Kadandale JS - Search Results

1

Variation at diabetes- and obesity-associated Loci may mirror neutral patterns of human population diversity and diabetes prevalence in India.

Raj SM, Halebeedu P, Kadandale JS, Mirazon Lahr M, Gallego Romero I, Yadhav JR, Iliescu M, Rai N, Crivellaro F, Chaubey G, Villems R, Thangaraj K, Muniyappa K, Chandra HS, Kivisild T. Raj SM, et al. Among authors: kadandale js. Ann Hum Genet. 2013 Sep;77(5):392-408. doi: 10.1111/ahg.12028. Epub 2013 Jul 1. Ann Hum Genet. 2013. PMID: 23808542

2

A novel leaky splice variant in centromere protein J (CENPJ)-associated Seckel syndrome.

Yadav N, Kirola L, Geetha TS, Mittal K, Kadandale J, Yogev Y, Birk OS, Gupta N, Balakrishnan P, Jana M, Gupta M, Kabra M, Thelma BK. Yadav N, et al. Ann Hum Genet. 2022 Sep;86(5):245-256. doi: 10.1111/ahg.12469. Epub 2022 Apr 22. Ann Hum Genet. 2022. PMID: 35451063

3

Splice, insertion-deletion and nonsense mutations that perturb the phenylalanine hydroxylase transcript cause phenylketonuria in India.

Bashyam MD, Chaudhary AK, Kiran M, Nagarajaram HA, Devi RR, Ranganath P, Dalal A, Bashyam L, Gupta N, Kabra M, Muranjan M, Puri RD, Verma IC, Nampoothiri S, Kadandale JS. Bashyam MD, et al. Among authors: kadandale js. J Cell Biochem. 2014 Mar;115(3):566-74. doi: 10.1002/jcb.24692. J Cell Biochem. 2014. PMID: 24130151

4

Next-Generation Sequencing Reveals Novel Mutations in X-linked Intellectual Disability.

Muthusamy B, Selvan LDN, Nguyen TT, Manoj J, Stawiski EW, Jaiswal BS, Wang W, Raja R, Ramprasad VL, Gupta R, Murugan S, Kadandale JS, Prasad TSK, Reddy K, Peterson A, Pandey A, Seshagiri S, Girimaji SC, Gowda H. Muthusamy B, et al. Among authors: kadandale js. OMICS. 2017 May;21(5):295-303. doi: 10.1089/omi.2017.0009. OMICS. 2017. PMID: 28481730 Free PMC article.

5

A de novo marker chromosome 15 in a child with isolated developmental delay.

Jeevan Kumar M, Gowrishankar K, Hemagowri V, Kadandale J. Jeevan Kumar M, et al. J Genet. 2020;99:72. J Genet. 2020. PMID: 33021245 Free article.

6

Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum.

Shetty M, Srikanth A, Kadandale J, Hegde S. Shetty M, et al. Mol Syndromol. 2015 Oct;6(4):187-92. doi: 10.1159/000440659. Epub 2015 Sep 11. Mol Syndromol. 2015. PMID: 26648835 Free PMC article.

7

Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia.

Shetty M, Kadandale J, Hegde S. Shetty M, et al. Mol Syndromol. 2016 Feb;6(5):248-53. doi: 10.1159/000442506. Epub 2015 Dec 17. Mol Syndromol. 2016. PMID: 26997946 Free PMC article.

8

Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

Sivasankaran A, Srikanth A, Kulshreshtha PS, Anuradha D, Kadandale JS, Samuel CR. Sivasankaran A, et al. Among authors: kadandale js. Mol Syndromol. 2016 Feb;6(6):287-96. doi: 10.1159/000443708. Epub 2016 Feb 3. Mol Syndromol. 2016. PMID: 27022330 Free PMC article.

9

Primed in situ labeling (PRINS) for evaluation of gene deletions in cancer.

Tharapel SA, Kadandale JS. Tharapel SA, et al. Among authors: kadandale js. Am J Med Genet. 2002 Jan 15;107(2):123-6. doi: 10.1002/ajmg.10105. Am J Med Genet. 2002. PMID: 11807886

10

Pre- and Postnatal Diagnosis of 5q35.1 and 8p23.1 Deletion in Congenital Heart Disease.

Shetty M, Srikanth A, Kulshreshtha P, Kadandale J, Hegde S. Shetty M, et al. Indian J Pediatr. 2016 Nov;83(12-13):1484-1485. doi: 10.1007/s12098-016-2158-3. Epub 2016 Jun 8. Indian J Pediatr. 2016. PMID: 27272050 No abstract available.

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