Verma IC - Search Results

1

Vascular Endothelial Growth Factor (VEGF) Gene Promoter Polymorphisms and Disease Progression in North Indian Cohort with Autosomal Dominant Polycystic Kidney Disease.

Pandita S, Maurya D, Ramachandran V, Verma J, Kohli S, Saxena R, Verma IC. Pandita S, et al. Among authors: verma j, verma ic. Int J Mol Cell Med. 2017 Summer;6(3):164-173. doi: 10.22088/acadpub.BUMS.6.3.164. Epub 2017 Sep 26. Int J Mol Cell Med. 2017. PMID: 29682488 Free PMC article.

2

Mutation studies in the CFTR gene in Asian Indian subjects with congenital bilateral absence of vas deferens: report of two novel mutations and four novel variants.

Sachdeva K, Saxena R, Majumdar A, Chadha S, Verma IC. Sachdeva K, et al. Among authors: verma ic. Genet Test Mol Biomarkers. 2011 May;15(5):307-12. doi: 10.1089/gtmb.2010.0156. Epub 2011 Jan 22. Genet Test Mol Biomarkers. 2011. PMID: 21254931

3

Use of ethnicity-specific sequence tag site markers for Y chromosome microdeletion studies.

Sachdeva K, Saxena R, Majumdar A, Chadda S, Verma IC. Sachdeva K, et al. Among authors: verma ic. Genet Test Mol Biomarkers. 2011 Jun;15(6):451-9. doi: 10.1089/gtmb.2010.0159. Epub 2011 Mar 4. Genet Test Mol Biomarkers. 2011. PMID: 21375402

4

Mutation analysis of the CFTR gene in 225 children: identification of five novel severe and seven reported severe mutations.

Sachdeva K, Saxena R, Puri R, Bijarnia S, Kohli S, Verma IC. Sachdeva K, et al. Among authors: verma ic. Genet Test Mol Biomarkers. 2012 Jul;16(7):798-801. doi: 10.1089/gtmb.2011.0283. Epub 2012 Feb 2. Genet Test Mol Biomarkers. 2012. PMID: 22299590 Clinical Trial.

5

Molecular characterisation and prenatal diagnosis of Asparto-acylase deficiency (Canavan disease)--report of two novel and two known mutations from the Indian subcontinent.

Bijarnia S, Kohli S, Puri RD, Jacob RJ, Saxena R, Jalan A, Sistermans EA, Mahmood S, Verma IC. Bijarnia S, et al. Among authors: verma ic. Indian J Pediatr. 2013 Jan;80(1):26-31. doi: 10.1007/s12098-012-0862-1. Epub 2012 Aug 10. Indian J Pediatr. 2013. PMID: 22878930

6

Variability in CYP2C9 allele frequency: a pilot study of its predicted impact on warfarin response among healthy South and North Indians.

Nahar R, Deb R, Saxena R, Puri RD, Verma IC. Nahar R, et al. Among authors: verma ic. Pharmacol Rep. 2013;65(1):187-94. doi: 10.1016/s1734-1140(13)70977-0. Pharmacol Rep. 2013. PMID: 23563037 Free article.

7

Molecular evaluation of a novel missense mutation & an insertional truncating mutation in SUMF1 gene.

Kotecha UH, Movva S, Sharma D, Verma J, Puri RD, Verma IC. Kotecha UH, et al. Among authors: verma j, verma ic. Indian J Med Res. 2014 Jul;140(1):55-9. Indian J Med Res. 2014. PMID: 25222778 Free PMC article.

8

Noninvasive Diagnosis of Fetal Gender: Utility of Combining DYS14 and SRY.

Jacob RR, Saxena R, Verma IC. Jacob RR, et al. Among authors: verma ic. Genet Test Mol Biomarkers. 2015 Sep;19(9):505-11. doi: 10.1089/gtmb.2015.0040. Epub 2015 Jun 29. Genet Test Mol Biomarkers. 2015. PMID: 26121024

9

Identification of mutations, genotype-phenotype correlation and prenatal diagnosis of maple syrup urine disease in Indian patients.

Gupta D, Bijarnia-Mahay S, Saxena R, Kohli S, Dua-Puri R, Verma J, Thomas E, Shigematsu Y, Yamaguchi S, Deb R, Verma IC. Gupta D, et al. Among authors: verma j, verma ic. Eur J Med Genet. 2015 Sep;58(9):471-8. doi: 10.1016/j.ejmg.2015.08.002. Epub 2015 Aug 7. Eur J Med Genet. 2015. PMID: 26257134

10

Seventeen Novel Mutations in PCCA and PCCB Genes in Indian Propionic Acidemia Patients, and Their Outcomes.

Gupta D, Bijarnia-Mahay S, Kohli S, Saxena R, Puri RD, Shigematsu Y, Yamaguchi S, Sakamoto O, Gupta N, Kabra M, Thakur S, Deb R, Verma IC. Gupta D, et al. Among authors: verma ic. Genet Test Mol Biomarkers. 2016 Jul;20(7):373-82. doi: 10.1089/gtmb.2016.0017. Epub 2016 May 26. Genet Test Mol Biomarkers. 2016. PMID: 27227689

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