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Stem Cell Research|November 4, 2019
Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disabilityT A Shnaider, I E Pristyazhnyuk, A G Menzorov, et al.
Vavilovskii Zhurnal Genetiki I Selektsii|September 26, 2025
A family case of a rare Xq28 duplicationA E Kopytova, E N Tolmacheva, D A Emelina, et al.
American Journal of Medical Genetics. Part A|February 25, 2026
Novel Biallelic Variants in IQSEC1 in a Patient With Intellectual Developmental Disorder With Short Stature and Behavioral Abnormalities (IDDSSBA) and Corpus Callosum DysgenesisA A Kashevarova, L I Minaycheva, E A Fonova, et al.
Vavilovskii Zhurnal Genetiki I Selektsii|March 16, 2023
Expression of the NUP153 and YWHAB genes from their canonical promoters and alternative promoters of the LINE-1 retrotransposon in the placenta of the first trimester of pregnancyV V Demeneva, E N Tolmacheva, T V Nikitina, et al.
Stem Cell Research|October 18, 2020
Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,-8 mosaicismM M Gridina, T V Nikitina, P A Orlova, et al.
Scientific Reports|February 23, 2021
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogrammingT V Nikitina, A A Kashevarova, M M Gridina, et al.
Stem Cell Research|March 18, 2022
Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4M M Gridina, A R Nurislamov, J M Minina, et al.
Stem Cell Research|January 8, 2019
Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplicationA A Khabarova, I E Pristyazhnyuk, T V Nikitina, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 11, 2013
[Clinical and genetic analysis of idiopathic intellectual disability based on array comparative genomic hybridization]A A Kashevarova, N A Skryabin, A D Cheremnykh, et al.
Molecular Genetics & Genomic Medicine|December 31, 2024
Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single-Gene BDH1 DuplicationsA A Kashevarova, M E Lopatkina, O Yu Vasilyeva, et al.
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