Works by Kiseleva, Anna A.


Results: 44
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    A Novel Bradycardia-Associated Variant in HCN4 as a Candidate Modifier in Type 3 Long QT Syndrome: Case Report and Deep In Silico Analysis.

    Published in:
    Biomedicines, 2025, v. 13, n. 4, p. 1008, doi. 10.3390/biomedicines13041008
    By:
    • Bukaeva, Anna A.;
    • Blokhina, Anastasia V.;
    • Kharlap, Maria S.;
    • Zaicenoka, Marija;
    • Zotova, Evgenia D.;
    • Petukhova, Anna V.;
    • Garbuzova, Elizaveta V.;
    • Zharikova, Anastasia A.;
    • Divashuk, Mikhail G.;
    • Kiseleva, Anna V.;
    • Ershova, Alexandra I.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
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    Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases.

    Published in:
    Journal of Personalized Medicine, 2022, v. 12, n. 7, p. 1132, doi. 10.3390/jpm12071132
    By:
    • Sotnikova, Evgeniia A.;
    • Kiseleva, Anna V.;
    • Kutsenko, Vladimir A.;
    • Zharikova, Anastasia A.;
    • Ramensky, Vasily E.;
    • Divashuk, Mikhail G.;
    • Vyatkin, Yuri V.;
    • Klimushina, Marina V.;
    • Ershova, Alexandra I.;
    • Revazyan, Karina Z.;
    • Skirko, Olga P.;
    • Zaicenoka, Marija;
    • Efimova, Irina A.;
    • Pokrovskaya, Maria S.;
    • Kopylova, Oksana V.;
    • Glechan, Anush M.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
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    A Data-Driven Approach to Carrier Screening for Common Recessive Diseases.

    Published in:
    Journal of Personalized Medicine, 2020, v. 10, n. 3, p. 140, doi. 10.3390/jpm10030140
    By:
    • Kiseleva, Anna V.;
    • Klimushina, Marina V.;
    • Sotnikova, Evgeniia A.;
    • Divashuk, Mikhail G.;
    • Ershova, Alexandra I.;
    • Skirko, Olga P.;
    • Kurilova, Olga V.;
    • Zharikova, Anastasia A.;
    • Khlebus, Eleonora Yu.;
    • Efimova, Irina A.;
    • Pokrovskaya, Maria S.;
    • Slominsky, Petr A.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
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    Cystic Fibrosis Polymorphic Variants in a Russian Population.

    Published in:
    Pharmacogenomics & Personalized Medicine, 2020, v. 13, p. 679, doi. 10.2147/PGPM.S278806
    By:
    • Kiseleva, Anna;
    • Klimushina, Marina;
    • Sotnikova, Evgeniia;
    • Skirko, Olga;
    • Divashuk, Mikhail;
    • Kurilova, Olga;
    • Ershova, Alexandra;
    • Khlebus, Eleonora;
    • Zharikova, Anastasia;
    • Efimova, Irina;
    • Pokrovskaya, Maria;
    • Slominsky, Petr A;
    • Shalnova, Svetlana;
    • Meshkov, Alexey;
    • Drapkina, Oxana
    Publication type:
    Article
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    Back Cover, Volume 40, Issue 6.

    Published in:
    Human Mutation, 2019, v. 40, n. 6, p. ii, doi. 10.1002/humu.23796
    By:
    • Marakhonov, Andrey V.;
    • Brodehl, Andreas;
    • Myasnikov, Roman P.;
    • Sparber, Peter A.;
    • Kiseleva, Anna V.;
    • Kulikova, Olga V.;
    • Meshkov, Alexey N.;
    • Zharikova, Anastasia A.;
    • Koretsky, Serguey N.;
    • Kharlap, Maria S.;
    • Stanasiuk, Caroline;
    • Mershina, Elena A.;
    • Sinitsyn, Valentin E.;
    • Shevchenko, Alexey O.;
    • Mozheyko, Natalia P.;
    • Drapkina, Oksana M.;
    • Boytsov, Sergey A.;
    • Milting, Hendrik;
    • Skoblov, Mikhail Yu.
    Publication type:
    Article
    14

    Noncompaction cardiomyopathy is caused by a novel in‐frame desmin (DES) deletion mutation within the 1A coiled‐coil rod segment leading to a severe filament assembly defect.

