Anuranjan Anand

Anuranjan Anand

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Anuranjan Anand

Anuranjan Anand

Publications by authors named "Anuranjan Anand"

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18Publications

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A genetic locus for sensory epilepsy precipitated by contact with hot water maps to chromosome 9p24.3-p23.

J Genet 2018 Jun;97(2):391-398

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru 560 064, India.

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June 2018

Mutations in & genes as major causes of hearing impairment in Dhadkai village, Jammu & Kashmir, India.

Indian J Med Res 2017 10;146(4):489-497

Molecular Biology & Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, India.

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October 2017

Microtubule-associated defects caused by EFHC1 mutations in juvenile myoclonic epilepsy.

Hum Mutat 2017 07 2;38(7):816-826. Epub 2017 May 2.

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore, Karnataka, India.

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July 2017

Rare SLC1A1 variants in hot water epilepsy.

Hum Genet 2017 06 21;136(6):693-703. Epub 2017 Mar 21.

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Bangalore, 560 064, India.

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June 2017

Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma.

Ann Hum Genet 2016 Jan 30;80(1):11-9. Epub 2015 Nov 30.

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India.

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January 2016

A locus for juvenile myoclonic epilepsy maps to 2q33-q36.

Hum Genet 2010 Aug 14;128(2):123-30. Epub 2010 May 14.

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560 064, India.

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August 2010

Familial autosomal dominant reflex epilepsy triggered by hot water maps to 4q24-q28.

Hum Genet 2009 Nov 14;126(5):677-83. Epub 2009 Jul 14.

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore 560064, India.

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November 2009

A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3.

Hum Genet 2009 Jun 6;125(5-6):541-9. Epub 2009 Mar 6.

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India.

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June 2009

Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss.

Eur J Hum Genet 2009 Apr 22;17(4):502-9. Epub 2008 Oct 22.

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India.

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April 2009

A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3.

Hum Genet 2009 Jan 22;124(6):669-75. Epub 2008 Nov 22.

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India.

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January 2009

An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene.

Ann Neurol 2008 Aug;64(2):158-67

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India.

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August 2008

A novel genetic locus for juvenile myoclonic epilepsy at chromosome 5q12-q14.

Hum Genet 2007 Jul 13;121(6):655-62. Epub 2007 Apr 13.

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560064, Karnataka, India.

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July 2007

Implications in disclosing auditory genetic mutation to a family: a case study.

Int J Audiol 2007 Jul;46(7):384-7

Ali Yavar Jung National Institute for the Hearing Handicapped, Mumbai, India.

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July 2007

Sex determining signal in Drosophila melanogaster.

Authors:
Anuranjan Anand

J Genet 2004 Aug;83(2):121-3

Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, PO Box 6436, Jakkur, Bangalore 560 064, India.

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August 2004