Sergey A Klyushnikov (Sergey Klyushnikov)

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 7

Top Topics

Intellectual Disability

Gene Expression

Top Venues

International journal of molecular sciences

Journal of neurology

European journal of human genetics : EJHG

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

Publications

Maria Sergeevna Protasova, Tatiana V Andreeva, Sergey A Klyushnikov, Sergey Nikolaevich Illarioshkin, Evgeny I Rogaev
Genetic Variant in GRM1 Underlies Congenital Cerebellar Ataxia with No Obvious Intellectual Disability. International journal of molecular sciences 24 (2) (2023)
Maria Sergeevna Protasova, Tatiana V Andreeva, Sergey A Klyushnikov, Sergey Nikolaevich Illarioshkin, Evgeny I Rogaev
Genetic Variant in GRM1 Underlies Congenital Cerebellar Ataxia with No Obvious Intellectual Disability. International journal of molecular sciences 24 (2) (2023)
Maria Sergeevna Protasova, Tatiana V Andreeva, Sergey A Klyushnikov, Sergey Nikolaevich Illarioshkin, Evgeny I Rogaev
Genetic Variant in GRM1 Underlies Congenital Cerebellar Ataxia with No Obvious Intellectual Disability. International journal of molecular sciences 24 (2) (2023)
Maria Sergeevna Protasova, Tatiana V Andreeva, Sergey A Klyushnikov, Sergey Nikolaevich Illarioshkin, Evgeny I Rogaev
Genetic Variant in GRM1 Underlies Congenital Cerebellar Ataxia with No Obvious Intellectual Disability. International journal of molecular sciences 24 (2) (2023)
Maria Sergeevna Protasova, Tatiana V Andreeva, Sergey A Klyushnikov, Sergey Nikolaevich Illarioshkin, Evgeny I Rogaev
Genetic Variant in GRM1 Underlies Congenital Cerebellar Ataxia with No Obvious Intellectual Disability. International journal of molecular sciences 24 (2) (2023)
Maria S Protasova, Fedor E Gusev, Tatiana V Andreeva, Sergey A Klyushnikov, Sergey N Illarioshkin, Evgeny I Rogaev
Novel genes bearing mutations in rare cases of early-onset ataxia with cerebellar hypoplasia. European journal of human genetics : EJHG 30 (6) (2022)
Alexandra Belyakova-Bodina, Mikhail Ratanov, Erich Schneider, Yury Seliverstov, Evgenii Nuzhnyi, Sergey A Klyushnikov, Amayak Broutian
Uncovering bilateral vestibulopathy in patients with SANDO syndrome caused by mutations in POLG gene: a case series. Journal of neurology 268 (10) (2021)