology and Experimental Neurology100 citations Open access
Semantic Scholar
Improved 6‐year overall survival in AT/RT – results of the registry study Rhabdoid 2007
K. Bartelheim, K. Nemes, A. Seeringer, K. Kerl +20 more
2016Cancer Medicine85 citations Open access
Semantic Scholar
A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE.
R. Schneppenheim, J. Michiels, T. Obser, F. Oyen +5 more
2010Blood78 citations
Semantic Scholar
A common origin of the 4143insA ADAMTS13 mutation
R. Schneppenheim, J. K. Hovinga, T. Becker, U. Budde +11 more
2006Thrombosis and Haemostasis78 citations
Semantic Scholar
Cribriform neuroepithelial tumor: molecular characterization of a SMARCB1‐deficient non‐rhabdoid tumor with favorable long‐term outcome
P. Johann, V. Hovestadt, C. Thomas, A. Jeibmann +22 more
2017Brain Pathology67 citations Open access
Semantic Scholar
Gene conversions are a common cause of von Willebrand disease
P. K. Gupta, E. Adamtziki, U. Budde, M. Jaiprakash +8 more
2005British Journal of Haematology56 citations
Semantic Scholar
Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults
C. Thomas, A. Wefers, S. Bens, K. Nemes +25 more
2019Acta Neuropathologica50 citations
Semantic Scholar
Sellar Region Atypical Teratoid/Rhabdoid Tumors (ATRT) in Adults Display DNA Methylation Profiles of the ATRT-MYC Subgroup
P. Johann, S. Bens, F. Oyen, R. Wagener +18 more
2018American Journal of Surgical Pathology49 citations
Semantic Scholar
Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysis
T. Holsten, S. Bens, F. Oyen, K. Nemes +6 more
2018European Journal of Human Genetics49 citations Open access
Semantic Scholar
A common 253‐kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3
R. Schneppenheim, G. Castaman, Augusto B. Federici, W. Kreuz +4 more
2007Journal of Thrombosis and Haemostasis41 citations Open access
Semantic Scholar
Characterisation of mutations and molecular studies of type 2 von Willebrand disease
F. Ahmad, R. Jan, M. Kannan, T. Obser +5 more
2012Thrombosis and Haemostasis36 citations
Semantic Scholar
Small cell undifferentiated (SCUD) hepatoblastomas: All malignant rhabdoid tumors?
C. Vokuhl, F. Oyen, B. Häberle, D. V. von Schweinitz +2 more
2016Genes, Chromosomes and Cancer35 citations
Semantic Scholar
Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor Suppressor.
V. Stahn, I. Nagel, S. Fischer-Huchzermeyer, F. Oyen +9 more
2016American Journal of Pathology34 citations Open access
Semantic Scholar
von Willebrand disease type 2A phenotypes IIC, IID and IIE: A day in the life of shear-stressed mutant von Willebrand factor
M. Brehm, V. Huck, C. Aponte-Santamaría, T. Obser +8 more
2014Thrombosis and Haemostasis33 citations
Semantic Scholar
The Prevalence of Sickle Cell Disease and Its Implication for Newborn Screening in Germany (Hamburg Metropolitan Area)
R. Grosse, Z. Lukács, P. Cobos, F. Oyen +4 more
2016Pediatric Blood & Cancer32 citations
Semantic Scholar
Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.
P. Gupta, Rajiv K. Saxena, E. Adamtziki, U. Budde +3 more
2008Blood Cells, Molecules & Diseases31 citations
Semantic Scholar
An Alu‐mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary
A. Mohl, R. Marschalek, T. Masszi, E. Nagy +5 more
2008Journal of Thrombosis and Haemostasis30 citations Open access
Semantic Scholar
Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization
R. Schneppenheim, H. Lenk, T. Obser, J. Oldenburg +5 more
2004Thrombosis and Haemostasis29 citations
Semantic Scholar
Recurrent loss, but lack of mutations, of the SMARCB1 tumor suppressor gene in T-cell prolymphocytic leukemia with TCL1A-TCRAD juxtaposition.
S. Bug, J. Durig, F. Oyen, L. Klein-Hitpass +8 more
2009Cancer Genetics and Cytogenetics25 citations Open access
Semantic Scholar
Administration of recombinant erythropoietin alone does not improve the phenotype in iron refractory iron deficiency anemia patients
K. Lehmberg, R. Grosse, M. Muckenthaler, S. Altamura +7 more
2013Annals of Hematology24 citations
Semantic Scholar
Natural and cryptic peptides dominate the immunopeptidome of atypical teratoid rhabdoid tumors
A. Marcu, A. Schlosser, A. Keupp, N. Trautwein +17 more
2021Journal for ImmunoTherapy of Cancer22 citations Open access
Semantic Scholar
Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS.
L. Baronciani, I. Peake, R. Schneppenheim, A. Goodeve +30 more
2021Blood Advances21 citations Open access
Semantic Scholar
Phenotypic and molecular characterisation of type 3 von Willebrand disease in a cohort of Indian patients
F. Ahmad, U. Budde, R. Jan, F. Oyen +3 more
2013Thrombosis and Haemostasis21 citations
Semantic Scholar
Intracranial hemorrhage in a term newborn with severe von Willebrand disease type 3 associated with sinus venous thrombosis.
