Vinod Scaria
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Indian biochemist
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Biology
Vinod Scaria's Degrees
- PhD Bioinformatics Jawaharlal Nehru University
Why Is Vinod Scaria Influential?
(Suggest an Edit or Addition)According to Wikipedia, Dr. Vinod Scaria FRSB, FRSPH is an Indian biologist, medical researcher pioneering in Precision Medicine and Clinical Genomics in India. He is best known for sequencing the first Indian genome. He was also instrumental in the sequencing of The first Sri Lankan Genome, analysis of the first Malaysian Genome sequencing and analysis of the Wild-type strain of Zebrafish and the IndiGen programme on Genomics for Public Health in India
Vinod Scaria's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Mapping Human Genetic Diversity in Asia (2009) (559)
- Global, regional, and national age-sex-specific mortality and life expectancy, 1950–2017: a systematic analysis for the Global Burden of Disease Study 2017 (2018) (538)
- Systematic Transcriptome Wide Analysis of lncRNA-miRNA Interactions (2012) (413)
- Human cellular microRNA hsa-miR-29a interferes with viral nef protein expression and HIV-1 replication (2008) (272)
- Genetic landscape of the people of India: a canvas for disease gene exploration (2008) (254)
- Targets for human encoded microRNAs in HIV genes. (2005) (209)
- Host-virus interaction: a new role for microRNAs (2006) (207)
- Inhibition of translation in living eukaryotic cells by an RNA G-quadruplex motif. (2008) (195)
- Genomic characterization and epidemiology of an emerging SARS-CoV-2 variant in Delhi, India (2021) (186)
- in vivo protein trapping produces a functional expression codex of the vertebrate proteome (2011) (168)
- Genome-Wide Association Study for Type 2 Diabetes in Indians Identifies a New Susceptibility Locus at 2q21 (2013) (164)
- Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding (2016) (159)
- Asymptomatic reinfection in two healthcare workers from India with genetically distinct SARS-CoV-2 (2020) (151)
- Upregulation of miR-23a∼27a∼24-2 Cluster Induces Caspase-Dependent and -Independent Apoptosis in Human Embryonic Kidney Cells (2009) (148)
- lncRNome: a comprehensive knowledgebase of human long noncoding RNAs (2013) (138)
- Genome-wide analysis reveals distinct patterns of epigenetic features in long non-coding RNA loci (2012) (117)
- High throughput detection and genetic epidemiology of SARS-CoV-2 using COVIDSeq next-generation sequencing (2020) (99)
- MicroRNA-mediated up-regulation of an alternatively polyadenylated variant of the mouse cytoplasmic β-actin gene (2008) (97)
- High Resolution Methylome Map of Rat Indicates Role of Intragenic DNA Methylation in Identification of Coding Region (2012) (94)
- Dynamic Expression of Long Non-Coding RNAs (lncRNAs) in Adult Zebrafish (2013) (92)
- Comparative analysis of human mitochondrial methylome show distinct patterns of epigenetic regulation in mitochondria (2014) (88)
- MicroRNAs: novel therapeutic targets in neurodegenerative diseases. (2009) (85)
- Quadfinder: server for identification and analysis of quadruplex-forming motifs in nucleotide sequences (2006) (84)
- Consensus miRNA expression profiles derived from interplatform normalization of microarray data. (2010) (83)
- Host–virus genome interactions: macro roles for microRNAs (2007) (66)
- Asymptomatic Reinfection in 2 Healthcare Workers From India With Genetically Distinct Severe Acute Respiratory Syndrome Coronavirus 2 (2020) (65)
- Open source drug discovery--a new paradigm of collaborative research in tuberculosis drug development. (2011) (65)
- Genomic variations in non-coding RNAs: Structure, function and regulation. (2016) (64)
- dbSMR: a novel resource of genome-wide SNPs affecting microRNA mediated regulation (2009) (64)
- Conceptual approaches for lncRNA drug discovery and future strategies (2012) (55)
- Potential G-quadruplexes in the human long non-coding transcriptome (2012) (53)
- Computational approaches towards understanding human long non-coding RNA biology (2015) (50)
- Insights into structural variations and genome rearrangements in prokaryotic genomes (2015) (50)
- A Distinct Phylogenetic Cluster of Indian Severe Acute Respiratory Syndrome Coronavirus 2 Isolates (2020) (50)
