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Tatiana S. Beskorovainaya

Observed names: T. Beskorovainaya, T. S. Beskorovainaya, T.S. Beskorovainaya, Tatiana Beskorovainaya, Tatyana Beskorovainaya, Tatyana S. Beskorovainaya, Бескоровайная, Т.С., Т. С. Бескоровайная, Т.С. Бескоровайная
ORCID: 0000-0001-5656-2561
Observed ORCID: 0000-0001-5656-2561
OpenAlex ID: A5002185157
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
The frequency and spectrum of mutations and the IVS8-T polymorphism of the CFTR gene in Russian infertile men
2010 · V. B. Chernykh, A. A. Stepanova, et al. · Russian Journal of Genetics · 13
Types of Y chromosome deletions and their frequency in infertile men
2006 · V. B. Chernykh, A. L. Chukhrova, et al. · Russian Journal of Genetics · 10
Pathogenic Variants and Genotypes of the CFTR Gene in Russian Men with Cystic Fibrosis and CBAVD Syndrome
2023 · Vyacheslav Chernykh, Stanislav Krasovsky, et al. · International Journal of Molecular Sciences · 6
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A Family Case of Congenital Myasthenic Syndrome-22 Induced by Different Combinations of Molecular Causes in Siblings
2020 · Olga Shchagina, Ludmila Bessonova, et al. · Genes · 5
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Hemophilia B Leyden: Literature and Our Data
2021 · T. S. Beskorovainaya, V. V. Zabnenkova, et al. · Russian Journal of Genetics · 4
CFTR Gene Variants and Genotypes in Russian Patients with CBAVD Syndrome
2020 · E. G. Marnat, T. A. Adyan, et al. · Russian Journal of Genetics · 4
Molecular genetic analysis of Rubinstein–Taybi syndrome in Russian patients
2025 · Olga R. Ismagilova, Tagui A. Adyan, et al. · Frontiers in Genetics · 3
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FOXL2 mutations in Blepharophimosis-Ptosis-Epicanthus inversus syndrome
2019 · О.А. Щагина, Н.А. Демина, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 3
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Complex Molecular Diagnostics of Hemophilia A in Russian Patients
2019 · T. S. Beskorovainaya, T. B. Milovidova, et al. · Russian Journal of Genetics · 3
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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CAGn Polymorphic Locus of Androgen Receptor (AR) Gene in Russian Infertile and Fertile Men
2024 · Vyacheslav Chernykh, Olga Solovova, et al. · International Journal of Molecular Sciences · 2
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Phenotype Variations in a Family with Various Rearrangements in the Locus of the SHOX Gene
2026 · Tatiana S. Beskorovainaya, Tatiana V. Markova, et al. · International Journal of Molecular Sciences · 1
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Гемофилия в Лейден: литературные и собственные данные
2021 · Т. С. Бескоровайная, В. В. Забненкова, et al. · Генетика · 1
Case Report: Complicated Molecular Diagnosis of MECP2 Gene Structural Rearrangement in a Proband with Rett Syndrome
2020 · Tatiana Beskorovainaya, Fedor Konovalov, et al. · Journal of Autism and Developmental Disorders · 1
Comparison of the CFTR gene variants and genotypes in Russian patients with various forms of pathozoospermia and CBAVD syndrome
2020 · Е.Г. Марнат, Т.А. Адян, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 1
Complex F8 Gene Rearrangements
2019 · T.S. Beskorovainaya, T.B. Milovidova, et al. · Molekulyarnaya Meditsina (Molecular medicine) · 1
P022 Reproductive examination in differential diagnosis of cystic fibrosis and CFTR-related disorders in male patients
2024 · V. Chernykh, T. Sorokina, et al. · Journal of Cystic Fibrosis
The role of the QF-PCR method in the detection of frequent aneuploidies
2023 · Т.С. Бескоровайная, А.Л. Чухрова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
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The spectrum of the F9 gene mutations in Russian patients with hemophilia B
2022 · Бескоровайная, Т.С., Череватова, Т.Б., et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
Molecular-genetic analysis of Rubinstein-Taybi syndrome in Russia
2022 · Исмагилова, О.Р., Адян, Т.А., et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
Rubinstein-teibi Syndrome
2021 · O.R. Ismagilova, T.S. Beskorovainaya, et al. · PEDIATRIA Journal named after G N SPERANSKY
An influence of the CFTR genotype on semen parameters in CBAVD syndrome patients
2021 · Е.Г. Марнат, Т.М. Сорокина, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
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Варианты гена CFTR у российских пациентов с синдромом CBAVD
2020 · Е. Г. Марнат, Т. А. Адян, et al. · Генетика
Комплексная диагностика гемофилии А у российских больных
2019 · Т. С. Бескоровайная, Т. Б. Миловидова, et al. · Генетика
Works count: 27
Citation count: 87
H-index: 5
I10-index: 3
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