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Email:
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jana.neupauerova@upjs.sk | |
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Homepage:
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https://www.upjs.sk/LF/zamestnanec/jana.neupauerova | |
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Faculty:
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LF UPJŠ
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Pavol Jozef Šafárik University in Košice Faculty of Medicine
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Department:
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ULBL
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Department of Medical Biology
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Office:
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MA5O518 | |
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Phone:
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+421 55 234 3349 | |
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ORCID ID:
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0000-0001-7438-2062 |
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Profile courses
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Biology 1 - General medicine, I.+II. degree
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Selected publications
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Neupauerová J., Vraná M., Ratajová E., Nazarová S., Půbalová Š., Šálek C., Crivello P., Březinová J., Beličková M., Dyr J.E. The formation of a somatic mutation in the HLA-B gene throughout the development of the disease from severe aplastic anaemia to acute myeloid leukaemia. HLA. 94, (2019). 30–33. |
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Sedláčková, L., Laššuthová, P., Štěrbová, K., Haberlová, J., Vyhnálková, E., Neupauerová, J., Staněk, D., Šedivá, M., Kršek, P., Seeman, P.: UBTF Mutation Causes Complex Phenotype of Neurodegeneration and Severe Epilepsy in Childhood. Neuropediatrics. 50, 1 (2019), 57 – 60. |
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Neupauerová J., Štěrbová K., Komárek V., Gřegořová A., Vlčková M., Staněk D., Seeman P., Laššuthová P., Havlovicová M. Schinzel--Giedion Syndrome: First Czech Patients Confirmed by Molecular Genetic Analysis. Journal of Pediatric Neurology. 17, 3 (2019), 125 - 127. |
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Selected projects
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Project: Precise identification of rare and unique HLA allele detected at Department of HLA and their registration in IMGT/HLA database, 2018 – 2019, Prague, Czech Republic |
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International mobilities and visits
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Centro de Investigación Príncipe Felipe, Unit of Rare Neurodegenerative Diseases, Spain, Valencia, One week/July/2016, Internship abroad
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