Raviraj V. Suresh

Copy Number Variations Burden on miRNA Genes Reveals Layers of Complexities Involved in the Regulation of Pathways and Phenotypic Expression

S. Vishweswaraiah, N. Ramachandra, Avinash M. Veerappa, 2014, PloS one.

Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.

P. Padakannaya, S. Vishweswaraiah, N. Ramachandra, 2015, Genetics research.

Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays.

S. Vishweswaraiah, N. Ramachandra, Avinash M. Veerappa, 2014, Genetics research.

Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations.

Nallur B Ramachandra, N. Ramachandra, Megha N. Murthy, 2016, Diabetes research and clinical practice.

Comprehensive in silico mutational-sensitivity analysis of PTEN establishes signature regions implicated in pathogenesis of Autism Spectrum Disorders.

N. Ramachandra, Raviraj V. Suresh, Ashitha S Niranjana Murthy, 2020, Genomics.

Association of RFC1 A80G gene polymorphism with advanced maternal age in risk of Down syndrome

Savitha, N. Ramachandra, Kusuma Lingaiah, 2017 .

Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach

N. Ramachandra, Avinash M. Veerappa, Kusuma Lingaiah, 2017, The Indian journal of medical research.

Global Spectrum of Copy Number Variations Reveals Genome Organizational Plasticity and Proposes New Migration Routes

S. Vishweswaraiah, N. Ramachandra, Avinash M. Veerappa, 2015, PloS one.

Insertion-deletions burden in copy number polymorphisms of the Tibetan population

Tejaswini, S. Vishweswaraiah, N. Ramachandra, 2014, Indian journal of human genetics.