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Author

Maria Orlova

Observed names: M. D. Orlova, M.D. Orlova, Orlova M.D
ORCID: 0000-0002-3743-094X
Observed ORCID: 0000-0002-3743-094X
OpenAlex ID: A5018577300
Accumulation of Circulating Cell-Free CpG-Enriched Ribosomal DNA Fragments on the Background of High Endonuclease Activity of Blood Plasma in Schizophrenic Patients
2019 · E. S. Ershova, E. M. Jestkova, et al. · International Journal of Genomics · 35
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NRF2 and HMOX1 Gene Expression against the Background of Systemic Oxidative Stress in Patients with Acute Psychosis
2020 · G. V. Shmarina, M. D. Orlova, et al. · Russian Journal of Genetics · 11
Generation of two induced pluripotent stem cell lines (RCMGi005-A/B) from human skin fibroblasts of a cystic fibrosis patient with homozygous F508del mutation in CFTR gene
2022 · Irina Panchuk, Ekaterina Kondrateva, et al. · Stem Cell Research · 6
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Generation of induced pluripotent stem cell line (RCMGi008-A) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/CFTRdele2.3 mutations in CFTR gene
2022 · Ekaterina Kondrateva, Irina Panchuk, et al. · Stem Cell Research · 5
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A Case Report of Auditory Neuropathy Due to TWNK Gene Mutations
2025 · Tufatulin G.Sh, Garbaruk E.S, et al. · The Journal of International Advanced Otology · 3
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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
The Missing Piece of the Puzzle: Unveiling the Role of PTPN11 Gene in Multiple Osteochondromas in a Large Cohort Study
2024 · Artem Borovikov, Nailya Galeeva, et al. · Human Mutation · 3
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Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12
2023 · I.O. Panchuk, O.V. Grigorieva, et al. · Stem Cell Research · 3
Beyond the Known: Expanding the Clinical and Genetic Spectrum of Rare RPL13-Related Spondyloepimetaphyseal Dysplasia
2025 · Daria Gorodilova, Elena Dadali, et al. · International Journal of Molecular Sciences · 2
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Case Report: The widening genetic and phenotypic spectrum of ultra-rare PDE4D-related acroscyphodysplasia
2025 · Anna Morgul, Margarita Sharova, et al. · Frontiers in Medicine · 1
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Generation of induced pluripotent stem cell line (RCMGi009-A) from urine cells of patient with fibrodysplasia ossificans progressiva
2023 · Ekaterina Kondrateva, Olga Grigorieva, et al. · Stem Cell Research · 1
Diagnostic utility of exome sequencing for inherited peripheral neuropathies
2020 · O. A. Shchagina, O. P. Ryzhkova, et al. · Neuromuscular Diseases · 1
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Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia
2020 · A. F. Murtazina, O. A. Shchagina, et al. · Neuromuscular Diseases · 1
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Kyphoscoliotic Ehlers–Danlos syndrome: case reports and literature review
2026 · G. E. Rudenskaya, T. V. Markova, et al. · Neuromuscular Diseases
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Case Report: Dual pathogenic mechanism of a PRKG2 missense variant underlies an attenuated phenotype of acromesomelic dysplasia
2026 · Daria Akimova, Tatiana Markova, et al. · Frontiers in Genetics
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Mitochondrial Complex IV Deficiency Nuclear Type 11 Caused by a Novel Start-Lost Variant in the COX20 Gene
2025 · Anna Kuchina, Artem Borovikov, et al. · Genes
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Works count: 16
Citation count: 75
H-index: 4
I10-index: 2
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