| Development of validated stability-indicating assay methods—critical review M Bakshi, S Singh Journal of pharmaceutical and biomedical analysis 28 (6), 1011-1040, 2002 | 1186 | 2002 |
| Stress test to determine inherent stability of drugs S Singh, M Bakshi Pharm Technol 4, 1-14, 2000 | 572 | 2000 |
| Lipophilic drug derivatives in liposomes M Gulati, M Grover, S Singh, M Singh International journal of pharmaceutics 165 (2), 129-168, 1998 | 318 | 1998 |
| Forced degradation studies to assess the stability of drugs and products S Singh, M Junwal, G Modhe, H Tiwari, M Kurmi, N Parashar, P Sidduri TrAC Trends in Analytical Chemistry 49, 71-88, 2013 | 231 | 2013 |
| A critical review on the use of modern sophisticated hyphenated tools in the characterization of impurities and degradation products S Singh, T Handa, M Narayanam, A Sahu, M Junwal, RP Shah Journal of pharmaceutical and biomedical analysis 69, 148-173, 2012 | 223 | 2012 |
| Stress degradation studies on ezetimibe and development of a validated stability-indicating HPLC assay S Singh, B Singh, R Bahuguna, L Wadhwa, R Saxena Journal of pharmaceutical and biomedical analysis 41 (3), 1037-1040, 2006 | 212 | 2006 |
| Strategies for characterizing sildenafil, vardenafil, tadalafil and their analogues in herbal dietary supplements, and detecting counterfeit products containing these drugs S Singh, B Prasad, AA Savaliya, RP Shah, VM Gohil, A Kaur TrAC Trends in Analytical Chemistry 28 (1), 13-28, 2009 | 209 | 2009 |
| Quantitative structure–property relationships in pharmaceutical research–Part 1 M Grover, B Singh, M Bakshi, S Singh Pharmaceutical science & technology today 3 (1), 28-35, 2000 | 162 | 2000 |
| Metabolite identification by liquid chromatography-mass spectrometry B Prasad, A Garg, H Takwani, S Singh TrAC Trends in Analytical Chemistry 30 (2), 360-387, 2011 | 144 | 2011 |
| A critical review of the probable reasons for the poor variable bioavailability of rifampicin from anti-tubercular fixed-dose combination (FDC) products, and the likely … S Singh, TT Mariappan, R Shankar, N Sarda, B Singh International journal of pharmaceutics 228 (1-2), 5-17, 2001 | 143 | 2001 |
| The ICH guidance in practice: stress degradation studies on ornidazole and development of a validated stability-indicating assay M Bakshi, B Singh, A Singh, S Singh Journal of pharmaceutical and biomedical analysis 26 (5-6), 891-897, 2001 | 137 | 2001 |
| LC and LC-MS study of stress decomposition behaviour of isoniazid and establishment of validated stability-indicating assay method H Bhutani, S Singh, S Vir, KK Bhutani, R Kumar, AK Chakraborti, ... Journal of pharmaceutical and biomedical analysis 43 (4), 1213-1220, 2007 | 127 | 2007 |
| Alteration in dissolution characteristics of gelatin-containing formulations S Singh, KVR Rao, K Venugopal, R Manikandan Pharmaceutical technology 26 (4), 36-54, 2002 | 117 | 2002 |
| Regional gastrointestinal permeability of rifampicin and isoniazid (alone and their combination) in the rat TT Mariappan, S Singh The international Journal of Tuberculosis and Lung Disease 7 (8), 797-803, 2003 | 112 | 2003 |
| Quality by design (QbD) in analytical sciences: an overview H Bhutani, M Kurmi, S Singh, S Beg, B Singh Quality Assurance 3, 39-45, 2004 | 106 | 2004 |
| The reason for an increase in decomposition of rifampicin in the presence of isoniazid under acid conditions S Singh, TT Mariappan, N Sharda, S Kumar, AK Chakraborti Pharmacy and Pharmacology Communications 6 (9), 405-410, 2000 | 101 | 2000 |
| Quantitative structure–property relationships in pharmaceutical research–Part 2 M Grover, B Singh, M Bakshi, S Singh Pharmaceutical science & technology today 3 (2), 50-57, 2000 | 100 | 2000 |
| Structure-based virtual screening to discover potential lead molecules for the SARS-CoV-2 main protease A Gahlawat, N Kumar, R Kumar, H Sandhu, IP Singh, S Singh, ... Journal of chemical information and modeling 60 (12), 5781-5793, 2020 | 97 | 2020 |
| Critical practical aspects in the application of liquid chromatography–mass spectrometric studies for the characterization of impurities and degradation products M Narayanam, T Handa, P Sharma, S Jhajra, PK Muthe, PK Dappili, ... Journal of pharmaceutical and biomedical analysis 87, 191-217, 2014 | 95 | 2014 |
| Study of forced degradation behavior of enalapril maleate by LC and LC–MS and development of a validated stability-indicating assay method SP Bhardwaj, S Singh Journal of pharmaceutical and biomedical analysis 46 (1), 113-120, 2008 | 85 | 2008 |
