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преподаватель Ерходжаева Нигара Халмахамметовна
Dr. Nigara Yerkhojayeva is a neurologist specializing in neurogenetics, pediatric neurology, and the diagnosis of rare inherited neurological diseases. She has over ten years of clinical experience, including work in a stroke center and pediatric neurology practice. Her academic and research activities focus on the integration of deep phenotyping and exome sequencing to improve diagnostic yield in complex neurological phenotypes.
She leads and participates in several national and international research projects, including a grant-funded study on pharmacoresistant epilepsy in Central Asia. Dr. Yerkhojayeva has presented her work at major European conferences, including the European Academy of Neurology (EAN) and the European Paediatric Neurology Society (EPNS), and has authored peer-reviewed publications on genomic diagnostics and sustainable healthcare models for rare diseases.
She is an active member of the EPNS, EAN, and the International Parkinson and Movement Disorder Society (MDS). Her research fellowship at the UCL Queen Square Institute of Neurology (London, UK) in 2024 further strengthened her expertise in neurogenetics and translational neurology.