Koneev K 1

1. BRAT1–related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients
2. Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and Transcaucasia
3. Phenotypic continuum of NFU1-related disorders
4. Clinico-radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiency
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