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Joshi N, Yan J, Levy S, Bhagchandani S, Slaughter KV, Sherman NE, Amirault J, Wang Y, Riegel L, He X, Rui TShi, Valic M, Vemula PK, Miranda OR, Levy O, Gravallese EM, Aliprantis AO, Ermann J, Karp JM.  2018.  Towards an arthritis flare-responsive drug delivery system.. Nat Commun. 9(1):1275. DOI:10.1038/s41467-018-03691-1.
Johnson NNaveen, Amirtham SManickam, B Rani S, Sathishkumar S, Rebekah G, Vinod E.  2022.  Assessment of the inherent chondrogenic potential of human articular cartilage-derived chondroprogenitors in pellet culture using a novel whole pellet processing approach.. J Orthop. 31:45-51. DOI:10.1016/j.jor.2022.03.007.
John G., Nagarajan S., Vemula P.K, Silverman J.R., Pillai C.KS.  2019.  Natural monomers: A mine for functional and sustainable materials – Occurrence, chemical modification and polymerization. Progress in Polymer Science. 92
Jijumon AS, Bodakuntla S, Genova M, Bangera M, Sackett V, Besse L, Maksut F, Henriot V, Magiera MM, Sirajuddin M, Janke C.  2022.  Lysate-based pipeline to characterize microtubule-associated proteins uncovers unique microtubule behaviours.. Nat Cell Biol. 24(2):253-267. DOI:10.1038/s41556-021-00825-4.
Javali A, Lakshmanan V, Palakodeti D, Sambasivan R.  2020.  Modulation of β-catenin levels regulates cranial neural crest patterning and dispersal into first pharyngeal arch.. Dev Dyn. DOI:10.1002/dvdy.208.
Javali A, Misra A, Leonavicius K, Acharyya D, Vyas B, Sambasivan R.  2017.  Co-expression of Tbx6 and Sox2 identifies a novel transient neuromesoderm progenitor cell state.. Development. 144(24):4522-4529. DOI:10.1242/dev.153262.
Jain A, Dhiman S, Dhayani A, Vemula PK, George SJ.  2019.  Chemical fuel-driven living and transient supramolecular polymerization.. Nat Commun. 10(1):450. DOI:10.1038/s41467-019-08308-9.
Jain PKumar, Jayappa S, Sairam T, Mittal A, Paul S, Rao VJ, Chittora H, Kashyap DK, Palakodeti D, Thangaraj K, Shenthar J, Koranchery R, Rajendran R, Alireza H, Mohanan KSreedharan, Rathinavel A, Dhandapany PS.  2021.  Ribosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathy.. J Med Genet. DOI:10.1136/jmedgenet-2021-107866.