| Common variants of FTO and the risk of obesity and type 2 diabetes in Indians G Chauhan, R Tabassum, A Mahajan, OP Dwivedi, Y Mahendran, I Kaur, ... Journal of human genetics 56 (10), 720-726, 2011 | 84 | 2011 |
| Genetic susceptibility to schizophrenia: role of dopaminergic pathway gene polymorphisms M Gupta, C Chauhan, P Bhatnagar, S Gupta, S Grover, PK Singh, ... Pharmacogenomics 10 (2), 277-291, 2009 | 62 | 2009 |
| Genetic profile of patients with epilepsy on first-line antiepileptic drugs and potential directions for personalized treatment S Grover, M Gourie-Devi, R Baghel, S Sharma, K Bala, M Gupta, ... Pharmacogenomics 11 (7), 927-941, 2010 | 54 | 2010 |
| Chromosome 22q11. 2 microdeletion in monozygotic twins with discordant phenotype and deletion size A Halder, M Jain, I Chaudhary, B Varma Molecular cytogenetics 5, 1-8, 2012 | 51 | 2012 |
| Ayurgenomics for stratified medicine: TRISUTRA consortium initiative across ethnically and geographically diverse Indian populations B Prasher, B Varma, A Kumar, BK Khuntia, R Pandey, A Narang, P Tiwari, ... Journal of ethnopharmacology 197, 274-293, 2017 | 36 | 2017 |
| Spectrum of large copy number variations in 26 diverse Indian populations: potential involvement in phenotypic diversity P Gautam, P Jha, D Kumar, S Tyagi, B Varma, D Dash, A Mukhopadhyay, ... Human genetics 131, 131-143, 2012 | 22 | 2012 |
| Genetic determinants of immune-response to a polysaccharide vaccine for typhoid PP Majumder, HF Staats, N Sarkar-Roy, B Varma, T Ghosh, S Maiti, ... The HUGO journal 3, 17-30, 2009 | 18 | 2009 |
| Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India A Narang, B Uppilli, A Vivekanand, S Naushin, A Yadav, K Singhal, ... Human Mutation 41 (11), 1833-1847, 2020 | 14 | 2020 |
| Targeted exome sequencing in anti-factor H antibody negative HUS reveals multiple variations RW Thergaonkar, A Narang, BS Gurjar, P Tiwari, M Puraswani, H Saini, ... Clinical and Experimental Nephrology 22, 653-660, 2018 | 14 | 2018 |
| Human brain harbors single nucleotide somatic variations in functionally relevant genes possibly mediated by oxidative stress A Sharma, AH Ansari, R Kumari, R Pandey, R Rehman, B Mehani, ... F1000Research 5, 2016 | 6 | 2016 |
| The somatic chromosomes of five species of Aristolochia AK Sharma, B Varma Phyton. Rev. Internac. Bot. Expt. Argentina 12, 101-108, 1959 | 6 | 1959 |
| Floury leaf spot of Bean caused by Ramularia phaseolina Petrak. HS Sohi, SL Sharma, BR Verma, KB Sachdeva | 5 | 1965 |
| Polymorphisms in renin-angiotensin-aldosterone system and vascular endothelial growth factor may cross talk in preeclampsia: a pilot study of maternal and fetal dyads in Indian … S Sharma, S Bhaskaran, SB Tripathi, N Vaid, B Varma Int J Res Med Sci 4, 1666-72, 2016 | 2 | 2016 |
| Genetic discovery in vesicoureteral reflux using exome sequencing: A pilot study RW Thergaonkar, V Manchanda, G Bansal, A Yadav, J Singh, B Varma, ... Medical Journal Armed Forces India, 2024 | | 2024 |
| Unique mutation and gene expression in High Hyperdiploid Acute Lymphoblastic Leukaemia with whole chromosome uniparental isodisomy M Parihar, D Ganguli, A Banerjee, R Islam, S Basu, C Bhattacharya, ... | | 2022 |
| Development of a targeted sequencing panel for Indian patients with acute Lymphoblastic Leukaemia D Ganguli, M Parihar, R Islam, D Saha, A Basu, P Roy, S Dhar, N Arora, ... Pediatric Hematology Oncology Journal 2 (2), S3-S4, 2017 | | 2017 |
| Targeted exome sequencing in patients with atypical hemolytic uremic syndrome (aHUS) and negative anti-complement factor H (FH) antibodies reveals multiple variations R Thergaonkar, A Narang, BS Gurjar, M Puraswani, A Sinha, A Yadav, ... PEDIATRIC NEPHROLOGY 31 (10), 1742-1742, 2016 | | 2016 |
| Identification Of Mutations In Bcr-Abl Gene In Newly Diagnosed Indian Patients With Chronic Myelogenous Leukemia (CML) BVMJ Aggarwal Shyam, Binuja Verma Blood 122 (5), 169, 2013 | | 2013 |
| Feto-Maternal Polymorphisms in Genes of Renin Angiotensin System and Angiogenesis Pathway in Preeclampsia/Eclampsia N Vaid, S Bhaskaran, A Suneja, K Narayanswamy, B Varma HYPERTENSION IN PREGNANCY 27 (4), 692-692, 2008 | | 2008 |
| Human brain harbors single nucleotide somatic variations A Sharma, AH Ansan, R Kumari, R Pandey, R Rehman, B Mehani, ... Proc Natl Acad Sci US A 98 (5), 2532-2537, 2001 | | 2001 |
