| Hat1 acetylates histone H4 and modulates the transcriptional program in Drosophila embryogenesis J Varga, S Korbai, A Neller, N Zsindely, L Bodai Scientific reports 9 (1), 17973, 2019 | 13 | 2019 |
| Acetylation state of lysine 14 of histone H3. 3 affects mutant huntingtin induced pathogenesis A Faragó, N Zsindely, A Farkas, A Neller, F Siági, MR Szabó, T Csont, ... International Journal of Molecular Sciences 23 (23), 15173, 2022 | 4 | 2022 |
| Genetic etiology of nonsyndromic hearing loss in Hungarian patients M Pál, D Nagy, A Neller, K Farkas, D Leprán-Török, N Nagy, D Füstös, ... International Journal of Molecular Sciences 24 (8), 7401, 2023 | 1 | 2023 |
| Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease N Nagy, M Pal, J Kun, B Galik, P Urban, M Medvecz, B Fabos, A Neller, ... International Journal of Molecular Sciences 25 (2), 1271, 2024 | | 2024 |
| Unique patient stratification method identified susceptibility and protective factors for the severe COVID-19 disease in the Hungarian population A Neller, M Bukva, B Galik, J Kun, A Gyenesei, M Szell EUROPEAN JOURNAL OF HUMAN GENETICS 32, 688-688, 2024 | | 2024 |
| Genetic etiology of non-syndromic hearing loss in Hungarian patients with cochlear implant M Pal, D Nagy, A Neller, K Farkas, D Lepran-Torok, N Nagy, D Fustos, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 121-121, 2024 | | 2024 |
| LB1721 A novel pathogenic TPCN2 mutation detected for the first time in a Caucasian patient confirms the dominant inheritance of albinism N Nagy, M Pal, J Kun, G Bence, P Urban, M Medvecz, B Fábos, A Neller, ... Journal of Investigative Dermatology 143 (9), B20, 2023 | | 2023 |
| 814 Epigenetically altered expression of the CYLD interacting BAG6 gene is a putative phenotype modifying factor in CYLD cutaneous syndrome N Nagy, M Pal, E Adam, J Danis, A Neller, J Kun, P Urban, A Gyenesei, ... Journal of Investigative Dermatology 143 (5), S140, 2023 | | 2023 |
