Phani NM - Search Results

1

Replication and Relevance of Multiple Susceptibility Loci Discovered from Genome Wide Association Studies for Type 2 Diabetes in an Indian Population.

Phani NM, Adhikari P, Nagri SK, D'Souza SC, Satyamoorthy K, Rai PS. Phani NM, et al. PLoS One. 2016 Jun 16;11(6):e0157364. doi: 10.1371/journal.pone.0157364. eCollection 2016. PLoS One. 2016. PMID: 27310578 Free PMC article.

2

Genetic Variants Identified from GWAS for Predisposition to Type 2 Diabetes Predict Sulfonylurea Drug Response.

Phani NM, Vohra M, Adhikari P, Nagri SK, Shashikiran U, D'Souza SC, Kalluri PRR, Satyamoorthy K, Rai PS. Phani NM, et al. Curr Mol Med. 2017;17(8):580-586. doi: 10.2174/1566524018666180222122653. Curr Mol Med. 2017. PMID: 29473503

3

Population specific impact of genetic variants in KCNJ11 gene to type 2 diabetes: a case-control and meta-analysis study.

Phani NM, Guddattu V, Bellampalli R, Seenappa V, Adhikari P, Nagri SK, D Souza SC, Mundyat GP, Satyamoorthy K, Rai PS. Phani NM, et al. PLoS One. 2014 Sep 23;9(9):e107021. doi: 10.1371/journal.pone.0107021. eCollection 2014. PLoS One. 2014. PMID: 25247988 Free PMC article. Review.

4

Implications of critical PPARγ2, ADIPOQ and FTO gene polymorphisms in type 2 diabetes and obesity-mediated susceptibility to type 2 diabetes in an Indian population.

Phani NM, Vohra M, Rajesh S, Adhikari P, Nagri SK, D'Souza SC, Satyamoorthy K, Rai PS. Phani NM, et al. Mol Genet Genomics. 2016 Feb;291(1):193-204. doi: 10.1007/s00438-015-1097-4. Epub 2015 Aug 5. Mol Genet Genomics. 2016. PMID: 26243686

5

Association of HSD11B1 gene polymorphisms with type 2 diabetes and metabolic syndrome in South Indian population.

Devang N, Satyamoorthy K, Rai PS, Nandini M, Rao S, Phani NM, Adhikari P. Devang N, et al. Among authors: phani nm. Diabetes Res Clin Pract. 2017 Sep;131:142-148. doi: 10.1016/j.diabres.2017.07.011. Epub 2017 Jul 13. Diabetes Res Clin Pract. 2017. PMID: 28750217

6

Implication of critical pharmacokinetic gene variants on therapeutic response to metformin in Type 2 diabetes.

Phani NM, Vohra M, Kakar A, Adhikari P, Nagri SK, D'Souza SC, Umakanth S, Satyamoorthy K, Rai PS. Phani NM, et al. Pharmacogenomics. 2018 Jul 1;19(11):905-911. doi: 10.2217/pgs-2018-0041. Epub 2018 Jun 19. Pharmacogenomics. 2018. PMID: 29914345

7

Genetic association of KCNJ10 rs1130183 with seizure susceptibility and computational analysis of deleterious non-synonymous SNPs of KCNJ10 gene.

Phani NM, Acharya S, Xavy S, Bhaskaranand N, Bhat MK, Jain A, Rai PS, Satyamoorthy K. Phani NM, et al. Gene. 2014 Feb 25;536(2):247-53. doi: 10.1016/j.gene.2013.12.026. Epub 2013 Dec 27. Gene. 2014. PMID: 24378235

8

Significance of 5,10-methylenetetrahydrofolate reductase gene variants in acute lymphoblastic leukemia in Indian population: an experimental, computational and meta-analysis.

Bellampalli R, Phani NM, Bhat KG, Prasad K, Bhaskaranand N, Guruprasad KP, Rai PS, Satyamoorthy K. Bellampalli R, et al. Among authors: phani nm. Leuk Lymphoma. 2015 May;56(5):1450-9. doi: 10.3109/10428194.2014.953154. Epub 2014 Nov 5. Leuk Lymphoma. 2015. PMID: 25115513

9

Paraoxonase: Its antiatherogenic role in chronic renal failure.

Prakash M, Phani NM, Kavya R, Supriya M. Prakash M, et al. Among authors: phani nm. Indian J Nephrol. 2010 Jan;20(1):9-14. doi: 10.4103/0971-4065.62088. Indian J Nephrol. 2010. PMID: 20535264 Free PMC article.

10

Neonatal Screening for Congenital Adrenal Hyperplasia in Indian Newborns with Reflex Genetic Analysis of 21-Hydroxylase Deficiency.

Tippabathani J, Seenappa V, Murugan A, Phani NM, Hampe MH, Appaswamy G, Sadashiv Gambhir P. Tippabathani J, et al. Among authors: phani nm. Int J Neonatal Screen. 2023 Feb 21;9(1):9. doi: 10.3390/ijns9010009. Int J Neonatal Screen. 2023. PMID: 36975848 Free PMC article.

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