Name and surname:
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doc. Mgr. Andrej Ficek, PhD.
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Document type:
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Research/art/teacher profile of a person
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The name of the university:
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Comenius University Bratislava
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The seat of the university:
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Šafárikovo námestie 6, 818 06 Bratislava
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III.a - Occupation-position | III.b - Institution | III.c - Duration |
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associate professor | Comenius University in Bratislava, Faculty of Natural Sciences | 2022-present |
assistant professor | Comenius University in Bratislava, Faculty of Natural Sciences | 2003 - 2021 |
V.1.a - Name of the profile course | V.1.b - Study programme | V.1.c - Degree | V.1.d - Field of study |
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Human Genetics | Biológia/Medicínska biológia | I. | Biology |
Human Molecular Genetics | Molecular Biology | II. | Biology |
Advanced DNA Analysis Methods in the Identification and Typisation of Organisms | Molecular Biology | II. | Biology |
Biotechnology and Biomedicine | Molecular Biology | II. | Biotechnology |
V.2.a - Name of the study programme | V.2.b - Degree | V.2.c - Field of study |
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Molecular biology | II. | Biology |
Molecular biology | III. | Biology |
V.3.a - Name of the field of habilitation procedure and inaugural procedure | V.3.b - Study field to which it is assigned |
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Molecular biology | Molecular biology |
V.5.a - Name of the course | V.5.b - Study programme | V.5.c - Degree | V.5.d - Field of study |
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Seminar on human genetics | Molecular Biology | II. | Biology |
Human Genomics | Molecular Biology | II. | Biology |
Practical course in human genetics | Biology | I. | Biology |
Medova V, Hulinkova I, Laiferova N, Urdova V, Ciznar P, Dolnikova D, Krasnanova V, Fabri O, Ficek A, Soltysova A. The importance of defining the age-specific TREC/KREC levels for detection of various inborn errors of immunity in pediatric and adult patients. Clin Immunol. 2022 Dec;245:109155. doi: 10.1016/j.clim.2022.109155. Epub 2022 Oct 13. PMID: 36243346.
Krivoňáková N, Šoltýsová A, Tamáš M, Takáč Z, Krahulec J, Ficek A, Gál M, Gall M, Fehér M, Krivjanská A, Horáková I, Belišová N, Bímová P, Škulcová AB, Mackuľak T. Mathematical modeling based on RT-qPCR analysis of SARS-CoV-2 in wastewater as a tool for epidemiology. Sci Rep. 2021 Sep 30;11(1):19456. doi: 10.1038/s41598-021-98653-x. PMID: 34593871; PMCID: PMC8484274.
Etzler J, Peyrl A, Zatkova A, Schildhaus HU, Ficek A, Merkelbach-Bruse S, Kratz CP, Attarbaschi A, Hainfellner JA, Yao S, Messiaen L, Slavc I, Wimmer K. RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference. Hum Mutat. 2008 Feb;29(2):299-305. doi: 10.1002/humu.20657. PMID: 18030674.
Minárik G, Ferák V, Feráková E, Ficek A, Poláková H, Kádasi L. High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL). Gen Physiol Biophys. 2003 Dec;22(4):549-56. PMID: 15113126.
Dusinská M, Ficek A, Horská A, Raslová K, Petrovská H, Vallová B, Drlicková M, Wood SG, Stupáková A, Gasparovic J, Bobek P, Nagyová A, Kováciková Z, Blazícek P, Liegebel U, Collins AR. Glutathione S-transferase polymorphisms influence the level of oxidative DNA damage and antioxidant protection in humans. Mutat Res. 2001 Oct 1;482(1-2):47-55. doi: 10.1016/s0027-5107(01)00209-3. PMID: 11535248.
Medova V, Hulinkova I, Laiferova N, Urdova V, Ciznar P, Dolnikova D, Krasnanova V, Fabri O, Ficek A, Soltysova A. The importance of defining the age-specific TREC/KREC levels for detection of various inborn errors of immunity in pediatric and adult patients. Clin Immunol. 2022 Dec;245:109155. doi: 10.1016/j.clim.2022.109155. Epub 2022 Oct 13. PMID: 36243346.
