Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Maria Harsanyova"'
Autor:
Marcel Kucharik, Andrej Gnip, Michaela Hyblova, Jaroslav Budis, Lucia Strieskova, Maria Harsanyova, Ondrej Pös, Zuzana Kubiritova, Jan Radvanszky, Gabriel Minarik, Tomas Szemes
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0238245 (2020)
To study the detection limits of chromosomal microaberrations in non-invasive prenatal testing with aim for five target microdeletion syndromes, including DiGeorge, Prader-Willi/Angelman, 1p36, Cri-Du-Chat, and Wolf-Hirschhorn syndromes. We used know
Externí odkaz:
https://doaj.org/article/bb1161995b534136bb456d23dfbea83c
Autor:
Martin Maronek, Barbora Gromova, Robert Liptak, Barbora Konecna, Michal Pastorek, Barbora Cechova, Maria Harsanyova, Jaroslav Budis, David Smolak, Jan Radvanszky, Tomas Szemes, Jana Harsanyiova, Alzbeta Kralova Trancikova, Roman Gardlik
Publikováno v:
Cells, Vol 10, Iss 1, p 81 (2021)
Circulating extracellular DNA (ecDNA) is known to worsen the outcome of many diseases. ecDNA released from neutrophils during infection or inflammation is present in the form of neutrophil extracellular traps (NETs). It has been shown that higher ecD
Externí odkaz:
https://doaj.org/article/f7e31031a00c4950a0b8308b48a46fb1
Autor:
Michaela Hyblova, Maria Harsanyova, Diana Nikulenkov-Grochova, Jitka Kadlecova, Marcel Kucharik, Jaroslav Budis, Gabriel Minarik
Publikováno v:
Diagnostics, Vol 10, Iss 8, p 569 (2020)
Detection of copy number variants as an integral part of noninvasive prenatal testing is increasingly used in clinical practice worldwide. We performed validation on plasma samples from 34 pregnant women with known aberrations using cell-free DNA seq
Externí odkaz:
https://doaj.org/article/a4da95914c724003b0ee9a01f8d2d894
Autor:
Martina Sekelska, Anita Izsakova, Katarina Kubosova, Petra Tilandyova, Erika Csekes, Zaneta Kuchova, Michaela Hyblova, Maria Harsanyova, Marcel Kucharik, Jaroslav Budis, Tomas Szemes, Gabriel Minarik
Publikováno v:
Diagnostics, Vol 9, Iss 4, p 138 (2019)
Noninvasive prenatal testing (NIPT) is one of the most common prenatal screening tests used worldwide. Trisomy Test® belongs to NIPT tests based on low-coverage whole-genome sequencing. In our prospective study, 7279 samples of pregnant women collec
Externí odkaz:
https://doaj.org/article/148ba3d0439a4c5ba6185952da69540b
Autor:
Jana Harsanyiova, Robert Liptak, Barbora Gromova, Martin Maronek, Barbora Konečná, Michal Pastorek, Roman Gardlik, Alzbeta Trancikova, David Smolak, Maria Harsanyova, Barbora Cechova, Tomáš Szemes, Jaroslav Budis, Jan Radvanszky
Publikováno v:
Cells
Cells, Vol 10, Iss 81, p 81 (2021)
Volume 10
Issue 1
Cells, Vol 10, Iss 81, p 81 (2021)
Volume 10
Issue 1
Circulating extracellular DNA (ecDNA) is known to worsen the outcome of many diseases. ecDNA released from neutrophils during infection or inflammation is present in the form of neutrophil extracellular traps (NETs). It has been shown that higher ecD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::953533bdcdbebe42cd658bf7a68ed143
http://europepmc.org/articles/PMC7825321
http://europepmc.org/articles/PMC7825321
Autor:
Michaela Hyblova, Gabriel Minarik, Zuzana Kubiritova, Andrej Gnip, Tomáš Szemes, Jaroslav Budis, Ondrej Pös, Jan Radvanszky, Marcel Kucharik, Maria Harsanyova, Lucia Strieskova
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 8, p e0238245 (2020)
PLoS ONE, Vol 15, Iss 8, p e0238245 (2020)
To study the detection limits of chromosomal microaberrations in non-invasive prenatal testing with aim for five target microdeletion syndromes, including DiGeorge, Prader-Willi/Angelman, 1p36, Cri-Du-Chat, and Wolf-Hirschhorn syndromes. We used know
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3b4fa30f0b86740a85cfc4405d8adbf
https://pubmed.ncbi.nlm.nih.gov/32845907
https://pubmed.ncbi.nlm.nih.gov/32845907
Autor:
Lucia Strieskova, Tomáš Szemes, Frantisek Duris, Michaela Hyblova, Jaroslav Budis, Jan Radvanszky, Andrej Gnip, Gabriel Minarik, Maria Harsanyova, Marcel Kucharik
ObjectiveTo study the detection limits of chromosomal microaberrations in non-invasive prenatal testing with aim for five target microdeletion syndromes, including DiGeorge, Prader-Willi/Angelman, 1p36, Cri-Du-Chat, and Wolf-Hirschhorn syndromes.Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccbf1be8719a6f173082916bdfba6339
https://doi.org/10.1101/686345
https://doi.org/10.1101/686345
Autor:
Ludevit Kadasi, Zuzana Kubiritova, Frantisek Duris, Maria Harsanyova, Michaela Hyblova, Juraj Gazdarica, Tomáš Szemes, Jaroslav Budis, Jan Radvanszky, Rastislav Hekel, Marianna Gyurászová, Emilia Nagyova
Publikováno v:
Journal of biotechnology. 298
Although massively parallel sequencing (MPS) is becoming common practice in both research and routine clinical care, confirmation requirements of identified DNA variants using alternative methods are still topics of debate. When evaluating variants d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef8bac96db46b74f50d26a4d5de7652b
https://pubmed.ncbi.nlm.nih.gov/30998956
https://pubmed.ncbi.nlm.nih.gov/30998956
Autor:
Frantisek Duris, Bálint Nagy, Gabriel Minarik, Tomáš Szemes, Juraj Gazdarica, Martina Sekelska, Jaroslav Budis, Jan Radvanszky, Iveta Gazdaricova, Richard Frno, Maria Harsanyova, Lucia Strieskova
Low-coverage massively parallel genome sequencing for non-invasive prenatal testing (NIPT) of common aneuploidies is one of the most rapidly adopted and relatively low-cost DNA tests. Since aggregation of reads from a large number of samples allows o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69550f335548ee4cc607114bbf9c7d47
Autor:
Gabor Szucs, Frantisek Duris, Jan Turna, Iveta Gazdaricova, Marcel Kucharik, Martina Sekelska, Bálint Nagy, Juraj Gazdarica, Gabriel Minarik, Maria Harsanyova, Tomáš Szemes, Lucia Strieskova, Jaroslav Budis, Jan Radvanszky
MotivationNon-invasive prenatal testing or NIPT is currently among the top researched topic in obstetric care. While the performance of the current state-of-the-art NIPT solutions achieve high sensitivity and specificity, they still struggle with a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d97ffc30dd10a4001aede0680335cd8
https://doi.org/10.1101/353862
https://doi.org/10.1101/353862