| Functional variants of interleukin-23 receptor gene confer risk for rheumatoid arthritis but not for systemic sclerosis B Faragó, L Magyari, E Sáfrány, V Csöngei, L Járomi, K Horvatovich, ... Annals of the rheumatic diseases 67 (2), 248-250, 2008 | 154 | 2008 |
| Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome A Maasz, P Kisfali, K Horvatovich, M Mohás, L Markó, V Csöngei, ... Pathology & Oncology Research 13, 243-247, 2007 | 83 | 2007 |
| Apolipoprotein A5 gene promoter region T-1131C polymorphism associates with elevated circulating triglyceride levels and confers susceptibility for development of ischemic stroke V Havasi, Z Szolnoki, G Talián, J Bene, K Komlósi, A Maász, ... Journal of molecular neuroscience 29, 177-183, 2006 | 74 | 2006 |
| Genetic variability and haplotype profile of MDR1 (ABCB1) in Roma and Hungarian population samples with a review of the literature C Sipeky, V Csongei, L Jaromi, E Safrany, A Maasz, I Takacs, J Beres, ... Drug metabolism and pharmacokinetics 26 (2), 206-215, 2011 | 63 | 2011 |
| Apolipoprotein A5 gene IVS3+ G476A allelic variant confers susceptibility for development of ischemic stroke A Maasz, P Kisfali, L Jaromi, K Horvatovich, Z Szolnoki, V Csongei, ... Circulation Journal 72 (7), 1065-1070, 2008 | 52 | 2008 |
| Haplotype analysis of the apolipoprotein A5 gene in patients with the metabolic syndrome P Kisfali, M Mohás, A Maász, N Polgar, F Hadarits, L Markó, P Brasnyó, ... Nutrition, Metabolism and Cardiovascular Diseases 20 (7), 505-511, 2010 | 50 | 2010 |
| GCKR gene functional variants in type 2 diabetes and metabolic syndrome: do the rare variants associate with increased carotid intima-media thickness? M Mohás, P Kisfali, L Járomi, A Maász, E Fehér, V Csöngei, N Polgár, ... Cardiovascular Diabetology 9, 1-7, 2010 | 49 | 2010 |
| Apolipoprotein A5 gene C56G variant confers risk for the development of large-vessel associated ischemic stroke A Maász, P Kisfali, Z Szolnoki, F Hadarits, B Melegh Journal of neurology 255, 649-654, 2008 | 44 | 2008 |
| Apolipoprotein A5 IVS3+ 476A allelic variant associates with increased trigliceride levels and confers risk for development of metabolic syndrome in Hungarians P Kisfali, M Mohás, A Maasz, F Hadarits, L Markó, K Horvatovich, ... Circulation Journal 72 (1), 40-43, 2008 | 43 | 2008 |
| Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation A Maasz, K Komlosi, K Hadzsiev, Z Szabo, PJ Willems, I Gerlinger, ... Current medicinal chemistry 15 (13), 1257-1262, 2008 | 39 | 2008 |
| Coexistence of angiotensin II type-1 receptor A1166C and angiotensin-converting enzyme D/D polymorphism suggests susceptibility for small-vessel-associated ischemic stroke Z Szolnoki, A Maasz, L Magyari, K Horvatovich, B Farago, F Somogyvari, ... Neuromolecular Medicine 8, 353-360, 2006 | 36 | 2006 |
| A polymorphism within the fructosamine-3-kinase gene is associated with HbA1c Levels and the onset of type 2 diabetes mellitus M Mohás, P Kisfali, E Baricza, A Mérei, A Maász, J Cseh, E Mikolás, ... Experimental and clinical endocrinology & diabetes 118 (03), 209-212, 2010 | 34 | 2010 |
| Functional variants of glucokinase regulatory protein and apolipoprotein A5 genes in ischemic stroke L Járomi, V Csöngei, N Polgár, Z Szolnoki, A Maász, K Horvatovich, ... Journal of molecular neuroscience 41, 121-128, 2010 | 32 | 2010 |
| Haplotype analysis of the apolipoprotein A5 gene in obese pediatric patients K Horvatovich, S Bokor, Á Baráth, A Maász, P Kisfali, L Járomi, N Polgár, ... International Journal of Pediatric Obesity 6 (sup3), e318-325, 2011 | 31 | 2011 |
| Triglyceride level modifying functional variants of GALTN2 and MLXIPL in patients with ischaemic stroke N Polgár, L Járomi, V Csöngei, A Maász, C Sipeky, E Sáfrány, M Szabo, ... European journal of neurology 17 (8), 1033-1039, 2010 | 23 | 2010 |
| Mitochondrial DNA 11777C> A mutation associated Leigh syndrome: case report with a review of the previously described pedigrees K Hadzsiev, A Maasz, P Kisfali, E Kalman, E Gomori, E Pal, E Berenyi, ... Neuromolecular medicine 12, 277-284, 2010 | 22 | 2010 |
| Prevalence of functional haplotypes of the peptidylarginine deiminase citrullinating enzyme gene in patients with rheumatoid arthritis: no influence of the presence of anti … B Farago, GC Talian, A Maasz, L Magyari, K Horvatovich, B Kovacs, ... Clinical and experimental rheumatology 25 (4), 523, 2007 | 21 | 2007 |
| Mutations of the apolipoprotein A5 gene with inherited hypertriglyceridaemia: review of the current literature B I Melegh, B Duga, K Sumegi, P Kisfali, A Maász, K Komlósi, K Hadzsiev, ... Current medicinal chemistry 19 (36), 6163-6170, 2012 | 20 | 2012 |
| Functional variants of lipid level modifier MLXIPL, GCKR, GALNT2, CILP2, ANGPTL3 and TRIB1 genes in healthy Roma and Hungarian populations K Sumegi, L Jaromi, L Magyari, E Kovesdi, B Duga, R Szalai, A Maasz, ... Pathology & Oncology Research 21, 743-749, 2015 | 19 | 2015 |
| Hodgkin disease therapy induced second malignancy susceptibility 6q21 functional variants in roma and hungarian population samples D Varszegi, B Duga, BI Melegh, K Sumegi, P Kisfali, A Maasz, B Melegh Pathology & Oncology Research 20, 529-533, 2014 | 17 | 2014 |