- Antagomirzymes: oligonucleotide enzymes that specifically silence microRNA function. (2009) (49)
- Genomic survey of SARS-CoV-2 vaccine breakthrough infections in healthcare workers from Kerala, India (2021) (49)
- Integrative transcriptome analysis suggest processing of a subset of long non-coding RNAs to small RNAs (2012) (48)
- Effectiveness of ChAdOx1 nCoV-19 vaccine against SARS-CoV-2 infection during the delta (B.1.617.2) variant surge in India: a test-negative, case-control study and a mechanistic study of post-vaccination immune responses (2021) (48)
- Does the buck stop with the bugs?: an overview of microbial dysbiosis in rheumatoid arthritis (2016) (48)
- Proximity of H2A.Z containing nucleosome to the transcription start site influences gene expression levels in the mammalian liver and brain (2012) (45)
- Predictive models for anti-tubercular molecules using machine learning on high-throughput biological screening datasets (2011) (42)
- A sequence-based variation map of zebrafish. (2013) (41)
- Human 45,X Fibroblast Transcriptome Reveals Distinct Differentially Expressed Genes Including Long Noncoding RNAs Potentially Associated with the Pathophysiology of Turner Syndrome (2014) (40)
- Crowd Sourcing a New Paradigm for Interactome Driven Drug Target Identification in Mycobacterium tuberculosis (2012) (39)
- miRvar: A comprehensive database for genomic variations in microRNAs (2011) (39)
- RNA sequencing of db/db mice liver identifies lncRNA H19 as a key regulator of gluconeogenesis and hepatic glucose output (2017) (39)
- Comparative Whole-Genome Analysis of Clinical Isolates Reveals Characteristic Architecture of Mycobacterium tuberculosis Pangenome (2015) (38)
- microRNAs in viral oncogenesis (2007) (38)
- Reverse Genetics Screen in Zebrafish Identifies a Role of miR-142a-3p in Vascular Development and Integrity (2012) (37)
- A distinct phylogenetic cluster of Indian SARS-CoV-2 isolates (2020) (36)
- Computational analysis and predictive modeling of small molecule modulators of microRNA (2012) (36)
- Computational models for in-vitro anti-tubercular activity of molecules based on high-throughput chemical biology screening datasets (2012) (35)
- Navigating the dynamic landscape of long noncoding RNA and protein-coding gene annotations in GENCODE (2016) (35)
- Predictive modeling of anti-malarial molecules inhibiting apicoplast formation (2013) (34)
- Genetic epidemiology of pharmacogenetic variations in CYP2C9, CYP4F2 and VKORC1 genes associated with warfarin dosage in the Indian population. (2014) (33)
- Rescue of neural crest-derived phenotypes in a zebrafish CHARGE model by Sox10 downregulation. (2016) (32)
- Bronchial Epithelial Cells from Cystic Fibrosis Patients Express a Specific Long Non-coding RNA Signature upon Pseudomonas aeruginosa Infection (2017) (32)
- Cheminformatic models based on machine learning for pyruvate kinase inhibitors of Leishmania mexicana (2013) (32)
- Symptomatic reinfection of SARS‐CoV‐2 with spike protein variant N440K associated with immune escape (2021) (31)
- Circad: a comprehensive manually curated resource of circular RNA associated with diseases (2020) (31)
- Large scale changes in the transcriptome of Eisenia fetida during regeneration (2018) (30)
- SCA‐LSVD: A repeat‐oriented locus‐specific variation database for genotype to phenotype correlations in spinocerebellar ataxias (2009) (30)
- Barcoding of Asian seabass across its geographic range provides evidence for its bifurcation into two distinct species (2014) (30)
- mit‐o‐matic: A Comprehensive Computational Pipeline for Clinical Evaluation of Mitochondrial Variations from Next‐Generation Sequencing Datasets (2015) (28)
- Screening Currency Notes for Microbial Pathogens and Antibiotic Resistance Genes Using a Shotgun Metagenomic Approach (2015) (28)
- IndiGenomes: a comprehensive resource of genetic variants from over 1000 Indian genomes (2020) (27)
- DyNAVacS: an integrative tool for optimized DNA vaccine design (2006) (27)
- al mena: a comprehensive resource of human genetic variants integrating genomes and exomes from Arab, Middle Eastern and North African populations (2017) (26)
- Mitoepigenetics: The different shades of grey. (2015) (26)
