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Vigneshwar Senthivel
Vigneshwar Senthivel
CSIR-IGIB
Verified email at acsir.res.in
Title
Cited by
Cited by
Year
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
3332021
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
882021
Genomics of rare genetic diseases—experiences from India
S Sivasubbu, V Scaria
Human genomics 13 (1), 52, 2019
692019
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
672021
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
472021
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
312018
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
282022
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
252018
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
172021
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
122022
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
92019
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
72022
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
72021
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
62021
CoV-2 Genomics Consortium (INSACOG) Gupta RK
MS Dhar, R Marwal, R Vs, K Ponnusamy, B Jolly, RC Bhoyar, V Sardana, ...
52021
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
42023
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
42022
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
32024
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
32022
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
32016
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