Dr Sundaresan .P
Senior Scientist
ARAVIND EYE HOSPITALAND PG INSTITUTE OF OPHTHAMOLOGY (Inst. Code - 043), MADURAI
Tamil Nadu
Expertise:
Genetics and Heredity
84
Publications
1
Projects
87
Scopus Citations
2290
CrossRef
29 Years 4 Months Total Experience
Scopus
87
Citations
6
h-index
CrossRef
2,290
Citations
25
h-index
Google Scholar
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Professional Recognition
ICMR AWARD and Prize for biomedical research for scientists belonging to underprivileged communities
2006
Indian Council of Medical Research
ICMR award and Prize For Biomedical Research Conducted in Underdeveloped Areas in India
2009
Indian Council of Medical Research
Tamilnadu Scientist Award (TANSA 2013) under the discipline -Biological Sciences
2013
TANSA, Tamilnadu government. India
Hari Om Ashram Alembic Research Award
2010
Medical Council of India. Received from Our Honourable President at Rashtrapati Bhawan, New Delhi
Community & Membership
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The Indian Society of Human Genetics
Life memberSociety for Mitochondiral Research and Medicine
Life memberIndian Eye Research Group
Life memberThe association for research in vision and ophthalmology
MemberAll India Ophthalmic Society
Non-memberPersonal Details
Doctor of Philosophy
1990
N/A
Senior Scientist
Mar 2000 – Present
ARAVIND EYE HOSPITALAND PG INSTITUTE OF OPHTHAMOLOGY (Inst. Code - 043), MADURAI
Lecturer
Jun 1990 – Mar 1993
B.M. Birla Science and Technology Centre
Medical and Health Sciences
Scholarly Work
TRANSLATIONAL GENOMICS OF PAEDIATRIC EYE DISEASES
OtherMolecular Analysis of PAX6 gene in Indian aniridic patients April 2007
Studies on Myocilin (TIGR/MYOC) gene mutations and protein in Indian patients with Primary Open Angle Glaucoma
Understanding the Molecular Genetics of Cataract
Involvement of Transcription Factor genes PAX6/FOXL2 in various ocular anomalies
Serological and Molecular characterization of Rubella virus in children with Ocular defects of Congenital Rubella Syndrome
Molecular genetics of diabetic retinopathy
Studies on Molecular Mechanism of Diabeti Retinopathy
Genetic and Functional Analysis of Fuchs Endothelial Corneal Dystrophy (FECD) and Congenital Hereditary Endothelial Dystrophy (CHED) in Indian Patients
Understanding pathogenesis of human mycotic keratitis – A proteome wide analysis
Molecular Genetics and Functional analysis of Albinism Patients in India
Identification and characterization of mutations in Candidate genes involved in major congenital Globe Anomalies
Molecular studies of Leber Congenital Amaurosis (LCA) in Indian population
Molecular genetics and functional studies of genes Associated with Primary Open Angle Glaucoma 2016
Investigating the role of nuclear mitochondrial genome and micro RNA in the pathogenesis of Diabetic Retinopathy
Mitochondrial genes involvement in Leber’s Hereditary Optic Neuropathy (LHON
Molecular genetic studies of primary angle closure glaucoma in south Indian population
Molecular analyses of various risk factors involved in Pseudoexfoliation Syndrome
Genetic and functional approaches to understand the pathogenicity of the primary Open Angle Glaucoma
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Scholarly Publications
Analysis of the SALL4 gene in patients with Duane retraction syndrome in a South Indian population.
10.3109/13816810.2011.559652
Crossref: 2
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes.
10.1093/hmg/ddp008
Crossref: 86
Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II.
Genotype/phenotype association in Indian congenital aniridia.
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern India.
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies.
10.1093/hmg/ddp496
Crossref: 135
Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India.
10.1186/1471-2415-10-3
Crossref: 20
Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 gene.
10.1097/ico.0b013e3181ae9038
Crossref: 14
Showing 1 to 8 of 84 publications