    Published in:
    Human Mutation, 2019, v. 40, n. 6, p. 734, doi. 10.1002/humu.23747
    By:
    • Marakhonov, Andrey V.;
    • Brodehl, Andreas;
    • Myasnikov, Roman P.;
    • Sparber, Peter A.;
    • Kiseleva, Anna V.;
    • Kulikova, Olga V.;
    • Meshkov, Alexey N.;
    • Zharikova, Anastasia A.;
    • Koretsky, Serguey N.;
    • Kharlap, Maria S.;
    • Stanasiuk, Caroline;
    • Mershina, Elena A.;
    • Sinitsyn, Valentin E.;
    • Shevchenko, Alexey O.;
    • Mozheyko, Natalia P.;
    • Drapkina, Oksana M.;
    • Boytsov, Sergey A.;
    • Milting, Hendrik;
    • Skoblov, Mikhail Yu.
    Publication type:
    Article
    15

    Murine SEC24D can substitute functionally for SEC24C during embryonic development.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-00579-x
    By:
    • Adams, Elizabeth J.;
    • Khoriaty, Rami;
    • Kiseleva, Anna;
    • Cleuren, Audrey C. A.;
    • Tomberg, Kärt;
    • van der Ent, Martijn A.;
    • Gergics, Peter;
    • Tang, Vi T.;
    • Zhu, Guojing;
    • Hoenerhoff, Mark J.;
    • O'Shea, K. Sue;
    • Saunders, Thomas L.;
    • Ginsburg, David
    Publication type:
    Article
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    Spectrum and Prevalence of Rare APOE Variants and Their Association with Familial Dysbetalipoproteinemia.

    Published in:
    International Journal of Molecular Sciences, 2024, v. 25, n. 23, p. 12651, doi. 10.3390/ijms252312651
    By:
    • Blokhina, Anastasia V.;
    • Ershova, Alexandra I.;
    • Kiseleva, Anna V.;
    • Sotnikova, Evgeniia A.;
    • Zharikova, Anastasia A.;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri V.;
    • Ramensky, Vasily E.;
    • Kutsenko, Vladimir A.;
    • Garbuzova, Elizaveta V.;
    • Divashuk, Mikhail G.;
    • Litinskaya, Olga A.;
    • Pokrovskaya, Maria S.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
    20

    The Yield of Genetic Testing and Putative Genetic Factors of Disease Heterogeneity in Long QT Syndrome Patients.

    Published in:
    International Journal of Molecular Sciences, 2024, v. 25, n. 22, p. 11976, doi. 10.3390/ijms252211976
    By:
    • Bukaeva, Anna;
    • Ershova, Alexandra;
    • Kharlap, Maria;
    • Kiseleva, Anna;
    • Kutsenko, Vladimir;
    • Sotnikova, Evgeniia;
    • Divashuk, Mikhail;
    • Pokrovskaya, Maria;
    • Garbuzova, Elizaveta;
    • Blokhina, Anastasia;
    • Kopylova, Oksana;
    • Zotova, Evgenia;
    • Petukhova, Anna;
    • Zharikova, Anastasia;
    • Ramensky, Vasily;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri;
    • Meshkov, Alexey;
    • Drapkina, Oxana
    Publication type:
    Article
    21

    A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.

    Published in:
    International Journal of Molecular Sciences, 2024, v. 25, n. 14, p. 7556, doi. 10.3390/ijms25147556
    By:
    • Bukaeva, Anna;
    • Myasnikov, Roman;
    • Kulikova, Olga;
    • Meshkov, Alexey;
    • Kiseleva, Anna;
    • Petukhova, Anna;
    • Zotova, Evgenia;
    • Sparber, Peter;
    • Ershova, Alexandra;
    • Sotnikova, Evgeniia;
    • Kudryavtseva, Maria;
    • Zharikova, Anastasia;
    • Koretskiy, Sergey;
    • Mershina, Elena;
    • Ramensky, Vasily;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri;
    • Muraveva, Alisa;
    • Abisheva, Alexandra;
    • Nikityuk, Tatiana
    Publication type:
    Article
    22

    Applicability of Diagnostic Criteria and High Prevalence of Familial Dysbetalipoproteinemia in Russia: A Pilot Study.

    Published in:
    International Journal of Molecular Sciences, 2023, v. 24, n. 17, p. 13159, doi. 10.3390/ijms241713159
    By:
    • Blokhina, Anastasia V.;
    • Ershova, Alexandra I.;
    • Kiseleva, Anna V.;
    • Sotnikova, Evgeniia A.;
    • Zharikova, Anastasia A.;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri V.;
    • Ramensky, Vasily E.;
    • Kutsenko, Vladimir A.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
    23

    The Double Mutation DSG2 -p.S363X and TBX20 -p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 6775, doi. 10.3390/ijms22136775
    By:
    • Myasnikov, Roman;
    • Brodehl, Andreas;
    • Meshkov, Alexey;
    • Kulikova, Olga;
    • Kiseleva, Anna;
    • Pohl, Greta Marie;
    • Sotnikova, Evgeniia;
    • Divashuk, Mikhail;
    • Klimushina, Marina;
    • Zharikova, Anastasia;
    • Pokrovskaya, Maria;
    • Koretskiy, Sergey;
    • Kharlap, Maria;
    • Mershina, Elena;
    • Sinitsyn, Valentin;
    • Basargina, Elena;
    • Gandaeva, Leila;
    • Barskiy, Vladimir;
    • Boytsov, Sergey;
    • Milting, Hendrik
    Publication type:
    Article
    24

    Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3786, doi. 10.3390/ijms22073786
    By:
    • Brodehl, Andreas;
    • Meshkov, Alexey;
    • Myasnikov, Roman;
    • Kiseleva, Anna;
    • Kulikova, Olga;
    • Klauke, Bärbel;
    • Sotnikova, Evgeniia;
    • Stanasiuk, Caroline;
    • Divashuk, Mikhail;
    • Pohl, Greta Marie;
    • Kudryavtseva, Maria;
    • Klingel, Karin;
    • Gerull, Brenda;
    • Zharikova, Anastasia;
    • Gummert, Jan;
    • Koretskiy, Sergey;
    • Schubert, Stephan;
    • Mershina, Elena;
    • Gärtner, Anna;
    • Pilus, Polina
    Publication type:
    Article
    25

    Loss of Pkd1 limits susceptibility to colitis and colorectal cancer.

    Published in:
    Oncogenesis, 2023, v. 12, n. 1, p. 1, doi. 10.1038/s41389-023-00486-y
    By:
    • Nikonova, Anna S.;
    • Deneka, Alexander Y.;
    • Silva, Flaviane N.;
    • Pirestani, Shabnam;
    • Tricarico, Rossella;
    • Kiseleva, Anna A.;
    • Zhou, Yan;
    • Nicolas, Emmanuelle;
    • Flieder, Douglas B.;
    • Grivennikov, Sergei I.;
    • Golemis, Erica A.
    Publication type:
    Article
    26

    The genetic regulatory signature of type 2 diabetes in human skeletal muscle.

    Published in:
    Nature Communications, 2016, v. 7, n. 6, p. 11764, doi. 10.1038/ncomms11764
    By:
    • Scott, Laura J.;
    • Erdos, Michael R.;
    • Huyghe, Jeroen R.;
    • Welch, Ryan P.;
    • Beck, Andrew T.;
    • Wolford, Brooke N.;
    • Chines, Peter S.;
    • Didion, John P.;
    • Narisu, Narisu;
    • Stringham, Heather M.;
    • Taylor, D. Leland;
    • Jackson, Anne U.;
    • Vadlamudi, Swarooparani;
    • Bonnycastle, Lori L.;
    • Kinnunen, Leena;
    • Saramies, Jouko;
    • Sundvall, Jouko;
    • Albanus, Ricardo D'Oliveira;
    • Kiseleva, Anna;
    • Hensley, John
    Publication type:
    Article
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    Uniparental Genetic Heritage of Belarusians: Encounter of Rare Middle Eastern Matrilineages with a Central European Mitochondrial DNA Pool.

    Published in:
    PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066499
    By:
    • Kushniarevich, Alena;
    • Sivitskaya, Larysa;
    • Danilenko, Nina;
    • Novogrodskii, Tadeush;
    • Tsybovsky, Iosif;
    • Kiseleva, Anna;
    • Kotova, Svetlana;
    • Chaubey, Gyaneshwer;
    • Metspalu, Ene;
    • Sahakyan, Hovhannes;
    • Bahmanimehr, Ardeshir;
    • Reidla, Maere;
    • Rootsi, Siiri;
    • Parik, Jüri;
    • Reisberg, Tuuli;
    • Achilli, Alessandro;
    • Hooshiar Kashani, Baharak;
    • Gandini, Francesca;
    • Olivieri, Anna;
    • Behar, Doron M.
    Publication type:
    Article
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    Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region.

    Published in:
    Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.709419
    By:
    • Ramensky, Vasily E.;
    • Ershova, Alexandra I.;
    • Zaicenoka, Marija;
    • Kiseleva, Anna V.;
    • Zharikova, Anastasia A.;
    • Vyatkin, Yuri V.;
    • Sotnikova, Evgeniia A.;
    • Efimova, Irina A.;
    • Divashuk, Mikhail G.;
    • Kurilova, Olga V.;
    • Skirko, Olga P.;
    • Muromtseva, Galina A.;
    • Belova, Olga A.;
    • Rachkova, Svetlana A.;
    • Pokrovskaya, Maria S.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
    34

    A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.

