Concomitant CNVs in healthy carriers with 7q31.1 microdeletions may suppress intellectual disability and autism spectrum disorders phenotype

por Belyaeva, E., Kashevarova, A., Drozdov, G., Fedotov, D., Lebedev, I.
Publicado 2022

Identification of candidate genes of intellectual disability by single-gene deletions/amplifications mapping using chromosomal microarray analysis

por Kashevarova, A., Lopatkina, M., Belyaeva, E., Fedotov, D., Drozdov, G., Nazarenko, L., Lebedev, I.
Publicado 2022

Influence of human peripheral blood samples preprocessing on the quality of Hi-C libraries

por Gridina, M.M., Vesna, E., Minzhenkova, M.E., Shilova, N.V., Ryzhkova, O.P., Nazarenko, L.P., Belyaeva, E.O., Lebedev, I.N., Fishman, V.S.
Publicado 2023

Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies

por Fonova, E. A., Kashevarova, A. A., Lopatkina, M. E., Sivtsev, A. A., Zarubin, A. A., Demeneva, V. V., Seitova, G. N., Minaycheva, L. I., Salyukova, O. A., Fadyushina, S. V., Petrova, V. V., Belyaeva, E. O., Nazarenko, L. P., Lebedev, I. N.
Publicado 2023

Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability

por Kashevarova, A. A., Belyaeva, E. O., Fonova, E. A., Lopatkina, M. E., Vasilyeva, O. Y., Fedotov, D. A., Zarubin, A. A., Sivtsev, A. A., Demeneva, V. V., Salyukova, O. A., Petrova, V. V., Fadiushina, S. V., Minaycheva, L. I., Seitova, G. N., Nazarenko, L. P., Lebedev, I. N.
Publicado 2023