| Marked differences in frequencies of statin therapy relevant SLCO1B1 variants and haplotypes between Roma and Hungarian populations A Nagy, C Sipeky, R Szalai, BI Melegh, P Matyas, A Ganczer, K Toth, ... BMC genetics 16, 1-7, 2015 | 27 | 2015 |
| Increased prevalence of functional minor allele variants of drug metabolizing CYP2B6 and CYP2D6 genes in Roma population samples A Weber, R Szalai, C Sipeky, L Magyari, M Melegh, L Jaromi, P Matyas, ... Pharmacological Reports 67, 460-464, 2015 | 26 | 2015 |
| Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions G Büki, A Zsigmond, M Czakó, R Szalai, G Antal, V Farkas, G Fekete, ... Frontiers in Genetics 12, 673025, 2021 | 20 | 2021 |
| 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 |
| Kleefstra syndrome in Hungarian patients: additional symptoms besides the classic phenotype K Hadzsiev, K Komlosi, M Czako, B Duga, R Szalai, A Szabo, E Postyeni, ... Molecular Cytogenetics 9, 1-6, 2016 | 17 | 2016 |
| Interethnic variability of CYP4F2 (V433M) in admixed population of Roma and Hungarians C Sipeky, A Weber, BI Melegh, P Matyas, I Janicsek, R Szalai, I Szabo, ... Environmental toxicology and pharmacology 40 (1), 280-283, 2015 | 13 | 2015 |
| Marked differences of haplotype tagging SNP distribution, linkage, and haplotype profile of IL23 receptor gene in Roma and Hungarian population samples L Magyari, D Varszegi, P Sarlos, L Jaromi, BI Melegh, B Duga, P Kisfali, ... Cytokine 65 (2), 148-152, 2014 | 13 | 2014 |
| Cytochrome P450 drug metabolizing enzymes in Roma population samples: systematic review of the literature R Szalai, K Hadzsiev, B Melegh Current Medicinal Chemistry 23 (31), 3632-3652, 2016 | 12 | 2016 |
| Extreme differences in SLCO1B3 functional polymorphisms in Roma and Hungarian populations A Nagy, R Szalai, L Magyari, J Bene, K Toth, B Melegh Environmental toxicology and pharmacology 39 (3), 1246-1251, 2015 | 12 | 2015 |
| Admixture of beneficial and unfavourable variants of GLCCI1 and FCER2 in Roma samples can implicate different clinical response to corticosteroids R Szalai, P Matyas, D Varszegi, M Melegh, L Magyari, L Jaromi, K Sumegi, ... Molecular biology reports 41, 7665-7669, 2014 | 12 | 2014 |
| Genetic polymorphisms in promoter and intronic regions of CYP1A2 gene in Roma and Hungarian population samples R Szalai, L Magyari, P Matyas, B Duga, Z Banfai, A Szabo, E Kovesdi, ... Environmental Toxicology and Pharmacology 38 (3), 814-820, 2014 | 11 | 2014 |
| Age-Related Hearing Impairment Associated NAT2, GRM7, GRHL2 Susceptibility Gene Polymorphisms and Haplotypes in Roma and Hungarian Populations P Matyas, E Postyeni, K Komlosi, R Szalai, J Bene, L Magyari, B Melegh, ... Pathology & Oncology Research 25, 1349-1355, 2019 | 8 | 2019 |
| A rare form of ion channel gene mutation identified as underlying cause of generalized epilepsy Á Till, R Szalai, M Hegyi, E Kövesdi, G Büki, K Hadzsiev, B Melegh Orvosi Hetilap 160 (21), 835-838, 2019 | 8 | 2019 |
| Lower carrier rate of GJB2 W24X ancestral Indian mutation in Roma samples from Hungary: implication for public health intervention C Sipeky, P Matyas, M Melegh, I Janicsek, R Szalai, I Szabo, R Varnai, ... Molecular biology reports 41, 6105-6110, 2014 | 8 | 2014 |
| Maternal mosaicism underlies the inheritance of a rare germline AKT3 variant which is responsible for megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome in two … R Szalai, BI Melegh, A Till, R Ripszam, G Csabi, A Acharya, I Schrauwen, ... Experimental and molecular pathology 115, 104471, 2020 | 7 | 2020 |
| Interethnic differences of cytochrome P450 gene polymorphisms may influence outcome of taxane therapy in Roma and Hungarian populations R Szalai, A Ganczer, L Magyari, P Matyas, J Bene, B Melegh Drug Metabolism and Pharmacokinetics 30 (6), 453-456, 2015 | 6 | 2015 |
| Correlation between large FBN1 deletions and severe cardiovascular phenotype in Marfan syndrome: Analysis of two novel cases and analytical review of the … G Buki, R Szalai, A Pinter, K Hadzsiev, B Melegh, T Rauch, J Bene Molecular Genetics & Genomic Medicine 11 (7), e2166, 2023 | 1 | 2023 |
| Overlapping Interstitial Deletions of the Region 9q22. 33 to 9q33. 3 of Three Patients Allow Pinpointing Candidate Genes for Epilepsy and Cleft Lip and Palate R Szalai, A Till, A Szabo, B Melegh, K Hadzsiev, M Czako Molecular Syndromology 14 (2), 109-122, 2023 | 1 | 2023 |
| Generalizált epilepszia hátterében azonosított ioncsatorna-génmutáció ritka formája Á Till, R Szalai, M Hegyi, E Kövesdi, G Büki, K Hadzsiev, B Melegh Orvosi Hetilap 160 (21), 835-838, 2019 | 1 | 2019 |
| NGS-Based Identification of Two Novel PCDH19 Mutations in Female Patients with Early-Onset Epilepsy R Szalai, K Hadzsiev, A Till, A Fogarasi, T Bodo, G Buki, Z Banfai, J Bene International Journal of Molecular Sciences 25 (11), 5732, 2024 | | 2024 |
