Chatrath A, Kiran M, Kumar P, Ratan A, Dutta A(2018) The Germline Variants rs61757955 and rs34988193 are Predictive of Survival in Low Grade Glioma Patients, Mol Cancer Res. , ,
10.1158/1541-7786.MCR-18-0996.
Kiran M, Chatrath A, Xiwei T, Keenan DM, Dutta A(2018) A prognostic signature for gliomas based on expression of long noncoding RNAs, Molecular Neurobiology , ,
1-13.
Reon B, Karia B, Kiran M, Dutta A(2018) LINC00152 Promotes Invasion Through a 3'-hairpin Structure and Associates with Prognosis in Glioblastoma, Mol Cancer Res , 16(10),
1470-1482.
Cichewicz M, Kiran M, Przanowska R, Dutta A(2018) MUNC, an eRNA upstream from the MYOD gene, induces a subgroup of myogenic transcripts in trans, independently of MyoD, Mol Cell Biol , MCB.00655-17,
Equal First Author Contribution-.
Kuscu C, Kumar P, Kiran M, Su Z, Malik A, Dutta A. (2018) tRNA fragments (tRFs) guide Ago to regulate gene expression post-transcriptionally in a Dicer independent manner, RNA , 10.1261/rna.066126.1,
-.
Shibata E, Kiran M, Shibata Y, Singh S, Kiran S, Dutta A. (2016) Two subunits of human ORC are dispensable for DNA replication and proliferation, eLife , 5:e19084,
-.
Kiran M and Nagarajaram HA(2016) Interaction and localization diversities of global and local hubs in human protein-protein interaction networks, Molecular BioSystems , 12(9),
2875-2882.
Dutta A, Kumar P, Kiran M, Kuscu C(2016) . Transfer RNA Fragments (tRFs): a Novel Class of Non-micro Short RNAs that Uses Ago1, 3 and 4 to Repress Specific Target RNAs Through 5' Seed Sequences, The FASEB Journal , 30 (1 Supplement),
1054.5-.
Kiran S, Anwar T, Kiran M, Ramakrishna G. (2015) Sirtuin 7 in cell proliferation, stress and disease: Rise of the Seventh Sirtuin! , Cellular Signalling , 27(3),
673-682.
Bashyam MD, Chaudhary AK, Kiran M, Reddy V, Nagarajaram HA, Dalal A., Bashyam L., Gupta N, Kabra M, Puri R, Verma IC, RamaDevi R, Ghosh VB, Kapoor S, Danda S. (2013) Molecular analyses of novel ASAH1 mutations causing Farber lipogranulomatosis: characterization of exonic splicing enhancer inactivating mutation, Clinical Genetics , 86(6),
530-538.
Bashyam MD, Chaudhary AK, Kiran M, Nagarajaram HA, Devi AR, Ranganath P, Dalal A, Bashyam L, Gupta N, Muranjan MKM, Puri RD, Verma IC, Nampoothiri S, Kadandale JS(2013) Splice, insertion-deletion and nonsense mutations that perturb the Phenylalanine hydroxylase transcript cause Phenylketonuria in India, Journal of Cellular Biochemistry , 115(3),
566-574.
Kiran M and Nagarajaram HA(2013) Global versus local hubs in human protein-protein interaction network., Journal of Proteome Research , 12(12),
5436-5446.
Bashyam, MD, Chaudhary, AK, Kiran M, Nagarajaram HA, Devi AR, Bashyam L, Reddy EC, Dalal A(2012) Molecular genetic analysis of MSUD from India reveals mutations causing altered protein truncation affecting the C- termini of E1alpha and E1beta., Journal of Cellular Biochemistry , 113(10),
3122-3132.