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

Protective and susceptibility effects of hSKCa3 allelic variants on juvenile myoclonic epilepsy

Open Access
Journal Article
Journal of Medical Genetics. Year: 2005. Volume: 42 , Issue: 5 , Pages: 439-442 .
Authors: J Vijai; A Kapoor; H M Ravishankar; P J Cherian; G Kuruttukulam; B Rajendran; R Sridharan; G Rangan; A S Girija; S Jayalakshmi; S Mohandas; K S Mani; K Radhakrishnan; A Anand

Sex determining signal in Drosophila melanogaster

Note
Journal of Genetics. Year: 2004. Volume: 83 , Issue: 2 , Pages: 121-123 .
Authors: Anuranjan Anand

Molecular analysis of Huntington's disease and linked polymorphisms in the Indian population

Journal Article
ACTA NEUROLOGICA SCANDINAVICA (ELECTRONIC). Year: 2003. Volume: 108 , Issue: 4 , Pages: 281-286 .
Authors: Q. Saleem; S. Roy; U. Murgood; R. Saxena; I. C. Verma; A. Anand; U. Muthane; S. Jain; S. K. Brahmachari

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

Journal Article
Human Genetics. Year: 2009. Volume: 125 , Issue: 5-6 , Pages: 541-549 .
Authors: Rinki Ratnapriya; Parthasarthy Satishchandra; S. Dilip Kumar; Girish Gadre; Ramesh Reddy; Anuranjan Anand

Clinical characteristics of a South Indian cohort of juvenile myoclonic epilepsy probands

Open Access
Journal Article
Seizure. Year: 2003. Volume: 12 , Issue: 7 , Pages: 490-496 .
Authors: J VIJAI; P.J CHERIAN; P.N SYLAJA; A ANAND; K RADHAKRISHNAN

Absence of GABRA1 Ala322Asp mutation in juvenile myoclonic epilepsy families from India

Journal Article
Journal of Genetics. Year: 2003. Volume: 82 , Issue: 1-2 , Pages: 17-21 .
Authors: A. Kapoor; J. Vijai; H. M. Ravishankar; P. Satishchandra; K. Radhakrishnan; A. Anand

Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.

Open Access
Journal Article
Journal of Medical Genetics. Year: 2003. Volume: 40 , Issue: 5 , Pages: e68 .
Authors: M RamShankar; S Girirajan; O Dagan; H M Ravi Shankar; R Jalvi; R Rangasayee; K B Avraham; A Anand

Common psychiatric diseases and human genetic variation

Journal Article
Public Health Genomics. Year: 2002. Volume: 5 , Issue: 3 , Pages: 171-177 .
Authors: O. Mukherjee; Q. Saleem; M. Purushottam; A. Anand; S.K. Brahmachari; S. Jain
Showing 9 to 16 of 41 publications