Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH

by Marcel Kucharík, Jaroslav Budiš, Michaela Hýblová, Gabriel Minárik, Tomáš Szemes
Published 2021-04-01

Validation of Copy Number Variants Detection from Pregnant Plasma Using Low-Pass Whole-Genome Sequencing in Noninvasive Prenatal Testing-Like Settings

by Michaela Hyblova, Maria Harsanyova, Diana Nikulenkov-Grochova, Jitka Kadlecova, Marcel Kucharik, Jaroslav Budis, Gabriel Minarik
Published 2020-08-01

Testosterone and Androgen Receptor Sensitivity in Relation to Hyperactivity Symptoms in Boys with Autism Spectrum Disorders.

by Anna Pivovarciova, Jaroslava Durdiakova, Katarina Babinska, Aneta Kubranska, Lenka Vokalova, Gabriel Minarik, Peter Celec, Marianna Murin, Daniela Ostatnikova
Published 2016-01-01

Development of 14 Microsatellite Markers for Zoonotic Tapeworm <i>Dibothriocephalus dendriticus</i> (Cestoda: Diphyllobothriidea)

by Eva Bazsalovicsová, Gabriel Minárik, Katarína Šoltys, Alžbeta Radačovská, Jesper A. Kuhn, Egil Karlsbakk, Karl Skírnisson, Ivica Králová-Hromadová
Published 2020-07-01

Decreased methylation in the SNAI2 and ADAM23 genes associated with de-differentiation and haematogenous dissemination in breast cancers

by Lenka Kalinkova, Iveta Zmetakova, Bozena Smolkova, Gabriel Minarik, Tatiana Sedlackova, Viera Horvathova Kajabova, Zuzana Cierna, Michal Mego, Ivana Fridrichova
Published 2018-09-01

Genetic polymorphisms related to testosterone metabolism in intellectually gifted boys.

by Peter Celec, Denisa Tretinárová, Gabriel Minárik, Andrej Ficek, Tomáš Szemes, Silvia Lakatošová, Eva Schmidtová, Ján Turňa, Ľudevít Kádaši, Daniela Ostatníková
Published 2013-01-01

Impact of MMP2 rs243865 and MMP3 rs3025058 Polymorphisms on Clinical Findings in Alzheimer’s Disease Patients

by Vladimira Durmanova, Juraj Javor, Zuzana Parnicka, Gabriel Minarik, Agata Ocenasova, Barbora Vaseckova, Veronika Reznakova, Maria Kralova, Tomas Hromadka, Ivana Shawkatova
Published 2021-01-01

Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions.

by Marcel Kucharik, Andrej Gnip, Michaela Hyblova, Jaroslav Budis, Lucia Strieskova, Maria Harsanyova, Ondrej Pös, Zuzana Kubiritova, Jan Radvanszky, Gabriel Minarik, Tomas Szemes
Published 2020-01-01

Plasma Nucleosomes in Primary Breast Cancer

by Michal Mego, Katarina Kalavska, Marian Karaba, Gabriel Minarik, Juraj Benca, Tatiana Sedlackova, Paulina Gronesova, Dana Cholujova, Daniel Pindak, Jozef Mardiak, Peter Celec
Published 2020-09-01

Inflammation-Based Scores Increase the Prognostic Value of Circulating Tumor Cells in Primary Breast Cancer

by Svetlana Miklikova, Gabriel Minarik, Tatiana Sedlackova, Jana Plava, Marina Cihova, Silvia Jurisova, Katarina Kalavska, Marian Karaba, Juraj Benca, Bozena Smolkova, Michal Mego
Published 2020-05-01

A Novel Association of Polymorphism in the ITGA4 Gene Encoding the VLA-4 α4 Subunit with Increased Risk of Alzheimer’s Disease

by Vladimira Durmanova, Zuzana Parnicka, Juraj Javor, Gabriel Minarik, Lubomir Vrazda, Barbora Vaseckova, Karin Gmitterova, Maria Kralova, Jan Pecenak, Peter Filipcik, Ivana Shawkatova
Published 2018-01-01

Result of Prospective Validation of the Trisomy Test^® for the Detection of Chromosomal Trisomies

by Martina Sekelska, Anita Izsakova, Katarina Kubosova, Petra Tilandyova, Erika Csekes, Zaneta Kuchova, Michaela Hyblova, Maria Harsanyova, Marcel Kucharik, Jaroslav Budis, Tomas Szemes, Gabriel Minarik
Published 2019-10-01

Uncovering Microbial Composition in Human Breast Cancer Primary Tumour Tissue Using Transcriptomic RNA-seq

by Dominik Hadzega, Gabriel Minarik, Marian Karaba, Katarina Kalavska, Juraj Benca, Sona Ciernikova, Tatiana Sedlackova, Petra Nemcova, Martin Bohac, Daniel Pindak, Lubos Klucar, Michal Mego
Published 2021-08-01

Spinal muscular atrophy caused by a novel Alu‐mediated deletion of exons 2a‐5 in SMN1 undetectable with routine genetic testing

by Ivana Jedličková, Anna Přistoupilová, Lenka Nosková, Filip Majer, Viktor Stránecký, Hana Hartmannová, Kateřina Hodaňová, Helena Trešlová, Michaela Hýblová, Peter Solár, Gabriel Minárik, Mária Giertlová, Stanislav Kmoch
Published 2020-07-01

Utilization of Benchtop Next Generation Sequencing Platforms Ion Torrent PGM and MiSeq in Noninvasive Prenatal Testing for Chromosome 21 Trisomy and Testing of Impact of In Silico...

by Gabriel Minarik, Gabriela Repiska, Michaela Hyblova, Emilia Nagyova, Katarina Soltys, Jaroslav Budis, Frantisek Duris, Rastislav Sysak, Maria Gerykova Bujalkova, Barbora Vlkova-Izrael, Orsolya Biro, Balint Nagy, Tomas Szemes
Published 2015-01-01

Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy

by Andrea Soltysova, Tatiana Sedlackova, Dana Dvorska, Karin Jasek, Pooneh Chokhachi Baradaran, Viera Horvathova Kajabova, Lucia Demkova, Verona Buocikova, Terezia Kurucova, Darina Lyskova, Alena Furdova, Gabriel Minarik, Pavel Babal, Zuzana Dankova, Bozena Smolkova
Published 2020-12-01

Increased Stromal Infiltrating Lymphocytes Are Associated with the Risk of Disease Progression in Mesenchymal Circulating Tumor Cell-Positive Primary Breast Cancer Patients

by Bozena Smolkova, Zuzana Cierna, Katarina Kalavska, Svetlana Miklikova, Jana Plava, Gabriel Minarik, Tatiana Sedlackova, Dana Cholujova, Paulina Gronesova, Marina Cihova, Karolina Majerova, Marian Karaba, Juraj Benca, Daniel Pindak, Jozef Mardiak, Michal Mego
Published 2020-12-01

Expression of SOCS1 and CXCL12 Proteins in Primary Breast Cancer Are Associated with Presence of Circulating Tumor Cells in Peripheral Blood

by Bozena Smolkova, Michal Mego, Viera Horvathova Kajabova, Zuzana Cierna, Ludovit Danihel, Tatiana Sedlackova, Gabriel Minarik, Iveta Zmetakova, Tomas Krivulcik, Paulina Gronesova, Marian Karaba, Juraj Benca, Daniel Pindak, Jozef Mardiak, James M. Reuben, Ivana Fridrichova
Published 2016-06-01