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

Modeling the QBO—Improvements resulting from higher‐model vertical resolution

por Geller, Marvin A., Zhou, Tiehan, Shindell, D., Ruedy, R., Aleinov, I., Nazarenko, L., Tausnev, N. L., Kelley, M., Sun, S., Cheng, Y., Field, R. D., Faluvegi, G.
Publicado 2016

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 pregnancy

por Demeneva, V.V., Tolmacheva, E.N., Nikitina, T.V., Sazhenova, E.A., Yuriev, S.Yu., Makhmutkhodzhaev, A.Sh., Zuev, A.S., Filatova, S.A., Dmitriev, A.E., Darkova, Ya.A., Nazarenko, L.P., Lebedev, I.N., Vasilyev, S.A.
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