Lundy L, Fatta-Kassinos D, Slobodnik J, Karaolia P, Cirka L, Kreuzinger N, Castiglioni S, Bijlsma L, Dulio V, Deviller G, Lai FY, Alygizakis N, Barneo M, Baz-Lomba JA, Béen F, Cíchová M, Conde-Pérez K, Covaci A, Donner E, Ficek A, Hassard F, Hedström A, Hernandez F, Janská V, Jellison K, Hofman J, Hill K, Hong PY, Kasprzyk-Hordern B, Kolarević S, Krahulec J, Lambropoulou D, de Llanos R, Mackuľak T, Martinez-García L, Martínez F, Medema G, Micsinai A, Myrmel M, Nasser M, Niederstätter H, Nozal L, Oberacher H, Očenášková V, Ogorzaly L, Papadopoulos D, Peinado B, Pitkänen T, Poza M, Rumbo-Feal S, Sánchez MB, Székely AJ, Soltysova A, Thomaidis NS, Vallejo J, van Nuijs A, Ware V, Viklander M. Making Waves: Collaboration in the time of SARS-CoV-2 - rapid development of an international co-operation and wastewater surveillance database to support public health decision-making. Water Res. 2021 Jul 1;199:117167. doi: 10.1016/j.watres.2021.117167. Epub 2021 Apr 22. PMID: 34015748; PMCID: PMC8060897.
Kluckova D, Kolnikova M, Lacinova L, Jurkovicova-Tarabova B, Foltan T, Demko V, Kadasi L, Ficek A, Soltysova A. A Study among the Genotype, Functional Alternations, and Phenotype of 9 SCN1A Mutations in Epilepsy Patients. Sci Rep. 2020 Jun 24;10(1):10288. doi: 10.1038/s41598-020-67215-y. PMID: 32581296; PMCID: PMC7314844.
Zahradníková, E., Ficek, A., Brejová, B., Vinař, T., & Mičieta, K. (2020). Mosaicism in old trees and its patterns. Trees, 34(2), 357-370.
Budiš J, Kucharík M, Ďuriš F, Gazdarica J, Zrubcová M, Ficek A, Szemes T, Brejová B, Radvanszky J. Dante: genotyping of known complex and expanded short tandem repeats. Bioinformatics. 2019 Apr 15;35(8):1310-1317. doi: 10.1093/bioinformatics/bty791. PMID: 30203023.
Polak, E., Ficek, A., Radvanszky, J., Soltysova, A., Urge, O., Cmelova, E., ... & Kadasi, L. (2013). Phenylalanine hydroxylase deficiency in the Slovak population: Genotype–phenotype correlations and genotype-based predictions of BH4-responsiveness. Gene, 526(2), 347-355. : Blau, N. Genetics of Phenylketonuria: Then and Now (2016) Human Mutation, 37 (6), pp. 508-515.
Radvansky, J., Ficek, A., & Kadasi, L. (2011). Upgrading molecular diagnostics of myotonic dystrophies: multiplexing for simultaneous characterization of the DMPK and ZNF9 repeat motifs. Molecular and Cellular Probes, 25(4), 182-185. Yum, K., Wang, E.T., Kalsotra, A. Myotonic dystrophy: disease repeat range, penetrance, age of onset, and relationship between repeat size and phenotypes (2017) Current Opinion in Genetics and Development, 44, pp. 30-37.
Etzler, J., Peyrl, A., Zatkova, A., Schildhaus, H. U., Ficek, A., Merkelbach‐Bruse, S., ... & Wimmer, K. (2008). RNA‐based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference. Human mutation, 29(2), 299-305.: Ripperger, T., Schlegelberger, B. Acute lymphoblastic leukemia and lymphoma in the context of constitutional mismatch repair deficiency syndrome (2016) European Journal of Medical Genetics, 59 (3), pp. 133-142.
Kluckova, D., Kolnikova, M., Lacinova, L., Jurkovicova-Tarabova, B., Foltan, T., Demko, V., ... & Soltysova, A. (2020). A study among the genotype, functional alternations, and phenotype of 9 SCN1A mutations in epilepsy patients. Scientific Reports, 10(1), 1-13.: Meisler, M.H., Hill, S.F., Yu, W. Sodium channelopathies in neurodevelopmental disorders (2021) Nature Reviews Neuroscience, 22 (3), pp. 152-166.
Soltysova, A., Tothova Tarova, E., Ficek, A., Baldovic, M., Polakova, H., Kayserova, H., & Kadasi, L. (2018). Comprehensive genetic study of cystic fibrosis in Slovak patients in 25 years of genetic diagnostics. The Clinical Respiratory Journal, 12(3), 1197-1206.: Scotet, V., L’hostis, C., Férec, C. The changing epidemiology of cystic fibrosis: Incidence, survival and impact of the CFTRGene discovery (2020) Genes, 11 (6), art. no. 589, .
VEGA 1/0190/19 Identifikácia genetických determinantov vrodených porúch imunity. Principal investigator
VEGA 1/0434/24 Možnosti epigenetickej modulácie pomocou CRISPR/Cas9 pri štúdiu génov s významnou úlohou v získanej chemorezistencii.
APVV-23-0294 Cielená modulácia chromatínovej štruktúry v liečbe malígneho melanómu uvey so zlou prognózou.
APVV-21-0197 Preprogramovanie mikroprostredia duktálneho adenokarcinómu pankreasu voči imunoterapii.