| Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia I Balogh, G Szôke, L Kárpáti, U Wartiovaara, E Katona, I Komáromi, ... Blood, The Journal of the American Society of Hematology 96 (7), 2479-2486, 2000 | 198 | 2000 |
| Analysis of Gas6 in human platelets and plasma I Balogh, S Hafizi, J Stenhoff, K Hansson, B Dahlbäck Arteriosclerosis, thrombosis, and vascular biology 25 (6), 1280-1286, 2005 | 166 | 2005 |
| Effect of Val34Leu polymorphism on the activation of the coagulation factor XIII-A U Wartiovaara, H Mikkola, G Szoke, G Haramura, L Karpati, I Balogh, ... Thrombosis and haemostasis 84 (10), 595-600, 2000 | 131 | 2000 |
| A modified, optimized kinetic photometric assay for the determination of blood coagulation factor XIII activity in plasma L Karpati, B Penke, E Katona, I Balogh, G Vamosi, L Muszbek Clinical chemistry 46 (12), 1946-1955, 2000 | 121 | 2000 |
| A European spectrum of pharmacogenomic biomarkers: implications for clinical pharmacogenomics C Mizzi, E Dalabira, J Kumuthini, N Dzimiri, I Balogh, N Başak, R Böhm, ... PloS one 11 (9), e0162866, 2016 | 115 | 2016 |
| Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups H Jiao, B Tóth, M Erdős, I Fransson, É Rákóczi, I Balogh, Z Magyarics, ... Molecular immunology 46 (1), 202-206, 2008 | 101 | 2008 |
| Factor V Leiden as a risk factor for miscarriage and reduced fertility SN Bare, R Poka, I Balogh, E Ajzner Australian and New Zealand Journal of Obstetrics and Gynaecology 40 (2), 186-190, 2000 | 72 | 2000 |
| Human epididymis protein 4: a novel serum inflammatory biomarker in cystic fibrosis B Nagy Jr, B Nagy, L Fila, LA Clarke, F Gönczy, O Bede, D Nagy, ... Chest 150 (3), 661-672, 2016 | 59 | 2016 |
| The effect of small molecules on sterol homeostasis: measuring 7-dehydrocholesterol in Dhcr7-deficient Neuro2a cells and human fibroblasts Z Korade, HYH Kim, KA Tallman, W Liu, K Koczok, I Balogh, L Xu, ... Journal of medicinal chemistry 59 (3), 1102-1115, 2016 | 58 | 2016 |
| Severe coagulation factor V deficiency caused by 2 novel frameshift mutations: 2952delT in exon 13 and 5493insG in exon 16 of factor 5 gene E Ajzner, I Balogh, T Szabó, A Marosi, G Haramura, L Muszbek Blood, The Journal of the American Society of Hematology 99 (2), 702-705, 2002 | 51 | 2002 |
| The P28T mutation in the GALK1 gene accounts for galactokinase deficiency in Roma (Gypsy) patients across Europe M Hunter, E Heyer, F Austerlitz, D Angelicheva, V Nedkova, P Briones, ... Pediatric research 51 (5), 602-606, 2002 | 49 | 2002 |
| Anti-factor V auto-antibody in the plasma and platelets of a patient with repeated gastrointestinal bleeding E Ajzner, I Balogh, G Haramura, Z Boda, K Kalmar, G Pfliegler, ... Journal of Thrombosis and Haemostasis 1 (5), 943-949, 2003 | 41 | 2003 |
| Analysis of the population heterogeneity in Hungary using fifteen forensically informative STR markers B Egyed, S Füredi, M Angyal, I Balogh, L Kalmar, Z Padar Forensic science international 158 (2-3), 244-249, 2006 | 37 | 2006 |
| 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 | 34 | 2018 |
| Analysis of complement factor H Y402H, LOC387715, HTRA1 polymorphisms and ApoE alleles with susceptibility to age‐related macular degeneration in Hungarian patients G Losonczy, Á Fekete, Z Vokó, L Takács, I Káldi, É Ajzner, M Kasza, ... Acta ophthalmologica 89 (3), 255-262, 2011 | 33 | 2011 |
| Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system G Ivády, L Madar, E Dzsudzsák, K Koczok, J Kappelmayer, V Krulisova, ... BMC genomics 19, 1-8, 2018 | 32 | 2018 |
| Complete recovery from psychosis upon miglustat treatment in a juvenile Niemann–Pick C patient K Szakszon, I Szegedi, Á Magyar, É Oláh, M Andrejkovics, P Balla, ... european journal of paediatric neurology 18 (1), 75-78, 2014 | 31 | 2014 |
| Monogenic forms of diabetes mellitus Z Gaál, I Balogh Genetics of Endocrine Diseases and Syndromes, 385-416, 2019 | 30 | 2019 |
| Severe Shwachman-Diamond syndrome phenotype caused by compound heterozygous missense mutations in the SBDS gene M Erdős, K Alapi, I Balogh, G Oroszlán, É Rákóczi, J Sümegi, L Maródi Experimental hematology 34 (11), 1517-1521, 2006 | 30 | 2006 |
| Altered microRNAs expression levels of sperm and seminal plasma in patients with infertile ejaculates compared with normozoospermic males A Mokánszki, Z Molnár, E Varga Tóthné, B Bodnár, A Jakab, BL Bálint, ... Human Fertility 23 (4), 246-255, 2020 | 27 | 2020 |
László MuszbekProfessor emeritus, University of Debrecen, Research Professor, Hungarian Academy of SciencesEmail verificata su med.unideb.hu
