Items where Author is "Lingaiah, K."

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Number of items: 7.

Article

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

Lingaiah, K. and Ramachandra, N. B. (2014) An insight into the understanding of 5-HTR2A variants leading to schizophrenia. Indian Journal of Medical Research, 140 (DEC). pp. 713-715. ISSN 0971-5916

Veerappa, A. M. and Vishweswaraiah, S. and Lingaiah, K. and Murthy, M. and Manjegowda, D. S. and Nayaka, R. and Ramachandra, N. B. (2013) Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays. PLoS ONE, 8 (7).

Dinesh, S. M. and Lingaiah, K. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) GATA4 specific nonsynonymous single-nucleotide polymorphisms in congenital heart disease patients of Mysore, India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (10). pp. 715-720.

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