Items where Author is "Avinash, M. V."

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Yogita Kattimani and Avinash, M. V. (2018) Complex interaction between mutant HNRNPA1 and gE of varicella zoster virus in pathogenesis of multiple sclerosis. Autoimmunity, 51 (4). pp. 147-151. ISSN 1607-842X

Yogita Kattimani and Avinash, M. V. (2018) Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis. Multiple Sclerosis and Related Disorders, 22. 153 - 156. ISSN 2211-0356

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

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

Avinash, M. V. and Prakash, P. and Ramachandra, N. B. (2016) Copy number variation of UGT 2B genes in Indian families using whole genome scans. Journal of Nucleic Acids. ISSN 2090-021X

Megha Murthy, N. and Avinash, M. V. and Seshachalam, K. B. and Ramachandra, N. B. (2016) High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts. Neurological Research, 38 (9). pp. 775-785.

Avinash, M. V. and Saldanha, Marita and Prakash, P. and Ramachandra, N. B. (2014) Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 165 (7). pp. 572-580. ISSN 1552-485X

This list was generated on Sat Jul 4 21:51:08 2020 IST.