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Dinesh Velayutham

Biographic Data

ID7978184
NAMEDinesh Velayutham
GIVEN NAMESDinesh
FAMILY NAMEVelayutham
SIGNATUREVELAYUTHAM D
AFFILIATIONSHamad bin Khalifa University
ORCID0000-0002-9425-7266
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2023
LATEST PUBLICATION YEAR2024
H-INDEX0
  • Forging the path to precision medicine in Qatar

    Open Access•Kholoud Bastaki, Dinesh Velayutham et al.•ARTICLE•Frontiers in Public Health•2024

    Pharmacogenomics (PGx) is an important component of precision medicine that promises tailored treatment approaches based on an individual’s genetic information. Exploring the initiatives in research that help to integrate PGx test into clinical setting, identifying the potential barriers and challenges as well as planning the future directions, are all important for fruitful PGx implementation in any population. Qatar serves as an exemplar case s…

  • Identification of two novel autism genes, TRPC4 and SCFD2, in Qatar simplex families through exome sequencing

    Open Access•Vijay Gupta, Afif Ben‐Mahmoud et al.•ARTICLE•Frontiers in Psychiatry•2023

    This study investigated the genetic underpinnings of autism spectrum disorder (ASD) in a Middle Eastern cohort in Qatar using exome sequencing. The study identified six candidate autism genes in independent simplex families, including both four known and two novel autosomal dominant and autosomal recessive genes associated with ASD. The variants consisted primarily of de novo and homozygous missense and splice variants. Multiple individuals displ…

No prominent works on this page.

  • Identification of two novel autism genes, TRPC4 and SCFD2, in Qatar simplex families through exome sequencing

    Open Access•Vijay Gupta, Afif Ben‐Mahmoud et al.•ARTICLE•Frontiers in Psychiatry•2023

    This study investigated the genetic underpinnings of autism spectrum disorder (ASD) in a Middle Eastern cohort in Qatar using exome sequencing. The study identified six candidate autism genes in independent simplex families, including both four known and two novel autosomal dominant and autosomal recessive genes associated with ASD. The variants consisted primarily of de novo and homozygous missense and splice variants. Multiple individuals displ…

  • Forging the path to precision medicine in Qatar

    Open Access•Kholoud Bastaki, Dinesh Velayutham et al.•ARTICLE•Frontiers in Public Health•2024

    Pharmacogenomics (PGx) is an important component of precision medicine that promises tailored treatment approaches based on an individual’s genetic information. Exploring the initiatives in research that help to integrate PGx test into clinical setting, identifying the potential barriers and challenges as well as planning the future directions, are all important for fruitful PGx implementation in any population. Qatar serves as an exemplar case s…

Medicine (2 works) · Autism (1 work) · Autism spectrum disorder (1 work) · Autism Spectrum Disorder Research (1 work) · Berberine and alkaloids research (1 work) · Bioinformatics (1 work) · Biology (1 work) · Biosimilars and Bioanalytical Methods (1 work) · Candidate gene (1 work) · Computer Science (1 work)

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