Zhanna Markova
8PUBLICATIONS
51CO-AUTHORS
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Publications (8)
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|Oct 16, 2025
13q Deletion Syndrome Presenting with Lymphopenia Detected Through Newborn Screening for Primary Immunodeficiencies.Irina Efimova, Anna Mukhina, Zhanna Markova
|Sep 13, 2025
Clinical and Molecular Presentation of a Patient with Paternal Uniparental Isodisomy of Chromosome 16.Elizaveta Panchenko, Natalia Semenova, Olga Sereda
|Aug 28, 2025
Chromosomal Aberrations in Induced Pluripotent Stem Cells: Identification of Breakpoints in the Large DCC Gene and HIST2 Histone Gene Cluster.Diana Zheglo, Victoria O Pozhitnova, Anastasiia V Kislova
|Apr 05, 2024
Newborn Screening for Severe T and B Cell Lymphopenia Using TREC/KREC Detection: A Large-Scale Pilot Study of 202,908 Newborns.Andrey V Marakhonov, Irina Yu Efimova, Anna A Mukhina
|Mar 11, 2023
Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report.Tatyana A Vasilyeva, Andrey V Marakhonov, Inna S Tebieva
|Dec 23, 2022
Previously Undescribed Gross HACE1 Deletions as a Cause of Autosomal Recessive Spastic Paraplegia.Valeriia A Kovalskaia, Victoriia V Zabnenkova, Marina S Petukhova
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Frequent Collaborators
4 joint publications
Nadezhda V Shilova
3 joint publications
Andrey V Marakhonov
3 joint publications
Rena Zinchenko
2 joint publications
Viktoriia V Zabnenkova
2 joint publications
Oxana P Ryzhkova
2 joint publications
Dmitry Pershin
2 joint publications
Irina Yu Efimova
2 joint publications
Natalya V Balinova
1 joint publications
Anastasiya Aleksandrovna Tarlycheva
1 joint publications
Yunna Petrusenko
