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Á. Szilágyi · SciRah

Researcher profile · Semantic Scholar

Á. Szilágyi

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Á. Szilágyi — researcher profile on SciRah

h-index: 23
Works: 110
Citations: 1,690

Most-cited papers

Efficacy of Eculizumab in a Patient With Immunoadsorption-Dependent Catastrophic Antiphospholipid Syndrome: A Case Report
Andreas Kronbichler, R. Frank, M. Kirschfink, Á. Szilágyi +5 more
2014Medicine100 citations Open access
Semantic Scholar
Multivariate Analysis of Dopaminergic Gene Variants as Risk Factors of Heroin Dependence
A. Vereczkei, Z. Demetrovics, A. Székely, P. Sarkozy +4 more
2013PLoS ONE82 citations Open access
Semantic Scholar
Structural Basis for the Function of Complement Component C4 within the Classical and Lectin Pathways of Complement
S. Mortensen, R. Kidmose, S. Petersen, Á. Szilágyi +2 more
2015Journal of Immunology81 citations Open access
Semantic Scholar
The role of complement in Streptococcus pneumoniae-associated haemolytic uraemic syndrome.
Á. Szilágyi, N. Z. Kiss, C. Bereczki, G. Tálosi +10 more
2013Nephrology, Dialysis and Transplantation79 citations Open access
Semantic Scholar
Novel duplication in the F12 gene in a patient with recurrent angioedema.
N. Z. Kiss, E. Barabás, Katalin Várnai, A. Halász +4 more
2013Clinical Immunology77 citations
Semantic Scholar
Hereditary angioedema: molecular and clinical differences among European populations.
M. Speletas, Á. Szilágyi, F. Psarros, D. Moldovan +11 more
2015Journal of Allergy and Clinical Immunology75 citations
Semantic Scholar
Maternal and Fetal Outcomes of Pregnancies in Women with Atypical Hemolytic Uremic Syndrome.
M. Gaggl, C. Aigner, D. Csuka, Á. Szilágyi +7 more
2018Journal of the American Society of Nephrology70 citations Open access
Semantic Scholar
The Major Autoantibody Epitope on Factor H in Atypical Hemolytic Uremic Syndrome Is Structurally Different from Its Homologous Site in Factor H-related Protein 1, Supporting a Novel Model for Induction of Autoimmunity in This Disease
A. Bhattacharjee, S. Reuter, Eszter Trojnar, R. Kołodziejczyk +8 more
2015Journal of Biological Chemistry70 citations Open access
Semantic Scholar
F12‐46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema
M. Speletas, Á. Szilágyi, D. Csuka, N. Koutsostathis +8 more
2015Allergy. European Journal of Allergy and Clinical Immunology48 citations
Semantic Scholar
Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations.
A. Bors, D. Csuka, L. Varga, H. Farkas +3 more
2013Journal of Allergy and Clinical Immunology44 citations
Semantic Scholar
Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndrome.
N. Szarvas, Á. Szilágyi, D. Csuka, Beáta Takács +12 more
2016Molecular Immunology41 citations
Semantic Scholar
Contribution of Serotonin Transporter Gene Polymorphisms to Pediatric Migraine
Á. Szilágyi, K. Boór, I. Orosz, E. Szántai +4 more
2006Headache40 citations
Semantic Scholar
Polymorphisms of TNF-alpha and LT-alpha genes in multiple myeloma.
K. Kadar, M. Kovács, I. Karádi, B. Melegh +7 more
2008Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis37 citations
Semantic Scholar
Muscle strength is associated with vitamin D receptor gene variants
Árpád Bozsódi, Sara Boja, Á. Szilágyi, A. Somhegyi +2 more
2016Journal of Orthopaedic Research36 citations Open access
Semantic Scholar
Heterogeneity but individual constancy of epitopes, isotypes and avidity of factor H autoantibodies in atypical hemolytic uremic syndrome.
P. Nozal, Maria E. Bernabéu-Herrero, B. Uzonyi, Á. Szilágyi +6 more
2016Molecular Immunology32 citations
Semantic Scholar
Concentration and Subclass Distribution of Anti-ADAMTS13 IgG Autoantibodies in Different Stages of Acquired Idiopathic Thrombotic Thrombocytopenic Purpura
György Sinkovits, Á. Szilágyi, P. Farkas, D. Inotai +5 more
