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Ashitha, S. N. and Ramachandra, N. B. (2020) Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders. Neuroscience, 438. pp. 25-40. ISSN 1873-7544
Gholipoorfeshkecheh, R. and Agarwala, S. and Kavya, G. and Krishnappa, S. and Savitha, M. R. and Ramachandra, N. B. (2020) Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects. Egyptian Journal of Medical Human Genetics, 21 (1).
Gholipoorfeshkecheh, R. and Agarwala, S. and Krishnappa, S. and Savitha, M. R. and Narayanappa, D. and Ramachandra, N. B. (2020) Variants in HEY genes manifest in ventricular septal defects of congenital heart disease. Gene Reports, 19.
Gholipoorfeshkecheh, R. and Swati Agarwala and Santhosh, K. and Savitha, M. R. and Narayanappa, D. and Ramachandra, N. B. (2020) Nuclear Co-repressor 1: A Potential Candidate Gene in the Manifestation of Congenital Heart Diseases. International Journal of Human Genetics, 20 (2). pp. 55-65. ISSN 2456-6330
Maleki, A. and Naveen, J. A. and Ramachandra, N. B. (2020) The possible role of point mutations and activation of the CDC27 Gene in progression of multiple myeloma. Meta Gene, 26.
Prakash, T. and Ramachandra, N.B. (2020) Integrated network and gene ontology analysis identifies key genes and pathways for coronary artery diseases. Avicenna Journal of Medical Biotechnology, 13 (1). pp. 12-23.
