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Ashish Kapoor

Research Profile

Disorders

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India

Chemicals & Drugs

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Physiology

Anatomy

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Publications

TOP 3
Ashish Kapoor; Parthasarathy Satishchandra; Rinki Ratnapriya; Ramesh Reddy; Jayaram Kadandale; Susarla K Shankar; Anuranjan Anand
An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene.
Ashish Kapoor; R Ratnapriya; Gigy Kuruttukulam; Anuranjan Anand
A novel genetic locus for juvenile myoclonic epilepsy at chromosome 5q12-q14.
J Vijai; Ashish Kapoor; HM Ravishankar; P Joseph Cherian; G Kuruttukulam; B Rajendran; R Sridharan; G Rangan; A S Girija; S Sita Jayalakshmi; S Mohandas; K S Mani; Kurupath Radhakrishnan; Anuranjan Anand
Protective and susceptibility effects of hSKCa3 allelic variants on juvenile myoclonic epilepsy.

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All Publications

2008: Ashish Kapoor; Parthasarathy Satishchandra; Rinki Ratnapriya; Ramesh Reddy; Jayaram Kadandale; Susarla K Shankar; Anuranjan Anand
An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene.
Annals of neurology 2008;64(2):158-67.
2007: Ashish Kapoor; R Ratnapriya; Gigy Kuruttukulam; Anuranjan Anand
A novel genetic locus for juvenile myoclonic epilepsy at chromosome 5q12-q14.
Human genetics 2007;121(6):655-62.
2005: J Vijai; Ashish Kapoor; HM Ravishankar; P Joseph Cherian; G Kuruttukulam; B Rajendran; R Sridharan; G Rangan; A S Girija; S Sita Jayalakshmi; S Mohandas; K S Mani; Kurupath Radhakrishnan; Anuranjan Anand
Protective and susceptibility effects of hSKCa3 allelic variants on juvenile myoclonic epilepsy.
Journal of medical genetics 2005;42(5):439-42.
2003: J Vijai; Ashish Kapoor; HM Ravishankar; P Joseph Cherian; A S Girija; B Rajendran; G Rangan; S Sita Jayalakshmi; S Mohandas; Kurupath Radhakrishnan; Anuranjan Anand
Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population.
Human genetics 2003;113(5):461-3.
2003: Ashish Kapoor; J Vijai; HM Ravishankar; P Satishchandra; Kurupath Radhakrishnan; Anuranjan Anand
Absence of GABRA1 Ala322Asp mutation in juvenile myoclonic epilepsy families from India.
Journal of genetics 2003;82(1-2):17-21.

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