 | Up a level |
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
Veerappa, A. M. and Suresh, R. V. and Vishweswaraiah, S. and Lingaiah, K. and Murthy, M. and Manjegowda, D. S. and Padakannaya, P. and Ramachandra, N. B. (2015) Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization. GENETICS RESEARCH, 97. ISSN 1469-5073
Veerappa, A. M. and Vishweswaraiah, S. and Lingaiah, K. and Murthy, M. and Suresh, R. V. and Manjegowda, D. S. and Ramachandra, N. B. (2015) Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes. PLOS ONE, 10 (4). ISSN 1932-6203
Veerappa, A. M. and Murthy, M. and Vishweswaraiah, S. and Lingaiah, K. and Suresh, R. V. and Nachappa, S. A. and Prashali, N. and Yadav, S. N. and Srikanta, M. A. and Manjegowda, D. S. and Seshachalam, K. B. and Ramachandra, N. B. (2014) Copy number variations burden on mirna genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression. PLoS ONE, 9 (2). ISSN 1932-6203
Veerappa, A. M. and Lingaiah, K. and Vishweswaraiah, S. and Murthy, M. N. and Suresh, R. V. and Manjegowda, D. S. and Ramachandra, N. B. (2014) Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays. Genetics Research, 96. ISSN 0016-6723
