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3. Whole genome sequencing of families diagnosed with cardiac channelopathies reveals structural variants missed by whole exome sequencing

5. Forward genetic screen using a gene-breaking trap approach identifies a novel role of grin2bb-associated RNA transcript (grin2bbART) in zebrafish heart function.

6. Development of pathophysiologically relevant models of sickle cell disease and β-thalassemia for therapeutic studies

7. Impact of COVID-19 outbreak on healthcare workers in a Tertiary Healthcare Center in India: a cross sectional study

14. Whole genome sequencing followed by functional analysis of genomic deletion encompassing ERCC8 and NDUFAF2 genes in a non-consanguineous Indian family reveals dysfunctional mitochondrial bioenergetics leading to infant mortality

25. 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

26. Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India

29. BRCAIndica: a Resource for ACMG/AMP classified BRCA1 and BRCA2 Variants

30. Forward genetic screen using a gene-breaking trap approach identifies a novel role of grin2bb-associated RNA transcript (grin2bbART) in zebrafish heart function

31. Landscape of pharmacogenetic variants associated with non-insulin antidiabetic drugs in the Indian population

34. A Rapid and Scalable Multiplex PCR-Based Next-Generation Amplicon Sequencing Method for Familial Hypercholesterolemia Genetic Screening

36. The genomic landscape of CYP2D6 variation in the Indian population

38. Scalable noninvasive amplicon-based precision sequencing (SNAPseq) for genetic diagnosis and screening of β-thalassemia and sickle cell disease using a next-generation sequencing platform

39. Genetic epidemiology of monogenic dyslipidemia and statin-associated adverse drug phenotypes in Indian population from whole-genomes of 1029 self-declared healthy individuals

40. Genetic epidemiology of autoinflammatory disease variants in Indian population from 1029 whole genomes

44. Systematic transcriptome wide analysis of lncRNA-miRNA interactions

45. LncRNA VEAL2 regulates PRKCB2 to modulate endothelial permeability in diabetic retinopathy

46. WilsonGenAI a deep learning approach to classify pathogenic variants in Wilson Disease.

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