2018Frontiers in Immunology31 citations Open access
Semantic Scholar
Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patients.
F. Mohlin, Sara C. Nilsson, T. K. Levart, E. Golubović +10 more
2015Molecular Immunology31 citations
Semantic Scholar
Real-time PCR quantification of human complement C4A and C4B genes
Á. Szilágyi, B. Blaskó, Denes Szilassy, G. Fust +2 more
2006BMC Genetics28 citations Open access
Semantic Scholar
Validation of distinct pathogenic patterns in a cohort of membranoproliferative glomerulonephritis patients by cluster analysis
Nóra Garam, Z. Prohászka, Á. Szilágyi, C. Aigner +57 more
2019Clinical Kidney Journal26 citations Open access
Semantic Scholar
Risk factors of non-specific spinal pain in childhood
Julia Szita, Sara Boja, Á. Szilágyi, A. Somhegyi +2 more
2018European spine journal26 citations
Semantic Scholar
Fine-tuned characterization of RCCX copy number variants and their relationship with extended MHC haplotypes
Z. Bánlaki, M. Doleschall, K. Rajczy, G. Fust +1 more
2012Genes and Immunity26 citations
Semantic Scholar
Comparative analysis of IL6 promoter and receptor polymorphisms in myelodysplasia and multiple myeloma.
István Aladzsity, M. Kovács, Á. Semsei, A. Falus +5 more
2009Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis26 citations
Semantic Scholar
Diseases associated with the low copy number of the C4B gene encoding C4, the fourth component of complement
Á. Szilágyi, G. Füst
2009Cytogenetic and Genome Research23 citations
Semantic Scholar
Capillary gel electrophoresis analysis of G-quartet forming oligonucleotides used in DNA-protein interaction studies.
Á. Szilágyi, G. Bonn, A. Guttman
2007Journal of Chromatography A23 citations
Semantic Scholar
Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups
L. Hurler, Á. Szilágyi, F. Mescia, L. Bergamaschi +24 more
2023Frontiers in Immunology22 citations Open access
Semantic Scholar
C4 nephritic factor in patients with immune-complex-mediated membranoproliferative glomerulonephritis and C3-glomerulopathy
Nóra Garam, Z. Prohászka, Á. Szilágyi, C. Aigner +57 more
2019Orphanet Journal of Rare Diseases22 citations Open access
Semantic Scholar
The role of human leukocyte antigen DRB1-DQB1 haplotypes in the susceptibility to acquired idiopathic thrombotic thrombocytopenic purpura.
György Sinkovits, Á. Szilágyi, P. Farkas, D. Inotai +5 more
2017Human Immunology22 citations
Semantic Scholar
International consensus on the use of genetics in the management of hereditary angioedema.
A. E. Germenis, M. Margaglione, J. Pesquero, H. Farkas +60 more
2020Journal of Allergy and Clinical Immunology: In Practice21 citations Open access
Semantic Scholar
Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene
Z. Banlaki, J. Szabó, Á. Szilágyi, A. Patócs +3 more
2012Genome Biology and Evolution21 citations Open access
Semantic Scholar
Serum concentration of immunoglobulin G‐type antibodies against the whole Epstein–Barr nuclear antigen 1 and its aa35–58 or aa398–404 fragments in the sera of patients with systemic lupus erythematosus and multiple sclerosis
D. Csuka, D. Simon, R. Hóbor, K. Uray +13 more
2013Clinical and Experimental Immunology19 citations Open access
Semantic Scholar
Frequent occurrence of conserved extended haplotypes (CEHs) in two Caucasian populations.
Á. Szilágyi, Z. Banlaki, É. Pozsonyi, E. Yunis +7 more
2010Molecular Immunology19 citations
Semantic Scholar
Atypical hemolytic uremic syndrome triggered by mRNA vaccination against SARS-CoV-2: Case report
R. Ryšavá, M. Peiskerová, V. Tesar, J. Beneš +4 more
2022Frontiers in Immunology18 citations Open access
Semantic Scholar
FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy
Nóra Garam, M. Cserhalmi, Z. Prohászka, Á. Szilágyi +64 more
2021Frontiers in Immunology18 citations Open access
Semantic Scholar
HLA-association of serum levels of natural antibodies.
