Thangaraj K - Search Results

1

Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.

Breuss M, Heng JI, Poirier K, Tian G, Jaglin XH, Qu Z, Braun A, Gstrein T, Ngo L, Haas M, Bahi-Buisson N, Moutard ML, Passemard S, Verloes A, Gressens P, Xie Y, Robson KJ, Rani DS, Thangaraj K, Clausen T, Chelly J, Cowan NJ, Keays DA. Breuss M, et al. Among authors: thangaraj k. Cell Rep. 2012 Dec 27;2(6):1554-62. doi: 10.1016/j.celrep.2012.11.017. Epub 2012 Dec 13. Cell Rep. 2012. PMID: 23246003 Free PMC article. Clinical Trial.

2

Mitochondrial DNA haplogroup 'R' is associated with Noonan syndrome of south India.

Rani DS, Dhandapany PS, Nallari P, Govindaraj P, Singh L, Thangaraj K. Rani DS, et al. Among authors: thangaraj k. Mitochondrion. 2010 Mar;10(2):166-73. doi: 10.1016/j.mito.2009.12.146. Epub 2009 Dec 16. Mitochondrion. 2010. PMID: 20006740

3

Haplotypes on 9p21 modify the risk for coronary artery disease among Indians.

AshokKumar M, Emmanuel C, Dhandapany PS, Rani DS, SaiBabu R, Cherian KM, Thangaraj K. AshokKumar M, et al. Among authors: thangaraj k. DNA Cell Biol. 2011 Feb;30(2):105-10. doi: 10.1089/dna.2010.1046. Epub 2010 Sep 21. DNA Cell Biol. 2011. PMID: 20858033

4

Cardiac Troponin T (TNNT2) mutations are less prevalent in Indian hypertrophic cardiomyopathy patients.

Rani DS, Nallari P, Dhandapany PS, Tamilarasi S, Shah A, Archana V, AshokKumar M, Narasimhan C, Singh L, Thangaraj K. Rani DS, et al. Among authors: thangaraj k. DNA Cell Biol. 2012 Apr;31(4):616-24. doi: 10.1089/dna.2011.1366. Epub 2011 Oct 21. DNA Cell Biol. 2012. PMID: 22017532

5

High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians.

Rani DS, Nallari P, Priyamvada S, Narasimhan C, Singh L, Thangaraj K. Rani DS, et al. Among authors: thangaraj k. BMC Med Genet. 2012 Aug 10;13:69. doi: 10.1186/1471-2350-13-69. BMC Med Genet. 2012. PMID: 22876777 Free PMC article.

6

A novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM).

Rani DS, Dhandapany PS, Nallari P, Narasimhan C, Thangaraj K. Rani DS, et al. Among authors: thangaraj k. PLoS One. 2014 Jul 3;9(7):e101451. doi: 10.1371/journal.pone.0101451. eCollection 2014. PLoS One. 2014. PMID: 24992688 Free PMC article.

7

A Complete Absence of Missense Mutation in Myosin Regulatory and Essential Light Chain Genes of South Indian Hypertrophic and Dilated Cardiomyopathies.

Rani DS, Nallari P, Rani J, Nizamuddin S, Seelamneni T, Narasimhan C, Thangaraj K. Rani DS, et al. Among authors: thangaraj k. Cardiology. 2018;141(3):156-166. doi: 10.1159/000495027. Epub 2019 Jan 3. Cardiology. 2018. PMID: 30605904

8

High frequencies of Non Allelic Homologous Recombination (NAHR) events at the AZF loci and male infertility risk in Indian men.

Rani DS, Rajender S, Pavani K, Chaubey G, Rasalkar AA, Gupta NJ, Deendayal M, Chakravarty B, Thangaraj K. Rani DS, et al. Among authors: thangaraj k. Sci Rep. 2019 Apr 18;9(1):6276. doi: 10.1038/s41598-019-42690-0. Sci Rep. 2019. PMID: 31000748 Free PMC article.

9

Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy.

Rani DS, Vijaya Kumar A, Nallari P, Sampathkumar K, Dhandapany PS, Narasimhan C, Rathinavel A, Thangaraj K. Rani DS, et al. Among authors: thangaraj k. CJC Open. 2021 Aug 8;4(1):1-11. doi: 10.1016/j.cjco.2021.07.020. eCollection 2022 Jan. CJC Open. 2021. PMID: 35072022 Free PMC article.

10

Novel MYBPC3 Mutations in Indian Population with Cardiomyopathies.

Rani DS, Kasala A, Dhandapany PS, Muthusami U, Kunnoth S, Rathinavel A, Ayapati DR, Thangaraj K. Rani DS, et al. Among authors: thangaraj k. Pharmgenomics Pers Med. 2023 Sep 20;16:883-893. doi: 10.2147/PGPM.S407179. eCollection 2023. Pharmgenomics Pers Med. 2023. PMID: 37750083 Free PMC article.

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