V. Wetzstein, U. Budde, F. Oyen, Xiaoqi Ding +3 more
2006Haematologica19 citations
Semantic Scholar
Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw–Schulman Syndrome Investigated in Germany
W. Hassenpflug, T. Obser, J. Bode, F. Oyen +4 more
2018Thrombosis and Haemostasis16 citations
Semantic Scholar
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
R. Pathak, Francesca Zin, C. Thomas, S. Bens +15 more
2021Acta Neuropathologica13 citations Open access
Semantic Scholar
Identifying molecular markers for the sensitive detection of residual atypical teratoid rhabdoid tumor cells.
Tu-Lan Vu-Han, M. Frühwald, M. Hasselblatt, K. Kerl +5 more
2014Cancer Genetics11 citations
Semantic Scholar
Atypical Teratoid/Rhabdoid Tumor (AT/RT) With Molecular Features of Pleomorphic Xanthoastrocytoma
C. Thomas, A. Federico, M. Sill, S. Bens +14 more
2021American Journal of Surgical Pathology10 citations
Semantic Scholar
Platelet-free shear flow assay facilitates analysis of shear-dependent functions of VWF and ADAMTS13.
Emma Kraus, Kristina Kraus, T. Obser, F. Oyen +3 more
2014Thrombosis Research9 citations
Semantic Scholar
Clinical and genetic features of rhabdoid tumors of the heart registered with the European Rhabdoid Registry (EU-RHAB).
K. Bartelheim, D. Sumerauer, U. Behrends, D. Kodetová +10 more
2014Cancer Genetics9 citations
Semantic Scholar
Difficulties in Diagnosing Congenital Thrombotic Thrombocytopenic Purpura
A. Klukowska, Edyta Niewiadomska, U. Budde, F. Oyen +1 more
2010Journal of pediatric hematology/oncology9 citations
Semantic Scholar
Isolated molecular Defects of von Willebrand Factor Binding to Collagen do not correlate with Bleeding Symptoms
R. Schneppenheim, T. Obser, E. Drewke, U. Gross-Wieltsch +6 more
20039 citations
Semantic Scholar
Lack of SMARCB1 expression characterizes a subset of human and murine peripheral T-cell lymphomas
A. Fischer, T. Albert, N. Moreno, M. Interlandi +51 more
2024Nature Communications8 citations Open access
Semantic Scholar
Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumor
C. Thomas, Kathrin Oehl-Huber, S. Bens, Patrick Soschinski +8 more
2021Genes, Chromosomes and Cancer8 citations Open access
Semantic Scholar
Two molecularly distinct atypical teratoid/rhabdoid tumors (or tumor components) occurring in an infant with rhabdoid tumor predisposition syndrome 1
C. Thomas, F. Knerlich-Lukoschus, H. Reinhard, P. Johann +17 more
2019Acta Neuropathologica8 citations
Semantic Scholar
The problem of novel FVIII missense mutations for haemophilia A genetic counseling
R. Schneppenheim, J. Schröder, T. Obser, F. Oyen +2 more
2009Hämostaseologie8 citations
Semantic Scholar
Response to DDAVP in children with von Willebrand disease type 2
R. Schneppenheim, U. Budde, Karin Beutel, W. Hassenpflug +5 more
2009Hämostaseologie7 citations
Semantic Scholar
Inherited Thrombotic Thrombocytopenic Purpura (Upshaw Schulman Syndrome) as Differential Diagnosis to Neonatal Septicaemia with Disseminated Intravascular Coagulation – a Case Series
K. Lehmberg, W. Hassenpflug, I. Klaassen, G. Hillebrand +4 more
2016Zeitschrift für Geburtshilfe und Neonatologie6 citations
Semantic Scholar
Characterisation of two novel large F8 deletions in patients with severe haemophilia A and factor VIII inhibitors
L. Roth, R. Marschalek, J. Oldenburg, F. Oyen +1 more
2010Thrombosis and Haemostasis6 citations
Semantic Scholar
Analysis of the CC chemokine receptor 5Δ32 polymorphism in pediatric liver transplant recipients
Louise Fischer-Maas, R. Schneppenheim, F. Oyen, E. Grabhorn +3 more
2008Pediatric Transplantation6 citations
Semantic Scholar
Beyond genotype: challenges in predicting disease risk for carriers of biallelic perforin variants
Oliver Wegehaupt, Oleg Borisov, E. Sieni, F. Oyen +21 more
2025Blood5 citations Open access
Semantic Scholar
Constitutional mosaicism of pathogenic variants in SMARCB1 in a subset of patients with sporadic rhabdoid tumors.
Lara S. Fleischmann, K. Nemes, S. Glaser, Alexandra G. Kouroukli +9 more
2024Neuro-Oncology5 citations Open access
Semantic Scholar

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