Gunda Padma
Hyderabad, TG, India
Last Updated: 09/26/2026
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Found 8 publications
Identification of a Novel Variant c.163delG in HBB Gene Resulting in a Beta Null Phenotype in a Proband with Thalassemia Intermedia.
Journal: Hemoglobin
Published: January 23, 2024
Establishment and characterization of induced pluripotent stem cell line (IGIBi002-A) from a β-thalassemia patient with IVS1-5 mutation by non-integrating reprogramming approach.
Journal: Stem cell research
Published: November 13, 2020
Haplotype association and synergistic effect of human aldosterone synthase (CYP11B2) gene polymorphisms causing susceptibility to essential hypertension in Indian patients.
Journal: Clinical and experimental hypertension (New York, N.Y. : 1993)
Published: December 10, 2016
Risk conferred by tagged SNPs of AGT gene in causing susceptibility to essential hypertension.
Journal: Clinical and experimental hypertension (New York, N.Y. : 1993)
Published: February 05, 2014
Novel variants detected in AGT gene among patients with essential hypertension.
Journal: Journal of the renin-angiotensin-aldosterone system : JRAAS
Published: August 13, 2013
Novel mutations affecting the secondary structure of MT-RNR1 gene: a causal relationship with profound nonsyndromic hearing impairment.
Journal: Genetic testing and molecular biomarkers
Published: August 03, 2012
High risk for essential hypertension in males conferred by g.15241A>G polymorphism in intron 3 of AGT gene.
Journal: Clinical and experimental hypertension (New York, N.Y. : 1993)
Published: July 18, 2012
Estimation of risk and interaction of single nucleotide polymorphisms at angiotensinogen locus causing susceptibility to essential hypertension: a case control study.
Journal: Journal of the renin-angiotensin-aldosterone system : JRAAS
Published: May 10, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026