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Nature Communications|May 14, 2014
Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiencyFabio Iannelli, Agnese Collino, Shruti Sinha, et al.Nature Communications|March 15, 2025
Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseasesShruti Sinha, Fatma Rabea, Sathishkumar Ramaswamy, et al.Stem Cells (Dayton, Ohio)|April 4, 2019
TNF-Stimulated Gene-6 Is a Key Regulator in Switching Stemness and Biological Properties of Mesenchymal Stem CellsBarbara Romano, Sudharshan Elangovan, Marco Erreni, et al.Current Issues in Molecular Biology|September 9, 2017
Status and Prospects of Next Generation Sequencing Technologies in Crop PlantsT R Sharma, B N Devanna, Kanti Kiran, et al.Genetics in Medicine Open|September 2, 2025
Pathogenic variation underlying rare diseases in an Arab population: Implications for screening programsRuchi Jain, Sami Bizzari, Sathishkumar Ramaswamy, et al.Nature Genetics|January 18, 2022
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustionFederica Marasca, Shruti Sinha, Rebecca Vadalà, et al.Cell|April 2, 2013
Endogenous retrotransposition activates oncogenic pathways in hepatocellular carcinomaRuchi Shukla, Kyle R Upton, Martin Muñoz-Lopez, et al.Nature Medicine|April 21, 2026
Citywide premarital genomic screening in a Middle Eastern populationKhulood Alblooshi, Radwa Sharaf, Shruti Shenbagam, et al.American Journal of Human Genetics|April 11, 2025
FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signatureNavin B Ramakrishna, Umar Bin Mohamad Sahari, Yoshikazu Johmura, et al.Pageof 6