Дроздов Глеб Владимирович

Lebedev, I.N.; Karamysheva, T.V.; Elisaphenko, E.A.; Makunin, A.I.; Zhigalina, D.I.; Lopatkina, M.E.; Drozdov, G.V.; Cheremnykh, A.D.; Torkhova, N.B.; Seitova, G.N.; Vasilyev, S.A.; Kashevarova, A.A.; Nazarenko, L.P.; Rubtsov, N.B. Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing. Biomedicines 2021, 9, 1030.

Belyaeva, E., Kashevarova, A., Drozdov, G., Fedotov, D., Lebedev, I. Concomitant CNVs in healthy carriers with 7q31.1 microdeletions may suppress intellectual disability and autism spectrum disorders phenotype. European Psychiatry. 2022. 65(S1):S382-S383.

Kashevarova, A., Lopatkina, M., Belyaeva, E., Fedotov, D., Drozdov, G., Nazarenko, L., Lebedev, I. Identification of candidate genes of intellectual disability by single-gene deletions/amplifications mapping using chromosomal microarray analysis. European Psychiatry. 2022. 65. S382-S383.

A Kashevarova, G Drozdov, T Nikitina, E Sazhenova, E Fonova, E Tolmacheva, I Lebedev, P-546 The structure of genome variations at CNV level differs in recurrent and sporadic pregnancy loss, Human Reproduction, Volume 37, Issue Supplement_1, July 2022, deac107.504.

I Lebedev, G Drozdov, T Nikitina, E Sazhenova, E Tolmacheva, E Fonova, A Kashevarova, P-547 Confined placental mosaicism for inherited segmental aneuploidies in miscarriages traces early karyotype self-correction events, Human Reproduction, Volume 37, Issue Supplement_1, July 2022.

Drozdov G.V., Kashevarova A.A., Nikitina T.V., Tolmacheva, E.N., Fonova E.A., Sazhenova E.A., Lebedev I.N. Mosaic runs of homozygosity in first trimester spontaneous abortions with normal karyotype. European Society of Human Genetics. Hybrid Conference Vienna, Austria june 11–14, 2022.

Грант РНФ № 21-65-00017 «Патогенетика наследственных форм умственной отсталости: клеточные, молекулярные и онтогенетические аспекты» 2021 – 2024, исполнитель проекта