SWARKAR SHARMA

About

Ph.D. in Human Genetics. PostDoctoral Fellow in Molecular Genetics, TSRH & UTSW, Dallas USA. A Genetics consultant and Scientist.Former Assistant Professor at SMVDU Katra. Associate Professor in Central University of Jammu.

Employment

• Central University of Jammu Associate Professor
  2023 - Present
• Shri Mata Vaishno Devi University ASSISTANT PROFESSOR
  2012 - 2023
• Texas Scottish Rite Hospital for Children POSTDOCTORAL RESEARCHER
  2008 - 2012

Education

• Guru Nanak Dev University PHD
  2003 - 2008

Projects & Funding

Projects & funding information is unavailable.

Publications (69)

• CNTNAP2, a neurodevelopmental pathway gene variants association with adolescent idiopathic scoliosis predisposition in northwest Indians
  Human Gene 2026 DOI: 10.1016/J.HUMGEN.2026.201581
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• Assessment of Degree, Pattern, and Associated Risk Factors of Congenital Hearing Loss among the Population of Village Paralkot, District Poonch, J and K
  Biosciences Biotechnology Research Asia 2026 DOI: 10.13005/bbra/3534
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• SBSPON gene association with type 2 diabetes mellitus and its impact on leukocyte telomere length
  Frontiers in Endocrinology 2026 DOI: 10.3389/FENDO.2026.1799481
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• ESR1 as a candidate gene for adolescent idiopathic scoliosis pathogenesis in North-West Indian population
  European Spine Journal 2026 DOI: 10.1007/S00586-026-10065-5
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• ARL15 Gene Variant rs255758 Provides Susceptibility to Rheumatoid Arthritis in Northwest Indian Population
  International Journal of Applied and Basic Medical Research 2025 DOI: 10.4103/IJABMR.IJABMR_156_24
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• Association of Vascular Endothelial Growth Factor (VEGF) and Mouse Model Minute 2 (MDM2) Polymorphisms With Diabetic Retinopathy in a Northwest Indian Population: A Case-Control Study
  Cureus 2024 DOI: 10.7759/CUREUS.62996
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• SOX9 gene shows association with adolescent idiopathic scoliosis predisposition in Northwest Indians
  European Journal of Medical Research 2024 DOI: 10.1186/S40001-024-01635-8
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• Human Y Chromosome: Genetic Markers, Implications, and Pathologies
  2023 DOI: 10.1201/9781003220404-18
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• Antigen Gene Variants rs13192471 and rs6457617 with Rheumatoid Arthritis Susceptibility: A Case-control Study from North-western India
  Journal of Clinical and Diagnostic Research 2023 DOI: 10.7860/JCDR/2023/63436.17887
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• Cost-effective Whole Exome Sequencing discovers pathogenic variant causing Neurofibromatosis type 1 in a family from Jammu and Kashmir, India
  Scientific Reports 2023 DOI: 10.1038/S41598-023-34941-Y
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