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Ashitha, S. N. and Avinash, M. V. and Ramachandra, N. B. (2017) Whole exome sequencing of discordant diseases in Monozygotic twins with Down syndrome reveals mutations for Congenital Heart Defect and epileptic seizures. Meta Gene, 12. 134 - 137. ISSN 2214-5400
Megha, Murthy N. and Ramachandra, N. B. (2017) Prioritization of differentially expressed genes in substantia nigra transcriptomes of Parkinson's disease reveals key protein interactions and pathways. Meta Gene, 14. 12 - 18. ISSN 2214-5400
Megha Murthy, N. and Blauwendraat, Cornelis and Hardy, John and Sebastian, Guelfi and Lewis, Patrick A. and Trabzuni, Daniah (2017) Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3. Neurogenetics, 18 (3). pp. 121-133. ISSN 1364-6753
Naik, Srilata Puru and Mahesh, P. A. and Jayaraj, B. S. and Madhunapantula, M. V. and Jahromi, Sarah Raeiszadeh and Yadav, Manish Kumar (2017) Evaluation of inflammatory markers interleukin-6 (IL-6) and matrix metalloproteinase-9 (MMP-9) in asthma. Journal of Asthma, 54 (6). pp. 584-593. ISSN 1532-4303
Rohith, B. N. and Shyamala, B. V. (2017) Scalloped a member of the Hippo tumor suppressor pathway controls mushroom body size in Drosophila brain by non-canonical regulation of neuroblast proliferation. Developmental Biology, 432 (2). 203 - 214. ISSN 0012-1606
Suresh, R. V. and Narayannapa and Savitha and Ambika S. Udupa and Kusuma, L. and Sunil Kumar, P. and Ramachandra, N. B. (2017) Association of RFC1 A80G gene polymorphism with advanced maternal age in risk of Down syndrome. Current Medicine Research and Practice, 7 (1). 6 - 10. ISSN 2352-0817
Suresh, Raviraj V. and Kusuma, L. and Avinash, M. V. and Ramachandra, N. B. (2017) Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: a copy number variation approach. Indian Journal of Medical Research, 145 (1). pp. 39-50. ISSN 0975-9174
Tejaswini, Prakash and Avinash, V. and Ramachandra, N. B. (2017) Complex interaction between HNRNPD mutations and risk polymorphisms is associated with discordant Crohn’s disease in monozygotic twins. Autoimmunity, 50 (5). pp. 275-276. ISSN 1607-842X
