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Gene|September 25, 2015
Identification of a novel, CF-causing compound genotype (p.S1159P and p.Y569H) using an NGS-based assay: Novel CF-causing compound p.S1159P and p.Y569H genotypeTamara Simakova, Elena Kondratyeva, Lusine Avakian, et al.
International Journal of Neonatal Screening|October 19, 2020
Newborn Screening for Cystic Fibrosis in Russia: A Catalyst for Improved CareVictoria Sherman, Elena Kondratyeva, Nataliya Kashirskaya, et al.
Plos Computational Biology|October 27, 2025
A semi-automated algorithm for image analysis of respiratory organoidsAnna Demchenko, Maxim Balyasin, Elena Kondratyeva, et al.
International Journal of Molecular Sciences|January 11, 2024
The Effect of Complex Alleles of the <i>CFTR</i> Gene on the Clinical Manifestations of Cystic Fibrosis and the Effectiveness of Targeted TherapyMaria Krasnova, Anna Efremova, Artem Bukhonin, et al.
Journal of Personalized Medicine|February 23, 2024
Advances in the Study of Common and Rare <i>CFTR</i> Complex Alleles Using Intestinal OrganoidsMaria Krasnova, Anna Efremova, Diana Mokrousova, et al.
International Journal of Molecular Sciences|December 11, 2025
L467F;F508del Complex Allele in a Heterozygous State with CFTRdele2,3: What to Expect from CFTR Modulators?Elena Kondratyeva, Anna Efremova, Yuliya Melyanovskaya, et al.
International Journal of Molecular Sciences|October 16, 2024
Estimation of Chloride Channel Residual Function and Assessment of Targeted Drugs Efficiency in the Presence of a Complex Allele [L467F;F508del] in the <i>CFTR</i> GeneAnna Efremova, Yuliya Melyanovskaya, Maria Krasnova, et al.
International Journal of Molecular Sciences|November 25, 2023
Pathogenic Variants and Genotypes of the <i>CFTR</i> Gene in Russian Men with Cystic Fibrosis and CBAVD SyndromeVyacheslav Chernykh, Stanislav Krasovsky, Olga Solovova, et al.
International Journal of Molecular Sciences|March 13, 2024
Comprehensive Assessment of <i>CFTR</i> Modulators' Therapeutic Efficiency for N1303K VariantAnna Efremova, Nataliya Kashirskaya, Stanislav Krasovskiy, et al.
Genes|January 8, 2025
Expanding the Genotypic and Phenotypic Spectrum of <i>OFD1</i>-Related Conditions: Three More CasesTatiana Kyian, Artem Borovikov, Inga Anisimova, et al.
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