| Genomic characterization and epidemiology of an emerging SARS-CoV-2 variant in Delhi, India MS Dhar, R Marwal, R Vs, K Ponnusamy, B Jolly, RC Bhoyar, V Sardana, ... Science 374 (6570), 995-999, 2021 | 340 | 2021 |
| IndiGenomes: a comprehensive resource of genetic variants from over 1000 Indian genomes A Jain, RC Bhoyar, K Pandhare, A Mishra, D Sharma, M Imran, ... Nucleic acids research 49 (D1), D1225-D1232, 2021 | 91 | 2021 |
| Genomics of rare genetic diseases—experiences from India S Sivasubbu, V Scaria Human genomics 13 (1), 52, 2019 | 70 | 2019 |
| Genomic survey of SARS-CoV-2 vaccine breakthrough infections in healthcare workers from Kerala, India B Jolly, N John, RC Bhoyar, N Majeed, V Senthivel, CP Fairoz, M Rophina, ... Journal of Infection 83 (2), 237-279, 2021 | 68 | 2021 |
| Symptomatic reinfection of SARS‐CoV‐2 with spike protein variant N440K associated with immune escape PR Rani, M Imran, JV Lakshmi, B Jolly, A Jain, A Surekha, V Senthivel, ... Journal of Medical Virology 93 (7), 4163, 2021 | 47 | 2021 |
| Pharmacogenetic Landscape of DPYD Variants in South Asian Populations by Integration of Genome-Scale Data JM Hariprakash, SK Vellarikkal, P Keechilat, A Verma, R Jayarajan, ... Pharmacogenomics 19 (3), 227-241, 2018 | 31 | 2018 |
| Variants of concern responsible for SARS‐CoV‐2 vaccine breakthrough infections from India UB Singh, M Rophina, R Chaudhry, V Senthivel, K Bala, RC Bhoyar, ... Journal of medical virology 94 (4), 1696-1700, 2022 | 29 | 2022 |
| SAGE: a comprehensive resource of genetic variants integrating South Asian whole genomes and exomes JM Hariprakash, SK Vellarikkal, A Verma, AS Ranawat, R Jayarajan, ... Database 2018, bay080, 2018 | 25 | 2018 |
| An optimized, amplicon-based approach for sequencing of SARS-CoV-2 from patient samples using COVIDSeq assay on Illumina MiSeq sequencing platforms RC Bhoyar, V Senthivel, B Jolly, M Imran, A Jain, MK Divakar, V Scaria, ... STAR protocols 2 (3), 100755, 2021 | 18 | 2021 |
| Pharmacogenomic landscape of Indian population using whole genomes S Sahana, RC Bhoyar, A Sivadas, A Jain, M Imran, M Rophina, ... Clinical and Translational Science 15 (4), 866-877, 2022 | 13 | 2022 |
| Organellar transcriptome sequencing reveals mitochondrial localization of nuclear encoded transcripts A Sabharwal, D Sharma, SK Vellarikkal, R Jayarajan, A Verma, ... Mitochondrion 46, 59-68, 2019 | 9 | 2019 |
| SARS-CoV-2 vaccine breakthrough infection following a previous infection in a healthcare worker A Gupta, R Bhoyar, S Mirza, B Jolly, V Senthivel, A Shamnath, MK Divakar, ... The Journal of Infection 84 (3), 418, 2022 | 8 | 2022 |
| Pharmacogenomic landscape of COVID-19 therapies from Indian population genomes S Sahana, A Sivadas, M Mangla, A Jain, RC Bhoyar, K Pandhare, ... Pharmacogenomics 22 (10), 603-618, 2021 | 7 | 2021 |
| Genomic analysis of symptomatic SARS-CoV-2 vaccine breakthrough infections from a tertiary care centre in India UB Singh, M Rophina, DR Chaudhry, V Senthivel, K Bala, RC Bhoyar, ... OSF Preprints 10, 2021 | 6 | 2021 |
| Whole-genome sequencing of 1029 Indian individuals reveals unique and rare structural variants MK Divakar, A Jain, RC Bhoyar, V Senthivel, B Jolly, M Imran, D Sharma, ... Journal of Human Genetics 68 (6), 409-417, 2023 | 5 | 2023 |
| CoV-2 Genomics Consortium (INSACOG) Gupta RK MS Dhar, R Marwal, R Vs, K Ponnusamy, B Jolly, RC Bhoyar, V Sardana, ... | 5 | 2021 |
| Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India GM Govindaraj, A Jain, A Edavazhippurath, RC Bhoyar, D Dhanasooraj, ... Human Immunology 83 (4), 335-345, 2022 | 4 | 2022 |
| Genetic epidemiology of monogenic dyslipidemia and statin-associated adverse drug phenotypes in Indian population from whole-genomes of 1029 self-declared healthy individuals M Imran, RC Bhoyar, A Jain, S Sahana, M Rophina, VR Arvinden, ... Human Gene 39, 201252, 2024 | 3 | 2024 |
| 1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants A Bajaj, V Senthivel, R Bhoyar, A Jain, M Imran, M Rophina, MK Divakar, ... Human Genomics 16 (1), 30, 2022 | 3 | 2022 |
| Case Report: whole exome sequencing reveals a novel frameshift deletion mutation p. G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa S Karuthedath Vellarikkal, R Jayarajan, A Verma, S Nair, R Ravi, ... F1000Research 5, 900, 2016 | 3 | 2016 |
