Skálová A, Taheri T, Bradová M, Vaněček T, Franchi A, Slouka D, et al. SMARCB1-deficient sinonasal adenocarcinoma: a rare variant of SWI/SNF-deficient malignancy often misclassified as high-grade non-intestinal-type sinonasal adenocarcinoma or myoepithelial carcinoma. Virchows Arch. 2024;485(2):245-56.
Skálová A, Klubíčková N, Bradová M, Agaimy A, Rupp NJ, Damjanov I, et al. Discovery of Novel TULP4/ACTN4/EWSR1/ACTB::MYB and ESRRG::DNM3 Fusions Expands Molecular Landscape of Adenoid Cystic Carcinoma Beyond Fusions Between MYB/MYBL1 and NFIB Genes. Am J Surg Pathol. 2024;48(12):1503-11.
Skálová A, Bradová M, Michal M, Jr., Mosaieby E, Klubíčková N, Vaněček T, et al. Molecular pathology in diagnosis and prognostication of head and neck tumors. Virchows Arch. 2024;484(2):215-31.
Skálová A, Baněčková M, Laco J, Di Palma S, Agaimy A, Ptáková N, et al. Sclerosing Polycystic Adenoma of Salivary Glands: A Novel Neoplasm Characterized by PI3K-AKT Pathway Alterations-New Insights Into a Challenging Entity. Am J Surg Pathol. 2022;46(2):268-80.
Pancsa T, Klubíčková N, Dashti NK, Machado I, Llombart-Bosch A, Linos K, et al. GLI1::FOXO4-rearranged kidney tumors: a potentially distinct renal subtype within the spectrum of GLI1-altered tumors? Virchows Arch. 2025;486(4):751-7.
Michal M, Ud Din N, Švajdler M, Klubíčková N, Ptáková N, Hájková V, et al. TFG::MET-rearranged soft tissue tumor: A rare infantile neoplasm with a distinct low-grade triphasic morphology. Genes Chromosomes Cancer. 2023;62(5):290-6.
Michal M, Kuruc J, Hájková V, Michalová K, Klubíčková N. S100 and CD34 positive spindle cell tumors of the uterine cervix with EGFR mutation: a hitherto unrecognized neoplasm phenotypically and epigenetically overlapping with "NTRK-rearranged spindle cell neoplasms" of the uterus. Virchows Arch. 2024.
Michal M, Agaimy A, Croce S, Mechtersheimer G, Gross JM, Xing D, et al. PLAG1-Rearranged Uterine Sarcomas: A Study of 11 Cases Showing a Wide Phenotypical Spectrum Not Limited to Myxoid Leiomyosarcoma-Like Morphology. Mod Pathol. 2024;37(9):100552.
Meyer A, Klubíčková N, Mosaieby E, Grossmann P, Kalmykova A, Koshyk O, et al. Biphenotypic sinonasal sarcoma with PAX3::MAML3 fusion transforming into high-grade rhabdomyosarcoma: report of an emerging rare phenomenon. Virchows Arch. 2023;482(4):777-82.
Macedo RT, Baranovska-Andrigo V, Pancsa T, Klubíčková N, Rubin BP, Kilpatrick SE, et al. Nuclear DUX4 immunohistochemistry is a highly sensitive and specific marker for the presence of CIC::DUX4 fusion in CIC-rearranged sarcomas: a study of 48 molecularly confirmed cases. Histopathology. 2025;86(3):423-32.
Lenz J, Klubíčková N, Ptáková N, Hájková V, Grossmann P, Šteiner P, et al. Extraskeletal myxoid chondrosarcoma: A study of 17 cases focusing on the diagnostic utility of INSM1 expression and presenting rare morphological variants associated with non-EWSR1::NR4A3 fusions. Hum Pathol. 2023;134:19-29.
Lasota J, Chłopek M, Kaczorowski M, Natálie K, Ryś J, Kopczyński J, et al. Utility of Immunohistochemistry With Antibodies to SS18-SSX Chimeric Proteins and C-Terminus of SSX Protein for Synovial Sarcoma Differential Diagnosis. Am J Surg Pathol. 2024;48(1):97-105.
João D, Feltri M, Klubickova N, Michal M, Kacerovská D, Skálová A. Apocrine variant of intraductal carcinoma of the parotid gland with sebaceous-like differentiation: expanding morphological and molecular spectrum of an enigmatic entity. Virchows Arch. 2024.
Koshyk O, Dehner CA, van den Hout M, Bempt IV, Sciot R, Huang HY, et al. EWSR1::POU2AF3(COLCA2) Sarcoma: An Aggressive, Polyphenotypic Sarcoma With a Head and Neck Predilection. Mod Pathol. 2023;36(12):100337.
Klubíčková N, Mosaieby E, Ptáková N, Trinquet A, Laé M, Costes-Martineau V, et al. High-grade non-intestinal type sinonasal adenocarcinoma with ETV6::NTRK3 fusion, distinct from secretory carcinoma by immunoprofile and morphology. Virchows Arch. 2023;483(2):187-95.
Klubíčková N, Michal M, Kinkor Z, Soukup J, Ryška A, Brtková J, et al. Poorly differentiated extra-axial extraskeletal chordoma diagnosed by methylation profiling: case report and analysis of brachyury expression in SWI/SNF-deficient tumors. Virchows Arch. 2024;484(4):621-7.
