Muralitharan Shanmugakonar

Absence of deafness-associated connexin-26 (GJB2) gene mutations in the Omani population

Mehmet Şımşek, Nadia Al-Wardy, Aisha Al‐Khayat et al. · Human Mutation · 2001 · 46 citations · Full text

Cadmium: An Emerging Role in Adipose Tissue Dysfunction

Sarra Mohammed Attia, V. Kavitha, Muralitharan Shanmugakonar et al. · Exposure and Health · 2021 · 28 citations · Full text

Metabolic Disorder, Adipose Tissue Macrophages, Adipokines +20

Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia

Anne Hempelmann, Santosh Kumar, Muralitharan Shanmugakonar et al. · Neuroscience Letters · 2006 · 27 citations

Mendelian Disorder, Genetic Disorder, Omani Family +7

Genotyping of the three major allelic variants of the human mannose-binding lectin gene by denaturing gradient gel electrophoresis

Martine Gabolde, Muralitharan Shanmugakonar, Claude Besmond · Human Mutation · 1999 · 22 citations

NF-κB Essential Modulator (NEMO) Is Critical for Thyroid Function

Carla Reale, Anna Iervolino, Ivan Scudiero et al. · Journal of Biological Chemistry · 2016 · 20 citations · Full text