| Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion NÁ Varga, K Pentelényi, P Balicza, A Gézsi, V Reményi, V Hársfalvi, ... Behavioral and Brain Functions 14, 1-14, 2018 | 51 | 2018 |
| Comprehensive analysis of rare variants of 101 autism-linked genes in a Hungarian cohort of autism spectrum disorder patients P Balicza, NÁ Varga, B Bolgár, K Pentelényi, R Bencsik, A Gál, A Gézsi, ... Frontiers in genetics 10, 434, 2019 | 21 | 2019 |
| Parkinsonet: estimation of updrs score using hubness-aware feedforward neural networks K Buza, NÁ Varga Applied Artificial Intelligence 30 (6), 541-555, 2016 | 20 | 2016 |
| Deep brain stimulation or thalamotomy in fragile X-associated tremor/ataxia syndrome? Case report G Tamás, N Kovács, NÁ Varga, P Barsi, L Erőss, MJ Molnár, I Balás Neurologia i Neurochirurgia Polska 50 (4), 303-308, 2016 | 7 | 2016 |
| Implementation of personalized medicine in Central-Eastern Europe: pitfalls and potentials based on citizen’s attitude P Balicza, A Terebessy, Z Grosz, NA Varga, A Gal, BA Fekete, MJ Molnar EPMA Journal 9, 103-112, 2018 | 4 | 2018 |
| Melatonin and mitochondrial dysfunction are key players in the pathophysiology of sepsis N Varga, JC Ruiz-Rodríguez, R Ferrer Enferm. infecc. microbiol. clín.(Ed. impr.), 535-538, 2018 | 4 | 2018 |
| Multilevel evidence of MECP2-associated mitochondrial dysfunction and its therapeutic implications P Balicza, A Gezsi, M Fedor, JC Sagi, A Gal, NA Varga, MJ Molnar Frontiers in Psychiatry 14, 1301272, 2024 | 1 | 2024 |
| Impact of emerging diagnostic technologies on diagnostic rate of ataxia: experience of a Hungarian expert centre for rare neurological diseases V Molnar, M Menyei-Kiss, P Balicza, NA Varga, Z Grosz, B Trombitas, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 265-265, 2022 | | 2022 |
| SPG7 mutations in Hungarian cohorts: new insights and possible genotype-phenotype correlations IJ Jimoh, P Balicza, D Csaban, Z Grosz, N Varga, V Molnar, B Fekete, ... EUROPEAN JOURNAL OF NEUROLOGY 28, 845-845, 2021 | | 2021 |
| Az autizmus spektrum zavar genetikai hátterének vizsgálata egy magyar betegpopulációban NÁ Varga | | 2021 |
| Genetic characterization of Hungarian patients with early onset dementia D Csaban, R Bencsik, A Illes, V Molnar, P Balicza, A Gezsi, Z Grosz, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 385-385, 2020 | | 2020 |
| Krónikus obstruktív tüdőbetegségben a bal kamra diasztolés funkciózavara gyakori és rossz prognózissal társul= Left ventricular diastolic dysfunction is common in patients with … M Hajdu, K Krämer, V Vértes, Á Nógrádi, N Varga, MB Illés, V Sárosi, ... Cardiologia Hungarica 50 (6), 410-416, 2020 | | 2020 |
| Burden test of selected autism-associated genes in a Hungarian cohort P Balicza, NA Varga, K Pentelenyi, R Bencsik, A Gal, C Prekop, V Molnar, ... EUROPEAN JOURNAL OF NEUROLOGY 26, 208-208, 2019 | | 2019 |
| Az agresszió megjelenése a gyermekrajzokban N Varga pk, 2018 | | 2018 |
| Genetic epidemiology analysis of Hungarian Charcot-Marie-Tooth patients GM Milley, Z Grosz, E Varga, NA Varga, J Boczan, Z Aranyi, P Dioszeghy, ... EUROPEAN JOURNAL OF NEUROLOGY 24, 606-606, 2017 | | 2017 |
| Targeted next-generation sequencing (NGS) as a diagnostic tool in syndromic autism spectrum disorder (ASD) NA Varga, K Pentelenyi, P Balicza, R Bencsik, A Illes, A Gezsi, C Prekop, ... EUROPEAN JOURNAL OF NEUROLOGY 24, 424-424, 2017 | | 2017 |
| mtDNA alterations and autism associated nuclear gene variants in the background of autism spectrum disorder NA Varga, K Pentelenyi, P Balicza, V Remenyi, V Harsfalvi, R Bencsik, ... EUROPEAN JOURNAL OF NEUROLOGY 23, 840-840, 2016 | | 2016 |
| The implementation of the next generation sequencing (NGS) to identify the genetic background of the autism spectrum disorder (ASD) in Hungarian patients NA Varga, K Pentelenyi, P Balicza, V Harsfalvi, V Remenyi, J Koller, ... EUROPEAN JOURNAL OF NEUROLOGY 22, 165-165, 2015 | | 2015 |
| Fragile X-associated tremor/ataxia syndrome, differential diagnosis of essential tremor: a case report G Tamas, N Kovacs, MJ Molnar, P Barsi, L Eross, NA Varga, I Balas EUROPEAN JOURNAL OF NEUROLOGY 22, 814-814, 2015 | | 2015 |
| A Leigh-szindróma a genetikailag legheterogénebb mitokondriális betegség NÁ Varga, B Péter, MJ Molnár | | 2015 |
