Search Results - Bukaeva, Anna A

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  1. 1
    Allelic Dropout Is a Common Phenomenon That Reduces the Diagnostic Yield of PCR-Based Sequencing of Targeted Gene Panels

    Allelic Dropout Is a Common Phenomenon That Reduces the Diagnostic Yield of PCR-Based Sequencing of Targeted Gene Panels by Shestak, Anna G, Bukaeva, Anna A, Saber, Siamak, Zaklyazminskaya, Elena V

    Published in Frontiers in genetics
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  2. 2
    A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy

    A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy 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, Yudin, Sergey M, Drapkina, Oxana M

    Published in Genes
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  3. 3
    A Splice Variant of the IMYH7/I Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy

    A Splice Variant of the IMYH7/I Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy 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, Yudin, Sergey M, Drapkina, Oxana M

    Published in Genes
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  4. 4
    A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities

    A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities 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, Sinitsyn, Valentin, Divashuk, Mikhail, Dadali, Elena, Pokrovskaya, Maria, Drapkina, Oxana

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  5. 5
    Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy – a pilot study

    Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy – a pilot study by Zaklyazminskaya, Elena, Mikhailov, Vadim, Bukaeva, Anna, Kotlukova, Natalia, Povolotskaya, Inna, Kaimonov, Vladimir, Dombrovskaya, Anna, Dzemeshkevich, Sergey

    Published in Scientific reports
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  6. 6
    The Yield of Genetic Testing and Putative Genetic Factors of Disease Heterogeneity in Long QT Syndrome Patients

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

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  7. 7
    The LDLR , APOB , and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia

    The LDLR , APOB , and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia 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, Akinshina, Alexsandra, Mitrofanov, Sergey, Kashtanova, Daria, Makarov, Valentin, Kukharchuk, Valeriy, Boytsov, Sergey, Yudin, Sergey, Drapkina, Oxana

    Published in Genes
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  8. 8
    A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene

    A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene 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, Mershina, Elena, Sinitsyn, Valentin, Kogan, Evgeniya, Blagova, Olga, Drapkina, Oxana

    Published in Genes
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  9. 9
    A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene

    A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene 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, Mershina, Elena, Sinitsyn, Valentin, Kogan, Evgeniya, Blagova, Olga, Drapkina, Oxana

    Published in Genes
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