doc. RNDr. Petr Kuglík, CSc.

2019

• 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

2018

• Circulating exosomal long noncoding RNA PRINS-First findings in monoclonal gammopathies

  SEDLAŘÍKOVÁ Lenka BOLLOVÁ Božena RADOVÁ Lenka BROŽOVÁ Lucie JARKOVSKÝ Jiří ALMÁŠI Martina PENKA Miroslav KUGLÍK Petr SANDECKÁ Viera ŠTORK Martin POUR Luděk ŠEVČÍKOVÁ Sabina

  Article in Periodical

  Hematological Oncology, year: 2018, volume: 36, edition: 5, DOI

• Chromothripsis 18 in multiple myeloma patient with rapid extramedullary relapse

  SMETANA Jan OPPELT Jan ŠTORK Martin POUR Luděk KUGLÍK Petr

  Article in Periodical

  MOLECULAR CYTOGENETICS, year: 2018, volume: 11, edition: JAN, DOI

2017

• Deregulated expression of long non-coding RNA UCA1 in multiple myeloma

  SEDLAŘÍKOVÁ Lenka GROMESOVÁ Barbora KUBACZKOVÁ Veronika RADOVÁ Lenka FILIPOVA Jana JARKOVSKÝ Jiří BROŽOVÁ Lucie VELICHOVÁ Roberta ALMÁŠI Martina PENKA Miroslav BEZDĚKOVÁ Renata ŠTORK Martin ADAM Zdeněk POUR Luděk KREJČÍ Marta KUGLÍK Petr HÁJEK Roman ŠEVČÍKOVÁ Sabina

  Article in Periodical

  European Journal of Haematology, year: 2017, volume: 99, edition: 3, DOI

• The clinical impact of targeted „next-generation“ sequencing in molecular diagnostics of intellectual disabilities and multiple congenital abnormalities

  WAYHELOVÁ Markéta OPPELT Jan SMETANA Jan PARDY Filip FILKOVÁ Hana GAILLYOVÁ Renata KUGLÍK Petr

  Appeared in Conference without Proceedings

  Year: 2017, type: Appeared in Conference without Proceedings

• The clinical utility of array-CGH and targeted NGS in idiopathic intellectual disabilities and developmental delays: a case report of SCN2A p.Ala263Val variant

  WAYHELOVÁ Markéta OPPELT Jan VESELÁ Denisa SMETANA Jan PARDY Filip FILKOVÁ Hana MATUCHOVÁ Dita ŠOUKALOVÁ Jana GAILLYOVÁ Renata KUGLÍK Petr

  Conference abstract

  Year: 2017, type: Conference abstract

• The spectrum of somatic mutations in monoclonal gammopathy of undetermined significance indicates a less complex genomic landscape than that in multiple myeloma

  MIKULÁŠOVÁ Aneta WARDELL Christopher P. MURISON Alexander BOYLE Eileen M. JACKSON Graham H. SMETANA Jan KUFOVA Zuzana POUR Luděk SANDECKÁ Viera ALMÁŠI Martina VŠIANSKÁ Pavla GREGORA Evzen KUGLÍK Petr HÁJEK Roman DAVIES Faith E. MORGAN Gareth J. WALKER Brian A.

  Article in Periodical

  Haematologica, year: 2017, volume: 102, edition: 9, DOI

2016

• Clonal cytogenetics changes in progression of multiple myeloma to extramedullary relapse and plasmocellular leukemia: a case report

  SMETANA Jan KUGLÍK Petr GREŠLIKOVÁ Henrieta KUPSKÁ Renata NĚMEC Pavel MIKULÁŠOVÁ Aneta VALÁŠKOVÁ Iveta OPPELT Jan ALMÁŠI Martina KREJČÍ Marta ADAM Zdeněk POUR Luděk HÁJEK Roman

  Article in Periodical

  International Journal of Clinical and Experimental Pathology, year: 2016, volume: 9, edition: 1

• Cytogenetics in multiple myeloma patients progressing into extramedullary disease

  BEŠŠE Lenka SEDLAŘÍKOVÁ Lenka GREŠLIKOVÁ Henrieta KUPSKÁ Renata ALMASI Martina PENKA Miroslav JELINEK Tomas POUR Luděk ADAM Zdeněk KUGLÍK Petr KREJČÍ Marta HÁJEK Roman ŠEVČÍKOVÁ Sabina

  Article in Periodical

  European Journal of Haematology, year: 2016, volume: 97, edition: 1, DOI

• 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