Get started
Author

Fatima Bostanova

Observed names: Bostanova, Fatima M., F. M. Bostanova, F.M. Bostanova, Fatima M. Bostanova, Ф. М. Бостанова, Ф.М. Бостанова
ORCID: 0000-0002-5337-1775
Observed ORCID: 0000-0002-5337-1775
OpenAlex ID: A5066468095
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia
2023 · Denis Kistol, Polina Tsygankova, et al. · International Journal of Molecular Sciences · 20
PDF
The Genetic Basis of the First Patient with Wiedemann–Rautenstrauch Syndrome in the Russian Federation
2024 · Valeriia A. Kovalskaia, Anastasiia L. Kungurtseva, et al. · Genes · 6
PDF
A novel FBXW11 variant in a patient with neurodevelopmental, jaw, eye, and digital syndrome
2025 · Anna Maznina, Daria Molodtsova-Zolotukhina, et al. · Neurogenetics · 3
New Case of Spinocerebellar Ataxia, Autosomal Recessive 4, Due to VPS13D Variants
2024 · Denis Kistol, Polina Tsygankova, et al. · International Journal of Molecular Sciences · 3
A case of rare hereditary Siddiqi syndrome with novel neuropsychiatric signs
2024 · G.E. Rudenskaya, F.M. Bostanova, et al. · S S Korsakov Journal of Neurology and Psychiatry · 3
The first case of a point pathogenic variant in the RREB1 gene in Noonan‐like Rasopathy
2024 · Olga Shatokhina, Fatima Bostanova, et al. · Clinical Genetics · 3
PDF
Identification of a Novel Indel Variant in the DARS2 Gene in Russian Patients with Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
2024 · Fatima M. Bostanova, Polina G. Tsygankova, et al. · Genes · 2
Special clinical manifestations and genetic characteristics of schaaf–Yang syndrome in Russian patients
2024 · E. L. Dadali, T. V. Markova, et al. · Neuromuscular Diseases · 2
PDF
Ethical problems of genetic testing for hereditary cardiovascular diseases
2022 · F. M. Bostanova, V. L. Izhevskaya · Сибирский журнал клинической и экспериментальной медицины · 2
PDF
Patients with Papillary Renal Cancer and Germline Duplication of MET Exons 5-21
2025 · Dmitry S. Mikhaylenko, Natalya B. Kuryakova, et al. · Biomedicines · 1
PDF
Clinical Case of Mild Tatton–Brown–Rahman Syndrome Caused by a Nonsense Variant in DNMT3A Gene
2024 · Fatima Bostanova, Olga Levchenko, et al. · Clinics and Practice · 1
PDF
Four Novel Disease-Causing Variants in the NOTCH3 Gene in Russian Patients with CADASIL
2023 · Fatima Bostanova, Polina Tsygankova, et al. · Genes · 1
PDF
Independent coexistence of diseases in neurogenetics: case reports and literature review
2026 · Galina E. Rudenskaya, A. S. Kuchina, et al. · Neuromuscular Diseases
PDF
Autosomal Dominant Dyskinesia Associated with the ADCY5 Gene
2026 · G. E. Rudenskaya, F. M. Bostanova, et al. · Neuroscience and Behavioral Physiology
Autosomal dominant dyskinesia associated with the ADCY5 gene
2026 · G.E. Rudenskaya, F.M. Bostanova, et al. · S S Korsakov Journal of Neurology and Psychiatry
Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
2026 · Valeriia A. Kovalskaia, Tatiana B. Cherevatova, et al. · Orphanet Journal of Rare Diseases
PDF
Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
2026 · Kovalskaia, Valeriia A., Cherevatova, Tatiana B., et al. · Figshare
Neuroimaging in hereditary neuromuscular disorders: a literature review and clinical case reports
2025 · Fatima M. Bostanova, I. V. Sharkova, et al. · Neuromuscular Diseases
PDF
FA2H gene-associated spastic paraplegia (SPG35) — familial case with late onset
2025 · G.E. Rudenskaya, F.M. Bostanova, et al. · S S Korsakov Journal of Neurology and Psychiatry
Klinefelter syndrome in a patient with double Y-autosomal translocation
2024 · V. B. Chernykh, F. M. Bostanova, et al. · Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)
PDF
Author response for "The first case of a point pathogenic variant in the RREB1 gene in Noonan‐like Rasopathy"
2024 · Olga Shatokhina, Fatima Bostanova, et al. · Publons reviews and discussion
Clinical and molecular cytogenetic characteristics of the unique pseudotricentric X chromosome
2023 · Ж.Г. Маркова, М.Е. Миньженкова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
PDF
Phenotypic variability in TRPV4-associated neuropathies and neuronopathies: a case series
2023 · A. F. Murtazina, P. N. Tsabay, et al. · Neuromuscular Diseases
PDF
Нейровизуализация при наследственных нервно-мышечных болезнях: обзор литературы с клиническими примерами
· Ф. М. Бостанова, И. В. Шаркова, et al. · CyberLeninK (CyberLeninka)
Works count: 26
Citation count: 47
H-index: 3
I10-index: 1
Year
Topic
Type