| NKX2-1 New Mutation Associated with Myoclonus, Dystonia, Pituitary Dysfunction and Empty Sella P Balicza, Z Grosz, V Molnar, A Illés, D Csaban, A Gezsi, L Dezsi, ... Frontiers in Genetics 9, 335, 2018 | 21* | 2018 |
| NKX2-1 new mutation associated with myoclonus, dystonia, and pituitary involvement P Balicza, Z Grosz, V Molnár, A Illés, D Csabán, A Gézsi, L Dézsi, ... Frontiers in genetics 9, 2018 | 21 | 2018 |
| The role of genetic testing in the clinical practice and research of early-onset Parkinsonian disorders in a Hungarian cohort: Increasing challenge in genetic counselling … A Illés, D Csabán, Z Grosz, P Balicza, A Gézsi, V Molnár, R Bencsik, A Gál, ... Frontiers in genetics 10, 1061, 2019 | 10 | 2019 |
| Positive association and future perspectives of mitochondrial DNA copy number and telomere length–a pilot twin study D Melicher, A Illés, L Littvay, ÁD Tárnoki, DL Tárnoki, A Bikov, L Kunos, ... Archives of Medical Science 15 (1), 2019 | 8 | 2019 |
| Importance of next generation sequencing in precision oncology approach of acute myeloid leukemia H Andrikovics, P Kövy, A Bors, D Csabán, N Meggyesi, Z Õrfi, A Borsy, ... Magyar onkologia 63 (4), 282, 2019 | | 2019 |
| Telomere length and mitochondrial DNA copy number changes as a biomarker in ALS BA Fekete, A Illes, D Csaban, H Zeke, V Molnar, IJ Jimoh, P Balicza, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1413-1413, 2019 | | 2019 |
| Coexistance of mutations and genetic risk factors in early onset Parkinson's disease challenge the genetic counseling Z Grosz, A Illes, P Balicza, D Csaban, A Gezsi, V Molnar, A Gal, ... EUROPEAN JOURNAL OF NEUROLOGY 26, 697-697, 2019 | | 2019 |
| Sequential approach to identify disease causing variants in patients with mitochondrial dysfunction of a Hungarian cohort V Molnar, A Gezsi, A Illes, P Balicza, B Berta, D Csaban, IJ Jimoh, A Gal, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 191-192, 2019 | | 2019 |
| Az új generációs szekvenálás jelentősége az akut mieloid leukémia precíziós onkológiai megközelítésében H Andrikovics, P Kövy, A Bors, D Csabán, N Meggyesi, Z Őrfi, A Borsy, ... leukemia 63, 282-287, 2019 | | 2019 |
| The phenotypic spectrum of rare variants in NBIA (neurodegeneration brain iron accumulation) associated genes M Molnar, R Bencsik, V Molnar, D Csaban, Z Grosz, P Balicza, A Lengyel, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 401-401, 2018 | | 2018 |
| Genomic studies in early onset Alzheimer's disease (EOAD) in Hungary D Csaban, R Bencsik, Z Grosz, B Antal, V Remenyi, BA Fekete, D Zadori, ... EUROPEAN JOURNAL OF NEUROLOGY 25, 95-95, 2018 | | 2018 |
| Assessing genetic risk factors for Alzheimer's disease in a Hungarian cohort Z Grosz, R Bencic, V Remenyi, D Csaban, B Szatmari, MJ Molnar EUROPEAN JOURNAL OF NEUROLOGY 23, 346-346, 2016 | | 2016 |
