Search Results - Igor N. Lebedev

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  1. 1

    Stem Cell-Based Trophoblast Models to Unravel the Genetic Causes of Human Miscarriages by Tatiana V. Nikitina, Igor N. Lebedev

    Published in Cells (2022-06-01)
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  2. 2

    A comparison of genome-wide DNA methylation patterns between different vascular tissues from patients with coronary heart disease. by Maria S Nazarenko, Anton V Markov, Igor N Lebedev, Maxim B Freidin, Aleksei A Sleptcov, Iuliya A Koroleva, Aleksei V Frolov, Vadim A Popov, Olga L Barbarash, Valery P Puzyrev

    Published in PLoS ONE (2015-01-01)
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  3. 3

    The Precise Breakpoint Mapping in Paracentric Inversion 10q22.2q23.3 by Comprehensive Cytogenomic Analysis, Multicolor Banding, and Single-Copy Chromosome Sequencing by Tatyana V. Karamysheva, Tatyana A. Gayner, Eugeny A. Elisaphenko, Vladimir A. Trifonov, Elvira G. Zakirova, Konstantin E. Orishchenko, Mariya A. Prokhorovich, Maria E. Lopatkina, Nikolay A. Skryabin, Igor N. Lebedev, Nikolay B. Rubtsov

    Published in Biomedicines (2022-12-01)
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  4. 4

    Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing by Igor N. Lebedev, Tatyana V. Karamysheva, Eugeny A. Elisaphenko, Alexey I. Makunin, Daria I. Zhigalina, Maria E. Lopatkina, Gleb V. Drozdov, Aleksander D. Cheremnykh, Natalia B. Torkhova, Gulnara N. Seitova, Stanislav A. Vasilyev, Anna A. Kashevarova, Ludmila P. Nazarenko, Nikolay B. Rubtsov

    Published in Biomedicines (2021-08-01)
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  5. 5

    Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disorders by Ekaterina N. Tolmacheva, Anna A. Kashevarova, Elizaveta A. Fonova, Olga A. Salyukova, Gulnara N. Seitova, Lyudmila P. Nazarenko, Anna A. Agafonova, Larisa I. Minaycheva, Ekaterina G. Ravzhaeva, Valeria V. Petrova, Maria E. Lopatkina, Elena O. Belyaeva, Svetlana L. Vovk, Dmitry A. Fedotov, Oksana Y. Vasilyeva, Nikolay A. Skryabin, Igor N. Lebedev

    Published in Molecular Cytogenetics (2025-02-01)
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  6. 6

    Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variants by Maria Gridina, Timofey Lagunov, Polina Belokopytova, Nikita Torgunakov, Miroslav Nuriddinov, Artem Nurislamov, Lyudmila P. Nazarenko, Anna A. Kashevarova, Maria E. Lopatkina, Stanislav Vasilyev, Andrey Zuev, Elena O. Belyaeva, Olga A. Salyukova, Aleksandr D. Cheremnykh, Natalia N. Sukhanova, Marina E. Minzhenkova, Zhanna G. Markova, Nina A. Demina, Yana Stepanchuk, Anna Khabarova, Alexandra Yan, Emil Valeev, Galina Koksharova, Elena V. Grigor’eva, Natalia Kokh, Tatiana Lukjanova, Yulia Maximova, Elizaveta Musatova, Elena Shabanova, Andrey Kechin, Evgeniy Khrapov, Uliana Boyarskih, Oxana Ryzhkova, Maria Suntsova, Alina Matrosova, Mikhail Karoli, Andrey Manakhov, Maxim Filipenko, Evgeny Rogaev, Nadezhda V. Shilova, Igor N. Lebedev, Veniamin Fishman

    Published in Genome Medicine (2025-05-01)
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