É. Pozsonyi, Bence György, T. Berki, Z. Banlaki +7 more
2009Molecular Immunology18 citations
Semantic Scholar
A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics
M. Doleschall, A. Luczay, Klára Koncz, K. Hadzsiev +14 more
2017European Journal of Human Genetics17 citations Open access
Semantic Scholar
Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome
Irene Gómez Delgado, F. Corvillo, P. Nozal, Emilia Arjona +8 more
2021Frontiers in Immunology16 citations Open access
Semantic Scholar
Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema
M. Iuraşcu, Zsuzsanna Balla, Catarina Pereira, Noémi Andrási +9 more
2023Clinical and Translational Allergy15 citations Open access
Semantic Scholar
Common Genetic Variants of the Human Steroid 21-Hydroxylase Gene (CYP21A2) Are Related to Differences in Circulating Hormone Levels
M. Doleschall, J. Szabó, J. Pazmandi, Á. Szilágyi +10 more
2014PLoS ONE15 citations Open access
Semantic Scholar
Analysis of the 8.1 ancestral MHC haplotype in severe, pneumonia-related sepsis.
István Aladzsity, K. Madách, Á. Szilágyi, J. Gal +3 more
2011Clinical Immunology15 citations
Semantic Scholar
Comparative analysis of IL6 and IL6 receptor gene polymorphisms in mastocytosis
Eszter Rausz, Á. Szilágyi, B. Nedoszytko, Magdalena Lange +11 more
2013British Journal of Haematology13 citations Open access
Semantic Scholar
Autoimmune-associated HLA-B8-DR3 haplotypes in Asian Indians are unique in C4 complement gene copy numbers and HSP-2 1267A/G.
G. Kaur, Neeraj Kumar, Á. Szilágyi, B. Blaskó +7 more
2008Human Immunology13 citations
Semantic Scholar
Analysis of Linear Antibody Epitopes on Factor H and CFHR1 Using Sera of Patients with Autoimmune Atypical Hemolytic Uremic Syndrome
Eszter Trojnar, M. Józsi, K. Uray, D. Csuka +13 more
2017Frontiers in Immunology12 citations Open access
Semantic Scholar
Hemolytic uremic syndrome in the setting of COVID-19 successfully treated with complement inhibition therapy: An instructive case report of a previously healthy toddler and review of literature
Matija Matošević, I. Kos, M. Davidović, M. Ban +9 more
2023Frontiers in Pediatrics11 citations Open access
Semantic Scholar
Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence
Noémi Andrási, Zsuzsanna Balla, B. Visy, Á. Szilágyi +3 more
2022Frontiers in Allergy11 citations Open access
Semantic Scholar
Variant Transthyretin Amyloidosis (ATTRv) in Hungary: First Data on Epidemiology and Clinical Features
Z. Pozsonyi, G. Peskó, H. Takács, D. Csuka +16 more
2021Genes11 citations Open access
Semantic Scholar
First-line therapy in atypical hemolytic uremic syndrome: consideration on infants with a poor prognosis
N. Szarvas, Á. Szilágyi, V. Tasic, Valbona Nushi-Stavileci +10 more
2014Italian Journal of Pediatrics10 citations Open access
Semantic Scholar
Both Positive and Negative Selection Pressures Contribute to the Polymorphism Pattern of the Duplicated Human CYP21A2 Gene
J. Szabó, Á. Szilágyi, Z. Doleschall, A. Patócs +5 more
2013PLoS ONE10 citations Open access
Semantic Scholar
ACTH‐induced cortisol release is related to the copy number of the C4B gene encoding the fourth component of complement in patients with non‐functional adrenal incidentaloma
Z. Banlaki, György Raizer, Bence Ács, J. Majnik +5 more
2012Clinical Endocrinology9 citations Open access
Semantic Scholar
Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema
E. Szabó, D. Csuka, Noémi Andrási, L. Varga +2 more
2022Frontiers in Allergy8 citations Open access
Semantic Scholar
The role of mannose binding lectin on fever episodes in pediatric oncology patients
Ferenc Fekete, Balázs Fadgyas, É. Papp, Á. Szilágyi +3 more
2015Pathology and Oncology Research8 citations
Semantic Scholar

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Z. Prohászka×27
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G. Füst×8
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