    Published in:
    Genes, 2022, v. 13, n. 2, p. 309, doi. 10.3390/genes13020309
    By:
    • Myasnikov, Roman;
    • Bukaeva, Anna;
    • Kulikova, Olga;
    • Meshkov, Alexey;
    • Kiseleva, Anna;
    • Ershova, Alexandra;
    • Petukhova, Anna;
    • Divashuk, Mikhail;
    • Zotova, Evgenia;
    • Sotnikova, Evgeniia;
    • Kharlap, Maria;
    • Zharikova, Anastasia;
    • Vyatkin, Yuri;
    • Ramensky, Vasily;
    • Abisheva, Alexandra;
    • Muraveva, Alisa;
    • Koretskiy, Sergey;
    • Kudryavtseva, Maria;
    • Popov, Sergey;
    • Utkina, Marina
    Publication type:
    Article
    35

    The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.

    Published in:
    Genes, 2021, v. 12, n. 1, p. 121, doi. 10.3390/genes12010121
    By:
    • Kulikova, Olga;
    • Brodehl, Andreas;
    • Kiseleva, Anna;
    • Myasnikov, Roman;
    • Meshkov, Alexey;
    • Stanasiuk, Caroline;
    • Gärtner, Anna;
    • Divashuk, Mikhail;
    • Sotnikova, Evgeniia;
    • Koretskiy, Sergey;
    • Kharlap, Maria;
    • Kozlova, Viktoria;
    • Mershina, Elena;
    • Pilus, Polina;
    • Sinitsyn, Valentin;
    • Milting, Hendrik;
    • Boytsov, Sergey;
    • Drapkina, Oxana
    Publication type:
    Article
    36

    The LDLR , APOB , and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.

    Published in:
    Genes, 2021, v. 12, n. 1, p. 66, doi. 10.3390/genes12010066
    By:
    • Meshkov, Alexey;
    • Ershova, Alexandra;
    • Kiseleva, Anna;
    • Zotova, Evgenia;
    • Sotnikova, Evgeniia;
    • Petukhova, Anna;
    • Zharikova, Anastasia;
    • Malyshev, Pavel;
    • Rozhkova, Tatyana;
    • Blokhina, Anastasia;
    • Limonova, Alena;
    • Ramensky, Vasily;
    • Divashuk, Mikhail;
    • Khasanova, Zukhra;
    • Bukaeva, Anna;
    • Kurilova, Olga;
    • Skirko, Olga;
    • Pokrovskaya, Maria;
    • Mikova, Valeriya;
    • Snigir, Ekaterina
    Publication type:
    Article
    37

    CRISPR-Based Editing of the Medicago truncatula LEC1 Gene.

    Published in:
    Plants (2223-7747), 2024, v. 13, n. 22, p. 3226, doi. 10.3390/plants13223226
    By:
    • Potsenkovskaia, Elina A.;
    • Tvorogova, Varvara E.;
    • Simonova, Veronika Y.;
    • Konstantinov, Zakhar S.;
    • Kiseleva, Anna S.;
    • Matveenko, Andrew G.;
    • Brynchikova, Anna V.;
    • Lutova, Ludmila A.
    Publication type:
    Article
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    A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.

    Published in:
    Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101750
    By:
    • Myasnikov, Roman P.;
    • Kulikova, Olga V.;
    • Meshkov, Alexey N.;
    • Bukaeva, Anna A.;
    • Kiseleva, Anna V.;
    • Ershova, Alexandra I.;
    • Petukhova, Anna V.;
    • Divashuk, Mikhail G.;
    • Zotova, Evgenia D.;
    • Sotnikova, Evgeniia A.;
    • Abisheva, Alexandra A.;
    • Muraveva, Alisa V.;
    • Koretskiy, Sergey N.;
    • Popov, Sergey V.;
    • Utkina, Marina V.;
    • Snigir, Ekaterina A.;
    • Mitrofanov, Sergey I.;
    • Konureeva, Ksenia D.;
    • Mershina, Elena A.;
    • Sinitsyn, Valentin E.
    Publication type:
    Article
    42

    Clinical and biochemical features of atherogenic hyperlipidemias with different genetic basis: A comprehensive comparative study.

    Published in:
    PLoS ONE, 2024, v. 19, n. 12, p. 1, doi. 10.1371/journal.pone.0315693
    By:
    • Blokhina, Anastasia V.;
    • Ershova, Alexandra I.;
    • Kiseleva, Anna V.;
    • Sotnikova, Evgeniia A.;
    • Zharikova, Anastasia A.;
    • Zaicenoka, Marija;
    • Vyatkin, Yuri V.;
    • Ramensky, Vasily E.;
    • Kutsenko, Vladimir A.;
    • Litinskaya, Olga A.;
    • Pokrovskaya, Maria S.;
    • Shalnova, Svetlana A.;
    • Meshkov, Alexey N.;
    • Drapkina, Oxana M.
    Publication type:
    Article
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