- zflncRNApedia: A Comprehensive Online Resource for Zebrafish Long Non-Coding RNAs (2015) (26)
- Systematic Pharmacogenomics Analysis of a Malay Whole Genome: Proof of Concept for Personalized Medicine (2013) (25)
- Variants of concern responsible for SARS‐CoV‐2 vaccine breakthrough infections from India (2021) (25)
- Genome-wide computational analysis of potential long noncoding RNA mediated DNA:DNA:RNA triplexes in the human genome (2017) (25)
- Aptamer-Assisted Detection of the Altered Expression of Estrogen Receptor Alpha in Human Breast Cancer (2016) (24)
- Genomics of rare genetic diseases—experiences from India (2019) (24)
- Prediction of viral microRNA precursors based on human microRNA precursor sequence and structural features (2009) (24)
- Machine learning and data mining techniques for medical complex data analysis (2018) (23)
- Analysis of the potential impact of genomic variants in global SARS-CoV-2 genomes on molecular diagnostic assays (2020) (23)
- Chamber Specific Gene Expression Landscape of the Zebrafish Heart (2016) (23)
- Hydroxymethyl cytosine marks in the human mitochondrial genome are dynamic in nature. (2016) (23)
- Hsp90-targeted miRNA-liposomal formulation for systemic antitumor effect. (2013) (23)
- Comparative analysis of human mitochondrial methylome show distinct patterns of epigenetic regulation in mitochondria (2014) (22)
- LncRNA VEAL2 regulates PRKCB2 to modulate endothelial permeability in diabetic retinopathy (2021) (22)
- Long Non-Coding RNAs in Infection Biology (2013) (22)
- tbvar: a comprehensive genome variation resource for Mycobacterium tuberculosis (2014) (22)
- Systematic analysis and functional annotation of variations in the genome of an Indian individual (2012) (22)
- A distinct phylogenetic cluster of Monkeypox genomes suggests an early and cryptic spread of the virus (2022) (22)
- FishMap: a community resource for zebrafish genomics. (2008) (21)
- Long noncoding RNAs could be potential key players in the pathophysiology of Sjögren's syndrome (2015) (20)
- TBrowse: an integrative genomics map of Mycobacterium tuberculosis. (2009) (20)
- Application of whole exome sequencing in elucidating the phenotype and genotype spectrum of junctional epidermolysis bullosa: A preliminary experience of a tertiary care centre in India. (2017) (20)
- SAGE: a comprehensive resource of genetic variants integrating South Asian whole genomes and exomes (2018) (19)
- Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale data. (2018) (19)
- Genetic epidemiology of familial Mediterranean fever through integrative analysis of whole genome and exome sequences from Middle East and North Africa (2018) (19)
- Cheminformatics Models for Inhibitors of Schistosoma mansoni Thioredoxin Glutathione Reductase (2014) (18)
- Genetic epidemiology of variants associated with immune escape from global SARS-CoV-2 genomes (2020) (18)
- “Locked onto the target”: increasing the efficiency of antagomirzymes using locked nucleic acid modifications. (2010) (18)
- Chemical and genetic rescue of an ep300 knockdown model for Rubinstein Taybi Syndrome in zebrafish. (2018) (18)
- From genomes to genomic medicine: enabling personalized and precision medicine in the Middle East. (2017) (17)
- MitoLSDB: A Comprehensive Resource to Study Genotype to Phenotype Correlations in Human Mitochondrial DNA Variations (2013) (17)
- Pharmacogenetic landscape of clopidogrel in north Indians suggest distinct interpopulation differences in allele frequencies. (2014) (17)
- Distinct Patterns of Genetic Variations in Potential Functional Elements in Long Noncoding RNAs (2014) (17)
- WilsonGen a comprehensive clinically annotated genomic variant resource for Wilson’s Disease (2020) (16)
- Abiotic stress mediated modulation of chromatin landscape in Arabidopsis thaliana. (2020) (16)
- Pharmacogenomic survey of Qatari populations using whole-genome and exome sequences (2018) (16)
- Incidental and clinically actionable genetic variants in 1005 whole exomes and genomes from Qatar (2017) (16)
- Landscape of warfarin and clopidogrel pharmacogenetic variants in Qatari population from whole exome datasets. (2016) (15)
- Short stories on zebrafish long noncoding RNAs. (2014) (15)
- A genome-wide map of circular RNAs in adult zebrafish (2017) (15)
