| GJB2 and GJB6 gene mutations found in Indian probands with congenital hearing impairment G Padma, PV Ramchander, UV Nandur, T Padma Journal of genetics 88, 267-272, 2009 | 73 | 2009 |
| Genetic polymorphisms of DNA repair genes XRCC1 and XRCC3 and risk of colorectal cancer in Chinese population Y Zhao, X Deng, Z Wang, Q Wang, Y Liu Asian Pacific Journal of Cancer Prevention 13 (2), 665-669, 2012 | 63 | 2012 |
| Polymorphisms in two DNA repair genes (XPD and XRCC1)–association with age related cataracts G Padma, M Mamata, KRK Reddy, T Padma Molecular vision 17, 127, 2011 | 56 | 2011 |
| Haplotype association and synergistic effect of human aldosterone synthase (CYP11B2) gene polymorphisms causing susceptibility to essential hypertension in … UM Vamsi, N Swapna, G Padma, S Vishnupriya, T Padma Clinical and Experimental Hypertension 38 (8), 659-665, 2016 | 25 | 2016 |
| Estimation of risk and interaction of single nucleotide polymorphisms at angiotensinogen locus causing susceptibility to essential hypertension: a case control study B Charita, G Padma, P Sushma, P Deepak, T Padma Journal of the Renin-Angiotensin-Aldosterone System 13 (4), 461-471, 2012 | 24 | 2012 |
| Risk conferred by tagged SNPs of AGT gene in causing susceptibility to essential hypertension G Padma, N Swapna, M Mamata, B Charita, T Padma Clinical and Experimental Hypertension 36 (8), 579-585, 2014 | 15 | 2014 |
| Novel variants detected in AGT gene among patients with essential hypertension G Padma, B Charita, N Swapna, M Mamata, T Padma Journal of the Renin-Angiotensin-Aldosterone System 16 (3), 642-646, 2015 | 12 | 2015 |
| Novel Mutations Affecting the Secondary Structure of MT-RNR1 Gene: A Causal Relationship with Profound Nonsyndromic Hearing Impairment G Padma, PV Ramchander, VU Nandur, KR Kumar, T Padma Genetic Testing and Molecular Biomarkers 16 (9), 1092-1097, 2012 | 11 | 2012 |
| High Risk for Essential Hypertension in Males Conferred by g.15241A>G Polymorphism in Intron 3 of AGT Gene G Padma, C Bhupatiraju, B Srinivas, T Padma Clinical and Experimental Hypertension 35 (2), 108-111, 2013 | 10 | 2013 |
| 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 P Thakur, N Bhargava, S Jaitly, P Gupta, SK Bhattacharya, G Padma, ... Stem Cell Research 50, 102124, 2021 | 4 | 2021 |
| A rare event of maternal UPD in a proband with congenital non-syndromic hearing impairment with homozygosity for GJB2 p. W24X mutation G Padma, PV Ramchander, UV Nandur, T Padma Int J Genet Mol Biol 2 (06), 126-129, 2010 | 3 | 2010 |
| Identification of a Novel Variant c.163delG in HBB Gene Resulting in a Beta Null Phenotype in a Proband with Thalassemia Intermedia M Mamata, G Padma, T Pragna Laxmi, K Saroja, D Ashwin, J Suman Hemoglobin 48 (1), 1-3, 2024 | 1 | 2024 |
| Angiotensinogen: A candidate gene involved in preeclampsia? A Amrani, F Mesli Taleb Bendieb, MB Baba Hamed, PM Kearney, ... Journal of Medical Sciences 14 (4), 217-223, 2005 | | 2005 |
