1. Thomas, W., P. Nallari, V.R. Sreekanth, K.V. Lakshmi, A. Ali, Y.R. Ahuja and Q. Hasan, 2018. Biomarkers for identifying individuals at risk of Alzheimer disease. Int. J. Emerg. Mental Health, 20: 1555-1562.
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2. Nagaraju, M., P.S. Reddy, S.A. Kumar, A. Kumar and P. Suravajhala et al., 2018. Genome-wide in silico analysis of dehydrins in Sorghum bicolor, Setaria italica and Zea mays and quantitative analysis of dehydrin gene expressions under abiotic stresses in Sorghum bicolor. Plant Gene, 13: 64-75.
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3. Kumar, C.S., A. Ali, S. Manchineela, A. Venkateshwari, C. Narasimhan and P. Nallari, 2018. Analyses of HSP90α gene polymorphism in arrhythmogenic right ventricular cardiomyopathy/dysplasia. J. Indian College Cardiol., 8: 127-131.
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4. Qureshi, F.S., A. Ali, A. Venkateshwari, H. Rao and M.P. Jayakrishnan, et al., 2016. Genotype-phenotype correlation in long QT syndrome families. Indian Pacing Electrophysiol. J., 15: 269-285.
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5. Kondapalli, M.S., R.K. Galimudi, K.K. Gundapaneni, C. Padala and A. Cingeetham et al., 2016. MMP 1 circulating levels and promoter polymorphism in risk prediction of coronary artery disease in asymptomatic first degree relatives. Gene, 595: 115-120.
6. Ali, A., S.F. Qureshi, M. Veronica, A. Venkateshwari and N. Calambur, et al., 2016. Heat shock protein 70 gene polymorphisms’ influence on the electrophysiology of long QT syndrome. J. Int. Cardiac Electrophysiol., 45: 119-130.
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7. Veronica M., A. Ali, A. Venkateshwari, D. Mamata, P. Nallari, 2015. Association of estrogen and progesterone receptor gene polymorphisms and their respective hormones in uterine leiomyomas. Tumor Bio., 6: 1-8.
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8. Qureshi, S.F., A. Ali, P. John, A.P. Jadhav and A. Venkateshwari et al., 2015. Mutational analysis of SCN5A gene in long QT syndrome. Metagene, 6: 26-35.
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9. Jadhav, A.P., M. Sairam, K.J. Princy, V. Viswamithra, C.S. Kumar, A. Ali and P. Nallari, 2015. Possibility of RNA editing in cardiomyopathies and channelopathies. J. Adv. Life Nat. Sci., 1: 1-7.
10. Chavah, S.K., A. James, A. Ali, S. Manchineela, C. Narasimhan and P. Nallari, 2015. Role of inflammation in arrhythmogenic right ventricular dysplasia/cardiomyopathy: An evidence based review. J. Adv. Life Nat. Sci., 1: 14-22.
11. Qureshi, S.F., A. Ali, A. Venkateshwari, H. Rao and M.P. Jayakrishnan et al., 2014. Atrial natriuretic peptide gene–a potential biomarker for long qt syndrome. EXCLI J., 13: 834-842.
12. Sameera S.C., FQ, A. Altaf, M.L. Satyanarayana, R. Advithi, A. Venkateshwari and N. Pratibha, 2013. Hidden magicians of genome evolution. Indian J. Med. Res., 137: 1052-1060.
13. Qureshi, S.F., A. Ali. Amol, P. Jadhav and A. Venkateshwari et al., 2013. KvLQT1 and KCNE1 K+channel gene polymorphisms in long QT syndrome. Br. J. Med. Med. Res., 3: 978-992.
14. Qureshi, S.F., A. Ali, A. Venkateshwari, M.P. Jayakrishnan, C. Narasimhan, K. Thangaraj and P. Nallari, 2013. Novel mutations of KCNQ1 in long QT syndrome. Ind. Heart J., 65: 552-560.
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15. Veronica, M., A. Ali, A. Venkateshwari, C. Narsimhan and P. Nallari, 2010. AAT: A comparative study in HCM and DCM. Int. J. Hum. Genet., 10: 235-238.
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16. Sujana, K., V. Shivani, M.L. Satyanarayana, A. Altaf, M. Mallikarjun, B.K.S. Sastry and N. Pratibha, 2009. Synergystic action of calcineurin and nitric oxide in idiopathic pulmonary hypertension (IPAH). J. Cell. Tiss. Res., 9: 1943-1946.
17. Ali, A., M. Veronica., V. Shivani, C. Narsimhan and N. Pratibha, 2009. Catalase and Nitric Oxide: A comparative study in HCM and DCM. J. Cell. Tiss. Res., 9: 2023-2026.