- Anti-HIV microRNA expression in a novel Indian cohort (2016) (15)
- Genetic epidemiology of pharmacogenetic variants in South East Asian Malays using whole-genome sequences (2016) (14)
- A new strain of white spot syndrome virus affecting Litopenaeus vannamei in Indian shrimp farms. (2018) (14)
- Antagonism of microRNA Function in Zebrafish Embryos by Using Locked Nucleic Acid Enzymes (LNAzymes) (2012) (14)
- BioSuite: a comprehensive bioinformatics software package (A unique industry-academia collaboration) (2007) (13)
- microRNA: an Emerging Therapeutic (2007) (13)
- ESC: a comprehensive resource for SARS-CoV-2 immune escape variants (2021) (12)
- Time for the zebrafish ENCODE (2013) (12)
- Cellular Immune Responses are Preserved and May Contribute to Chadox1 ChAdOx1 nCoV-19 Vaccine Effectiveness Against Infection Due to SARS-CoV-2 B·1·617·2 Delta Variant Despite Reduced Virus Neutralisation (2021) (12)
- The long noncoding RNA MALAT1 suppresses miR‐211 to confer protection from ultraviolet‐mediated DNA damage in vitiligo epidermis by upregulating sirtuin 1 * (2020) (11)
- Initial Insights Into the Genetic Epidemiology of SARS-CoV-2 Isolates From Kerala Suggest Local Spread From Limited Introductions (2020) (11)
- Chronic systemic exposure to IL6 leads to deregulation of glycolysis and fat accumulation in the zebrafish liver. (2021) (11)
- Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy (2019) (11)
- Genotype-Phenotype Correlations of Dystrophic Epidermolysis Bullosa in India: Experience from a Tertiary Care Centre. (2018) (11)
- RNA secondary structure profiling in zebrafish reveals unique regulatory features (2018) (10)
- Exome sequencing reveals a novel mutation, p.L325H, in the KRT5 gene associated with autosomal dominant Epidermolysis Bullosa Simplex Koebner type in a large family from western India (2014) (10)
- Maternal vitamin B12 deficiency in rats alters DNA methylation in metabolically important genes in their offspring (2020) (10)
- FMiR: A Curated Resource of Mitochondrial DNA Information for Fish (2015) (10)
- Whole‐exome sequencing solves diagnostic dilemma in a rare case of sporadic acrokeratosis verruciformis (2016) (10)
- Joining the long shots: emerging evidence on the role of long noncoding RNAs in rheumatoid arthritis (2014) (10)
- Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome (2020) (10)
- Distinct patterns of epigenetic marks and transcription factor binding sites across promoters of sense-intronic long noncoding RNAs (2015) (10)
- Diagnosis of Inherited Epidermolysis Bullosa in Resource-Limited Settings: Immunohistochemistry Revisited (2017) (9)
- Egyptian tale from India: application of whole‐exome sequencing in diagnosis of atypical familial Mediterranean fever (2017) (9)
- Population-scale genomics-Enabling precision public health. (2019) (9)
- Correction: Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding (2016) (9)
- FishMap Zv8 update--a genomic regulatory map of zebrafish. (2010) (8)
- Familial Hypertrophic Cardiomyopathy - Identification of cause and risk stratification through exome sequencing. (2018) (8)
- Asymptomatic reactivation of SARS-CoV-2 in a child with neuroblastoma characterised by whole genome sequencing (2020) (8)
- Systematic curation and analysis of genomic variations and their potential functional consequences in snoRNA loci (2012) (8)
- Draft Genome Sequence of Urease-Producing Sporosarcina pasteurii with Potential Application in Biocement Production (2014) (8)
- De novo identification of viral pathogens from cell culture hologenomes (2012) (7)
- Draft Genome Sequence of a Clinical Isolate of Multidrug-Resistant Mycobacterium tuberculosis East African Indian Strain OSDD271 (2013) (7)
- A novel cathepsin D mutation in 2 siblings with late infantile neuronal ceroid lipofuscinosis (2019) (7)
- X-Linked Agammaglobulinemia and COVID-19: Two Case Reports and Review of Literature. (2021) (7)
- Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis. (2015) (7)
- The Zebrafish GenomeWiki: a crowdsourcing approach to connect the long tail for zebrafish gene annotation (2014) (7)
- An optimized, amplicon-based approach for sequencing of SARS-CoV-2 from patient samples using COVIDSeq assay on Illumina MiSeq sequencing platforms (2021) (7)
