On the Complexity of Mechanisms and Consequences of Chromothripsis: An Update von Koltsova, Alla S, Pendina, Anna A, Efimova, Olga A, Chiryaeva, Olga G, Kuznetzova, Tatyana V, Baranov, Vladislav S

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Methylation levels of SLC23A2 and NCOR2 genes correlate with spinal muscular atrophy severity von Zheleznyakova, Galina Yu, Nilsson, Emil K, Kiselev, Anton V, Maretina, Marianna A, Tishchenko, Lyudmila I, Fredriksson, Robert, Baranov, Vladislav S, Schiöth, Helgi B

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Telomere Length in Metaphase Chromosomes of Human Triploid Zygotes von Pendina, Anna A., Krapivin, Mikhail I., Efimova, Olga A., Tikhonov, Andrei V., Mekina, Irina D., Komarova, Evgeniia M., Koltsova, Alla S., Gzgzyan, Alexander M., Kogan, Igor Yu, Chiryaeva, Olga G., Baranov, Vladislav S.

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Molecular Factors Involved in Spinal Muscular Atrophy Pathways as Possible Disease-modifying Candidates von Maretina, Marianna A, Zheleznyakova, Galina Y, Lanko, Kristina M, Egorova, Anna A, Baranov, Vladislav S, Kiselev, Anton V

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Telomere Length in Chromosomally Normal and Abnormal Miscarriages and Ongoing Pregnancies and Its Association with 5-hydroxymethylcytosine Patterns von Krapivin, Mikhail I., Tikhonov, Andrei V., Efimova, Olga A., Pendina, Anna A., Smirnova, Anna A., Chiryaeva, Olga G., Talantova, Olga E., Petrova, Lubov’ I., Dudkina, Vera S., Baranov, Vladislav S.

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Uterine Leiomyomas with an Apparently Normal Karyotype Comprise Minor Heteroploid Subpopulations Differently Represented in vivo and in vitro von Koltsova, Alla S., Efimova, Olga A., Pendina, Anna A., Chiryaeva, Olga G., Osinovskaya, Natalia S., Shved, Natalia Y., Yarmolinskaya, Maria I., Polenov, Nikolai I., Kunitsa, Vladislava V., Sagurova, Yanina M., Tral, Tatyana G., Tolibova, Gulrukhsor K., Baranov, Vladislav S.

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Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension von VASHUKOVA, ELENA S, GLOTOV, ANDREY S, FEDOTOV, PAVEL V, EFIMOVA, OLGA A, PAKIN, VLADIMIR S, MOZGOVAYA, ELENA V, PENDINA, ANNA A, TIKHONOV, ANDREI V, KOLTSOVA, ALLA S, BARANOV, VLADISLAV S

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Synergistic Anti-Angiogenic Effects Using Peptide-Based Combinatorial Delivery of siRNAs Targeting VEGFA, VEGFR1, and Endoglin Genes von Egorova, Anna A, Shtykalova, Sofia V, Maretina, Marianna A, Sokolov, Dmitry I, Selkov, Sergei A, Baranov, Vladislav S, Kiselev, Anton V

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The spectrum of pathogenic variants of the ATP7B gene in Wilson disease in the Russian Federation von Balashova, Mariya S., Tuluzanovskaya, Inna G., Glotov, Oleg S., Glotov, Andrey S., Barbitoff, Yury A., Fedyakov, Mikhail A., Alaverdian, Diana A., Ivashchenko, Tatiana E., Romanova, Olga V., Sarana, Andrey M., Scherbak, Sergey G., Baranov, Vladislav S., Filimonov, Marat I., Skalny, Anatoly V., Zhuchenko, Natalya A., Ignatova, Tatiana M., Asanov, Aliy Y.

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Genome-wide 5-hydroxymethylcytosine patterns in human spermatogenesis are associated with semen quality von Efimova, Olga A, Pendina, Anna A, Tikhonov, Andrei V, Parfenyev, Sergey E, Mekina, Irina D, Komarova, Evgeniia M, Mazilina, Mariia A, Daev, Eugene V, Chiryaeva, Olga G, Galembo, Ilona A, Krapivin, Mikhail I, Glotov, Oleg S, Stepanova, Irina S, Shlykova, Svetlana A, Kogan, Igor Yu, Gzgzyan, Alexander M, Kuznetzova, Tatyana V, Baranov, Vladislav S

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Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes von Glotov, Oleg S, Serebryakova, Elena A, Turkunova, Mariia E, Efimova, Olga A, Glotov, Andrey S, Barbitoff, Yury A, Nasykhova, Yulia A, Predeus, Alexander V, Polev, Dmitrii E, Fedyakov, Mikhail A, Polyakova, Irina V, Ivashchenko, Tatyana E, Shved, Natalia Y, Shabanova, Elena S, Tiselko, Alena V, Romanova, Olga V, Sarana, Andrey M, Pendina, Anna A, Scherbak, Sergey G, Musina, Ekaterina V, Petrovskaia-Kaminskaia, Anastasiia V, Lonishin, Liubov R, Ditkovskaya, Liliya V, Zhelenina, Liudmila А, Tyrtova, Ludmila V, Berseneva, Olga S, Skitchenko, Rostislav K, Suspitsin, Evgenii N, Bashnina, Elena B, Baranov, Vladislav S

