Name and surname:
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RNDr. Dušan Loderer, 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 | Jessenius Faculty of Medicine in Martin, Comenius University Bratislava | 2018-current |
IV.a - Activity description, course name, other | IV.b - Name of the institution | IV.c - Year |
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Nextseq 550Dx Training | GeneTiCA s.r.o | 2020 |
NovaSeq 6000 Training | GeneTiCA s.r.o | 2023 |
Grendár M, Loderer D, Laučeková Z, Švecová I, Hrtánková M, Hornáková A, Nagy B, Žúbor P, Lasabová Z, Danko J. Uncertainty of fetal fraction determination in Non-Invasive Prenatal Screening by highly polymorphic SNPs. J Biotechnol. 2019 Jun 20;299:32-36. doi: 10.1016/j.jbiotec.2019.04.020. Epub 2019 Apr 26. PMID: 31034863.
Grendár Marián, Loderer Dušan, Lasabová, Zora, Danko Ján. Method for determining the qualification of a sample for fetal aneuploidy status determination in Non-Invasive Prenatal Testing = EP17203198.1 [EP3447153, 10.09.2020]. – Mníchov (Nemecko) : European Patent Office, 08.12.2020. – 35 s. : text, tab.
Grendár Marián, Loderer Dušan, Lasabová Zora, Danko Ján. Method for determining the uncertainty of the degree of placental mosaicism of a sample in Non-Invasive Prenatal Screening = PCT/EP2020/054287 [WO 2020/169635A1, 27.08.2020]. – Ženeva (Švajčiarsko) : World Intellectual Property Organization, 28.04.2020. – 93 s. : text, graf.
Simurda T, Snahnicanova Z, Loderer D, Sokol J, Stasko J, Lasabova Z, Kubisz P. Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia. Semin Thromb Hemost. 2016 Jun;42(4):455-8. doi: 10.1055/s-0036-1581104. Epub 2016 May 5. PMID: 27148845.
Simurda T, Zolkova J, Snahnicanova Z, Loderer D, Skornova I, Sokol J, Hudecek J, Stasko J, Lasabova Z, Kubisz P. Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders. Int J Mol Sci. 2017 Dec 29;19(1):100. doi: 10.3390/ijms19010100. PMID: 29286337; PMCID: PMC5796050.
Simurda T, Zolkova J, Kolkova Z, Loderer D, Dobrotova M, Skornova I, Brunclíkova M, Grendar M, Lasabova Z, Stasko J, Kubisz P. Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia. Int J Hematol. 2020 Jun;111(6):795-802. doi: 10.1007/s12185-020-02842-9. Epub 2020 Mar 12. PMID: 32166693.
Tobiášová K, Barthová M, Janáková Ľ, Lešková K, Farkašová A, Loderer D, Grendár M, Plank L. Discordant ALK Status in Non-Small Cell Lung Carcinoma: A Detailed Reevaluation Comparing IHC, FISH, and NGS Analyses. Int J Mol Sci. 2024 Jul 26;25(15):8168. doi: 10.3390/ijms25158168. PMID: 39125737; PMCID: PMC11312000.
Janíková K, Váňová B, Grendár M, Samec M, Loderer D, Kašubová I, Škereňová M, Farkašová A, Scheerová K, Slávik P, Lasabová Z, Danková Z, Strnádel J, Halašová E, Plank L. Small-scale variants and large deletions in BRCA1/2 genes in Slovak high-grade serous ovarian cancer. Pathol Res Pract. 2023 Jun;246:154475. doi: 10.1016/j.prp.2023.154475. Epub 2023 Apr 20. PMID: 37121054.
Holubekova V, Loderer D, Grendar M, Mikolajcik P, Kolkova Z, Turyova E, Kudelova E, Kalman M, Marcinek J, Miklusica J, Laca L, Lasabova Z. Differential gene expression of immunity and inflammation genes in colorectal cancer using targeted RNA sequencing. Front Oncol. 2023 Oct 5;13:1206482. doi: 10.3389/fonc.2023.1206482. PMID: 37869102; PMCID: PMC10586664.
Loderer, D., Hornáková, A., Tobiášová, K., Lešková, K., Halašová, E., Danková, Z., Biringer, K., Kúdela, E., Rokos, T., Dzian, A., Miklušica, J., Mikolajčík, P., Smolár, M., Plank, L., Grendár, M."Comparison of next‑generation sequencing quality metrics and concordance in the detection of cancer‑specific molecular alterations between formalin‑fixed paraffin‑embedded and fresh‑frozen samples in comprehensive genomic profiling with the Illumina® TruSight Oncology 500 assay". Experimental and Therapeutic Medicine 29, no. 4 (2025): 64. https://doi.org/10.3892/etm.2025.12814
Mohsenian, Samin - Palla, Roberta - Menegatti, Marzia - Cairo, Andrea - Lecchi, Anna - Casini, Alessandro - Neerman-Arbez, Marguerite - Asselta, Rosanna - Scardo, Sara - Siboni, Simona Maria - Blatny, Jan - Zapletal, Ondrej - Schved, Jean Francois - Giansily-Blaizot, Muriel - Halimeh, Susan - Daoud, Mohamad Ayman - Platokouki, Helen - Pergantou, Helen - Schutgens, Roger E.G. - Van Haaften-Spoor, Monique - Brons, Paul - Laros-Van Gorkom, Britta - Van Pinxten, Elise - Borhany, Munira - Fatima, Naveena. Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database [elektronický dokument]. DOI 10.1182/bloodadvances.2023012186 In: Blood Advances. Washington: American Society of Hematology, 2024,
Nencini, Francesca - Bettiol, Alessandra - Argento, Flavia Rita - Borghi, Serena - Giurranna, Elvira - Emmi, Giacomo - Prisco, Domenico - Taddei, Niccolò - Fiorillo, Claudia - Becatti, Matteo. Post-translational modifications of fibrinogen: implications for clotting, fibrin structure and degradation [elektronický dokument]. DOI 10.1186/s43556-024-00214-x In: Molecular biomedicine. Singapur: Springer Nature,
Jung, Ana - Droit, Lindsay - Febles, Binita - Fronick, Catarina - Cook, Lisa - Handley, Scott A. - Parikh, Bijal A. - Wang, David. Tracking the prevalence and emergence of SARS-CoV-2 variants of concern using a regional genomic surveillance program [elektronický dokument]. DOI 10.1128/spectrum.04225-23 In: Microbiology Spectrum. Washington: American Society for Microbiology, 2024, Roč. 12, č. 8
Casini, Alessandro. Congenital Fibrinogen Disorders, Diagnosis, and Management [elektronický dokument]. DOI 10.1007/978-3-031-43156-2_6 In: Congenital Bleeding Disorders: Diagnosis and Management. Cham: Springer Nature, 2023, s. 175-190
van Beek, D. M. - Straver, R. - Weiss, M. M. - Boon, E. M. J. - Huijsdens-van Amsterdam, K. - Oudejans, C. B. M. - Reinders, M. J. T. - Sistermans, E. A. Článok [elektronický dokument] In: Prenatal Diagnosis: the Official Journal of the International Society for Prenatal Diagnosis. Charlottesville: International Society for Prenatal Diagnosis, 2017, Roč. 37, č. 12