Markéta Havlovicová

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Body Mass Index

Circulating Tumor

Top Venues

Molecular biology reports

Scientific reports

Annals of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Martin Schwarz, Matej Gazdarica, Eva Froňková, Michael Svatoň, Jiri Bronsky, Markéta Havlovicová, Anna Křepelová, Milan Macek
Functional studies associate novel DUOX2 gene variants detected in heterozygosity to Crohn's disease. Molecular biology reports 51 (1) (2024)
Martin Schwarz, Matej Gazdarica, Eva Froňková, Michael Svatoň, Jiri Bronsky, Markéta Havlovicová, Anna Křepelová, Milan Macek
Functional studies associate novel DUOX2 gene variants detected in heterozygosity to Crohn's disease. Molecular biology reports 51 (1) (2024)
Martin Schwarz, Jan Geryk, Markéta Havlovicová, Michaela Zelinová, Marek Turnovec, Lukáš Ryba, Júlia Martinková, Milan Macek, Richard Palmer, Karolina Kočandrlová, Jana Velemínská, Veronika Moslerová
Body mass index is an overlooked confounding factor in existing clustering studies of 3D facial scans of children with autism spectrum disorder. Scientific reports 14 (1) (2024)
Martin Schwarz, Jan Geryk, Markéta Havlovicová, Michaela Zelinová, Marek Turnovec, Lukáš Ryba, Júlia Martinková, Milan Macek, Richard Palmer, Karolina Kočandrlová, Jana Velemínská, Veronika Moslerová
Body mass index is an overlooked confounding factor in existing clustering studies of 3D facial scans of children with autism spectrum disorder. Scientific reports 14 (1) (2024)
Jana Čopíková, Jana Paděrová, Věra Románková, Markéta Havlovicová, Miroslava Balaščáková, Michaela Zelinová, Šárka Vejvalková, Martina Simandlová, Jana Štěpánková, Věra Hořínová, Eva Kantorová, Gabriela Křečková, Jana Pospíšilová, Arpád Boday, Anna Uhrová Mészárosová, Marek Turnovec, Pavel Votýpka, Petra Liskova, Radka Kremlíková Pourová
Expanding the phenotype spectrum associated with pathogenic variants in the COL2A1 and COL11A1 genes. Annals of human genetics 84 (5) (2020)