Works matching AU Shatalov, Peter A.

Results: 9
    1

    Experience in developing the human genome standard E701 Open Access.

    Published in:
    NAR Genomics & Bioinformatics, 2025, v. 7, n. 2, p. 1, doi. 10.1093/nargab/lqaf057
    By:
    • Vasiliadis, Iuliia;
    • Belova, Vera;
    • Shmitko, Anna;
    • Kuznetsova, Anna;
    • Samitova, Alina;
    • Suchalko, Oleg;
    • Goltsov, Andrey;
    • Shatalov, Peter;
    • Shegai, Peter;
    • Kulyabina, Elena;
    • Kulyabina, Tatiana;
    • Melkova, Olga;
    • Rebrikov, Denis;
    • Korostin, Dmitriy
    Publication type:
    Article
    2

    Prognostic Impact of Phenotypic and Genetic Features of Pancreatic Malignancies.

    Published in:
    Life (2075-1729), 2025, v. 15, n. 4, p. 635, doi. 10.3390/life15040635
    By:
    • Potievskiy, Mikhail B.;
    • Nekrasova, Lidia A.;
    • Korobov, Ivan V.;
    • Bykova, Ekaterina A.;
    • Moshurov, Ruslan I.;
    • Sokolov, Pavel V.;
    • Shatalov, Peter A.;
    • Falaleeva, Natalia A.;
    • Petrov, Leonid O.;
    • Trifanov, Vladimir S.;
    • Ivanov, Sergey A.;
    • Shegai, Peter V.;
    • Kaprin, Andrei D.
    Publication type:
    Article
    3
    4
    5

    Novel mutation in the MPZ gene causes early-onset but slow-progressive Charcot–Marie–Tooth disease in a Russian family: a case report.

    Published in:
    Journal of International Medical Research, 2022, v. 50, n. 12, p. 1, doi. 10.1177/03000605221139718
    By:
    • Kozina, Anastasiya Aleksandrovna;
    • Baryshnikova, Natalia Vladimirovna;
    • Ilinskaya, Anna Yurievna;
    • Kim, Anna Alexandrovna;
    • Plotnikov, Nikolay Alekseevich;
    • Pogodina, Nadezhda Andreevna;
    • Surkova, Ekaterina Ivanovna;
    • Shatalov, Peter Alekseevich;
    • Ilinsky, Valery Vladimirovich
    Publication type:
    Article
    6
    7

    A novel MFSD8 mutation in a Russian patient with neuronal ceroid lipofuscinosis type 7: a case report.

    Published in:
    BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0669-7
    By:
    • Kozina, Anastasiya Aleksandrovna;
    • Okuneva, Elena Grigorievna;
    • Baryshnikova, Natalia Vladimirovna;
    • Krasnenko, Anna Yurievna;
    • Tsukanov, Kirill Yurievich;
    • Klimchuk, Olesya Igorevna;
    • Kondakova, Olga Borisovna;
    • Larionova, Anna Nikolaevna;
    • Batysheva, Tatyana Timofeevna;
    • Surkova, Ekaterina Ivanovna;
    • Shatalov, Peter Alekseevich;
    • Ilinsky, Valery Vladimirovich
    Publication type:
    Article
    8
    9

    Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 7, p. 1, doi. 10.1002/mgg3.1228
    By:
    • Kozina, Anastasiya A.;
    • Okuneva, Elena G.;
    • Baryshnikova, Natalia V.;
    • Kondakova, Olga B.;
    • Nikolaeva, Ekaterina A.;
    • Fedoniuk, Inessa D.;
    • Mikhailova, Svetlana V.;
    • Krasnenko, Anna Y.;
    • Stetsenko, Ivan F.;
    • Plotnikov, Nikolay A.;
    • Klimchuk, Olesia I.;
    • Popov, Yaroslav V.;
    • Surkova, Ekaterina I.;
    • Shatalov, Peter A.;
    • Rakitko, Alexander S.;
    • Ilinsky, Valery V.
    Publication type:
    Article