- Methods for Annotation and Validation of Circular RNAs from RNAseq Data. (2019) (7)
- Draft Genome Sequence of the Extremely Halophilic Bacterium Halomonas salina Strain CIFRI1, Isolated from the East Coast of India (2015) (6)
- Organellar transcriptome sequencing reveals mitochondrial localization of nuclear encoded transcripts. (2019) (6)
- Pharmacogenomics in the Era of Personal Genomics: A Quick Guide to Online Resources and Tools (2013) (6)
- Investigating Coronary Artery Disease methylome through targeted bisulfite sequencing. (2019) (6)
- Modulation of microRNA function by synthetic ribozymes. (2010) (6)
- Computational Analysis and In silico Predictive Modeling for Inhibitors of PhoP Regulon in S. typhi on High-Throughput Screening Bioassay Dataset (2015) (5)
- Utility of whole‐exome sequencing in detecting novel compound heterozygous mutations in COL7A1 among families with severe recessive dystrophic epidermolysis bullosa in India – implications on diagnosis, prognosis and prenatal testing (2018) (5)
- The Sri Lankan Personal Genome Project: an overview (2011) (5)
- Normative range of blood biochemical parameters in urban Indian school-going adolescents (2019) (5)
- Computational Analysis and Phylogenetic Clustering of SARS-CoV-2 Genomes. (2021) (5)
- Data-mining of potential antitubercular activities from molecular ingredients of traditional Chinese medicines (2014) (5)
- Genome and transcriptome analysis of the mealybug Maconellicoccus hirsutus: Correlation with its unique phenotypes. (2021) (5)
- Pallidal Deep Brain Stimulation for KMT2B Related Dystonia in An Indian Patient (2021) (4)
- Distinct and Modular Organization of Protein Interacting Sites in Long Non-coding RNAs (2018) (4)
- Open, Online and Global: Benefits of BioMedical Journals Going Online and Open (2004) (4)
- Case Report: Application of whole exome sequencing for accurate diagnosis of rare syndromes of mineralocorticoid excess (2016) (4)
- Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia (2020) (4)
- Analysis of the potential impact of genomic variants in SARS-CoV-2 genomes from India on molecular diagnostic assays (2020) (4)
- Pharmacogenomic landscape of COVID-19 therapies from Indian population genomes (2021) (4)
- AB0188 Systematic Analysis of the Oral Microbiome in Primary SjÖgren's Syndrome Suggest Enrichment of Distinct Microbes (2015) (4)
- RNA sequencing reveals potential interacting networks between the altered transcriptome and ncRNome in the skeletal muscle of diabetic mice (2021) (4)
- Machine Learning Approaches Toward Building Predictive Models for Small Molecule Modulators of miRNA and Its Utility in Virtual Screening of Molecular Databases. (2017) (4)
- A Temporal Map of Gene Expression Pattern During Zebrafish Liver Regeneration. (2019) (4)
- FaviCoV -a comprehensive manually curated resource for functional genetic variants in SARS-CoV-2 (2020) (4)
- Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the SAMD12 gene (2020) (3)
- RNA sequencing of db/db mice liver identifies lncRNA H19 as a key regulator of gluconeogenesis and hepatic glucose output (2017) (3)
- Case Report: Application of whole exome sequencing for accurate diagnosis of rare syndromes of mineralocorticoid excess. (2016) (3)
- Insights from genomes and genetic epidemiology of SARS-CoV-2 isolates from the state of Andhra Pradesh (2021) (3)
- The Sri Lankan Personal Genome Project (2011) (3)
- Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency (2016) (3)
- Draft Genome Sequence of an Extensively Drug-Resistant Mycobacterium tuberculosis Clinical Isolate of the Ural Strain OSDD493 (2013) (3)
- Investigating Coronary Artery Disease methylome through targeted bisulfite sequencing (2019) (3)
- Do monogenic inborn errors of immunity cause susceptibility to severe COVID-19? (2021) (3)
- Whole exome sequencing in a multi-generation family from India reveals a genetic variation c.10C>T (p.Gln4Ter) in keratin 5 gene associated with Dowling–Degos disease (2018) (3)
- MitoepigenomeKB a comprehensive resource for human mitochondrial epigenetic data. (2017) (3)
- Cyber-pharmacies and emerging concerns on marketing drugs Online (2003) (3)
- HGV&TB: a comprehensive online resource on human genes and genetic variants associated with tuberculosis (2014) (3)
