Ekaterina Ivanovna Surkova (Ekaterina I Surkova, Surkova I Ekaterina, Surkova Ekaterina Ivanovna)

Scopus Author ID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 11

Top Venues

The Journal of international medical research

BMC medical genetics

Molecular genetics & genomic medicine

BMC pediatrics

Moscow State University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Moscow State University Sep 01 2003 - Jun 30 2008

Russia

PHD :: Biological

Publications

Anastasiya Aleksandrovna Kozina, Guria Kurbanovna Kanaeva, Natalia Vladimirovna Baryshnikova, Anna Yurievna Ilinskaya, Anna Alexandrovna Kim, Anastasia Vladimirovna Erofeeva, Nadezhda Andreevna Pogodina, Jamilya Payzutdinova Gadzhiyeva, Ekaterina Ivanovna Surkova, Valery Vladimirovich Ilinsky
A case of Joubert syndrome caused by novel compound heterozygous variants in the TMEM67 gene. The Journal of international medical research 51 (10) (2023)
Anastasiya Aleksandrovna Kozina, Natalia Vladimirovna Baryshnikova, Anna Yurievna Ilinskaya, Anna Alexandrovna Kim, Nikolay Alekseevich Plotnikov, Nadezhda Andreevna Pogodina, Ekaterina Ivanovna Surkova, Peter Alekseevich Shatalov, Valery Vladimirovich Ilinsky
Novel mutation in the MPZ gene causes early-onset but slow-progressive Charcot-Marie-Tooth disease in a Russian family: a case report. The Journal of international medical research 50 (12) (2022)
Anastasiya Aleksandrovna Kozina, Natalia Vladimirovna Baryshnikova, Anna Yurievna Ilinskaya, Anna Alexandrovna Kim, Nikolay Alekseevich Plotnikov, Nadezhda Andreevna Pogodina, Ekaterina Ivanovna Surkova, Peter Alekseevich Shatalov, Valery Vladimirovich Ilinsky
Novel mutation in the MPZ gene causes early-onset but slow-progressive Charcot-Marie-Tooth disease in a Russian family: a case report. The Journal of international medical research 50 (12) (2022)
Anastasiya Aleksandrovna Kozina, Natalia Vladimirovna Baryshnikova, Anna Yurievna Ilinskaya, Anna Alexandrovna Kim, Nikolay Alekseevich Plotnikov, Nadezhda Andreevna Pogodina, Ekaterina Ivanovna Surkova, Peter Alekseevich Shatalov, Valery Vladimirovich Ilinsky
Novel mutation in the MPZ gene causes early-onset but slow-progressive Charcot-Marie-Tooth disease in a Russian family: a case report. The Journal of international medical research 50 (12) (2022)
Anastasiya Aleksandrovna Kozina, Natalia Vladimirovna Baryshnikova, Anna Yurievna Ilinskaya, Anna Alexandrovna Kim, Nikolay Alekseevich Plotnikov, Nadezhda Andreevna Pogodina, Ekaterina Ivanovna Surkova, Peter Alekseevich Shatalov, Valery Vladimirovich Ilinsky
Novel mutation in the MPZ gene causes early-onset but slow-progressive Charcot-Marie-Tooth disease in a Russian family: a case report. The Journal of international medical research 50 (12) (2022)
Anastasiya Aleksandrovna Kozina, Elena Grigorievna Okuneva, Natalia Vladimirovna Baryshnikova, Inessa Dmitrievna Fedonyuk, Alexey Aleksandrovich Kholin, Elena Stepanovna Il'ina, Anna Yurievna Krasnenko, Ivan Fedorovich Stetsenko, Nikolay Alekseevich Plotnikov, Olesia Igorevna Klimchuk, Ekaterina Ivanovna Surkova, Valery Vladimirovich Ilinsky
Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report. BMC medical genetics 21 (1) (2020)
Anastasiya A Kozina, Elena G Okuneva, Natalia V Baryshnikova, Olga B Kondakova, Ekaterina A Nikolaeva, Inessa D Fedoniuk, Svetlana V Mikhailova, Anna Y Krasnenko, Ivan F Stetsenko, Nikolay A Plotnikov, Olesia I Klimchuk, Yaroslav V Popov, Ekaterina Ivanovna Surkova, Peter A Shatalov, Alexander S Rakitko, Valery V Ilinsky
Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers. Molecular genetics & genomic medicine 8 (7) (2020)
Kondakova Olga Borisovna, Krasnenko Anna Yurievna, Tsukanov Kirill Yurievich, Klimchuk Olesya Igorevna, Korostin Dmitriy Olegovich, Davidova Anna Igorevna, Batysheva Tatyana Timofeevna, Zhurkova Natalia Vyacheslavovna, Ekaterina Ivanovna Surkova, Shatalov Peter Alekseevich, Ilinsky Valery Vladimirovich
Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report. BMC pediatrics 19 (1) (2019)
Anastasiya A Kozina, Tatiana A Trofimova, Elena G Okuneva, Natalia V Baryshnikova, Varvara A Obuhova, Anna Yu Krasnenko, Kirill Yu Tsukanov, Olesya I Klimchuk, Ekaterina Ivanovna Surkova, Peter A Shatalov, Valery V Ilinsky
Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report. BMC nephrology 20 (1) (2019)
Kozina A Anastasiya, Okuneva G Elena, Baryshnikova V Natalia, Krasnenko Yu Anna, Tsukanov Yu Kirill, Klimchuk I Olesya, Nikishina A Tatiana, Fedoniuk D Inessa, Ekaterina Ivanovna Surkova, Shatalov A Peter, Ilinsky V Valery
Atypical onset of nephropathic infantile cystinosis in a Russian patient with rare CTNS mutation. Clinical case reports 6 (9) (2018)
Anastasiya Aleksandrovna Kozina, Elena Grigorievna Okuneva, Natalia Vladimirovna Baryshnikova, Anna Yurievna Krasnenko, Kirill Yurievich Tsukanov, Olesya Igorevna Klimchuk, Olga Borisovna Kondakova, Anna Nikolaevna Larionova, Tatyana Timofeevna Batysheva, Ekaterina Ivanovna Surkova, Peter Alekseevich Shatalov, Valery Vladimirovich Ilinsky
A novel MFSD8 mutation in a Russian patient with neuronal ceroid lipofuscinosis type 7: a case report. BMC medical genetics 19 (1) (2018)

Ekaterina Ivanovna Surkova.css-eqlu8i{font-size:small;padding-left:4px;} (Ekaterina I Surkova, Surkova I Ekaterina, Surkova Ekaterina Ivanovna)

Publication Activity (10 Years)

Top Topics

Top Venues

Ekaterina Ivanovna Surkova (Ekaterina I Surkova, Surkova I Ekaterina, Surkova Ekaterina Ivanovna)