Markéta Vlčková

4PUBLICATIONS
178CO-AUTHORS
Medical genetics (excl. cancer genetics)Genomics and transcriptomicsNeurology and neuromuscular diseasesBehavioural epidemiology
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Publications (4)

|Jan 29, 2024
Lessons from two series by physicians and caregivers' self-reported data in DDX3X-related disorders.

Valentin Ruault, Pauline Burger, Johanna Gradels-Hauguel

|Nov 12, 2023
The Human Phenotype Ontology in 2024: phenotypes around the world.

Michael A Gargano, Nicolas Matentzoglu, Ben Coleman

|Feb 25, 2023
A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype-phenotype correlation.

Marketa Vlckova, Darina Prchalova, Pavel Zimmermann

|Feb 16, 2021
A novel variant in YWHAG further supports phenotype of developmental and epileptic encephalopathy.

Lucie Sedláčková, Katalin Štěrbová, Markéta Vlčková

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Frequent Collaborators

2 joint publications

Miroslava Hancarova

1 joint publications

Lucie Sedláčková

1 joint publications

Darina Prchalova

1 joint publications

Pavel Zimmermann