| High-coverage whole-exome sequencing identifies candidate genes for suicide in victims with major depressive disorder D Tombácz, Z Maróti, T Kalmár, Z Csabai, Z Balázs, S Takahashi, ... Scientific reports 7 (1), 7106, 2017 | 68 | 2017 |
| Y-chromosome haplogroups from Hun, Avar and conquering Hungarian period nomadic people of the Carpathian Basin E Neparáczki, Z Maróti, T Kalmár, K Maár, I Nagy, D Latinovics, Á Kustár, ... Scientific Reports 9 (1), 16569, 2019 | 67 | 2019 |
| Mitogenomic data indicate admixture components of Central-Inner Asian and Srubnaya origin in the conquering Hungarians E Neparáczki, Z Maróti, T Kalmár, K Kocsy, K Maár, P Bihari, I Nagy, ... PLoS One 13 (10), e0205920, 2018 | 62 | 2018 |
| Revising mtDNA haplotypes of the ancient Hungarian conquerors with next generation sequencing E Neparáczki, K Kocsy, GE Tóth, Z Maróti, T Kalmár, P Bihari, I Nagy, ... PLoS One 12 (4), e0174886, 2017 | 51 | 2017 |
| The genetic origin of Huns, Avars, and conquering Hungarians Z Maróti, E Neparáczki, O Schütz, K Maár, GIB Varga, B Kovács, T Kalmár, ... Current Biology 32 (13), 2858-2870. e7, 2022 | 43 | 2022 |
| Genetic polymorphisms and the risk of progressive renal failure in elderly H ungarian patients M Zsom, T Fueloep, L Zsom, A Barath, Z Maroti, E ENDREFFY Hemodialysis International 15 (4), 501-508, 2011 | 37 | 2011 |
| Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third PL Nagy, J Olasz, E Neparáczki, N Rouse, K Kapuria, S Cano, H Chen, ... European Journal of Human Genetics 29 (1), 164-172, 2021 | 35 | 2021 |
| Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies T Szabó, P Orosz, E Balogh, E Jávorszky, I Máttyus, C Bereczki, Z Maróti, ... Pediatric Nephrology 33, 1713-1721, 2018 | 35 | 2018 |
| Cerebrospinal Fluid Neurofilament Light Chain Is Associated with Kynurenine Pathway Metabolite Changes in Multiple Sclerosis C Rajda, Z Galla, H Polyák, Z Maróti, K Babarczy, D Pukoli, L Vécsei International journal of molecular sciences 21 (8), 2665, 2020 | 28 | 2020 |
| Diffuse mesangial sclerosis in a PDSS2 mutation-induced coenzyme Q10 deficiency B Iványi, GZ Rácz, P Gál, K Brinyiczki, I Bódi, T Kalmár, Z Maróti, ... Pediatric Nephrology 33, 439-446, 2018 | 28 | 2018 |
| Partial RAG deficiency in a patient with varicella infection, autoimmune cytopenia, and anti-cytokine antibodies V Goda, A Malik, T Kalmar, Z Maroti, B Patel, B Ujhaz, K Csomos, JE Hale, ... The journal of allergy and clinical immunology. In practice 6 (5), 1769, 2018 | 25 | 2018 |
| Maternal Lineages from 10–11th Century Commoner Cemeteries of the Carpathian Basin K Maár, GIB Varga, B Kovács, O Schütz, Z Maróti, T Kalmár, E Nyerki, ... Genes 12 (3), 460, 2021 | 23 | 2021 |
| A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature M Zombor, T Kalmár, N Nagy, M Berényi, B Telcs, Z Maróti, O Brandau, ... Journal of applied genetics 60, 151-162, 2019 | 23 | 2019 |
| Heme oxygenase-1 expression in premature and mature neonates during the first week of life Z Maróti, M Katona, H Orvos, I Németh, I Farkas, S Túri European journal of pediatrics 166, 1033-1038, 2007 | 21 | 2007 |
| Increased heme oxygenase-1 expression in premature infants with respiratory distress syndrome I Farkas, Z Maróti, M Katona, E Endreffy, P Monostori, K Máder, S Túri European journal of pediatrics 167, 1379-1383, 2008 | 17 | 2008 |
| Myopia-26, the female-limited form of early-onset high myopia, occurring in a European family N Széll, T Fehér, Z Maróti, T Kalmár, D Latinovics, I Nagy, ZZ Orosz, ... Orphanet Journal of Rare Diseases 16, 1-13, 2021 | 16 | 2021 |
| Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis Z Maróti, Z Boldogkői, D Tombácz, M Snyder, T Kalmár BMC genomics 19, 1-13, 2018 | 16 | 2018 |
| Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation L Szpisjak, VL Nemeth, N Szepfalusi, D Zadori, Z Maroti, T Kalmar, ... The Cerebellum 16, 979-985, 2017 | 14 | 2017 |
| Heme oxygenase 1 expression in young uremic patients on hemodialysis Z Maróti, I Németh, S Túri, E Karg, P Ugocsai, E Endreffy Pediatric Nephrology 19, 426-431, 2004 | 14 | 2004 |
| Refinement and delineation of the breakpoint regions of a chromosome 1; 22 translocation in a patient with Costello syndrome Z Maróti, K Kutsche, M Sutajova, A Gal, HG Nothwang, AE Czeizel, ... American journal of medical genetics 109 (3), 234-237, 2002 | 14 | 2002 |
