Publications by authors named "Viktor Stranecky"

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Differential regulation of gene co-expression modules in muscles and liver of preterm newborns.
Petra Janovska, Tatyana Kobets, Lenka Steiner Mrazova, Michaela Svobodova, Marketa Tesarova, Viktor Stranecky

Front Cell Dev Biol· October 2025

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Long-Read Sequencing of the VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression.
Alena Vrbacká, Anna Přistoupilová, Kendrah O Kidd, Václav Janoušek, Martin Radina

bioRxiv· September 2025

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Faster postnatal decline in hepatic erythropoiesis than granulopoiesis in human newborns.
Petra Janovska, Kristina Bardova, Zuzana Prouzova, Ilaria Irodenko, Tatyana Kobets, Viktor Stranecky

Front Pediatr· May 2025

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Disruption of Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy.
Lubica Dudakova, Lenka Noskova, Stanislav Kmoch, Martin Filipec, Ales Filous, Viktor Stranecky

Hum Mutat· April 2025

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Misprocessing of α -Galactosidase A, Endoplasmic Reticulum Stress, and the Unfolded Protein Response.
Martina Živná, Gabriela Dostálová, Veronika Barešová, Dita Mušálková, Klára Svojšová

J Am Soc Nephrol· April 2025

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Genetic Predisposition to Male Breast Cancer.
Markéta Janatová, Marianna Borecká, Petra Zemánková, Kateřina Matějková, Petr Nehasil

Folia Biol (Praha)· January 2025

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Correction: Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease.
Magdaléna Neřoldová, Elżbieta Ciara, Janka Slatinská, Soňa Fraňková, Petra Lišková

PLoS One· January 2025

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Genotype is associated with left ventricular reverse remodelling and early events in recent-onset dilated cardiomyopathy.
Milos Kubanek, Jana Binova, Lenka Piherova, Alice Krebsova, Martin Kotrc, Viktor Stranecky

ESC Heart Fail· December 2024

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Genetic Landscape of Amyotrophic Lateral Sclerosis in Czech Patients.
Daniel Baumgartner, Zuzana Mušová, Jana Zídková, Petra Hedvičáková, Eva Vlčková

J Neuromuscul Dis· September 2024

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Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome.
Petr Pecina, Kristýna Čunátová, Vilma Kaplanová, Guillermo Puertas-Frias, Jan Šilhavý

Commun Biol· September 2024

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A comprehensive study evaluating germline FANCG variants in predisposition to breast and ovarian cancer.
Jana Soukupova, Barbora Stastna, Madiha Kanwal, Jan Hojny, Petra Zemankova, Viktor Stranecky

Cancer Med· August 2024

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A comprehensive analysis of germline predisposition to early-onset ovarian cancer.
Klara Horackova, Petra Zemankova, Petr Nehasil, Michal Vocka, Milena Hovhannisyan, Viktor Stranecky

Sci Rep· July 2024

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A Novel Monoallelic Variant Causing Late-Onset ADPKD and Tubulointerstitial Fibrosis.
Elhussein A E Elhassan, Tereza Kmochová, Katherine A Benson, Neil K Fennelly, Veronika Barešová

Kidney Int Rep· July 2024

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A deep intronic recurrent CHEK2 variant c.1009-118_1009-87delinsC affects pre-mRNA splicing and contributes to hereditary breast cancer predisposition.
Petra Zemankova, Marta Cerna, Klara Horackova, Corinna Ernst, Jana Soukupova, Viktor Stranecky

Breast· June 2024

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Sodium-glucose cotransporter 2 inhibitors induce anti-inflammatory and anti-ferroptotic shift in epicardial adipose tissue of subjects with severe heart failure.
Barbora Judita Kasperova, Milos Mraz, Petr Svoboda, Daniel Hlavacek, Helena Kratochvilova, Viktor Stranecky

Cardiovasc Diabetol· June 2024

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Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosis.
Tereza Kmochová, Kendrah O Kidd, Andrew Orr, Aleš Hnízda, Hana Hartmannová

Kidney Int· April 2024

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Increased burden of rare protein-truncating variants in constrained, brain-specific and synaptic genes in extremely impulsively violent males with antisocial personality disorder.
Dita Mušálková, Anna Přistoupilová, Ivana Jedličková, Hana Hartmannová, Helena Trešlová

Genes Brain Behav· February 2024

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Spontaneous nonsense mutation in the tuftelin 1 gene is associated with abnormal hair appearance and amelioration of glucose and lipid metabolism in the rat.
Jan Šilhavý, Petr Mlejnek, Miroslava Šimáková, František Liška, Hana Malínská

Physiol Genomics· January 2024

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ethnic-specific variant reducing binding of membrane-associated guanylate kinases causes focal epilepsy and behavioural disorder.
Lenka Nosková, Yuko Fukata, Viktor Stránecký, Jana Šaligová, Oxana Bodnárová

Brain Commun· October 2023

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Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease.
Magdaléna Neřoldová, Elżbieta Ciara, Janka Slatinská, Soňa Fraňková, Petra Lišková

PLoS One· July 2023

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A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype-phenotype correlation.
Marketa Vlckova, Darina Prchalova, Pavel Zimmermann, Jana Haberlova, Sarka Bendova, Viktor Stranecky

Mol Genet Genomic Med· June 2023

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Germline multigene panel testing of patients with endometrial cancer.
Jan Kral, Sandra Jelinkova, Petra Zemankova, Michal Vocka, Marianna Borecka, Viktor Stranecky

Oncol Lett· June 2023

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ATAD3A-related pontocerebellar hypoplasia: new patients and insights into phenotypic variability.
Martina Skopkova, Hana Stufkova, Vibhuti Rambani, Viktor Stranecky, Katarina Brennerova

Orphanet J Rare Dis· April 2023

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Ethical principles for the usage and sharing of genomic data from researc.
Věra Franková, Hana Svozilová, Viktor Stránecký, Kateřina Staňo Kozubík, Josef Srovnal

Cas Lek Cesk· March 2023

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Low Frequency of Cancer-Predisposition Gene Mutations in Liver Transplant Candidates with Hepatocellular Carcinoma.
Klara Horackova, Sona Frankova, Petra Zemankova, Petr Nehasil, Marta Cerna, Viktor Stranecky

Cancers (Basel)· December 2022

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