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Anita Maász

Observed names: A Maász, A. Maasz, A. Maász, Anita Maasz, Anita Maász, Maász, Anita
Institution: University of Pecs
Observed institution: University of Pecs
ORCID: 0000-0002-5051-7708
Observed ORCID: 0000-0002-5051-7708
OpenAlex ID: A5005314660
Functional variants of interleukin-23 receptor gene confer risk for rheumatoid arthritis but not for systemic sclerosis
2007 · B Faragó, L Magyari, et al. · Annals of the Rheumatic Diseases · 133
Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome
2007 · Anita Maász, Péter Kisfali, et al. · Pathology & Oncology Research · 61
Apolipoprotein A5 Gene Promoter Region T-1131C Polymorphism Associates With Elevated Circulating Triglyceride Levels and Confers Susceptibility for Development of Ischemic Stroke
2006 · Viktória Havasi, Zoltán Szolnoki, et al. · Journal of Molecular Neuroscience · 58
GCKR gene functional variants in type 2 diabetes and metabolic syndrome: do the rare variants associate with increased carotid intima-media thickness?
2010 · Márton Mohás, Péter Kisfali, et al. · Cardiovascular Diabetology · 51
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Genetic Variability and Haplotype Profile of MDR1 (ABCB1) in Roma and Hungarian Population Samples with a Review of the Literature
2010 · Csilla Sipeky, Veronika Csongei, et al. · Drug Metabolism and Pharmacokinetics · 50
Apolipoprotein A5 Gene IVS3+G476A Allelic Variant Confers Susceptibility for Development of Ischemic Stroke
2008 · Anita Maasz, Peter Kisfali, et al. · Circulation Journal · 44
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Haplotype analysis of the apolipoprotein A5 gene in patients with the metabolic syndrome
2009 · P. Kisfali, M. Mohás, et al. · Nutrition Metabolism and Cardiovascular Diseases · 37
Apolipoprotein A5 gene C56G variant confers risk for the development of large-vessel associated ischemic stroke
2008 · A. Maász, P. Kisfali, et al. · Journal of Neurology · 36
Phenotypic Variants of the Deafness-Associated Mitochondrial DNA A7445G Mutation
2008 · Anita Maasz, Katalin Komlosi, et al. · Current Medicinal Chemistry · 33
A Polymorphism within the Fructosamine-3-kinase Gene is Associated with HbA1c Levels and the Onset of Type 2 Diabetes Mellitus
2009 · M. Mohás, P. Kisfali, et al. · Experimental and Clinical Endocrinology & Diabetes · 31
Apolipoprotein A5 IVS3+476A Allelic Variant Associates With Increased Trigliceride Levels and Confers Risk for Development of Metabolic Syndrome in Hungarians
2007 · Péter Kisfali, Márton Mohás, et al. · Circulation Journal · 31
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Functional Variants of Glucokinase Regulatory Protein and Apolipoprotein A5 Genes in Ischemic Stroke
2009 · Luca Járomi, Veronika Csöngei, et al. · Journal of Molecular Neuroscience · 28
Haplotype analysis of the apolipoprotein A5 gene in obese pediatric patients
2010 · Katalin Horvatovich, Szilvia Bokor, et al. · International Journal of Pediatric Obesity · 27
Coexistence of angiotensin II type-1 receptor A1166C and angiotensin-converting enzyme D/D polymorphism suggests susceptibility for small-vessel-associated ischemic stroke
2006 · Zoltán Szolnoki, Anita Maasz, et al. · NeuroMolecular Medicine · 25
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Triglyceride level modifying functional variants of GALTN2 and MLXIPL in patients with ischaemic stroke
2010 · N. Polgár, L. Járomi, et al. · European Journal of Neurology · 18
Mitochondrial DNA 11777C>A Mutation Associated Leigh Syndrome: Case Report with a Review of the Previously Described Pedigrees
2010 · Kinga Hadzsiev, Anita Maasz, et al. · NeuroMolecular Medicine · 17
Three-Year Follow-Up after Intrauterine mTOR Inhibitor Administration for Fetus with TSC-Associated Rhabdomyoma
2023 · Anita Maász, Tímea Bodó, et al. · International Journal of Molecular Sciences · 16
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Mutations of the Apolipoprotein A5 Gene with Inherited Hypertriglyceridaemia: Review of the Current Literature
2012 · B. I. Melegh, B. Duga, et al. · Current Medicinal Chemistry · 16
TUBB4B gene mutation in Leber phenotype of congenital amaurosis syndrome associated with early-onset deafness
2022 · Anita Maasz, Kinga Hadzsiev, et al. · European Journal of Medical Genetics · 15
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Functional Variants of Lipid Level Modifier MLXIPL, GCKR, GALNT2, CILP2, ANGPTL3 and TRIB1 Genes in Healthy Roma and Hungarian Populations
2015 · Katalin Sumegi, Luca Jaromi, et al. · Pathology & Oncology Research · 15
Association of myasthenia gravis with polymorphisms in the gene of histamine N-methyltransferase
2013 · Blanka Kellermayer, Noemi Polgar, et al. · Human Immunology · 11
Common functional variants of APOA5 and GCKR accumulate gradually in association with triglyceride increase in metabolic syndrome patients
2011 · Ferenc Hadarits, Péter Kisfali, et al. · Molecular Biology Reports · 11
The combination of homozygous MTHFR 677T and angiotensin II type-1 receptor 1166C variants confers the risk of small-vessel-associated ischemic stroke
2007 · Zoltan Szolnoki, Anita Maasz, et al. · Journal of Molecular Neuroscience · 11
Hodgkin Disease Therapy Induced Second Malignancy Susceptibility 6q21 Functional Variants in Roma and Hungarian Population Samples
2013 · Dalma Varszegi, Balazs Duga, et al. · Pathology & Oncology Research · 10
Three periods of one and a half decade of ischemic stroke susceptibility gene research: lessons we have learned
2010 · Anita Maasz, Bela Melegh · Genome Medicine · 10
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Works count: 51
Citation count: 898
H-index: 16
I10-index: 26
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