RNDr. Vladimíra Vallová, Ph.D.

2021

• Whole-exome sequencing as an effective tool for the detection of DNA sequence and structural variants in the pathogenesis of neurodevelopmental disorders

  WAYHELOVÁ Markéta VALLOVÁ Vladimíra SMETANA Jan BROŽ Petr MIKULÁŠOVÁ Aneta LOUBALOVÁ Dominika GAILLYOVÁ Renata KUGLÍK Petr

  Conference abstract

  Year: 2021, type: Conference abstract

2020

• 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

• The clinical utility of targeted NGS in neurodevelopmental disorders: a case of a girl with pontocerebellar hypoplasia caused by TSEN54 gene pathogenic variants

  WAYHELOVÁ Markéta VALLOVÁ Vladimíra HLADÍLKOVÁ Eva FILKOVÁ Hana OPPELT Jan ŠOUKALOVÁ Jana KUGLÍK Petr

  Conference abstract

  Year: 2020, type: Conference abstract

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

• The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay

  WAYHELOVÁ Markéta SMETANA Jan VALLOVÁ Vladimíra HLADÍLKOVÁ Eva FILKOVÁ Hana HANÁKOVÁ Marta VILÉMOVÁ Marcela NIKOLOVÁ Petra GROMESOVÁ Barbora GAILLYOVÁ Renata KUGLÍK Petr

  Article in Periodical

  BMC MEDICAL GENOMICS, year: 2019, volume: 12, edition: 1, DOI

2016

• Detection of oncogenic mutations in cervical carcinoma using method "High Resolution Melting" (HRM).

  WAYHELOVÁ Markéta MIKULÁŠOVÁ Aneta SMETANA Jan VALLOVÁ Vladimíra BLAŽKOVÁ Dita FILKOVÁ Hana MOUKOVÁ Lucie KUGLÍK Petr

  Article in Periodical

  Neoplasma, year: 2016, volume: 63, edition: 5, DOI

2015

• A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms

  HLADÍLKOVÁ Eva BAROYA Tuva FANNEMELA Madeleine VALLOVÁ Vladimíra MISCEO Doriana BRYND Vesna SLÁMOVÁ Iva PRÁŠILOVÁ Šárka KUGLÍK Petr FRENGEN Eirik

  Article in Periodical

  MOLECULAR CYTOGENETICS, year: 2015, volume: 8, edition: 57, DOI

• Molecular cytogenetic analyses of hTERC (3q26) and MYC (8q24) genes amplifications in correlation with oncogenic human papillomavirus infection in Czech patients with cervical intraepithelial neoplasia and cervical carcinomas

  KUGLÍK Petr KAŠÍKOVÁ Kateřina SMETANA Jan VALLOVÁ Vladimíra LAŠTŮVKOVÁ Anna MOUKOVÁ Lucie CVANOVÁ Michaela BROŽOVÁ Lucie

  Article in Periodical

  Neoplasma, year: 2015, volume: 62, edition: 1, DOI

• První zkušenosti s preimplantačním genetickým screeningem chromozomových abnormalit pomocí komparativní genomové hybridizace na oligonukleotidových DNA mikročipech

  KUGLÍK Petr SMETANA Jan NĚMCOVÁ Darja VALLOVÁ Vladimíra MIKULÁŠOVÁ Aneta GAILLYOVÁ Renata HUBINKA Vít KOUDELKA Marek

  Article in Periodical

  Časopis lékařů českých, year: 2015, volume: 154, edition: 3

2014

• Genome-Wide Screening of Cytogenetic Abnormalities in Multiple Myeloma Patients Using Array-CGH Technique: A Czech Multicenter Experience

  SMETANA Jan FRÖHLICH Jan ZAORALOVÁ Romana VALLOVÁ Vladimíra GREŠLIKOVÁ Henrieta KUPSKÁ Renata NĚMEC Pavel MIKULÁŠOVÁ Aneta ALMAŠI Martina POUR Luděk ADAM Zdeněk SANDECKÁ Viera ZAHRADOVÁ Lenka HÁJEK Roman KUGLÍK Petr

  Article in Periodical

  BioMed Research International, year: 2014, volume: Neuveden, edition: MAY, DOI