| Genomics of rare genetic diseases--experiences from India A Bajaj, S Mathew, SK Vellarikkal, A Sivadas, RC Bhoyar, K Joshi, A Jain, ... Human Genomics 13 (1), 2019 | 53* | 2019 |
| RNA sequencing of db/db mice liver identifies lncRNA H19 as a key regulator of gluconeogenesis and hepatic glucose output N Goyal, A Sivadas, KV Shamsudheen, R Jayarajan, A Verma, ... Scientific reports 7 (1), 1-12, 2017 | 49 | 2017 |
| Saliva microbiome in primary Sjögren’s syndrome reveals distinct set of disease‐associated microbes D Sharma, P Sandhya, SK Vellarikkal, AK Surin, R Jayarajan, A Verma, ... Oral Diseases 26 (2), 295-301, 2020 | 44 | 2020 |
| Large scale changes in the transcriptome of Eisenia fetida during regeneration A Bhambri, N Dhaunta, SS Patel, M Hardikar, A Bhatt, N Srikakulam, ... PloS one 13 (9), e0204234, 2018 | 41 | 2018 |
| Chamber specific gene expression landscape of the zebrafish heart AR Singh, A Sivadas, A Sabharwal, SK Vellarikal, R Jayarajan, A Verma, ... PloS one 11 (1), e0147823, 2016 | 35 | 2016 |
| 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 | 29 | 2018 |
| A genome-wide map of circular RNAs in adult zebrafish D Sharma, P Sehgal, S Mathew, SK Vellarikkal, AR Singh, S Kapoor, ... Scientific reports 9 (1), 1-11, 2019 | 24 | 2019 |
| 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, 2018 | 24 | 2018 |
| Application of whole exome sequencing in elucidating the phenotype and genotype spectrum of junctional epidermolysis bullosa: A preliminary experience of a tertiary care centre … VK Yenamandra, SK Vellarikkal, M Kumar, MR Chowdhury, R Jayarajan, ... Journal of dermatological science 86 (1), 30-36, 2017 | 23 | 2017 |
| Genotype–Phenotype Correlations of Dystrophic Epidermolysis Bullosa in India: Experience from a Tertiary Care Centre VK Yenamandra, SK Vellarikkal, MR Chowdhury, R Jayarajan, A Verma, ... Acta dermato-venereologica 98 (9-10), 873-879, 2018 | 17 | 2018 |
| Genetic purity assessment of DxT hybrids in coconut with SSR markers JPM 33. Rajesh M.K, Thomas R.J, Rijith J, Shareefa M Indian J Genet 72 (4), 472-474, 2012 | 17* | 2012 |
| Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy A Biswas, A Raza, S Das, M Kapoor, R Jayarajan, A Verma, ... Purinergic signalling 15 (2), 205-210, 2019 | 16 | 2019 |
| Chronic systemic exposure to IL6 leads to deregulation of glycolysis and fat accumulation in the zebrafish liver MK Singh, R Jayarajan, S Varshney, S Upadrasta, A Singh, R Yadav, ... Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids …, 2021 | 15 | 2021 |
| Studies on genetic relationships and diversity in arecanut (Areca catechu L.) germplasm utilizing RAPD markers MKR B.G. Bharath, K.S. Ananda, J. Rijith, N.R. Nagaraja, K.P. Chandran ... Journal of Plantation Crops 43 (2), 117-125, 2015 | 13* | 2015 |
| Investigating Coronary Artery Disease methylome through targeted bisulfite sequencing S Ghose, S Ghosh, VS Tanwar, P Tolani, R Kutum, A Sharma, N Bhardwaj, ... Gene 721, 144107, 2019 | 12 | 2019 |
| RNA secondary structure profiling in zebrafish reveals unique regulatory features K Kaushik, A Sivadas, SK Vellarikkal, A Verma, R Jayarajan, S Pandey, ... BMC genomics 19 (1), 1-17, 2018 | 12 | 2018 |
| Familial Hypertrophic Cardiomyopathy-Identification of cause and risk stratification through exome sequencing A Biswas, S Das, M Kapoor, KV Shamsudheen, R Jayarajan, A Verma, ... Gene 660, 151-156, 2018 | 12 | 2018 |
| E gyptian tale from I ndia: application of whole‐exome sequencing in diagnosis of atypical familial M editerranean fever P Sandhya, SK Vellarikkal, A Nair, R Ravi, J Mathew, R Jayarajan, ... International journal of rheumatic diseases 20 (11), 1770-1775, 2017 | 10 | 2017 |
| Whole-exome sequencing solves diagnostic dilemma in a rare case of sporadic acrokeratosis verruciformis. A Gupta, YK Sharma, SK Vellarikkal, R Jayarajan, V Dixit, A Verma, ... Journal of the European Academy of Dermatology and Venereology: JEADV 30 (4 …, 2015 | 10 | 2015 |
| A novel cathepsin D mutation in 2 siblings with late infantile neuronal ceroid lipofuscinosis J Thottath, SK Vellarikkal, R Jayarajan, A Verma, M Manamel, A Singh, ... Neurology Genetics 5 (3), 2019 | 8 | 2019 |