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Genomic distribution of 5‐formylcytosine and 5‐carboxylcytosine in human preimplantation embryos von Pendina, Anna A., Efimova, Olga A., Krapivin, Mikhail I., Mekina, Irina D., Tikhonov, Andrei V., Koltsova, Alla S., Petrovskaia‐Kaminskaia, Anastasiia V., Chiryaeva, Olga G., Kogan, Igor Y., Gzgzyan, Alexander M., Baranov, Vladislav S.

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Molecular association of pathogenetic contributors to pre-eclampsia (pre-eclampsia associome) von Glotov, Andrey S, Tiys, Evgeny S, Vashukova, Elena S, Pakin, Vladimir S, Demenkov, Pavel S, Saik, Olga V, Ivanisenko, Timofey V, Arzhanova, Olga N, Mozgovaya, Elena V, Zainulina, Marina S, Kolchanov, Nikolay A, Baranov, Vladislav S, Ivanisenko, Vladimir A

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Inter-Cell and Inter-Chromosome Variability of 5-Hydroxymethylcytosine Patterns in Noncultured Human Embryonic and Extraembryonic Cells von Efimova, Olga A., Pendina, Anna A., Krapivin, Mikhail I., Kopat, Vladimir V., Tikhonov, Andrei V., Petrovskaia-Kaminskaia, Anastasiia V., Navodnikova, Polina M., Talantova, Olga E., Glotov, Oleg S., Baranov, Vladislav S.

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Case of chromothripsis in a large solitary non-recurrent uterine leiomyoma von Pendina, Anna A., Koltsova, Alla S., Efimova, Olga A., Malysheva, Olga V., Osinovskaya, Natalia S., Sultanov, Iskender Yu, Tikhonov, Andrei V., Shved, Natalia Yu, Chiryaeva, Olga G., Simareva, Anastasiia D., Kakhiani, Maka I., Baranov, Vladislav S.

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Genetic and expression studies of SMN2 gene in Russian patients with spinal muscular atrophy type II and III von Zheleznyakova, Galina Yu, Kiselev, Anton V, Vakharlovsky, Viktor G, Rask-Andersen, Mathias, Chavan, Rohit, Egorova, Anna A, Schiöth, Helgi B, Baranov, Vladislav S

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Identification of Genetic Risk Factors of Severe COVID-19 Using Extensive Phenotypic Data: A Proof-of-Concept Study in a Cohort of Russian Patients von Shcherbak, Sergey G, Changalidi, Anton I, Barbitoff, Yury A, Anisenkova, Anna Yu, Mosenko, Sergei V, Asaulenko, Zakhar P, Tsay, Victoria V, Polev, Dmitrii E, Kalinin, Roman S, Eismont, Yuri A, Glotov, Andrey S, Garbuzov, Evgeny Y, Chernov, Alexander N, Klitsenko, Olga A, Ushakov, Mikhail O, Shikov, Anton E, Urazov, Stanislav P, Baranov, Vladislav S, Glotov, Oleg S

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Chromosome hydroxymethylation patterns in human zygotes and cleavage-stage embryos von Efimova, Olga A, Pendina, Anna A, Tikhonov, Andrei V, Fedorova, Irina D, Krapivin, Mikhail I, Chiryaeva, Olga G, Shilnikova, Evgeniia M, Bogdanova, Mariia A, Kogan, Igor Yu, Kuznetzova, Tatyana V, Gzgzyan, Alexander M, Ailamazyan, Edward K, Baranov, Vladislav S

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Cytogenomic Profile of Uterine Leiomyoma: In Vivo vs. In Vitro Comparison von Koltsova, Alla S, Efimova, Olga A, Malysheva, Olga V, Osinovskaya, Natalia S, Liehr, Thomas, Al-Rikabi, Ahmed, Shved, Natalia Yu, Sultanov, Iskender Yu, Chiryaeva, Olga G, Yarmolinskaya, Maria I, Polenov, Nikolai I, Kunitsa, Vladislava V, Kakhiani, Maka I, Tral, Tatyana G, Tolibova, Gulrukhsor Kh, Bespalova, Olesya N, Kogan, Igor Yu, Glotov, Andrey S, Baranov, Vladislav S, Pendina, Anna A

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Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutations von Dzhemlikhanova, Lyailya Kh, Efimova, Olga A, Osinovskaya, Natalia S, Parfenyev, Sergey E, Niauri, Dariko A, Sultanov, Iskender Yu, Malysheva, Olga V, Pendina, Anna A, Shved, Natalia Yu, Ivashchenko, Tatyana E, Yarmolinskaya, Maria I, Kakhiani, Maka I, Gorovaya, Ekaterina A, Tkachenko, Antonina N, Baranov, Vladislav S

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