Bi-allelic <i>ACBD6</i> variants lead to a neurodevelopmental syndrome with progressive and complex movement disordersRauan Kaiyrzhanov, Ban A. Abdul–Majeed, Mislen Bauer et al.|Brain|2023Cited by 19
Clinical and Molecular Spectrum of Autosomal Recessive <scp><i>CA8</i></scp>‐Related Cerebellar AtaxiaRauan Kaiyrzhanov, Reza Maroofian, Karen Pysden et al.|Movement Disorders|2024Cited by 9
Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and TranscaucasiaRauan Kaiyrzhanov, Henry Houlden, Chingiz Shashkin et al.|Nature Genetics|2024Cited by 7