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Sergey V. Voronin

Observed names: S V Voronin, S. V. Voronin, S. Voronin, S.V. Voronin, Sergei V. Voronin, Sergey V Voronin, Sergey Voronin, Воронин, С.В.
ORCID: 0000-0002-9918-9565
Observed ORCID: 0000-0002-9918-9565
OpenAlex ID: A5024085654
Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions
2017 · Elena A Bliznetz, Maria R Lalayants, et al. · Journal of Human Genetics · 39
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Advanced neonatal screening for hereditary diseases in Russia: first results and future prospects
2024 · S.V. Voronin, E.Yu. Zakharova, et al. · PEDIATRIA Journal named after G N SPERANSKY · 30
Newborn Screening for Severe T and B Cell Lymphopenia Using TREC/KREC Detection: A Large-Scale Pilot Study of 202,908 Newborns
2024 · Andrey V. Marakhonov, Irina Yu. Efimova, et al. · Journal of Clinical Immunology · 27
Neonatal screening for hereditary diseases in Russia: yesterday, today, and tomorrow
2022 · S.V. Voronin, S.I. Kutsev · Neonatology News Opinions Training · 21
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Epidemiology of Spinal Muscular Atrophy Based on the Results of a Large-Scale Pilot Project on 202,908 Newborns
2024 · Irina Yu. Efimova, Rena A. Zinchenko, et al. · Pediatric Neurology · 12
Genetic characterization of cystic fibrosis patients in Russian Federation according to the National Register, 2014
2016 · S. A. Krasovskiy, N. Yu. Kashirskaya, et al. · PULMONOLOGIYA · 11
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Decreased TREC and KREC levels in newborns with trisomy 21
2024 · Andrey Marakhonov, Anna Mukhina, et al. · Frontiers in Pediatrics · 6
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Neonatal Screening, Postnatal Diagnosis and Tactics of Preclinical Treatment and Prevention of Primary Immunodeficiencies in Children. Guidelines by the Experts From the National Association of Experts in Primary Immunodeficiencies (naepid) and the Association of Medical Genetics (amg) of Russia
2023 · S.V. Voronin, R.A. Zinchenko, et al. · PEDIATRIA Journal named after G N SPERANSKY · 6
Guidelines for routing, monitoring and management tactics of immunocompromised children at risk and patients with congenital immune defects [Reviewed by Drs. O.V. Zaytseva, N.I. Zakharova and O.V. Kalyuzhin. Approved as official Guidelines for Practitioners by the Educational and Methodological Commission of the Research and Clinical Institute of Childhood with the Moscow Oblast Healthcare Ministry (Mytishchi, Moscow Oblast, Russia), Record No. 8 dated Nov. 11, 2024]
2024 · A.P. Prodeus, N.D. Odinayeva, et al. · PEDIATRIA Journal named after G N SPERANSKY · 5
Newborn screening for primary immunodeficiencies as a way to detect syndromal disorders in neonates: a clinical case of 22q11.2DS syndrome
2022 · E. Yu. Efimova, A. A. Mukhina, et al. · Pediatric Hematology/Oncology and Immunopathology · 5
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Prevention and diagnosis of congenital malformations
2021 · Maria A. Astrakhantseva, Pavel F. Kiku, et al. · Health Care of the Russian Federation · 5
First 2-year experience of nationwide newborn screening for severe forms of T and B cell immunodeficiency: 2.3 million newborns analyzed using TREC and KREC in Russia
2026 · Andrey Marakhonov, Anna Mukhina, et al. · Frontiers in Immunology · 4
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A Rare Case of TP63-Associated Lymphopenia Revealed by Newborn Screening Using TREC
2024 · Andrey Marakhonov, Elena Serebryakova, et al. · International Journal of Molecular Sciences · 4
Protein linking fatty acids and its genetic regulation in children having food allergy
2022 · N. G. Prikhodchenko, T. A. Shumatova, et al. · Pacific Medical Journal · 4
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13q Deletion Syndrome Presenting with Lymphopenia Detected Through Newborn Screening for Primary Immunodeficiencies
2025 · Irina Efimova, Anna Mukhina, et al. · International Journal of Molecular Sciences · 3
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Harmonizing TREC Thresholds in Newborn Screening for SCID : Insights From Russian Validation Cohort
2025 · Andrey Marakhonov, Ekaterina Kalinina, et al. · Journal of Clinical Laboratory Analysis · 3
Инновационные методы диагностики и терапии муковисцидоза
2025 · S.N. Avdeev, A.V. Abrukova, et al. · 3
Two Years of Expanded Newborn Screening in Russia: High-Throughput Detection of Inherited Metabolic Disorders by Tandem Mass Spectrometry with Next-Generation Sequencing Confirmation
2026 · Ekaterina Y. Zakharova, Galina V. Baydakova, et al. · International Journal of Neonatal Screening · 2
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Genotype Structure Alterations in 5q SMA Patients as a Result of the Newborn Screening Program Implementation in the Russian Federation
2025 · Maria A. Akhkiamova, Andrey V. Marakhonov, et al. · International Journal of Molecular Sciences · 2
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Results of neonatal screening for cystic fibrosis (18-year follow-up)
2025 · I. R. Fatkhullina, E. I. Kondratyeva, et al. · PULMONOLOGIYA · 1
Routing improvement in the expanded neonatal screening system for primary immunodeficiencies diagnosis
2024 · A.V. Marakhonov, A.A. Mukhina, et al. · PEDIATRIA Journal named after G N SPERANSKY · 1
Rare Variants of the SMN1 Gene Detected during Neonatal Screening
2024 · Maria Akhkiamova, Aleksander Polyakov, et al. · Genes · 1
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Duchenne Muscular Dystrophy and Its Early Diagnosis. Relevance, Problematics, Possibilities, Prospects
2024 · Т.А. Gremyakova, О.I. Gremyakova, et al. · PEDIATRIA Journal named after G N SPERANSKY · 1
The optimization of prenatal diagnostic of inherent malformations in population of the Primorsky Krai
2019 · S. V. Voronin, Pavel F. Kiku, et al. · Health Care of the Russian Federation · 1
Congenital anomalies in Primorsky region
2015 · P. Kiku, S. Voronin, et al. · International Journal of Risk & Safety in Medicine · 1
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Works count: 49
Citation count: 197
H-index: 6
I10-index: 6
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