Dr Sundaresan .P
vidwan id: 225098
Senior Scientist,
ARAVIND EYE HOSPITALAND PG INSTITUTE OF OPHTHAMOLOGY (Inst. Code - 043), MADURAI
Expertise
- Genetics and Heredity
Publications
Publications
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0
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Citations
45
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2
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Professional Recognition
ICMR AWARD and Prize for biomedical research for scientists belonging to underprivileged communities"
Indian Council of Medical ResearchICMR award and Prize For Biomedical Research Conducted in Underdeveloped Areas in India
Indian Council of Medical ResearchTamilnadu Scientist Award (TANSA 2013) under the discipline -Biological Sciences.
TANSA, Tamilnadu government. IndiaHari Om Ashram Alembic Research Award
Medical Council of India. Received from Our Honourable President at Rashtrapati Bhawan, New DelhiCommunity & Membership
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Society for Mitochondiral Research and Medicine
The Indian Society of Human Genetics
Indian Eye Research Group
The association for research in vision and ophthalmology
All India Ophthalmic Society
Bio
Dr.P.Sundaresan’s research focuses on the Molecular Genetics of eye diseases and molecular diagnosis for inherited eye diseases.
Personal Details
- Male
- Senior Scientist , ARAVIND EYE HOSPITALAND PG INSTITUTE OF OPHTHAMOLOGY (Inst. Code - 043), MADURAI
- Department of Genetics, Aravind Medical Research Foundation
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Assistant Professor
Assistant Professor
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Physical Director
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Assistant Professor
Dr Jyothi Alias Jyotsna Baragi
Assistant Professor
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N/A
Organisation (1)
Senior Scientist
Co-Authors (2)
Kannur University
THIAGARAJAR COLLEGE
Scholarly Work
TRANSLATIONAL GENOMICS OF PAEDIATRIC EYE DISEASES
Funding Agency: DBT
PI and Team Leader
> 5 Crores
2018 - Ongoing
“Molecular 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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