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		题名	作者	年代	出处	被引量
	1	Association of GSTP1 gene(I105V)polymorphism with acute leukaemia显示文摘	Dunna NR Vuree S Kagita S	2012	J Genet2012，91，1：	1
	2	NRAS mutations in de no- vo acute leukemia:prevalence and clinical significance显示文摘	Dunna NR Vuree S Anuradha C	2014	Indian J Biochem Biophys2014，51，3：	1
	3	Congenital midline cervical cleft with an underlying bronchogenic cyst 显示文摘	Vure S Pang K Hallam L	2009	Pediatr Surg Int2009，25，9：	1
	4	Deletion of GSTM1 and T1 genes as a risk factor for development of acute leukemia显示文摘	Dunna NR Vure S Sailaja K	2013	Asi- an Pac J Cancer Prev2013，14，4：	1
	5	Association of thymidylate synthase 5'-UTR 28bp tandem repeat and serine hydroxymethyl transfarase C1420T polymorphisms with susceptibility to acute leukemia显示文摘	Dunna NR Naushad SM Vuree S	2014	Asian Pac J Cancer Prev2014，15，4：	1
	6	Pharmacogenomics of drug resistance in breast cancer resistance protein(BCRP) and its mutated variants 显示文摘	VUREE S DUNNA N R KHAN 1 A	2013	J Pharm Res2013，6，7：	1
	7	Diabetes mellitus susceptibility with varied diseased phenotypes and its comparison with phenome interactome networks显示文摘An emerging area of interest in understanding disease phenotypes is systems genomics.Complex diseases such as diabetes have played an important role towards understanding the susceptible genes and mutations.A wide number of methods have been employed and strategies such as polygenic risk score and allele frequencies have been useful,but understanding the candidate genes harboring those mutations is an unmet goal.In this perspective,using systems genomic approaches,we highlight the application of phenome-interactome networks in diabetes and provide deep insights.LINC01128,which we previously described as candidate for diabetes,is shown as an example to discuss the approach.	Madhusmita Rout Bhumandeep Kour Sugunakar Vuree Sajitha S Lulu Krishna Mohan Medicherla Prashanth Suravajhala	2022	World Journal of Clinical Cases2022，10，18：	0

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