Items where Author is "Veerappa, Avinash M."

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Article

Veerappa, Avinash M. and Sangeetha, V. and Lingaiah, Kusuma and Megha Murthy, and Suresh, Raviraj V. and Manjegowda, Dinesh S. and Nallur B., Ramachandra (2015) Global Spectrum of Copy Number Variations Reveals Genome Organizational Plasticity and Proposes New Migration Routes. PLoS ONE, 10 (4). e0121846.

Sangeetha, V. and Veerappa, Avinash M. and Mahesh, P. A. and Jahromi, Sareh Raeiszadeh and Ramachandra, N. B. (2015) Copy number variation burden on asthma subgenome in normal cohorts identifies susceptibility markers. Allergy Asthma and Immunology Research, 7 (3). pp. 265-275. ISSN 2092-7355

Saldanha, Marita and Siddaiah, Anand and Veerappa, Avinash M. and Ramachandra, N. B. and Prakash, 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). pp. 1-8.

Veerappa, Avinash M. and Saldanha, Marita and Padakannaya, Prakash 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

Sangeetha, V. and Veerappa, Avinash M. and Mahesh, P. A. and Jayaraj, B. S. and Chaya, S. K. and Ramachandra, N. B. (2014) Molecular Interaction Network and Pathway Studies of ADAM33 Potentially Relevant to Asthma. Annals of Allergy, Asthma & Immunology, 133 (4). pp. 418-424.

Veerappa, Avinash M. and Kusuma, L. and Sangeetha, V. and Megha, N. Murthy and Suresh, Raviraj V. and Ramachandra, N. B. and Dinesh, S. M. (2014) Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays. Genetics research, 96. pp. 1-12. ISSN 1469-5073

Veerappa, Avinash M. and Sangeetha, V. and Kusuma, L. and Megha Murthy, N. and Suresh, Raviraj V. and Keshavan, B. and Ramachandra, N. B. and Tejaswini, and Niveditha, B. Patel and Supriya Gowda, P. K. (2014) Insertion-deletions burden in copy number polymorphisms of the Tibetan population. Indian Journal of Human Genetics, 20 (2). pp. 166-174. ISSN 0971-6866; 1998-362X

Veerappa, Avinash M. and Saldanha, Marita 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 (Copyri). ISSN 1435-232X

Veerappa, Avinash M. and Saldanha, Marita 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, Cop). pp. 889-897. ISSN 1552-4841

Veerappa, Avinash M. and Vishweswaraiah, S. and Kusuma, L. and Megha, N. Murthy and Manjegowda, D. S. and Radhika Nayaka, 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). pp. 1-14.

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