Hasil Pencarian - Vigneshwar Senthivel
- Menampilkan 1 - 7 hasil dari 7
-
1
Case Report: Whole exome sequencing reveals a novel frameshift deletion mutation p.G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa [version 2... oleh Shamsudheen Karuthedath Vellarikkal, Rijith Jayarajan, Ankit Verma, Sreelata Nair, Rowmika Ravi, Vigneshwar Senthivel, Sridhar Sivasubbu, Vinod Scaria
Diterbitkan 2016-07-01Dapatkan teks lengkap
Artikel -
2
Case Report: Whole exome sequencing reveals a novel frameshift deletion mutation p.G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa [version 1... oleh Shamsudheen Karuthedath Vellarikkal, Rijith Jayarajan, Ankit Verma, Sreelata Nair, Rowmika Ravi, Vigneshwar Senthivel, Sridhar Sivasubbu, Vinod Scaria
Diterbitkan 2016-05-01Dapatkan teks lengkap
Artikel -
3
An optimized, amplicon-based approach for sequencing of SARS-CoV-2 from patient samples using COVIDSeq assay on Illumina MiSeq sequencing platforms oleh Rahul C. Bhoyar, Vigneshwar Senthivel, Bani Jolly, Mohamed Imran, Abhinav Jain, Mohit Kumar Divakar, Vinod Scaria, Sridhar Sivasubbu
Diterbitkan 2021-09-01Dapatkan teks lengkap
Artikel -
4
Pharmacogenomic landscape of Indian population using whole genomes oleh S. Sahana, Rahul C. Bhoyar, Ambily Sivadas, Abhinav Jain, Mohamed Imran, Mercy Rophina, Vigneshwar Senthivel, Mohit Kumar Diwakar, Disha Sharma, Anushree Mishra, Sridhar Sivasubbu, Vinod Scaria
Diterbitkan 2022-04-01Dapatkan teks lengkap
Artikel -
5
Landscape of pharmacogenetic variants associated with non-insulin antidiabetic drugs in the Indian population oleh Anura V Kurpad, Disha Sharma, KM Venkat Narayan, Ambily Sivadas, Arpita Mukhopadhyay, Greg Gibson, Abhinav Jain, S Sahana, Bani Jolly, Rahul C Bhoyar, Mohamed Imran, Vigneshwar Senthivel, Mohit Kumar Divakar, Anushree Mishra, Sridhar Sivasubbu, Vinod Scaria
Diterbitkan 2024-04-01Dapatkan teks lengkap
Artikel -
6
1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants oleh Anjali Bajaj, Vigneshwar Senthivel, Rahul Bhoyar, Abhinav Jain, Mohamed Imran, Mercy Rophina, Mohit Kumar Divakar, Bani Jolly, Ankit Verma, Anushree Mishra, Disha Sharma, Siddharthan Deepti, Gautam Sharma, Raghav Bansal, Rakesh Yadav, Vinod Scaria, Nitish Naik, Sridhar Sivasubbu
Diterbitkan 2022-08-01Dapatkan teks lengkap
Artikel -
7
Genetic epidemiology of autoinflammatory disease variants in Indian population from 1029 whole genomes oleh Abhinav Jain, Rahul C. Bhoyar, Kavita Pandhare, Anushree Mishra, Disha Sharma, Mohamed Imran, Vigneshwar Senthivel, Mohit Kumar Divakar, Mercy Rophina, Bani Jolly, Arushi Batra, Sumit Sharma, Sanjay Siwach, Arun G. Jadhao, Nikhil V. Palande, Ganga Nath Jha, Nishat Ashrafi, Prashant Kumar Mishra, Vidhya A.K., Suman Jain, Debasis Dash, Nachimuthu Senthil Kumar, Andrew Vanlallawma, Ranjan Jyoti Sarma, Lalchhandama Chhakchhuak, Shantaraman Kalyanaraman, Radha Mahadevan, Sunitha Kandasamy, Pabitha B. M, Raskin Erusan Rajagopal, Ezhil Ramya J., Nirmala Devi P., Anjali Bajaj, Vishu Gupta, Samatha Mathew, Sangam Goswami, Mohit Mangla, Savinitha Prakash, Kandarp Joshi, Meyakumla, Sreedevi S., Devarshi Gajjar, Ronibala Soraisham, Rohit Yadav, Yumnam Silla Devi, Aayush Gupta, Mitali Mukerji, Sivaprakash Ramalingam, Binukumar B. K., Vinod Scaria, Sridhar Sivasubbu
Diterbitkan 2021-12-01Dapatkan teks lengkap
Artikel