| Photosensitivity and type I IFN responses in cutaneous lupus are driven by epidermal-derived interferon kappa MK Sarkar, GA Hile, LC Tsoi, X Xing, J Liu, Y Liang, CC Berthier, ... Annals of the rheumatic diseases 77 (11), 1653-1664, 2018 | 206 | 2018 |
| Genetic and functional identification of the likely causative variant for cholesterol gallstone disease at the ABCG5/8 lithogenic locus O Von Kampen, S Buch, M Nothnagel, L Azocar, H Molina, M Brosch, ... Hepatology 57 (6), 2407-2417, 2013 | 106 | 2013 |
| Matrix metalloproteinases in coronary artery disease B Mittal, A Mishra, A Srivastava, S Kumar, N Garg Advances in clinical chemistry 64, 1-72, 2014 | 91 | 2014 |
| De novo dominant ASXL3 mutations alter H2A deubiquitination and transcription in Bainbridge–Ropers syndrome A Srivastava, KC Ritesh, YC Tsan, R Liao, F Su, X Cao, MC Hannibal, ... Human molecular genetics 25 (3), 597-608, 2016 | 81 | 2016 |
| Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome A Shukla, M Hebbar, A Srivastava, R Kadavigere, P Upadhyai, A Kanthi, ... Journal of human genetics 62 (7), 723-727, 2017 | 67 | 2017 |
| Association of matrix metalloproteinases (MMP2, MMP7 and MMP9) genetic variants with left ventricular dysfunction in coronary artery disease patients A Mishra, A Srivastava, T Mittal, N Garg, B Mittal Clinica Chimica Acta 413 (19-20), 1668-1674, 2012 | 64 | 2012 |
| Hemoglobin A1c in nondiabetic patients: an independent predictor of coronary artery disease and its severity N Garg, N Moorthy, A Kapoor, S Tewari, S Kumar, A Sinha, A Shrivastava, ... Mayo Clinic Proceedings 89 (7), 908-916, 2014 | 60 | 2014 |
| Significant role of estrogen and progesterone receptor sequence variants in gallbladder cancer predisposition: a multi-analytical strategy A Srivastava, KL Sharma, N Srivastava, S Misra, B Mittal PLoS One 7 (7), e40162, 2012 | 56 | 2012 |
| Genetic analysis of CHARGE syndrome identifies overlapping molecular biology A Moccia, A Srivastava, JM Skidmore, JA Bernat, M Wheeler, JX Chong, ... Genetics in medicine 20 (9), 1022-1029, 2018 | 53 | 2018 |
| Role of inflammatory gene polymorphisms in left ventricular dysfunction (LVD) susceptibility in coronary artery disease (CAD) patients A Mishra, A Srivastava, T Mittal, N Garg, B Mittal Cytokine 61 (3), 856-861, 2013 | 51 | 2013 |
| Genotype–phenotype correlations in individuals with pathogenic RERE variants VK Jordan, B Fregeau, X Ge, J Giordano, RJ Wapner, TB Balci, MT Carter, ... Human mutation 39 (5), 666-675, 2018 | 45 | 2018 |
| Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome C Bélanger, FA Bérubé-Simard, E Leduc, G Bernas, PM Campeau, ... Proceedings of the National Academy of Sciences 115 (4), E620-E629, 2018 | 34 | 2018 |
| Role of ABCG8 D19H (rs11887534) variant in gallstone susceptibility in northern India A Srivastava, A Srivastava, K Srivastava, G Choudhuri, B Mittal Journal of gastroenterology and hepatology 25 (11), 1758-1762, 2010 | 32 | 2010 |
| Detection of nucleotide-specific CRISPR/Cas9 modified alleles using multiplex ligation detection R Kc, A Srivastava, JM Wilkowski, CE Richter, JA Shavit, DT Burke, ... Scientific reports 6 (1), 32048, 2016 | 29 | 2016 |
| Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction in coronary artery disease patients A Srivastava, N Garg, T Mittal, R Khanna, S Gupta, PK Seth, B Mittal PloS one 6 (9), e24123, 2011 | 28 | 2011 |
| Histone H2A monoubiquitination in neurodevelopmental disorders A Srivastava, B McGrath, SL Bielas Trends in Genetics 33 (8), 566-578, 2017 | 25 | 2017 |
| Impact of renin-angiotensin-aldosterone system gene polymorphisms on left ventricular dysfunction in coronary artery disease patients A Mishra, A Srivastava, T Mittal, N Garg, B Mittal Disease markers 32 (1), 33-41, 2012 | 24 | 2012 |
| A multigenic approach to evaluate genetic variants of PLCE1, LXRs, MMPs, TIMP, and CYP genes in gallbladder cancer predisposition KL Sharma, R Rai, A Srivastava, A Sharma, S Misra, A Kumar, B Mittal Tumor Biology 35, 8597-8606, 2014 | 23 | 2014 |
| Report of four novel variants in ASNS causing asparagine synthetase deficiency and review of literature C Galada, M Hebbar, L Lewis, S Soans, R Kadavigere, A Srivastava, ... Congenital anomalies 58 (5), 181, 2018 | 21 | 2018 |
| Genetic diversity of NDUFV1-dependent mitochondrial complex I deficiency A Srivastava, KR Srivastava, M Hebbar, C Galada, R Kadavigrere, F Su, ... European Journal of Human Genetics 26 (11), 1582-1587, 2018 | 19 | 2018 |
