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	1.	Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations. [electronic resource] by Prabhanjan, Manasa Suresh, Raviraj V Murthy, Megha N Ramachandra, Nallur B Producer: 20161110 In: Diabetes research and clinical practice vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts. [electronic resource] by Murthy, Megha N Veerappa, Avinash M Seshachalam, Keshava B Ramachandra, Nallur B Producer: 20170117 In: Neurological research vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3. [electronic resource] by Murthy, Megha N Blauwendraat, Cornelis Guelfi, Sebastian Hardy, John Lewis, Patrick A Trabzuni, Daniah Producer: 20180424 In: Neurogenetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays. [electronic resource] by Veerappa, Avinash M Vishweswaraiah, Sangeetha Lingaiah, Kusuma Murthy, Megha Manjegowda, Dinesh S Nayaka, Radhika Ramachandra, Nallur B Producer: 20140207 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes. [electronic resource] by Veerappa, Avinash M Vishweswaraiah, Sangeetha Lingaiah, Kusuma Murthy, Megha Suresh, Raviraj V Manjegowda, Dinesh S Ramachandra, Nallur B Producer: 20160119 In: PloS one vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays. [electronic resource] by Veerappa, Avinash M Lingaiah, Kusuma Vishweswaraiah, Sangeetha Murthy, Megha N Suresh, Raviraj V Manjegowda, Dinesh S Ramachandra, Nallur B Producer: 20150908 In: Genetics research vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization. [electronic resource] by Veerappa, Avinash M Suresh, Raviraj V Vishweswaraiah, Sangeetha Lingaiah, Kusuma Murthy, Megha Manjegowda, Dinesh S Padakannaya, Prakash Ramachandra, Nallur B Producer: 20160404 In: Genetics research vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression. [electronic resource] by Veerappa, Avinash M Murthy, Megha N Vishweswaraiah, Sangeetha Lingaiah, Kusuma Suresh, Raviraj V Nachappa, Somanna Ajjamada Prashali, Nelchi Yadav, Sangeetha Nuggehalli Srikanta, Manjula Arsikere Manjegowda, Dinesh S Seshachalam, Keshava B Ramachandra, Nallur B Producer: 20141028 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)