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Jan Lebl

7PUBLICATIONS
172CO-AUTHORS
NanomedicineNeurogeneticsInfant and child healthGene expression (incl. microarray and other genome-wide approaches)Medical infection agents (incl. prions)
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Publications (7)

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|Jan 23, 2026
Noonan syndrome spectrum disorders in real life: patient characteristics and response to growth hormone therapy in a genetically defined single-country multicenter cohort.

Barbora Jirova, Maria Najdekova, Jana Cerna

|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

|Mar 13, 2025
Early-onset growth hormone treatment in Prader-Willi syndrome attenuates transition to severe obesity.

Aneta Kodytková, Shenali Anne Amaratunga, Eva El-Lababidi

|Mar 13, 2025
Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration.

Stefan Groeneweg, Ferdy S van Geest, Mariano Martín

|Nov 22, 2024
Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C).

Evangelos Bellos, Dilys Santillo, Pierre Vantourout

|Oct 28, 2023
Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq.

Shenali A Amaratunga, Tara Hussein Tayeb, Rozhan N Muhamad Sediq

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Frequent Collaborators

4 joint publications

Stepanka Pruhova

3 joint publications

Barbora Obermannová

3 joint publications

Petra Dusatkova

3 joint publications

Zdeněk Šumník

2 joint publications

Shenali Anne Amaratunga

2 joint publications

Dana Novotná

2 joint publications

Marta Šnajderová

2 joint publications

Jiří Strnadel

2 joint publications

Ivana Kotvalová

2 joint publications

Stanislava Koloušková

Frequent Collaborators

4 joint publications

Stepanka Pruhova

3 joint publications

Barbora Obermannová

3 joint publications

Petra Dusatkova

3 joint publications

Zdeněk Šumník

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