- Personal genomes to precision medicine (2014) (3)
- Whole exome sequencing of pediatric leukemia reveals a novel InDel within FLT-3 gene in AML patient from Mizo tribal population, Northeast India (2022) (2)
- Predictive modeling of anti-malarial molecules inhibiting apicoplast formation (2013) (2)
- Case Report: Whole exome sequencing identifies a novel frameshift insertion c.1325dupT (p.F442fsX2) in the tyrosine kinase domain of BTK gene in a young Indian individual with X-linked agammaglobulinemia. (2016) (2)
- Rapid Transition of Facial Features from Early to Mid - Adolescence in Autosomal Dominant Hyper IgE Syndrome with a STAT3 Variation (2018) (2)
- A founder mutation MLC1 c.736delA associated with megalencephalic leukoencephalopathy with subcortical cysts‐1 in north Indian kindred (2018) (2)
- A temporal map of gene expression pattern during zebrafish liver regeneration (2019) (2)
- Collaborative Tools to Accelerate Neglected Disease Research: Open‐Source Drug Discovery Model (2011) (2)
- Computational Analysis and Predictive Cheminformatics Modeling of Small Molecule Inhibitors of Epigenetic Modifiers (2016) (2)
- Insights into regeneration from the genome, transcriptome and metagenome analysis of Eisenia fetida (2017) (2)
- Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency. (2016) (2)
- Methods to Study Long Noncoding RNA Expression and Dynamics in Zebrafish Using RNA Sequencing. (2019) (2)
- Exome sequencing analysis and interpretation: Handbook for clinicians (2015) (2)
- Case Report: Whole exome sequencing reveals a novel frameshift deletion mutation p.G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa. (2016) (2)
- Case Report: Whole exome sequencing reveals a novel frameshift deletion mutation p.G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa (2016) (2)
- OPEN SOURCE DRUG DISCOVERY: A GLOBAL COLLABORATIVE DRUG DISCOVERY MODEL FOR TUBERCULOSIS (2011) (2)
- Computational Analysis and In silico Predictive Modeling for Inhibitors of PhoP Regulon in S. typhi on High-Throughput Screening Bioassay Dataset (2015) (2)
- Genome-Wide Computational Analysis and Validation of Potential Long Noncoding RNA-Mediated DNA-DNA-RNA Triplexes in the Human Genome. (2020) (2)
- Genome and transcriptome analysis of the mealybug Maconellicoccus hirsutus: A model for genomic Imprinting (2020) (2)
- Pharmacogenomic analysis of a genetically distinct Indigenous population (2021) (2)
- Non-invasive detection of mycobacterium tuberculosis using IR and NIR spectroscopy (2012) (2)
- Draft Genome Sequence of Multidrug-Resistant Mycobacterium tuberculosis Clinical Isolate OSDD515, Belonging to the Uganda I Genotype (2013) (2)
- Functional long non-coding and circular RNAs in zebrafish. (2021) (2)
- Genetic Landscape of Rare Autoinflammatory Disease Variants in Qatar and Middle Eastern Populations Through the Integration of Whole-Genome and Exome Datasets (2021) (1)
- Expression of the human microRNA miR 29a in an Indian cohort of HIV patients (2014) (1)
- Autosomal recessive epidermolysis bullosa simplex: report of three cases from India (2017) (1)
- Case Report: Whole exome sequencing identifies a novel frameshift insertion c.1325dupT (p.F442fsX2) in the tyrosine kinase domain of BTK gene in a young Indian individual with X-linked agammaglobulinemia (2016) (1)
- ATP7A Clinical Genetics Resource – A comprehensive clinically annotated database and resource for genetic variants in ATP7A gene (2020) (1)
- Genome-wide comparison of DNA methylation between life cycle stages of Drosophila melanogaster using high-throughput sequencing techniques (2020) (1)
- Personal genomes, participatory genomics and the anonymity-privacy conundrum (2014) (1)
- Pharmacogenomics for Precision Medicine in the Era of Collaborative Co-creation and Crowdsourcing (2014) (1)
- BGvar - a comprehensive resource for blood group immunogenetics (2021) (1)
- Cheminformatic models based on machine learning for pyruvate kinase inhibitors of Leishmania mexicana (2013) (1)
- A Case for Pharmacogenomics in Management of Cardiac Arrhythmias (2012) (1)
- Pharmacogenomic landscape of Indian population using whole genomes (2022) (1)
