| A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation H Demond, Z Anvar, BN Jahromi, A Sparago, A Verma, M Davari, ... Genome medicine 11, 1-14, 2019 | 57 | 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), 8312, 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 |
| Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance MV Cubellis, L Pignata, A Verma, A Sparago, R Del Prete, M Monticelli, ... Clinical epigenetics 12, 1-13, 2020 | 43 | 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 | 40 | 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 |
| 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 | 24 | 2018 |
| The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to … A Sparago, A Verma, MG Patricelli, L Pignata, S Russo, L Calzari, ... Clinical Epigenetics 11, 1-10, 2019 | 23 | 2019 |
| 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), 873-879, 2018 | 17 | 2018 |
| 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, 205-210, 2019 | 16 | 2019 |
| 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, 1-17, 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 |
| Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs B Acurzio, A Verma, A Polito, C Giaccari, F Cecere, S Fioriniello, ... Scientific Reports 11 (1), 13802, 2021 | 10 | 2021 |
| 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 30 (4), 695-697, 2016 | 10 | 2016 |
| Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or … L Pignata, F Cecere, A Verma, B Hay Mele, M Monticelli, B Acurzio, ... Clinical Epigenetics 14 (1), 71, 2022 | 9 | 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 | 8 | 2019 |
