MUDr. Renata Gaillyová, Ph.D.

2020

• Next generation sequencing in newborn screening for cystic fibrosis

  VINOHRADSKÁ Jana VALÁŠKOVÁ Iveta GAILLYOVÁ Renata

  Conference abstract

  Year: 2020, type: Conference abstract

• Novel Familial IQSEC2 Pathogenic Sequence Variant Associated With Neurodevelopmental Disorders and Epilepsy

  WAYHELOVÁ Markéta RYZÍ Michal OPPELT Jan HLADÍLKOVÁ Eva VALLOVÁ Vladimíra KRSKOVÁ Lenka VILÉMOVÁ Marcela POLÁČKOVÁ Hana GAILLYOVÁ Renata KUGLÍK Petr

  Article in Periodical

  Neurogenetics, year: 2020, volume: 21, edition: 4, DOI

2019

• "Two hit" model as an explanation of variable expressivity of recurrent submicroscopic chromosomal rearrangements in children with intellectual disability and developmental delay

  WAYHELOVÁ Markéta HLADÍLKOVÁ Eva VALLOVÁ Vladimíra SMETANA Jan FILKOVÁ Hana GAILLYOVÁ Renata KUGLÍK Petr

  Conference abstract

  Year: 2019, type: Conference abstract

• Dystrophin Deficiency Leads to Genomic Instability in Human Pluripotent Stem Cells via NO Synthase-Induced Oxidative Stress

  JELÍNKOVÁ Šárka KOHUTOVÁ Aneta FOJTÍK Petr KRUTÁ Miriama VILOTIĆ Aleksandra PEŠL Martin VRBSKÝ Jan GAILLYOVÁ Renata VALÁŠKOVÁ Iveta FRÁK Ivan FORTE Giancarlo DVOŘÁK Petr MELI Albano ROTREKL Vladimír MARKOVÁ Lenka JURÁKOVÁ Tereza LACAMPAGNE Alain

  Article in Periodical

  Cells, year: 2019, volume: 8, edition: 1, DOI

• EPIDEMIOLOGY OF RARE DISEASES DETECTED BY NEWBORN SCREENING IN THE CZECH REPUBLIC

  DAVID Jan CHRASTINA Petr PEŠKOVÁ Karolína KOŽICH Viktor FRIEDECKÝ David ADAM Tomáš HLÍDKOVÁ Eva VINOHRADSKÁ Hana NOVOTNÁ Dana HEDELOVÁ Monika AL TAJI Eva HOLUBOVÁ Andrea SKALICKÁ Veronika MACEK Milan GAILLYOVÁ Renata VOTAVA Felix

  Article in Periodical

  Central European journal of public health, year: 2019, volume: 27, edition: 2, DOI

• Genetické testování v predikci nádorového rizika u IBD

  ZBOŘIL Vladimír GAILLYOVÁ Renata POREDSKÁ Karolina PROKOPOVÁ Lucie

  Conference abstract

  Year: 2019, type: Conference abstract

• Molecular analysis confirmed common ancestor of 10 Czech families with long QT syndrome carrying C926T-KCNQ1 variant

  SYNKOVÁ Iva VALÁŠKOVÁ Iveta GAILLYOVÁ Renata NOVOTNÝ Tomáš BÉBAROVÁ Markéta ANDRŠOVÁ Irena FLORIANOVA A. VÍT Pavel NAVRATIL R.

  Conference abstract

  Year: 2019, type: Conference abstract

• Mutace T309I asociovaná se syndromem dlouhého QT typu 1: akumulace IKs jako mechanismus ochrany srdce proti arytmii

  BÉBAROVÁ Markéta SYNKOVÁ Iva ANDRŠOVÁ Irena BAIAZITOVA Larisa ŠVECOVÁ Olga HOŠEK Jan PÁSEK Michal VÍT Pavel VALÁŠKOVÁ Iveta GAILLYOVÁ Renata NAVRÁTIL Rostislav NOVOTNÝ Tomáš

  Conference abstract

  Year: 2019, type: Conference abstract

• Mutation R591C associated with long QT syndrome type 1: clinical, genetic, and functional analysis

  ŠVECOVÁ Olga BÉBAROVÁ Markéta BAIAZITOVA Larisa POLICAROVÁ Marcela HOŠEK Jan ANDRŠOVÁ Irena VALÁŠKOVÁ Iveta SYNKOVÁ Iva GAILLYOVÁ Renata VÍT Pavel NOVOTNÝ Tomáš

  Conference abstract

  Year: 2019, type: Conference abstract

• Novel de novo frameshift variant in the ASXL3 gene in a child with microcephaly and global developmental delay

  WAYHELOVÁ Markéta OPPELT Jan SMETANA Jan HLADÍLKOVÁ Eva FILKOVÁ Hana MAKATUROVÁ Eva NIKOLOVÁ Petra BEHARKA Rastislav GAILLYOVÁ Renata KUGLÍK Petr

  Article in Periodical

  Molecular Medicine Reports, year: 2019, volume: 20, edition: 1, DOI