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Dušan Loderer · SciRah

Researcher profile · Semantic Scholar

Dušan Loderer

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Dušan Loderer — researcher profile on SciRah

h-index: 12
Works: 38
Citations: 502

Most-cited papers

Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype
T. Simurda, M. Brunclíková, R. Asselta, S. Caccia +8 more
2020International Journal of Molecular Sciences75 citations Open access
Semantic Scholar
Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management
T. Simurda, R. Asselta, J. Žolková, M. Brunclíková +8 more
2021Diagnostics64 citations Open access
Semantic Scholar
Association of Circulating miRNA Expression with Preeclampsia, Its Onset, and Severity
Z. Kolková, V. Holubeková, M. Grendár, M. Ňachajová +6 more
2021Diagnostics35 citations Open access
Semantic Scholar
Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders
T. Simurda, J. Žolková, Z. Sňahničanová, Dušan Loderer +6 more
2017International Journal of Molecular Sciences35 citations Open access
Semantic Scholar
Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and Thrombosis
M. Brunclíková, T. Simurda, J. Žolková, Miroslava Sterankova +8 more
2022Journal of Clinical Medicine33 citations Open access
Semantic Scholar
Diagnostic Potential of MicroRNAs as Biomarkers in the Detection of Preeclampsia
Andrea Hornáková, Z. Kolková, V. Holubeková, Dušan Loderer +3 more
2020Genetic Testing and Molecular Biomarkers33 citations
Semantic Scholar
A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype
T. Simurda, Rui Vilar, J. Žolková, E. Ceznerová +10 more
2020Biomedicines29 citations Open access
Semantic Scholar
Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia
T. Simurda, J. Žolková, Z. Kolková, Dušan Loderer +7 more
2020International journal of hematology29 citations
Semantic Scholar
Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop)
T. Simurda, S. Caccia, R. Asselta, J. Žolková +6 more
2019Journal of Thrombosis and Thrombolysis25 citations
Semantic Scholar
Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia
T. Simurda, Z. Sňahničanová, Dušan Loderer, J. Sokol +3 more
2016Seminars in Thrombosis and Hemostasis24 citations Open access
Semantic Scholar
Genetic Background of von Willebrand Disease: History, Current State, and Future Perspectives
J. Žolková, J. Sokol, T. Simurda, Ľ. Vádelová +8 more
2019Seminars in Thrombosis and Hemostasis22 citations
Semantic Scholar
Dual activities of emodin--DNA protectivity vs mutagenicity.
A. Ševčovičová, Kristína Bodnárová, Dušan Loderer, Petronela Imreová +2 more
2014Neuro - endocrinology letters13 citations
Semantic Scholar
Systematic Genomic Surveillance of SARS-CoV-2 Virus on Illumina Sequencing Platforms in the Slovak Republic—One Year Experience
Diana Rusňáková, T. Sedláčková, P. Radvák, M. Böhmer +29 more
2022Viruses10 citations Open access
Semantic Scholar
Comparison of SARS-CoV-2 Detection by Rapid Antigen and by Three Commercial RT-qPCR Tests: A Study from Martin University Hospital in Slovakia
Z. Danková, E. Nováková, M. Škereňová, V. Holubeková +27 more
2021International Journal of Environmental Research and Public Health10 citations Open access
Semantic Scholar
Association between 3'UTR polymorphisms in genes ACVR2A, AGTR1 and RGS2 and preeclampsia.
A. Mendelová, V. Holubeková, M. Grendár, P. Zubor +6 more
2018General Physiology and Biophysics10 citations Open access
Semantic Scholar
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
Dušan Loderer, Andrea Hornáková, Katarína Tobiášová, K. Lešková +11 more
2025Experimental and Therapeutic Medicine8 citations
Semantic Scholar
Diagnostic value of clot formation parameters determined by rotational thromboelastometry in 63 patients with congenital dysfibrinogenemia
T. Simurda, Rita Marchi, A. Casini, M. Neerman-Arbez +8 more
2024Blood Coagulation and Fibrinolysis6 citations Open access
Semantic Scholar
Differential gene expression of immunity and inflammation genes in colorectal cancer using targeted RNA sequencing
V. Holubeková, Dušan Loderer, M. Grendár, P. Mikolajčík +8 more
2023Frontiers in Oncology5 citations Open access
Semantic Scholar
CNHplus: the chromosomal copy number heterogeneity which respects biological constraints
M. Grendár, Petr Martínek, Dušan Loderer, O. Ondič
2022bioRxiv5 citations Open access
Semantic Scholar
Small-scale variants and large deletions in BRCA1/2 genes in Slovak high-grade serous ovarian cancer.
K. Janíková, B. Váňová, M. Grendár, Marek Samec +11 more
2023Pathology, Research and Practice4 citations
Semantic Scholar
High-grade serous ovarian carcinoma and detection of inactivated BRCA genes from biopsy material of Slovak patients.
K. Janíková, B. Váňová, M. Grendár, Marek Samec +9 more
