Items where Author is "Veerappa, A. M."

Vishweswaraiah, S. and Veerappa, A. M. and Mahesh, P. A. and Jahromi, S. R. and Ramachandra, N. B. (2015) Copy number variation burden on asthma subgenome in normal cohorts identifies susceptibility markers. ALLERGY ASTHMA & IMMUNOLOGY RESEARCH, 7 (3). pp. 265-275. ISSN 2092-7363

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

Saldanha, M. and Siddaiah, A. and Veerappa, A. M. and Ramachandra, N. B. and Padakannaya, P. (2014) Catch them before they fall: A simple test of sight-word and pseudo-word reading in Kannada for a quick and early assessment. SAGE Open, 4 (4). ISSN 2158-2440

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 Saldanha, M. and Padakannaya, 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 1552-4841

Manjegowda, D. S. and Prasad, M. and Veerappa, A. M. and Ramachandra, N. B. (2014) Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family. Genetics Research, 96. ISSN 0016-6723

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

Vishweswaraiah, S. and Veerappa, A. M. and Mahesh, P. A. and Jayaraj, B. S. and Krishnarao, C. S. and Ramachandra, N. B. (2014) Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma. Annals of Allergy, Asthma and Immunology, 113 (4). 418-424.e1. ISSN 1081-1206

Veerappa, A. M. and Padakannaya, P. and Ramachandra, N. B. (2013) Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the y chromosome. Functional and Integrative Genomics, 13 (3). pp. 285-293. ISSN 1438-793X

Veerappa, A. M. and Saldanha, M. and Padakannaya, P. and Ramachandra, N. B. (2013) Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity. Journal of Human Genetics, 58 (8). pp. 539-547. ISSN 1434-5161

Veerappa, A. M. and Saldanha, M. and Padakannaya, P. and Ramachandra, N. B. (2013) Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 162 (8). pp. 889-897. ISSN 1552-4841

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).