Rauan Kaiyrzhanov

20PUBLICATIONS
202CO-AUTHORS
Neurology and neuromuscular diseasesOther European languagesGene mappingNeonatologyNeurogenetics
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Publications (20)

|Apr 12, 2026
DRD1-driven infantile dystonia: towards a mechanism-informed framework for GPCR receptoropathies.

Gülsüm Kayhan, Ryosuke Tany, Reza Maroofian

|Sep 15, 2025
The LRRK2 p.A419V variant associates with risk of Parkinson's disease in the East Asian population and an evaluation on age of onset.

Kai Shi Lim, Maria Teresa Periñan, Elaine Guo Yan Chew

|Jul 17, 2025
The Global Landscape of Genetic Variation in Parkinson's disease: Multi-Ancestry Insights into Established Disease Genes and their Translational Relevance.

Lara M Lange, Zih-Hua Fang, Mary B Makarious

|Feb 18, 2025
Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment.

Rauan Kaiyrzhanov, Kyle Thompson, Stephanie Efthymiou

|Nov 23, 2024
Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and Transcaucasia.

Rauan Kaiyrzhanov, Nazira Zharkinbekova, Ulviyya Guliyeva

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