| AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ... Nature communications 10 (1), 3094, 2019 | 187 | 2019 |
| PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation V Chelban, MP Wilson, J Warman Chardon, J Vandrovcova, MN Zanetti, ... Annals of Neurology 86 (2), 225-240, 2019 | 67 | 2019 |
| Spike orientation may predict epileptogenic side across cerebral sulci containing the estimated equivalent dipole KA Salayev, N Nakasato, M Ishitobi, H Shamoto, A Kanno, K Iinuma Clinical neurophysiology 117 (8), 1836-1843, 2006 | 43 | 2006 |
| The strengths and difficulties questionnaire (SDQ) in autism spectrum disorders KA Salayev, B Sanne International Journal on Disability and Human Development 16 (3), 275-280, 2017 | 24 | 2017 |
| Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals K Saida, R Maroofian, T Sengoku, T Mitani, AT Pagnamenta, D Marafi, ... Genetics in Medicine 25 (1), 90-102, 2023 | 17 | 2023 |
| Psychiatric and behavioural problems in children and adolescents with epilepsy KA Salayev, B Sanne, R Salayev East Asian Archives of Psychiatry 27 (3), 106-114, 2017 | 13 | 2017 |
| Evaluation of Interhemispheric Time Difference by Magnetoencephalography Before and After Total Callosotomy—Two Case Reports— KA Salayev, N Nakasato, M Ishitobi, H Shamoto, A Kanno, T Tominaga, ... Neurologia medico-chirurgica 46 (3), 136-142, 2006 | 9 | 2006 |
| The discriminative ability of the Azeri version of the strengths and difficulties questionnaire in outpatient practice K Salayev, I Rustamov, N Gadjiyeva, R Salayev, B Sanne Community mental health journal 52, 1106-1112, 2016 | 8 | 2016 |
| PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations C Tremblay‐Laganière, R Kaiyrzhanov, R Maroofian, TTM Nguyen, ... Clinical genetics 99 (2), 313-317, 2021 | 5 | 2021 |
| Biallelic loss of EMC10 leads to mild to severe intellectual disability R Kaiyrzhanov, C Rocca, M Suri, S Gulieva, MS Zaki, NZ Henig, K Siquier, ... Annals of Clinical and Translational Neurology 9 (7), 1080-1089, 2022 | 4 | 2022 |
| GM1‐gangliosidosis type III associated parkinsonism R Kaiyrzhanov, U Guliyeva, S Gulieva, K Salayev, A Mursalova, ... Movement Disorders Clinical Practice 8 (Suppl 1), S21, 2021 | 3 | 2021 |
| A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease E Calì, SJ Lin, C Rocca, Y Sahin, A Al Shamsi, S El Chehadeh, ... Genetics in Medicine 24 (10), 2194-2203, 2022 | 1 | 2022 |
| Whole exome sequencing in 62 families with early-onset movement disorders, cerebellar ataxia and hereditary spastic paraplegia from Kazakhstan, Tajikistan, and Azerbaijan R Kaiyrzhanov, M Ganieva, K Salayev, U Guliyeva, S Gulieva, C Shashkin, ... Movement Disorders 37, S289-S290, 2022 | 1 | 2022 |
| Whole exome sequencing in 444 families with rare paediatric neurological disorders in Central Asia and Transcaucasia R Kaiyrzhanov, K Salayev, M Ganieva, B Sukhudyan, N Tabatadze, ... European Journal of Neurology 29, 164-164, 2022 | 1 | 2022 |
| Validation of the Azeri version of the pediatric epilepsy side effects questionnaire S Kamran, M Sharif, G Garay Child's Nervous System 35, 2379-2383, 2019 | 1 | 2019 |
| Evaluating the Decisional Capacity for Informed Consent of Transition age Children to Adolescents in Human Subject Research K Salayev, U Aslanova, K Munir Journal of Empirical Research on Human Research Ethics 19 (1-2), 28-36, 2024 | | 2024 |
| Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome V Salpietro, R Maroofian, MS Zaki, J Wangen, A Ciolfi, S Barresi, ... The American Journal of Human Genetics 111 (1), 200-210, 2024 | | 2024 |
| Assessment of Research Ethics Knowledge of Pediatricians K Salayev, U Aslanova, N Guliyeva, G Geraybeyli, K Munir Global Pediatric Health 11, 2333794X231224989, 2024 | | 2024 |
| Expanding SNX14-Associated Movement Disorders in a Genotype–Phenotype Spectrum EM Toepffer, NM Ojeda, S Bakhtiari, S Efthymiou, R Horvath, ... Neuropediatrics 54 (S 01), A-214, 2023 | | 2023 |
| Attitudes of Parents of Children with Rare Neurological Disorders Toward Clinical Genetic Testing K Salayev, U Guliyeva, S Guliyeva, R Kaiyrzhanov, U Aslanova, ... | | 2023 |
Rauan KaiyrzhanovInstitute of Neurology UCLVerified email at ucl.ac.uk
