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I. Guryanova · SciRah

Researcher profile · Semantic Scholar

I. Guryanova

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I. Guryanova — researcher profile on SciRah

h-index: 6
Works: 25
Citations: 124

Most-cited papers

Late-onset combined immune deficiency associated to skin granuloma due to heterozygous compound mutations in RAG1 gene in a 14 years old male.
S. Sharapova, A. Migas, I. Guryanova, S. Aleshkevich +3 more
2013Human Immunology32 citations
Semantic Scholar
Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene
I. Guryanova, C. Suffritti, D. Parolin, A. Zanichelli +9 more
2021Clinical and Molecular Allergy27 citations Open access
Semantic Scholar
Next generation sequencing revealed DNA ligase IV deficiency in a "developmentally normal" patient with massive brain Epstein-Barr virus-positive diffuse large B-cell lymphoma.
S. Sharapova, Elizabeth Chang, I. Guryanova, Inna V. Proleskovskaya +3 more
2016Clinical Immunology18 citations
Semantic Scholar
Molecular Characteristics, Clinical and Immunologic Manifestations of 11 Children with Omenn Syndrome in East Slavs (Russia, Belarus, Ukraine)
S. Sharapova, I. Guryanova, O. Pashchenko, I. Kondratenko +9 more
2015Journal of Clinical Immunology17 citations
Semantic Scholar
Recent thymic emigrants, T regulatory cells, and BAFF level in children with X-linked agammaglobulinaemia in association with chronic respiratory disease.
S. Sharapova, O. Pashchenko, I. Guryanova, Alexandr A. Migas +2 more
2018Allergologia et Immunopathologia10 citations Open access
Semantic Scholar
Novel LRBA Mutation and Possible Germinal Mosaicism in a Slavic Family
S. Sharapova, E. Haapaniemi, I. Sakovich, Jessica Rojas +7 more
2018Journal of Clinical Immunology6 citations
Semantic Scholar
Novel Mutations in SH2D1A Gene in X-linked Lymphoproliferative Syndrome, Diagnosed After B-Cell Non-Hodgkin Lymphoma
S. Sharapova, A. Fedorova, O. Pashchenko, Svetlana S Vahliarskaya +4 more
2017Journal of pediatric hematology/oncology6 citations
Semantic Scholar
Novel biallelic ATM mutations coexist with a mosaic form of triple X syndrome in an 11-year-old girl at remission after T cell acute leukemia
S. Sharapova, A. Valochnik, I. Guryanova, I. Sakovich +1 more
2018Immunogenetics4 citations
Semantic Scholar
Nijmegen breakage syndrome in two half sibs with peripheral T-cell lymphoma and cortical T-cell acute lymphoid leukemia
S. Sharapova, E. I. Golovataya, E. V. Shepelevich, Yuliya E. Mareika +3 more
2021Central European Journal of Immunology3 citations Open access
Semantic Scholar
Abstracts of the 14th C1-inhibitor Deficiency and Angioedema Workshop
Katalin Karikó, Steffen Thiel, A. E. Germenis, László Cervenak +158 more
2025Allergy, Asthma & Clinical Immunology1 citations Open access
Semantic Scholar
Molecular genetic diagnosis of hereditary angioedema
I. Guryanova, Y. Zharankova, E. Polyakova, V. V. Pugacheva +3 more
2021Proceedings of the National Academy of Sciences of Belarus Medical series1 citations Open access
Semantic Scholar
Role of multiplex ligation-dependent probe amplification in hemophilia A: analysis of large F8 variants
A. V. Liubushkin, E. Dmitriev, E. Polyakova, L. I. Volkova +1 more
2026Medical and Biological Problems of Life Activity0 citations Open access
Semantic Scholar
Newborn Screening Inborn Errors of Immunity in the Republic of Belarus: The First Pilot Study
E. Polyakova, T. Volodashchik, O. L. Zobikova, A. V. Liubushkin +10 more
2026Journal of Human Immunity0 citations Open access
Semantic Scholar
Newborn screening for inborn errors of immunity in the Republic of Belarus: a two-year pilot study and initial clinical results
E. Polyakova, T. Volodashchik, O. Zobikova, E. Kalinina +11 more
2026Immunopathology, Allergology, Infectology0 citations Open access
Semantic Scholar
Diagnostic significance of determining products of DNA rearrangments of the T-and-B cell receptor TREC/KREC in common variable immunodeficiency
E. Polyakova, I. Guryanova, S. Sharapova, I. Sakovich +9 more
2024Medical and Biological Problems of Life Activity0 citations Open access
Semantic Scholar
The use of next generation sequencing technologies for the diagnosis of inborn errors of immunity
E. Polyakova, I. Guryanova, V. Vertelko, A. V. Liubushkin +5 more
2023Pediatric Hematology/Oncology and Immunopathology0 citations Open access
Semantic Scholar
Diagnostic significance of determining TREC and KREC T- and B-cell receptor rearrangement products in patients with inborn immune errors
E. Polyakova, M. Stegantseva, I. Guryanova, D. Lutskovich +6 more
2023Proceedings of the National Academy of Sciences of Belarus Medical series0 citations Open access
Semantic Scholar
Molecular genetic diagnosis in the group of hemophilia A patients in Belarus: 12 new allelic variants in the F8 gene
A. V. Liubushkin, I. Guryanova, E. Dmitriev, V. Vertelko +3 more
2023Pediatric Hematology/Oncology and Immunopathology0 citations Open access
Semantic Scholar
Patients with hereditary angioedema and patients with SARS-CoV-2-associated pneumonia – what can be similar?
I. Guryanova, A. Liubushkin, V. Kazak, Y. Zharankova +3 more
2023Clinical Immunology0 citations Open access
Semantic Scholar
Clinical efficiency of the cleaved high-molecular-weight kininogen detection in the diagnosis of hereditary angioedema
I. Guryanova, E. Polyakova, Chiara Suffritti, L. Korosteleva +3 more
2023Medical and Biological Problems of Life Activity0 citations Open access
Semantic Scholar
The first results of genetic screening and exploration of genotype-phenotype correlations in retinoblastoma patients from Belarus
I. Guryanova, A. V. Liubushkin, O. O. Makarevich, D. Litvinova +5 more
2022Pediatric Hematology/Oncology and Immunopathology0 citations Open access
Semantic Scholar
Genetic defects in patients with primary immunodeficiencies in the Republic of Belarus
M. Belevtsev, V. V. Pugacheva, I. Guryanova, E. Polyakova +8 more
2020Proceedings of the National Academy of Sciences of Belarus Medical series0 citations Open access
Semantic Scholar
Mutational spectrum of the SERPING1 gene in patients with hereditary angioedema
I. Guryanova, K. Paliakova, M. Belevtsev, O. Aleynikova
2019Proceedings of the National Academy of Sciences of Belarus Medical series0 citations Open access
Semantic Scholar
Мутационный спектр гена SERPING1 у пациентов с врожденным ангионевротическим отеком
I. Guryanova, K. A. Paliakova, M. Belevtsev, O. V. Aleynikova
20190 citations Open access
Semantic Scholar
Novel biallelic ATM mutations coexist with a mosaic form of triple X syndrome in an 11-year-old girl at remission after T cell acute leukemia
S. Sharapova, A. Valochnik, I. Guryanova, I. Sakovich +1 more
2018Immunogenetics0 citations
Semantic Scholar

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