- Integrative transcriptome analysis suggest processing of a subset of long non-coding RNAs to small RNAs (2012) (1)
- Genomic analysis of early SARS-CoV-2 breakthrough infections from the state of Kerala suggest a preponderance of variants of concern (2021) (1)
- Clericuzio‐type poikiloderma with neutropenia in a patient from India (2020) (1)
- Open Access: At What Cost? (2017) (1)
- The genome sequence of the Lumpy Skin Disease virus from the outbreak in India suggests a distinct lineage of the virus (2022) (1)
- SARS-CoV-2 vaccine breakthrough infection following a previous infection in a healthcare worker (2021) (1)
- Peer review of scholarly communication in health: Perspectives in the Internet age (2003) (1)
- DALIA- a comprehensive resource of Disease Alleles in Arab population. (2021) (1)
- Draft Genome Sequence of a Multidrug-Resistant Clinical Isolate of Mycobacterium tuberculosis Belonging to a Novel Spoligotype (2013) (1)
- Software Platform for Metabolic Network Reconstruction of Mycobacterium tuberculosis (2013) (1)
- X-linked agammaglobulinemia and COVID-19: Two case reports and review of literature (2020) (1)
- Genomics of rare genetic diseases—experiences from India (2019) (0)
- Prognostic significance of protein-coding and long non-coding RNA expression profile in T-cell acute lymphoblastic leukemia (2021) (0)
- A genome-wide circular RNA transcriptome in rat (2021) (0)
- Genomics of rare genetic diseases—experiences from India (2019) (0)
- Genomic map of blood group alleles in Malaysian indigenous Orang Asli population from whole genome sequences (2021) (0)
- MitoLSDB: The Human Mitochondrial Locus Specific Database (2012) (0)
- Chronic exposure to IL6 leads to deregulation of glycolysis and fat accumulation in the zebrafish liver (2020) (0)
- MON-923 MENIN Gene Mutation: Unity Amidst Diversity (2020) (0)
- A Compendium of manually annotated genetic variants for Alkaptonuria-AKUHub (2023) (0)
- Conceptual approaches forlncRNA drug discovery and futurestrategies (2012) (0)
- Whole Genome Sequencing identifies novel structural variant in a large Indian family affected with X - linked agammaglobulinemia (2021) (0)
- Distinct patterns of epigenetic marks and transcription factor binding sites across promoters of sense-intronic long noncoding RNAs (2015) (0)
- Illustrates the comprehensive analyses of central proteins as potential drug targets. (2012) (0)
- De novo identification of viral pathogens from cell culture hologenomes (2012) (0)
- Hematopoietic Stem Cell Transplantation for Children With Inborn Errors of Immunity (2021) (0)
- Comprehensive Analysis of Immunophenotype and Transcriptome in Indian T-Acute Lymphoblastic Leukemia - a Prospective Study (2019) (0)
- MUSTARD—a comprehensive resource of mutation-specific therapies in cancer (2021) (0)
- WilsonGen a comprehensive clinically annotated genomic variant resource for Wilson’s Disease (2020) (0)
- Clinico-pathological and Genomic Characteristics among Children with SARS-CoV-2 Infection (2022) (0)
- Understanding genetic epidemiology and population disparities of inherited blood cancer syndromes from integrative analysis of population genomics datasets (2021) (0)
- Incidental and clinically actionable genetic variants in 1005 whole exomes and genomes from Qatar (2018) (0)
- An amplicon-based approach for sequencing of SARS-CoV-2 using COVIDSeq assay on Illumina MiSeq sequencing platforms (2021) (0)
- A genome-wide map of circular RNAs in adult zebrafish (2019) (0)
- Comprehensive Assessment of Indian Variations in the Druggable Kinome Landscape Highlights Distinct Insights at the Sequence, Structure and Pharmacogenomic Stratum (2021) (0)
- Genetic landscape of rare autoinflammatory disease variants in Qatar and Middle Eastern populations through the integration of genomic datasets (2020) (0)
- Genetic epidemiology of human neutrophil antigen variants suggest significant global variability (2022) (0)
- Enabling Genomic Medicine in Qatar - from Genomes to Translational Genomics (2017) (0)
- Autologous NeoHep Derived from Chronic Hepatitis B Virus Patients’ Blood Monocytes by Upregulation of c‐MET Signaling (2016) (0)
- Personal genomes to precision medicine (2014) (0)
- Correction: MitoLSDB: A Comprehensive Resource to Study Genotype to Phenotype Correlations in Human Mitochondrial DNA Variations (2020) (0)
