Kirill V Savostyanov

9PUBLICATIONS
47CO-AUTHORS
NeonatologyEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesMolecular targetsMajor global burdens of disease
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Publications (9)

|Aug 13, 2026
Hypophosphatasia: Results of a Country-Wide Selective Screening Program Using NGS Technology as a First-Tier Test.

|Jun 26, 2026
Molecular Genetic and Biochemical Characterization of Hyperphenylalaninemia Based on Expanded Neonatal Screening Data from 2023 to 2024 in the Russian Federation.

|Mar 27, 2026
Two Years of Expanded Newborn Screening in Russia: High-Throughput Detection of Inherited Metabolic Disorders by Tandem Mass Spectrometry with Next-Generation Sequencing Confirmation.

Ekaterina Y Zakharova, Galina V Baydakova, Polina V Baranova

|Dec 10, 2025
Extracellular Vesicles from iPSC-Derived Glial Progenitor Cells Prevent Glutamate-Induced Excitotoxicity by Stabilising Calcium Oscillations and Mitochondrial Depolarisation.

Margarita Shedenkova, Anastasiia Gurianova, Irina Krasilnikova

|Aug 28, 2025
Genotype Structure Alterations in 5q SMA Patients as a Result of the Newborn Screening Program Implementation in the Russian Federation.

Maria A Akhkiamova, Andrey V Marakhonov, Victoria V Zabnenkova

|Jun 26, 2025
A Unique Case of a Child with Two Rare Hereditary Diseases: Familial Dilated Cardiomyopathy and Arterial Calcification.

Yulia Burykina, Daria Chudakova, Olga Zharova

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Frequent Collaborators

4 joint publications

Ilya Zhanin

4 joint publications

Olga Shchagina

3 joint publications

Alexander L Koroteev

2 joint publications

Zanda Bakaeva