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Natarajan N. Srikrupa

Observed names: N.N. Srikrupa, Natarajan Srikrupa, Natarajan, Srikrupa N., Srikrupa N. Natarajan, Srikrupa N.N, Srikrupa Natarajan
ORCID: 0000-0003-2921-0477
Observed ORCID: 0000-0003-2921-0477
OpenAlex ID: A5008315620
Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families
2015 · Sundaramurthy Srilekha, Tharigopala Arokiasamy, et al. · PLoS ONE · 40
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Genetic profile and mutation spectrum of Leber congenital amaurosis in a larger Indian cohort using high throughput targeted re‐sequencing
2017 · N.N. Srikrupa, S. Srilekha, et al. · Clinical Genetics · 22
Leber’s Congenital Amaurosis as the Retinal Degenerative Phenotype in Thiamine Responsive Megaloblastic Anemia: A Case Report
2013 · Natarajan N. Srikrupa, Swaminathan Meenakshi, et al. · Ophthalmic Genetics · 16
CERKL mutation causing retinitis pigmentosa(RP) in Indian population – a genotype and phenotype correlation study
2020 · Parveen Sen, Puja Maitra, et al. · Ophthalmic Genetics · 15
Understanding variable disease severity in X-linked retinoschisis: Does RS1 secretory mechanism determine disease severity?
2018 · Dhandayuthapani Sudha, Srividya Neriyanuri, et al. · PLoS ONE · 15
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Next-generation sequencing-based genetic testing and phenotype correlation in retinitis pigmentosa patients from India
2023 · Parveen Sen, Natarajan Srikrupa, et al. · Indian Journal of Ophthalmology · 8
Whole-exome sequencing identifies two novel ALMS1 mutations in Indian patients with Leber congenital amaurosis
2021 · Natarajan N. Srikrupa, Sarangapani Sripriya, et al. · Human Genome Variation · 6
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An Overview on the Genetic Etiology, Testing, and Therapeutic Options for Retinitis Pigmentosa
2022 · Srikrupa N. Natarajan, Harshavardhini Gnanasekaran, et al. · Springer eBooks · 2
Whole-exome sequencing and molecular dynamics confirm pathogenicity of a novel SLC6A6 mutation in Leber congenital amaurosis
2025 · Srikrupa N. Natarajan, Samdani Ansar, et al. · Egyptian Journal of Medical Human Genetics · 1
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Next Generation Sequencing in presumptive diagnosis of syndromes in childhood retinal dystrophies - case series from India
2024 · Harshavardhini Gnanasekaran, Srikrupa N. Natarajan, et al. · Human Gene
RNA biomarker discovery in Polypoidal Choroidal Vasculopathy (PCV): Pharmacogenomics approach
2019 · Sinnakaruppan Mathavan, Lakshmi Priyankka Alagappan, et al. · Investigative Ophthalmology & Visual Science
Works count: 13
Citation count: 125
H-index: 6
I10-index: 5
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