Stem Cell-Based Trophoblast Models to Unravel the Genetic Causes of Human Miscarriages

por Nikitina, Tatiana V., Lebedev, Igor N.
Publicado 2022

Aneuploidy and DNA Methylation as Mirrored Features of Early Human Embryo Development

por Tolmacheva, Ekaterina N., Vasilyev, Stanislav A., Lebedev, Igor N.
Publicado 2020

Method of targeted bisulfite massive parallel sequencing of the human LINE-1 retrotransposon promoter

por Vasilyev, Stanislav A., Markov, Anton V., Vasilyeva, Oksana Yu., Tolmacheva, Ekaterina N., Zatula, Lada A., Sharysh, Diana V., Zhigalina, Daria I., Demeneva, Victoria V., Lebedev, Igor N.
Publicado 2021

A Comparison of Genome-Wide DNA Methylation Patterns between Different Vascular Tissues from Patients with Coronary Heart Disease

por Nazarenko, Maria S., Markov, Anton V., Lebedev, Igor N., Freidin, Maxim B., Sleptcov, Aleksei A., Koroleva, Iuliya A., Frolov, Aleksei V., Popov, Vadim A., Barbarash, Olga L., Puzyrev, Valery P.
Publicado 2015

Genomic structural variations for cardiovascular and metabolic comorbidity

por Nazarenko, Maria S., Sleptcov, Aleksei A., Lebedev, Igor N., Skryabin, Nikolay A., Markov, Anton V., Golubenko, Maria V., Koroleva, Iuliia A., Kazancev, Anton N., Barbarash, Olga L., Puzyrev, Valery P.
Publicado 2017

A cookbook for DNase Hi-C

por Gridina, Maria, Mozheiko, Evgeniy, Valeev, Emil, Nazarenko, Ludmila P., Lopatkina, Maria E., Markova, Zhanna G., Yablonskaya, Maria I., Voinova, Viktoria Yu, Shilova, Nadezhda V., Lebedev, Igor N., Fishman, Veniamin
Publicado 2021

Comparative Cytogenetic Analysis of Spontaneous Abortions in Recurrent and Sporadic Pregnancy Losses

por Nikitina, Tatiana V., Sazhenova, Elena A., Tolmacheva, Ekaterina N., Sukhanova, Natalia N., Kashevarova, Anna A., Skryabin, Nikolay A., Vasilyev, Stanislav A., Nemtseva, Tatiana N., Yuriev, Sergey Y., Lebedev, Igor N.
Publicado 2016

The Precise Breakpoint Mapping in Paracentric Inversion 10q22.2q23.3 by Comprehensive Cytogenomic Analysis, Multicolor Banding, and Single-Copy Chromosome Sequencing

por Karamysheva, Tatyana V., Gayner, Tatyana A., Elisaphenko, Eugeny A., Trifonov, Vladimir A., Zakirova, Elvira G., Orishchenko, Konstantin E., Prokhorovich, Mariya A., Lopatkina, Maria E., Skryabin, Nikolay A., Lebedev, Igor N., Rubtsov, Nikolay B.
Publicado 2022

Clinically relevant morphological structures in breast cancer represent transcriptionally distinct tumor cell populations with varied degrees of epithelial-mesenchymal transition a...

por Denisov, Evgeny V., Skryabin, Nikolay A., Gerashchenko, Tatiana S., Tashireva, Lubov A., Wilhelm, Jochen, Buldakov, Mikhail A., Sleptcov, Aleksei A., Lebedev, Igor N., Vtorushin, Sergey V., Zavyalova, Marina V., Cherdyntseva, Nadezhda V., Perelmuter, Vladimir M.
Publicado 2017

Identification of differentially methylated genes in first-trimester placentas with trisomy 16

por Tolmacheva, Ekaterina N., Vasilyev, Stanislav A., Nikitina, Tatiana V., Lytkina, Ekaterina S., Sazhenova, Elena A., Zhigalina, Daria I., Vasilyeva, Oksana Yu., Markov, Anton V., Demeneva, Victoria V., Tashireva, Liubov A., Kashevarova, Anna A., Lebedev, Igor N.
Publicado 2022

Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability

por Kashevarova, Anna A, Nazarenko, Lyudmila P, Schultz-Pedersen, Soren, Skryabin, Nikolay A, Salyukova, Olga A, Chechetkina, Nataliya N, Tolmacheva, Ekaterina N, Rudko, Aleksey A, Magini, Pamela, Graziano, Claudio, Romeo, Giovanni, Joss, Shelagh, Tümer, Zeynep, Lebedev, Igor N
Publicado 2014

46,XY,r(8)/45,XY,−8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study

por Kashevarova, Anna A., Nikitina, Tatyana V., Mikhailik, Larisa I., Belyaeva, Elena O., Vasilyev, Stanislav A., Lopatkina, Mariya E., Fedotov, Dmitry A., Fonova, Elizaveta A., Zarubin, Aleksei A., Sivtsev, Aleksei A., Skryabin, Nikolay A., Nazarenko, Lyudmila P., Lebedev, Igor N.
Publicado 2020

Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22

por Kashevarova, Anna A., Belyaeva, Elena O., Nikonov, Aleksandr M., Plotnikova, Olga V., Skryabin, Nikolay A., Nikitina, Tatyana V., Vasilyev, Stanislav A., Yakovleva, Yulia S., Babushkina, Nadezda P., Tolmacheva, Ekaterina N., Lopatkina, Mariya E., Savchenko, Renata R., Nazarenko, Lyudmila P., Lebedev, Igor N.
Publicado 2018

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing

por Lebedev, Igor N., Karamysheva, Tatyana V., Elisaphenko, Eugeny A., Makunin, Alexey I., Zhigalina, Daria I., Lopatkina, Maria E., Drozdov, Gleb V., Cheremnykh, Aleksander D., Torkhova, Natalia B., Seitova, Gulnara N., Vasilyev, Stanislav A., Kashevarova, Anna A., Nazarenko, Ludmila P., Rubtsov, Nikolay B.
Publicado 2021

Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortium

por Fedorenko, Olga Yu., Golimbet, Vera E., Ivanova, Svetlana А., Levchenko, Аnastasia, Gainetdinov, Raul R., Semke, Arkady V., Simutkin, German G., Gareeva, Аnna E., Glotov, Аndrey S., Gryaznova, Anna, Iourov, Ivan Y., Krupitsky, Evgeny M., Lebedev, Igor N., Mazo, Galina E., Kaleda, Vasily G., Abramova, Lilia I., Oleichik, Igor V., Nasykhova, Yulia A., Nasyrova, Regina F., Nikolishin, Anton E., Kasyanov, Evgeny D., Rukavishnikov, Grigory V., Timerbulatov, Ilgiz F., Brodyansky, Vadim M., Vorsanova, Svetlana G., Yurov, Yury B., Zhilyaeva, Tatyana V., Sergeeva, Anzhelika V., Blokhina, Elena A., Zvartau, Edwin E., Blagonravova, Anna S., Aftanas, Lyubomir I., Bokhan, Nikolay А., Kekelidze, Zurab I., Klimenko, Tatyana V., Anokhina, Irina P., Khusnutdinova, Elza K., Klyushnik, Tatyana P., Neznanov, Nikolay G., Stepanov, Vadim A., Schulze, Thomas G., Kibitov, Аleksandr О.
Publicado 2019