Júlia Martinková

3PUBLICATIONS
26CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsAnthropological genetics
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Publications (3)

|Jun 04, 2026
A c.89G>C p.(Gly30Ala) Variant in the DHCR7 Gene as a Cause of a Mild Phenotype in the Smith-Lemli-Opitz Syndrome.

|Jun 16, 2025
Cytogenetic anomalies are the predominant genetic alteration in children with nonfamilial tall stature: a comparative study with familial cases.

Katerina Gregorova, Lukas Plachy, Petra Dusatkova

|Apr 29, 2024
Body mass index is an overlooked confounding factor in existing clustering studies of 3D facial scans of children with autism spectrum disorder.

Martin Schwarz, Jan Geryk, Markéta Havlovicová

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Frequent Collaborators

2 joint publications

Martin Schwarz

2 joint publications

Lukáš Ryba

1 joint publications

Jan Geryk

1 joint publications

Markéta Havlovicová