Name and surname:
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Mgr. Martina Pečimonová, 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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Researcher | Geneton ltd. | 19.09.2017-31.10.2019 |
Researcher | Biomedical Research Center of the Slovak Academy of Sciences | 01.11.2019-31.01.2020 |
Researcher | Comenius University in Bratislava, Faculty of Natural Sciences | 15.03.2020 |
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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Practical Course in Human Genetics | Biology | I. | Biology |
Advanced Practical Course in Molecular Biology | Biology | I. | Biology |
Soltysova A., Dvorska D., Kajabova V. H., Pecimonova M., Cepcekova K., Ficek A., Demkova L., Buocikova V., Babal P., Juras I., Janikova K., Kasubova I., Samec M., Brany D., Lyskova D., Valaskova J., Dankova Z., Smolkova B., Furdova A. Uncovering accurate prognostic markers for high-risk uveal melanoma through DNA methylation profiling. Clinical and translational medicine. 2023; 13(7), e1317.
Pecimonova M, Radvanszky J, Smolak D, Budis J, Lichvar M, Kristinova D, Rozova I, Turna J, Szemes T. Admixed phenotype of NEDD4L associated periventricular nodular heterotopia: A case report. Medicine (Baltimore). 2021 Jun 4;100(22):e26136.
Pecimonova M, Kluckova D, Csicsay F, Reblova K, Krahulec J, Procházkova D, Skultety L, Kadasi L, Soltysova A. Structural and functional impact of seven missense variants of phenylalanine hydroxylase. Genes (Basel). 2019 Jun 15;10(6):459.
Pecimonova M, Polak E, Csicsay F, Reblova K, Stojiljkovic M, Levarski Z, Skultety L, Kadasi L, Soltysova A. Functional and structural characterisation of 5 missense mutations of the phenylalanine hydroxylase. Gen Physiol Biophys. 2017 Oct;36(4):361-371.
Dubinová M, Straka M, Predný J, Struhárňanská E, Pečimonová M, Verešpejová A, Lenártová PD, Oltman M, Koller T, Stuchlík S, Liptáková A, Kristian P.: Quantitative determination of pregenomic RNA as a new biomarker of viral hepatitis B in patients‘ plasma. Lekarsky Obzor, 2022; 71(4), pp. 163–167.
Soltysova A., Dvorska D., Kajabova V. H., Pecimonova M., Cepcekova K., Ficek A., Demkova L., Buocikova V., Babal P., Juras I., Janikova K., Kasubova I., Samec M., Brany D., Lyskova D., Valaskova J., Dankova Z., Smolkova B., Furdova A. Uncovering accurate prognostic markers for high-risk uveal melanoma through DNA methylation profiling. Clinical and translational medicine. 2023; 13(7), e1317.
Pecimonova M, Radvanszky J, Smolak D, Budis J, Lichvar M, Kristinova D, Rozova I, Turna J, Szemes T. Admixed phenotype of NEDD4L associated periventricular nodular heterotopia: A case report. Medicine (Baltimore). 2021 Jun 4;100(22):e26136.
Pecimonova M, Kluckova D, Csicsay F, Reblova K, Krahulec J, Procházkova D, Skultety L, Kadasi L, Soltysova A. Structural and functional impact of seven missense variants of phenylalanine hydroxylase. Genes (Basel). 2019 Jun 15;10(6):459.
Dubinová M, Straka M, Predný J, Struhárňanská E, Pečimonová M, Verešpejová A, Lenártová PD, Oltman M, Koller T, Stuchlík S, Liptáková A, Kristian P.: Quantitative determination of pregenomic RNA as a new biomarker of viral hepatitis B in patients‘ plasma. Lekarsky Obzor, 2022; 71(4), pp. 163–167.
Lalonde E, Li D, Ewens K, Shields CL, Ganguly A. Genome-Wide Methylation Patterns in Primary Uveal Melanoma: Development of MethylSig-UM, an Epigenomic Prognostic Signature to Improve Patient Stratification. Cancers (Basel). 2024;16(15):2650. Published 2024 Jul 25.
Pašalić D, Nikuševa-Martić T, Sekovanić A, Kaštelan S. Genetic and Epigenetic Features of Uveal Melanoma-An Overview and Clinical Implications. Int J Mol Sci. 2023;24(16):12807. Published 2023 Aug 15.
Fuentes-Rodriguez A, Mitchell A, Guérin SL, Landreville S. Recent Advances in Molecular and Genetic Research on Uveal Melanoma. Cells. 2024;13(12):1023. Published 2024 Jun 12.
Liu J, Hu J, Duan Y, et al. Genetic analysis of periventricular nodular heterotopia 7 caused by a novel NEDD4L missense mutation: Case and literature summary. Mol Genet Genomic Med. 2023;11(7):e2169.
Santilli C, Aggarwal A, Dailey C, McClelland C. Ophthalmic Findings Associated with NEDD4L-related Disorder. J AAPOS. 2022 Jun;26(3):164-167. doi: 10.1016/j.jaapos.2022.02.012. Epub 2022 May 13. PMID: 35577021.
APVV-0240-12 - member - Functional analysis of newly identified DNA variants in genes responsible for cystic fibrosis and phenylketonuria
ITMS 26240220058 - member - Diagnostics of socially important disorders in Slovakia, based on modern biotechnologies
VEGA 1/0434/24 - member - Epigenetic modulation using CRISPR/Cas9 in the study of genes with a significant role in acquired chemoresistance
APVV-23-0294 - member -Targeting high-order chromatin regulation for the treatment of poor prognosis uveal melanoma