Fedor A Konovalov (Fedor Konovalov, F A Konovalov)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 8

Top Topics

Top Venues

Life (Basel, Switzerland)

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

European journal of human genetics : EJHG

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

Publications

Anastasiia Danishevich, Anzhelika Chegodar, Natalia Bodunova, Fedor A Konovalov, Maria Nefedova, Natalya Kremneva, Nizhat Kurbanov, Airat Bilyalov, Sergey Nikolaev, Igor Khatkov, Galina Dudina
Myelodysplastic Syndrome: Clinical Characteristics and Significance of Preclinically Detecting Biallelic Mutations in the TET2 Gene. Life (Basel, Switzerland) 14 (5) (2024)
Anastasiia Danishevich, Anzhelika Chegodar, Natalia Bodunova, Fedor A Konovalov, Maria Nefedova, Natalya Kremneva, Nizhat Kurbanov, Airat Bilyalov, Sergey Nikolaev, Igor Khatkov, Galina Dudina
Myelodysplastic Syndrome: Clinical Characteristics and Significance of Preclinically Detecting Biallelic Mutations in the TET2 Gene. Life (Basel, Switzerland) 14 (5) (2024)
G E Rudenskaya, Fedor A Konovalov, Sergey Nikolaevich Illarioshkin, Olga A Shchagina
[Gerstmann-Sträussler disease: a familial case with common PRNP mutation and atypical features]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 123 (2) (2023)
Nika V Petrova, Andrey A Marakhonov, Natalia V Balinova, Anna V Abrukova, Fedor A Konovalov, Sergey I Kutsev, Rena A Zinchenko
Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population. Genes 12 (6) (2021)
G E Rudenskaya, V A Kadnikova, L A Bessonova, Peter A Sparber, Sergey Kurbatov, Olga Mironovich, Fedor A Konovalov, Oxana P Ryzhkova
[Autosomal dominant spastic paraplegias]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 121 (5) (2021)
Igor O Bychkov, Galina Baydakova, Alexandra Yu Filatova, Ochir Migiaev, Andrey A Marakhonov, Nataliya Pechatnikova, Ekaterina Pomerantseva, Fedor A Konovalov, Maria Ampleeva, Vladimir Kaimonov, Mikhail Yurevich Skoblov, Ekaterina Zakharova
Complex Transposon Insertion as a Novel Cause of Pompe Disease. International journal of molecular sciences 22 (19) (2021)
Andrey A Marakhonov, Magdalena Přechová, Fedor A Konovalov, Alexandra Yu Filatova, Maria A Zamkova, Ilya V Kanivets, Vladimir G Solonichenko, Natalia A Semenova, Rena A Zinchenko, Richard Treisman, Mikhail Yurevich Skoblov
Mutation in PHACTR1 associated with multifocal epilepsy with infantile spasms and hypsarrhythmia. Clinical genetics 99 (5) (2021)
Marcello Scala, Geok Lin Chua, Cheen Fei Chin, Hessa S Alsaif, Artem Borovikov, Saima Riazuddin, Sheikh Riazuddin, M Chiara Manzini, Mariasavina Severino, Alvin Kuk, Hao Fan, Yalda Jamshidi, Mehran Beiraghi Toosi, Mohammad Doosti, Ehsan Ghayoor Karimiani, Vincenzo Salpietro, Elena Dadali, Galina Baydakova, Fedor A Konovalov, Ekaterina Lozier, Emer O'Connor, Yasser Sabr, Abdullah Alfaifi, Farah Ashrafzadeh, Pasquale Striano, Federico Zara, Fowzan Sami Alkuraya, Henry Houlden, Reza Maroofian, David L Silver
Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features. European journal of human genetics : EJHG 28 (11) (2020)