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Lebedev Igor
Lebedev Igor
Institute of Medical Genetics
在 medgenetics.ru 的电子邮件经过验证
标题
引用次数
引用次数
年份
Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis
IN Lebedev, NV Ostroverkhova, TV Nikitina, NN Sukhanova, ...
European journal of human genetics 12 (7), 513-520, 2004
1122004
Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability
AA Kashevarova, LP Nazarenko, S Schultz-Pedersen, NA Skryabin, ...
Molecular Cytogenetics 7, 1-10, 2014
1012014
A comparison of genome-wide DNA methylation patterns between different vascular tissues from patients with coronary heart disease
MS Nazarenko, AV Markov, IN Lebedev, MB Freidin, AA Sleptcov, ...
PLoS One 10 (4), e0122601, 2015
762015
Mosaic aneuploidy in early fetal losses
I Lebedev
Cytogenetic and genome research 133 (2-4), 169-183, 2011
752011
Array CGH analysis of a cohort of Russian patients with intellectual disability
AA Kashevarova, LP Nazarenko, NA Skryabin, OA Salyukova, ...
Gene 536 (1), 145-150, 2014
642014
Genomic structural variations for cardiovascular and metabolic comorbidity
MS Nazarenko, AA Sleptcov, IN Lebedev, NA Skryabin, AV Markov, ...
Scientific reports 7 (1), 41268, 2017
602017
Karyotype of the blastocoel fluid demonstrates low concordance with both trophectoderm and inner cell mass
O Tšuiko, DI Zhigalina, T Jatsenko, NA Skryabin, OR Kanbekova, ...
Fertility and sterility 109 (6), 1127-1134. e1, 2018
522018
Clinically relevant morphological structures in breast cancer represent transcriptionally distinct tumor cell populations with varied degrees of epithelial-mesenchymal …
EV Denisov, NA Skryabin, TS Gerashchenko, LA Tashireva, J Wilhelm, ...
Oncotarget 8 (37), 61163, 2017
482017
Comparative cytogenetic analysis of spontaneous abortions in recurrent and sporadic pregnancy losses
TV Nikitina, EA Sazhenova, EN Tolmacheva, NN Sukhanova, ...
Biomedicine hub 1 (1), 1-11, 2016
442016
About the sex ratio in connection with early embryonic mortality in man
VN Evdokimova, TV Nikitina, IN Lebedev, NN Sukhanova, SA Nazarenko
Russian Journal of Developmental Biology 31, 204-210, 2000
372000
Allele-specific biased expression of the CNTN6 gene in iPS cell-derived neurons from a patient with intellectual disability and 3p26. 3 microduplication involving the CNTN6 gene
MM Gridina, NM Matveeva, VS Fishman, AG Menzorov, HA Kizilova, ...
Molecular Neurobiology 55, 6533-6546, 2018
312018
A mathematical model for evaluation of maternal cell contamination in cultured cells from spontaneous abortions: significance for cytogenetic analysis of prenatal selection factors
TV Nikitina, IN Lebedev, NN Sukhanova, EA Sazhenova, SA Nazarenko
Fertility and sterility 83 (4), 964-972, 2005
292005
Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells
EV Grigor’eva, TB Malankhanova, A Surumbayeva, SV Pavlova, ...
Cytotechnology 72, 649-663, 2020
252020
Karyotype evaluation of repeated abortions in primary and secondary recurrent pregnancy loss
TV Nikitina, EA Sazhenova, DI Zhigalina, EN Tolmacheva, NN Sukhanova, ...
Journal of Assisted Reproduction and Genetics 37 (3), 517-525, 2020
242020
Molecular cytogenetics of recurrent missed abortions
I Lebedev
Indian Journal of Medical Research 124 (1), 9-10, 2006
212006
Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortium
OY Fedorenko, VE Golimbet, SА Ivanova, А Levchenko, RR Gainetdinov, ...
Molecular Psychiatry 24 (8), 1099-1111, 2019
202019
A de novo microtriplication at 4q21. 21‐q21. 22 in a patient with a vascular malignant hemangioma, elongated sigmoid colon, developmental delay, and absence of speech
IN Lebedev, LP Nazarenko, NA Skryabin, NP Babushkina, ...
American Journal of Medical Genetics Part A 170 (8), 2089-2096, 2016
192016
A cookbook for DNase Hi-C
M Gridina, E Mozheiko, E Valeev, LP Nazarenko, ME Lopatkina, ...
Epigenetics & Chromatin 14 (1), 1-15, 2021
182021
Compound phenotype in a girl with r (22), concomitant microdeletion 22q13. 32-q13. 33 and mosaic monosomy 22
AA Kashevarova, EO Belyaeva, AM Nikonov, OV Plotnikova, NA Skryabin, ...
Molecular Cytogenetics 11 (1), 1-9, 2018
182018
Epimutations of the KCNQ1OT1 imprinting center of chromosome 11 in early human embryolethality
EA Sazhenova, IN Lebedev
Russian journal of genetics 44, 1394-1399, 2008
182008
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