Phenome-wide functional dissection of pleiotropic effects highlights key molecular pathways for human complex traits

por Shikov, Anton E., Skitchenko, Rostislav K., Predeus, Alexander V., Barbitoff, Yury A.
Publicado 2020

Census of halide-binding sites in protein structures

por Skitchenko, Rostislav K, Usoltsev, Dmitrii, Uspenskaya, Mayya, Kajava, Andrey V, Guskov, Albert
Publicado 2020

No More Tears: Mining Sequencing Data for Novel Bt Cry Toxins with CryProcessor

por Shikov, Anton E., Malovichko, Yury V., Skitchenko, Rostislav K., Nizhnikov, Anton A., Antonets, Kirill S.
Publicado 2020

Case report: Somatic mutations in microtubule dynamics-associated genes in patients with WNT-medulloblastoma tumors

por Skitchenko, Rostislav, Dinikina, Yulia, Smirnov, Sergey, Krapivin, Mikhail, Smirnova, Anna, Morgacheva, Daria, Artomov, Mykyta
Publicado 2023

Annotation of uORFs in the OMIM genes allows to reveal pathogenic variants in 5′UTRs

por Filatova, Alexandra, Reveguk, Ivan, Piatkova, Maria, Bessonova, Daria, Kuziakova, Olga, Demakova, Victoria, Romanishin, Alexander, Fishman, Veniamin, Imanmalik, Yerzhan, Chekanov, Nikolay, Skitchenko, Rostislav, Barbitoff, Yury, Kardymon, Olga, Skoblov, Mikhail
Publicado 2023

Estimation of amyloid aggregate sizes with semi-denaturing detergent agarose gel electrophoresis and its limitations

por Drozdova, Polina B., Barbitoff, Yury A., Belousov, Mikhail V., Skitchenko, Rostislav K., Rogoza, Tatyana M., Leclercq, Jeremy Y., Kajava, Andrey V., Matveenko, Andrew G., Zhouravleva, Galina A., Bondarev, Stanislav A.
Publicado 2020

A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report

por Zlotina, Anna, Melnik, Olesia, Fomicheva, Yulia, Skitchenko, Rostislav, Sergushichev, Alexey, Shagimardanova, Elena, Gusev, Oleg, Gazizova, Guzel, Loevets, Tatiana, Vershinina, Tatiana, Kozyrev, Ivan, Gordeev, Mikhail, Vasichkina, Elena, Pervunina, Tatiana, Kostareva, Anna
Publicado 2020

Whole‐exome sequencing provides insights into monogenic disease prevalence in Northwest Russia

por Barbitoff, Yury A., Skitchenko, Rostislav K., Poleshchuk, Olga I., Shikov, Anton E., Serebryakova, Elena A., Nasykhova, Yulia A., Polev, Dmitrii E., Shuvalova, Anna R., Shcherbakova, Irina V., Fedyakov, Mikhail A., Glotov, Oleg S., Glotov, Andrey S., Predeus, Alexander V.
Publicado 2019

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

por 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 A., Tyrtova, Ludmila V., Berseneva, Olga S., Skitchenko, Rostislav K., Suspitsin, Evgenii N., Bashnina, Elena B., Baranov, Vladislav S.
Publicado 2019