Radhakrishnan

Employment

• University Hospital of Basel Postdoc
  2024 - Present
• Kasturba Medical College, Manipal Assistant Professor
  2022 - 2024
• Suma Genomics Private Limited Scientist and Laboratory Director
  2020 - 2022
• Kasturba Medical College, Manipal Senior research fellow
  2017 - 2020

Education

• Manipal Academy of Higher Education P.hD.
  2016 - 2020
• Kasturba Medical College, Manipal Master in Medical Anatomy
  2010 - 2013
• Tamil Nadu Dr. M.G.R. Medical University Bachelor of physiotherapy
  2005 - 2009

Projects & Funding

Projects & funding information is unavailable.

Publications (30)

• Biallelic Splicing Variant c.12479+3A>G in FAT4 Causes Hennekam Lymphangiectasia‐Lymphedema Syndrome 2
  American Journal of Medical Genetics Part A 2026 DOI: 10.1002/ajmg.a.70166
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• Further evidence of biallelic NAV3 variants associated with recessive neurodevelopmental disorder with dysmorphism, developmental delay, intellectual disability, and behavioral abnormalities.
  Human genetics 2024 DOI: 10.1007/s00439-024-02718-6
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• Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype.
  American journal of human genetics 2024 DOI: 10.1016/j.ajhg.2024.11.007
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• Biallelic Variants in LRRC45 Impair Ciliogenesis and Cause a Severe Neurological Disorder.
  Clinical genetics 2024 DOI: 10.1111/cge.14663
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• Bi-Allelic Splicing Variant, c.153-2A > C in TOMM7 Is Associated With Leigh Syndrome.
  American journal of medical genetics. Part A 2024 DOI: 10.1002/ajmg.a.63892
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• Low-energy electric shock ameliorates cell proliferation, morphallaxis, and regeneration via driving key regenerative proteins in earthworm and 3T3 cells.
  Bioelectrochemistry (Amsterdam, Netherlands) 2024 DOI: 10.1016/j.bioelechem.2024.108824
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• Secondary Membranous Nephropathy and Immunodeficiency due to a Novel Biallelic Variant in CARMIL2.
  Indian journal of nephrology 2024 DOI: 10.25259/ijn_542_23
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• Genome sequencing enables diagnosis and treatment of SLC5A6 neuropathy.
  European journal of human genetics : EJHG 2024 DOI: 10.1038/s41431-024-01641-8
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• Intragenic homozygous duplication in HEPACAM is associated with megalencephalic leukoencephalopathy with subcortical cysts type 2A.
  Neurogenetics 2024 DOI: 10.1007/s10048-024-00743-1
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• A bi-allelic missense change c.638A > G in matrix metalloproteinase 15 in a patient with progressive familial intrahepatic cholestasis without cardiac anomalies.
  Clinical genetics 2022 DOI: 10.1111/cge.14263
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