ARSHIA ANGURAL

Employment

• JSS Academy of Higher Education and Research Assistant Professor
  2022 - Present

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (10)

• “Bridging the clinical, molecular and genetic perspectives on myocarditis in post-COVID-19 era”
  International Journal of Cardiology Cardiovascular Risk and Prevention 2026 DOI: 10.1016/j.ijcrp.2026.200576
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• Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India
  Frontiers in Genetics 2020 DOI: 10.3389/fgene.2020.00415
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• A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcifications
  Mitochondrion 2019 DOI: 10.1016/j.mito.2018.06.005
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• Replication of MACF1 gene variant rs2296172 with type 2 diabetes susceptibility in the Bania population group of Punjab, India
  International Journal of Diabetes in Developing Countries 2018 DOI: 10.1007/s13410-017-0598-6
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• A variation in PANK2 gene is causing Pantothenate kinase-associated Neurodegeneration in a family from Jammu and Kashmir-India
  Scientific Reports 2017 DOI: 10.1038/s41598-017-05388-9
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• Replication of newly identified type 2 diabetes susceptible loci in Northwest Indian population
  Diabetes Research and Clinical Practice 2017 DOI: 10.1016/j.diabres.2017.02.013
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• Whole Exome screening identifies novel and recurrent wisp3 mutations causing progressive pseudorheumatoid dysplasia in Jammu and Kashmir-India
  Scientific Reports 2016 DOI: 10.1038/srep27684
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• Evidence for genetic linkage between a polymorphism in the GNAS gene and malaria in South Indian population
  Acta Tropica 2013 DOI: 10.1016/j.actatropica.2013.08.005
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• Single nucleotide polymorphisms of ADRB2 gene and their association with susceptibility for Plasmodium falciparum malaria and asthma in an Indian population
  Infection, Genetics and Evolution 2013 DOI: 10.1016/j.meegid.2013.08.026
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• Missense Variation in TPP1 Gene causes Neuronal Ceroid Lipofuscinosis Type 2 in a Family from Jammu and Kashmir-India
  DOI: 10.20944/preprints202107.0661.v1
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