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Elena S. Merkuryeva

Observed names: E. S. Merkuryeva, Elena Merkuryeva, Elena Sergeevna Merkurieva
ORCID: 0000-0001-6902-253X
Observed ORCID: 0000-0001-6902-253X
OpenAlex ID: A5036639524
Clinical and Genetic Characteristics of Calvarial Doughnut Lesions with Bone Fragility in Three Families with a Reccurent SGMS2 Gene Variant
2023 · Elena Merkuryeva, Tatiana Markova, et al. · International Journal of Molecular Sciences · 11
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Does the c.-14C>T Mutation in the IFITM5 Gene Provide Identical Phenotypes for Osteogenesis Imperfecta Type V? Data from Russia and a Literature Review
2022 · Anton Tyurin, Elena Merkuryeva, et al. · Biomedicines · 11
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Molecular and Clinical Aspects of Osteogenesis Imperfecta Type VI: A Case Series with Novel SERPINF1 Gene Variants
2025 · Elena S. Merkuryeva, Tatyana S. Nagornova, et al. · International Journal of Molecular Sciences · 4
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Presentation of Rare Phenotypes Associated with the FKBP10 Gene
2024 · Elena S. Merkuryeva, Tatiana V. Markova, et al. · Genes · 4
Phenotypic variability in children with Bruck syndrome type 2: Clinical cases
2023 · Svetlana I. Trofimova, Evgeniia A. Kochenova, et al. · Pediatric Traumatology Orthopaedics and Reconstructive Surgery · 2
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Clinical Variability Within the PLOD2-Associated Phenotypic Continuum: Three Novel Variants in Four Patients from a Descriptive Case Series
2026 · Elena S. Merkuryeva, Evgeniya A. Melnik, et al. · Genes
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Rare Variants in the P3H1 Gene in Patients With Osteogenesis Imperfecta of Bashkir Origin From Russia
2025 · Aliya Ramilevna Zaripova, Dina Dayanovna Nadyrshina, et al. · Clinical Genetics
Author response for "Rare Variants in the P3H1 Gene in Patients With Osteogenesis Imperfecta of Bashkir Origin From Russia"
2025 · Aliya Ramilevna Zaripova, Dina Dayanovna Nadyrshina, et al.
Author response for "Rare Variants in the P3H1 Gene in Patients With Osteogenesis Imperfecta of Bashkir Origin From Russia"
2025 · Aliya Ramilevna Zaripova, Dina Dayanovna Nadyrshina, et al.
Clinico-radiological characteristics of two patients with geroderma osteodysplasticum caused by new nucleotide variants in the GORAB gene
2024 · E. S. Merkuryeva, T. V. Markova, et al. · Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)
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Clinical and radiological characteristics of two patients with osteoporosis–pseudoglioma syndrome caused by a pathogenic homozygotic variant in the LRP5 gene
2023 · Elena S. Merkuryeva, Tatiana V. Markova, et al. · Pediatric Traumatology Orthopaedics and Reconstructive Surgery
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Works count: 11
Citation count: 32
H-index: 4
I10-index: 2
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