Klubíčková N, Michal M, Agaimy A, Zidar N, Pavlovský M, Yorita K, et al. TIMP3::ALK fusions characterize a distinctive myxoid fibroblastic tumor of the vocal cords: a report of 7 cases. Virchows Arch. 2022;481(5):721-9.
Klubíčková N, Loghides F, van den Hout M, Costes-Martineau V, Ferrara G, Rito M, et al. Expanding the Molecular-genetic Spectrum of Canalicular Adenoma-like Subtype of Pleomorphic Adenoma of Salivary Glands. Am J Surg Pathol. 2025.
Klubíčková N, Kinkor Z, Michal M, Baněčková M, Hájková V, Michálek J, et al. Epithelioid Soft Tissue Neoplasm of the Soft Palate with a PTCH1-GLI1 Fusion: A Case Report and Review of the Literature. Head Neck Pathol. 2022;16(2):621-30.
Klubíčková N, Grossmann P, Šteiner P, Baněčková M, Mosaieby E, Koshyk O, et al. A minority of cases of acinic cell carcinoma of the salivary glands are driven by an NR4A2 rearrangement: the diagnostic utility of the assessment of NR4A2 and NR4A3 alterations in salivary gland tumors. Virchows Arch. 2023;482(2):339-45.
Klubíčková N, Gross JM, Comová K, Kuruc J, Michal M. A novel FUS::NFATC4 fusion detected in a sarcoma with morphological features overlapping with NFATC2 sarcomas. Histopathology. 2024;84(2):413-5.
Klubíčková N, Dermawan JK, Mosaieby E, Martínek P, Vaněček T, Hájková V, et al. Comprehensive clinicopathological, molecular, and methylation analysis of mesenchymal tumors with NTRK and other kinase gene aberrations. J Pathol. 2024;263(1):61-73.
Klubíčková N, Billings S, Dermawan JKT, Molligan JF, Fritchie K. Ossifying fibromyxoid tumours with lipomatous and cartilaginous differentiation: A diagnostic pitfall. Histopathology. 2025;86(6):891-9.
Klubíčková N, Agaimy A, Hájková V, Ptáková N, Grossmann P, Šteiner P, et al. RNA-sequencing of myxoinflammatory fibroblastic sarcomas reveals a novel SND1::BRAF fusion and 3 different molecular aberrations with the potential to upregulate the TEAD1 gene including SEC23IP::VGLL3 and TEAD1::MRTFB gene fusions. Virchows Arch. 2022;481(4):613-20.
Lectures
50. Sjezd českých patologů, 25.-26.9.2025, Plzeň:
Lecture: Diagnostická patologie nádorů slinných žláz: Imunohistochemické a molekulárně-genetické testování.
13th International Arkadi M. Rywlin Pathology Slide Seminar, 16.-18.6.2025, Plzeň, prezentováno doc. Michalem:
Lecture 1: EGFR mutated polypoid spindle cell tumor of the cervix,
Lecture 2: Ossifying fibromyxoid tumor with EP300::BCORL1 fusion.
114th USCAP, 22.-27.3.2025, Boston:
Lecture: Ossifying fibromyxoid tumor: From morphology to methylation profiling.
47. Sjezd českých patologů, 3.-5.11.2022, Praha:
Lecture: Tumory s diferenciací do příčně pruhované svaloviny: přehled novinek a diferenciální diagnostika.
34th European Congress of Pathology, 3-7.9.2022, Basilej:
Lecture 1: A single-institution experience with 128 cases of acinic cell carcinoma: diagnostic utility of NR4A3 and NR4A2 immunohistochemistry in salivary glands pathology,
Lecture 2: A single institution experience with 17 cases of extraskeletal myxoid chondrosarcoma: rare fusion, unusual morphology and the utility of INSM1 immunohistochemistry.
113th USCAP, 23.-28.3.2024, Baltimore, MD, USA
Poster 1: Ossifying fibromyxoid tumors with lipomatous and chondroid differentiation: A diagnostic pitfall,
Poster 2: HMGA2 gene alterations define a distinctive canalicular subtype of salivary pleomorphic adenoma.
112th USCAP, 11.-16.3.2023, New Orleans, LA, USA:
Poster 1: Targeted RNA sequencing of ossifying fibromyxoid tumors reveals novel PHF1 gene fusions and unusual morphologic features,
Poster 2: SMARCB1-deficient sinonasal adenocarcinoma: Rare variant of SWI/SNF-deficient malignancy often misclassified as high-grade non-intestinal adenocarcinoma or myoepithelial carcinoma
111th USCAP, 19.-24.3.2022, Los Angeles, CA, USA:
Poster 1: Targeted DNA and RNA sequencing of soft tissue spindle cell tumors reveals a rare MET::TFG and a novel PWWP2A::RET gene fusions as well as additional recurrent PIK3CA point mutations,
Poster 2: Solitary fibrous tumor with pure round cell morphology: immunohistochemical and molecular study of 15 cases.
Prizes
Jeremy Jass Prize for Research Excellence in Pathology, 2024.