- Autologous NeoHep Derived From Chronic Hepatitis B Virus Patients' Blood Monocytes by Upregulation of cMET Signaling. (2016) (0)
- An Alu insertion map of the Indian population: identification and analysis in 1021 genomes of the IndiGen project (2022) (0)
- Time for the zebrafish ENCODE (2013) (0)
- Intronic non-coding RNAs within ribosomal protein coding genes can regulate biogenesis of yeast ribosome (2018) (0)
- MON-509 RET Mutations in the MEN1 Syndrome: Is It an Innocent Bystander? (2020) (0)
- Personal genomes, participatory genomics and the anonymity-privacy conundrum (2014) (0)
- Anti-COVID-19 Activity of FDA Approved Drugs through RNA G-quadruplex Binding (2022) (0)
- Erratum for Behera et al., Draft Genome Sequence of the Extremely Halophilic Bacterium Halomonas salina Strain CIFRI1, Isolated from the East Coast of India (2015) (0)
- A study of biomedical information extraction systems : designing a tool to extract symptoms from clinical text (2017) (0)
- RNA secondary structure profiling in zebrafish reveals unique regulatory features (2018) (0)
- Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India. (2022) (0)
- Personal Genomics In Clinical Medicine: It Is Not In The Future Anymore (2016) (0)
- How The Public Access Health Information On The Internet: A Study Involving Public Internet Access Points (2003) (0)
- Navigating the dynamic landscape of long noncoding RNA and protein-coding gene annotations in GENCODE (2016) (0)
- Persistent SARS-CoV-2 infections in Immunocompromised hosts contribute to new variants (2022) (0)
- Whole-genome sequencing of 1029 Indian individuals reveals unique and rare structural variants (2023) (0)
- Genetic epidemiology of autoinflammatory disease variants in Indian population from 1029 whole genomes (2021) (0)
- What did we learn from the SARS-CoV-2 vaccine breakthrough infections? (2021) (0)
- Building on an Ad Hoc Covid-19 Response to Enhance Community-based Care for Vulnerable Children in Kerala, India (2020) (0)
- Pharmacogenomic survey of Qatari populations using whole-genome and exome sequences (2018) (0)
- Undiagnosed diseases: Needs and opportunities in 20 countries participating in the Undiagnosed Diseases Network International (2023) (0)
- Genetic landscape of Human neutrophil antigen variants in India from population-scale genomes (2022) (0)
- Whole exome sequencing of pediatric leukemia reveals a novel InDel within FLT-3 gene in AML patient from Mizo tribal population, Northeast India (2022) (0)
- DB120406 977..986 (2013) (0)
- Computational Modeling of Small Molecule Inhibitors of Mitochondrial Fusion (2017) (0)
- Systematic In-Silico Evaluation of the Diagnostic Impact of Mpox Genome Variants in the Current Outbreak (2022) (0)
- Genome-wide computational analysis of potential long noncoding RNA mediated DNA:DNA:RNA triplexes in the human genome (2017) (0)
- 1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants (2022) (0)
- Parental Experience of Hematopoietic Stem Cell Transplantation for Children with Primary Immune Deficiency Disorders (2020) (0)
- Genetic variants of human platelet antigens in the Indian population from 1029 whole genomes (2022) (0)
- IndiCleft – A web-based standardized research tool and resource for cleft anomalies (2022) (0)
- G4-binding drugs, chlorpromazine and prochlorperazine, repurposed against COVID-19 infection in hamsters (2023) (0)
- ZNF469 mutation in a case of Ehlers–Danlos syndrome presenting with glomerulonephritis (2018) (0)
- 1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants (2022) (0)
- Founder variants and population genomes-Toward precision medicine. (2021) (0)
- Micro RNA and non-coding DNA and repeats (2009) (0)
- Immunological consequences of compromised ocular immune privilege accelerate retinal degeneration in retinitis pigmentosa (2022) (0)
- Landscape of Variability in Chemosensory Genes Associated With Dietary Preferences in Indian Population: Analysis of 1029 Indian Genomes (2022) (0)
- Long noncoding RNAs in hematopoiesis (2018) (0)
- Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy (2019) (0)
- A Combined Evidence Approach to Prioritize Nipah Virus Inhibitors (2020) (0)
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