Anuranjan Anand
VIDWAN ID: 42658

Prof Anuranjan Anand

Male Doctor of Philosophy
Professor | Molecular Biology and Genetics Unit
Jawaharlal Nehru Centre for Advanced Scientific Research, Banaglore
Karnataka
Expertise: Genetics and Heredity
41 Publications
0 Projects
1384 Scopus Citations
1170 CrossRef
17 Years 5 Months Total Experience
Publications
41 Total
Articles
39
Chapters
2
Activity

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Scopus Scopus
1,384 Citations
16 h-index
CrossRef CrossRef
1,170 Citations
15 h-index
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Indian Academy of Sciences(FASc)
Member
The National Academy of Sciences, India
Member

Personal Details

Doctor of Philosophy
1999
Indian Institute of Technology, Delhi
Professor
Apr 2009 – Present
Jawaharlal Nehru Centre for Advanced Scientific Research, Banaglore | Molecular Biology and Genetics Unit
Medical and Health Sciences
Genetics and Heredity

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Scholarly Work

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Scholarly Publications

Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population

Journal Article
Human Genetics. Year: 2003. Volume: 113 , Issue: 5 , Pages: 461-463 .
Authors: J. Vijai; A. Kapoor; H. M. Ravishankar; P. J. Cherian; A. S. Girija; B. Rajendran; G. Rangan; S. Jayalakshmi; S. Mohandas; K. Radhakrishnan; A. Anand

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

Journal Article
Human Genetics. Year: 2009. Volume: 124 , Issue: 6 , Pages: 669-675 .
Authors: Arunima Chatterjee; Rajeev Jalvi; Nishtha Pandey; R. Rangasayee; Anuranjan Anand

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

Open Access
Journal Article
European Journal of Human Genetics. Year: 2009. Volume: 17 , Issue: 4 , Pages: 502-509 .
Authors: Ram Shankar Mani; Aparna Ganapathy; Rajeev Jalvi; C R Srikumari Srisailapathy; Vikas Malhotra; Shelly Chadha; Arun Agarwal; Arabandi Ramesh; Raghunath Rao Rangasayee; Anuranjan Anand

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

Journal Article
ANNALS OF NEUROLOGY. Year: 2008. Volume: 64 , Issue: 2 , Pages: 158-167 .
Authors: Ashish Kapoor; Parthasarathy Satishchandra; Rinki Ratnapriya; Ramesh Reddy; Jayaram Kadandale; Susarla K. Shankar; Anuranjan Anand

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

Journal Article
Human Genetics. Year: 2007. Volume: 121 , Issue: 6 , Pages: 655-662 .
Authors: Ashish Kapoor; R. Ratnapriya; Gigy Kuruttukulam; Anuranjan Anand

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

Journal Article
International Journal of Audiology. Year: 2007. Volume: 46 , Issue: 7 , Pages: 384-387 .
Authors: Giriraj Singh Shekhawat; M. Ramshankar; Rajeev R Jalvi; R. Rangasayee; Anuranjan Anand

A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy

Open Access
Journal Article
EPILEPSIA. Year: 2007. Volume: 48 , Issue: 4 , Pages: 706-712 .
Authors: Gianpiero L. Cavalleri; Nicole M. Walley; Nicole Soranzo; John Mulley; Colin P. Doherty; Ashish Kapoor; Chantal Depondt; John M. Lynch; Ingrid E. Scheffer; Armin Heils; Anne Gehrmann; Peter Kinirons; Sonia Gandhi; Parthasarathy Satishchandra; Nicholas W. Wood; Anuranjan Anand; Thomas Sander; Samuel F. Berkovic; Norman Delanty; David B. Goldstein; Sanjay M. Sisodiya

Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease

Open Access
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry. Year: 2005. Volume: 76 , Issue: 11 , Pages: 1588-1590 .
Authors: R H Madegowda
Showing 1 to 8 of 41 publications