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Agnes Selina

Osteogenesis imperfecta: Novel genetic variants and clinical observations from a clinical exome study of 54 Indian patients
2020 · Vrisha Madhuri, Agnes Selina, et al. · Annals of Human Genetics · 20
SERPINF1 gene variants causing late-onset progressive deforming osteogenesis imperfecta – A study of 18 patients from India
2023 · Agnes Selina, Madhavi Kandagaddala, et al. · Bone Reports · 13
MATN3 Mutation Causing Spondyloepimetaphyseal Dysplasia
2019 · L. G. Shyamasundar, Lakshmi Loganathan, et al. · The Indian Journal of Pediatrics · 8
COL1A1 and COL1A2 Gene Variants Causing Osteogenesis Imperfecta in a Major Referral Center of India
2025 · Agnes Selina, Madhavi Kandagaddala, et al. · American Journal of Medical Genetics Part A · 6
A Recurrent Biallelic Pathogenic Variant in TBXAS1 Gene Causing Ghosal Hematodiaphyseal Dysplasia
2020 · Agnes Selina, Madhavi Kandagaddala, et al. · The Indian Journal of Pediatrics · 6
Case report of a PRDM5 linked brittle cornea syndrome type 2 in association with a novel SLC6A5 mutation
2020 · Vrisha Madhuri, Agnes Selina, et al. · Indian Journal of Ophthalmology · 6
Novel TRPV4 Pathogenic Variant in Severe Metatropic Skeletal Dysplasia: A Case Report
2022 · James D, Subramanian L, et al. · Malaysian Orthopaedic Journal · 5
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A Novel Biallelic Splice Site Variant in the SPARC Gene Causing Severe Osteogenesis Imperfecta
2023 · Agnes Selina, Deeptiman James, et al. · The Indian Journal of Pediatrics · 3
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Corrigendum to “SERPINF1 gene variants causing late-onset progressive deforming osteogenesis imperfecta – A study of 18 patients from India” [Bone Rep. 2023 May 26;18:101690. doi: 10.1016/j.bonr.2023.101690]
2025 · Agnes Selina, Madhavi Kandagaddala, et al. · Bone Reports · 2
Atypical Fibrodysplasia Ossificans Progressiva with G328E Variant and Digit Reduction Abnormalities
2025 · Vrisha Madhuri, Agnes Selina, et al. · JBJS Case Connector · 1
Translational Research in Osteogenesis Imperfecta and Cell Therapy
2021 · Vrisha Madhuri, Sowmya Ramesh, et al. · 1
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Type V Osteogenesis Imperfecta in an Indian Cohort: Phenotypic Variability and Radiological Insights in IFITM5-Related Bone Fragility
2026 · Agnes Selina, Madhavi Kandagaddala, et al. · Indian Journal of Orthopaedics
Pengaruh Citra Merek Dan Promosi Terhadap Keputusan Pembelian Konsumen (studi Kasus Pada Kopi Taji Lereng Bromo)
2025 · Selina, Agnes · UMM Institutional Repository (University of Maine at Machias)
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An iMSC-Based iPSC Model for Osteogenesis Imperfecta: A Platform for Disease Modeling and Drug Screening
2025 · Ashis Kumar, Vignesh Kumar, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Pamidronate Response in a Novel Biallelic CREB3L1 Gene Mutation–Associated Osteogenesis Imperfecta
2024 · Agnes Selina, Madhavi Kandagaddala, et al. · JBJS Case Connector
Clinical and genetic landscape of Bruck syndrome in the Indian population
2024 · Agnes Selina, Madhavi Kandagaddala, et al. · Research Square
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Perthes-Like Disorder in a Child with Atypical Bohring-Opitz Syndrome
2023 · Mir Tariq Altaf, Madhavi Kandagaddala, et al. · JBJS Case Connector
Works count: 17
Citation count: 71
H-index: 6
I10-index: 2
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