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Sandhya Kiran Pemmasani

Observed names: Sandhya K. Pemmasani, SandhyaKiran Pemmasani
ORCID: 0000-0002-4382-0100
Observed ORCID: 0000-0002-4382-0100
OpenAlex ID: A5111680519
WIP1 Phosphatase as a Potential Therapeutic Target in Neuroblastoma
2015 · Mark Richter, Tajhal Dayaram, et al. · PLoS ONE · 67
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A Review on the Challenges in Indian Genomics Research for Variant Identification and Interpretation
2020 · Sandhya Kiran Pemmasani, Rasika Raman, et al. · Frontiers in Genetics · 17
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Genome-wide polygenic risk score for type 2 diabetes in Indian population
2023 · Sandhya Kiran Pemmasani, Shravya Atmakuri, et al. · Scientific Reports · 6
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Genetic variants associated with longevity in long-living Indians
2024 · Sandhya Kiran Pemmasani, Shakthiraju R G, et al. · npj Aging · 3
Genetic Susceptibility Versus Fibrosis Progression in North Indian Metabolic Dysfunction–Associated Steatotic Liver Disease: Distinct Roles of APOC3 and PNPLA3 in a Candidate Gene Study
2026 · Nandini Tomar, Sangeeta Choudhury, et al. · Journal of Clinical and Experimental Hepatology · 1
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COVID-19 and Indian population: a comparative genetic analysis
2021 · Saurabh Patil, Sandhya Kiran Pemmasani, et al. · medRxiv · 1
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Prevalence rates of ADIPOQ polymorphisms in Indian population and a comparison with other populations
2018 · SandhyaKiran Pemmasani, Rasika Raman, et al. · Indian Journal of Endocrinology and Metabolism · 1
Development and validation of neurological health score using machine learning algorithms
2026 · Sandhya Kiran Pemmasani, Shravya Atmakuri, et al. · medRxiv
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A novel homozygous mutation, c.662_672del, in DGUOK gene causing mitochondrial DNA depletion syndrome of type hepatocerebral – A case report
2024 · Kandula Radhakrishna, Batchu Rajsekhar, et al. · Clinics and Research in Hepatology and Gastroenterology
HNF1A gene mutation (c.811del, p.Arg271Glyfs) causing maturity onset of diabetes of the young 3: a case study of an Indian patient
2023 · Neelima Chitturi, Satish Sunkara, et al. · Research Square
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Comprehensive analysis of WGS and RNA-seq data to identify genetic variations in a patient with clear cell renal carcinoma
2021 · Sandhya Kiran Pemmasani, Neelima Chitturi, et al. · Molecular Genetics and Metabolism
Works count: 11
Citation count: 96
H-index: 3
I10-index: 2
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