Articles with public access mandates - Vinod ScariaLearn more
Not available anywhere: 29
Mapping human genetic diversity in Asia
HUGO Pan-Asian SNP Consortium, MA Abdulla, I Ahmed, ...
Science 326 (5959), 1541-1545, 2009
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Conceptual approaches for lncRNA drug discovery and future strategies
D Bhartiya, S Kapoor, S Jalali, S Sati, K Kaushik, C Sachidanandan, ...
Expert opinion on drug discovery 7 (6), 503-513, 2012
Mandates: Council of Scientific and Industrial Research, India
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
Mandates: Council of Scientific and Industrial Research, India
Hydroxymethyl cytosine marks in the human mitochondrial genome are dynamic in nature
S Ghosh, S Sengupta, V Scaria
Mitochondrion 27, 25-31, 2016
Mandates: Council of Scientific and Industrial Research, India
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
Mandates: Council of Scientific and Industrial Research, India, Department of Science …
The long noncoding RNA MALAT1 suppresses miR‐211 to confer protection from ultraviolet‐mediated DNA damage in vitiligo epidermis by upregulating sirtuin 1*
HD Brahmbhatt, R Gupta, A Gupta, S Rastogi, R Misri, A Mobeen, ...
British Journal of Dermatology 184 (6), 1132-1142, 2021
Mandates: Council of Scientific and Industrial Research, India, Department of …
Long noncoding RNAs could be potential key players in the pathophysiology of Sjögren's syndrome
P Sandhya, K Joshi, V Scaria
International journal of rheumatic diseases 18 (8), 898-905, 2015
Mandates: Council of Scientific and Industrial Research, India
Genetic epidemiology of Familial Mediterranean Fever through integrative analysis of whole genome and exome sequences from Middle East and North Africa
R Koshy, A Sivadas, V Scaria
Clinical genetics 93 (1), 92-102, 2018
Mandates: Council of Scientific and Industrial Research, India
Antagonism of microRNA function in zebrafish embryos by using locked nucleic acid enzymes (LNAzymes)
H Suryawanshi, MK Lalwani, S Ramasamy, R Rana, V Scaria, ...
ChemBioChem 13 (4), 584-589, 2012
Mandates: Council of Scientific and Industrial Research, India
Distinct patterns of genetic variations in potential functional elements in long noncoding RNAs
D Bhartiya, S Jalali, S Ghosh, V Scaria
Human mutation 35 (2), 192-201, 2014
Mandates: Council of Scientific and Industrial Research, India
From genomes to genomic medicine: enabling personalized and precision medicine in the Middle East
PV Jithesh, V Scaria
Personalized Medicine 14 (5), 377-382, 2017
Mandates: Council of Scientific and Industrial Research, India
Pharmacogenetic landscape of clopidogrel in north Indians suggest distinct interpopulation differences in allele frequencies
AK Giri, NM Khan, INDICO, A Basu, N Tandon, V Scaria, D Bharadwaj
Pharmacogenomics 15 (5), 643-653, 2014
Mandates: Council of Scientific and Industrial Research, India
Genetic epidemiology of pharmacogenetic variants in South East Asian Malays using whole-genome sequences
A Sivadas, MZ Salleh, LK Teh, V Scaria
The pharmacogenomics journal 17 (5), 461-470, 2017
Mandates: Council of Scientific and Industrial Research, India
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 & Venereology 30 (4), 2016
Mandates: Council of Scientific and Industrial Research, India
Pharmacogenomic analysis of a genetically distinct Indigenous population
A Jaya Shankar, S Jadhao, W Hoy, SJ Foote, HR Patel, V Scaria, ...
The Pharmacogenomics Journal 22 (2), 100-108, 2022
Mandates: National Health and Medical Research Council, Australia, Medical Research …
A founder mutation MLC1 c. 736delA associated with megalencephalic leukoencephalopathy with subcortical cysts-1 in north Indian kindred
SK Vellarikkal, R Jayarajan, A Verma, R Ravi, V Senthilvel, A Kumar, ...
Clinical genetics 94 (2), 271-273, 2018
Mandates: Council of Scientific and Industrial Research, India
AB0188 Systematic Analysis of the Oral Microbiome in Primary SjÖgren's Syndrome Suggest Enrichment of Distinct Microbes
P Sandhya, D Sharma, SK Vellarikkal, AK Surin, R Jayarajan, A Verma, ...
Annals of the Rheumatic Diseases 74, 953, 2015
Mandates: Council of Scientific and Industrial Research, India
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
Mandates: Council of Scientific and Industrial Research, India
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
Mandates: Council of Scientific and Industrial Research, India, Department of Science …
Building on an Ad Hoc Covid-19 Response to Enhance Community-based Care for Vulnerable Children in Kerala, India
GM Govindaraj, P Krishnakumar, V Scaria, E Athulya, VT Ajithkumar, ...
NEJM Catalyst Innovations in Care Delivery 1 (6), 2020
Mandates: Department of Science & Technology, India
Publication and funding information is determined automatically by a computer program