2021Neoplasma (Bratislava)4 citations Open access
Semantic Scholar
Uncertainty of fetal fraction determination in Non-Invasive Prenatal Screening by highly polymorphic SNPs.
M. Grendár, Dušan Loderer, Z. Laučeková, I. Švecová +6 more
2019Journal of Biotechnology4 citations Open access
Semantic Scholar
A comment on “Comparing methods for fetal fraction determination and quality control of NIPT samples”
M. Grendár, Dušan Loderer, Z. Lasabová, J. Danko
2017Prenatal Diagnosis4 citations
Semantic Scholar
Discordant ALK Status in Non-Small Cell Lung Carcinoma: A Detailed Reevaluation Comparing IHC, FISH, and NGS Analyses
Katarína Tobiášová, M. Barthová, Ľuboslava Janáková, K. Lešková +4 more
2024International Journal of Molecular Sciences3 citations Open access
Semantic Scholar
Detection of therapeutically relevant and concomitant rare somatic variants in colorectal cancer.
P. Mikolajčík, Z. Lasabová, Dušan Loderer, M. Grendár +12 more
2021Neoplasma (Bratislava)3 citations Open access
Semantic Scholar
Novel Fibrinogen Bbeta Chain Mutation as an Underlying Mechanism of Afibrinogenemia?
Lucia Stančiaková, T. Simurda, J. Staško, Z. Sňahničanová +3 more
2015Seminars in Thrombosis and Hemostasis3 citations Open access
Semantic Scholar
Establishment of PANDA - a new human pancreatic ductal adenocarcinoma cell line with 3D cell culture technology.
Romana Zahumenska, M. Kalman, J. Marcinek, S. Mersakova +22 more
2021Neoplasma (Bratislava)2 citations Open access
Semantic Scholar
Establishment of Coala: a novel 3D and 2D cancer cell line derived from colorectal cancer liver metastasis
S. Mersakova, J. Marcinek, D. Brany, Oľga Chodelková +30 more
2025Human Cell1 citations
Semantic Scholar
A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemia
M. Drotárová, R. Asselta, Sonia Caccia, I. Škorňová +6 more
2025Blood Coagulation and Fibrinolysis1 citations Open access
Semantic Scholar
SPP1 as a Potential Stage-Specific Marker of Colorectal Cancer
E. Túryová, P. Mikolajčík, M. Kalman, Dušan Loderer +7 more
2025Cancers1 citations
Semantic Scholar
The Importance and Complications of Sequencing of Von Willebrand Gene in Von Willebrand Disease
J. Žolková, J. Sokol, T. Simurda, Ľ. Vádelová +7 more
2019Acta Medica Martiniana1 citations Open access
Semantic Scholar
Preliminary miRNA profiling of plasma from patients infected with distinct SARS-CoV-2 variants
Ivana Baranová, Dana Dvorská, Andrea Kapinova, D. Brany +13 more
2026Molecular Biology Reports0 citations Open access
Semantic Scholar
PB1362 Functional, structural and biomechanical characterization of FGA variants in congenital dysfibrinogenemia
T. Simurda, E. Ceznerová, Z. Kolková, Dušan Loderer +8 more
2026Research and Practice in Thrombosis and Haemostasis0 citations Open access
Semantic Scholar
Identification of genetic variants in the FGB gene associated with congenital hypofibrinogenemia with divergent clinical phenotype
K. Belakova, R. Asselta, Sonia Caccia, Z. Kolková +8 more
2026Annals of Hematology0 citations Open access
Semantic Scholar
Targeted NGS of Preoperative Circulating Cell-Free DNA in Colorectal Cancer.
Mária Škereňová, E. Halašová, M. Šarlinová, Dušan Loderer +8 more
2026Current molecular medicine0 citations
Semantic Scholar
PB1379 Identification of pathogenic variants in the fibrinogen Bβ chain gene causing congenital hypofibrinogenemia
K. Belakova, T. Simurda, R. Asselta, S. Caccia +7 more
2026Research and Practice in Thrombosis and Haemostasis0 citations Open access
Semantic Scholar
A comment on “Predicting fetoplacental chromosomal mosaicism during non‐invasive prenatal testing”
M. Grendár, Dušan Loderer, Z. Lasabová, J. Danko
2018Prenatal Diagnosis0 citations
Semantic Scholar
P-1.134Mechanisms of emodin bioprotectivity
A. Ševčovičová, Kristína Bodnárová, Dušan Loderer, Petronela Imreová +2 more
20140 citations
Semantic Scholar

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Z. Lasabová×20
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Z. Lasabová — researcher profile on SciRah
M. Grendár×18
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M. Grendár — researcher profile on SciRah
T. Simurda×16
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T. Simurda — researcher profile on SciRah
J. Staško×16
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×15

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Z. Kolková — researcher profile on SciRah

J. Žolková×11

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I. Škorňová×11

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M. Brunclíková×9

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E. Halašová×9

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V. Holubeková×7

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Z. Sňahničanová×7

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