JK
Jeevan Kumar
Kasturba Medical College, Manipal, SRM Institute of Science and Technology, VIT, Sri Venkateswara University, Kanchi Kamakoti CHILDS Trust Hospital
0000-0002-2708-5513
About
Passionate medical geneticist. Extensive experience in clinical cytogenetics, next generation sequencing for disease gene identification. Strongly believe in collaborative work and the ability to work independently and in a team. Dedicated to leveraging my current skill sets and building upon them, and passionate about making a difference in the lives of patients through medical research.
Employment
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Kasturba Medical College, Manipal Postdoctoral Fellow2021 - Present
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SRM Institute of Science and Technology Research Assistant Professor2016 - 2021
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Kanchi Kamakoti CHILDS Trust Hospital Geneticist and Research scholar2006 - 2015
Education
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VIT Doctor of Philosophy2007 - 2014
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VIT Master of Science2003 - 2005
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Sri Venkateswara University Bachelor of Science1999 - 2002
Projects & Funding
Projects & funding information is unavailable.
Publications (10)
- “Heptadecanol” a phytochemical multi-target inhibitor of SMYD3 & GFPT2 proteins in non-small cell lung cancer: an in-silico & in-vitro investigation Save
- Green synthesized heteromorphic iron oxide nanoparticles (Fe₃O₄NPs) as potential food additive, food supplement & food colorant sensor and their physiological impact on Drosophila melanogaster Save
- De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India. Save
- The E262K mutation in Lamin A links nuclear proteostasis imbalance to laminopathy‐associated premature aging Save
- Genetic counseling education at the undergraduate level: An outreach initiative to promote professional recruitment and support workforce development Save
- A de novo marker chromosome 15 in a child with isolated developmental delay. Save
- Subtelomeric rearrangements in Indian children with idiopathic intellectual disability/developmental delay: Frequency estimation & clinical correlation using fluorescence in situ hybridization (FISH) Save
- Class II Analphoid Chromosome in a Child with Aberrant Chromosome 7: A Rare Cytogenetic Association Save
- Application of Fluorescence in situ Hybridization (FISH) Technique to Discern Complete/Partial Monosomy 21 Save
- Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic association Save