Taisiya O Kochetkova

ORCID

Publication Activity (10 Years)

Years Active: 2023-2023
Publications (10 Years): 9

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

Publications

Taisiya O Kochetkova, Dmitry N Maslennikov, Ekaterina R Tolmacheva, Jekaterina Shubina, Anna S Bolshakova, Dzhenneta I Suvorova, Anna V Degtyareva, Irina V Orlovskaya, Maria V Kuznetsova, Anastasia A Rachkova, Gennady T Sukhikh, Denis V Rebrikov, Dmitriy Yu Trofimov
De Novo Variant in the KCNJ9 Gene as a Possible Cause of Neonatal Seizures. Genes 14 (2) (2023)
Ekaterina R Tolmacheva, Jekaterina Shubina, Taisiya O Kochetkova, Lubov' V Ushakova, Ekaterina L Bokerija, Grigory S Vasiliev, Galina V Mikhaylovskaya, Ekaterina E Atapina, Nadezhda V Zaretskaya, Gennady T Sukhikh, Denis V Rebrikov, Dmitriy Yu Trofimov
CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report. Genes 14 (6) (2023)
Taisiya O Kochetkova, Dmitry N Maslennikov, Ekaterina R Tolmacheva, Jekaterina Shubina, Anna S Bolshakova, Dzhenneta I Suvorova, Anna V Degtyareva, Irina V Orlovskaya, Maria V Kuznetsova, Anastasia A Rachkova, Gennady T Sukhikh, Denis V Rebrikov, Dmitriy Yu Trofimov
De Novo Variant in the KCNJ9 Gene as a Possible Cause of Neonatal Seizures. Genes 14 (2) (2023)
Ekaterina R Tolmacheva, Jekaterina Shubina, Taisiya O Kochetkova, Lubov' V Ushakova, Ekaterina L Bokerija, Grigory S Vasiliev, Galina V Mikhaylovskaya, Ekaterina E Atapina, Nadezhda V Zaretskaya, Gennady T Sukhikh, Denis V Rebrikov, Dmitriy Yu Trofimov
CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report. Genes 14 (6) (2023)
Ekaterina R Tolmacheva, Jekaterina Shubina, Taisiya O Kochetkova, Lubov' V Ushakova, Ekaterina L Bokerija, Grigory S Vasiliev, Galina V Mikhaylovskaya, Ekaterina E Atapina, Nadezhda V Zaretskaya, Gennady T Sukhikh, Denis V Rebrikov, Dmitriy Yu Trofimov
CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report. Genes 14 (6) (2023)
Taisiya O Kochetkova, Dmitry N Maslennikov, Ekaterina R Tolmacheva, Jekaterina Shubina, Anna S Bolshakova, Dzhenneta I Suvorova, Anna V Degtyareva, Irina V Orlovskaya, Maria V Kuznetsova, Anastasia A Rachkova, Gennady T Sukhikh, Denis V Rebrikov, Dmitriy Yu Trofimov
De Novo Variant in the KCNJ9 Gene as a Possible Cause of Neonatal Seizures. Genes 14 (2) (2023)
Taisiya O Kochetkova, Dmitry N Maslennikov, Ekaterina R Tolmacheva, Jekaterina Shubina, Anna S Bolshakova, Dzhenneta I Suvorova, Anna V Degtyareva, Irina V Orlovskaya, Maria V Kuznetsova, Anastasia A Rachkova, Gennady T Sukhikh, Denis V Rebrikov, Dmitriy Yu Trofimov
De Novo Variant in the KCNJ9 Gene as a Possible Cause of Neonatal Seizures. Genes 14 (2) (2023)
Ekaterina R Tolmacheva, Jekaterina Shubina, Taisiya O Kochetkova, Lubov' V Ushakova, Ekaterina L Bokerija, Grigory S Vasiliev, Galina V Mikhaylovskaya, Ekaterina E Atapina, Nadezhda V Zaretskaya, Gennady T Sukhikh, Denis V Rebrikov, Dmitriy Yu Trofimov
CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report. Genes 14 (6) (2023)
Taisiya O Kochetkova, Dmitry N Maslennikov, Ekaterina R Tolmacheva, Jekaterina Shubina, Anna S Bolshakova, Dzhenneta I Suvorova, Anna V Degtyareva, Irina V Orlovskaya, Maria V Kuznetsova, Anastasia A Rachkova, Gennady T Sukhikh, Denis V Rebrikov, Dmitriy Yu Trofimov
De Novo Variant in the KCNJ9 Gene as a Possible Cause of Neonatal Seizures. Genes 14 (2) (2023)

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Publication Activity (10 Years)

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Taisiya O Kochetkova