Items where Author is "Kusuma, L."

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Number of items: 14.

Article

Avinash, M. V. and Suresh, R. V. and Sangeetha, V. and Kusuma, L. and Megha Murthy, and Dinesh, S. M. and Prakash, 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. pp. 1-12.

Ramachandra, N. B. and Kusuma, L. (2015) An understanding of spinocerebellar ataxia. The Indian Journal of Medical Research, 141 (2). pp. 148-150. ISSN 0971-5916

Kusuma, L. and Ramachandra, N. B. (2014) An insight into the understanding of 5-HTR2A variants leading to schizophrenia. The Indian Journal of Medical Research, 140 (6). pp. 713-715. ISSN 0971-5916; 0975-9174

Avinash, M. V. and Megha, N. Murthy and Sangeetha, V. and Kusuma, L. and Suresh, R. V. and Nachappa, S. A. and Prashali, Nelchi and Sangeetha, N. Y. and Manjula, A. S. 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. Plosone, 9 (2).

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 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.

Santhosh Kumar, K. and Kusuma, L. and Ramachandra, N. B. and Mala, Nair Vijay (2012) Genetic variations among Ecologically diverse species of Anurans at the level of Genus based on ISSR Marker. Res. J. Biological Sci, 1 (7). pp. 11-19.

Dinesh, S. M. and Kusuma, L. 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.

Kusuma, L. and Dinesh, S. M. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) A Maiden Report on CRELD1 Single-Nucleotide Polymorphism Association in Congenital Heart Disease Patients of Mysore, South India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (7-8). pp. 483-487.

Kusuma, L. and Dinesh, S. M. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) Mutations of TFAP2B in congenital heart disease patients in Mysore, South India. Indian Journal of Medical Research, 134 (5). pp. 621-626. ISSN 0971-5916

Dinesh, S. M. and Kusuma, L. and Smitha, R. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2010) Single-Nucleotide Polymorphisms of NKX2.5 Found in Congenital Heart Disease Patients of Mysore, South India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 14 (6). pp. 873-879.

Kusuma, L. and Parshwanath, Bharath A. and Savitha , R. M. and Krishnamurthy, B. and Ramachandra, N. B. (2010) A rare case of congenital heart disease with ambiguous genitalia. Indian Journal of Human Genetics., 16 (3).

Kusuma, L. and Parshwanath, Bharath A. and Savitha , R. M. and Krishnamurthy, B. and Ramachandra, N. B. (2010) A rare case of congenital heart disease with ambiguous genitalia. Indian journal of human genetics, 16 (3, Cop). pp. 166-168. ISSN 0971-6866

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