M.Sc., PhD in Biomedical Science-Ophthalmic Genetics
RESEARCH, TEACHING, or OTHER INTERESTS
General Biochemistry, Genetics and Molecular Biology, Molecular Medicine, Molecular Biology, Biotechnology
35
Scholar Citations
3
Scholar h-index
1
Scholar i10-index
RECENT SCHOLAR PUBLICATIONS
Cutaneous freckling: Possible new clinical marker for the diagnosis of Hermansky-Pudlak syndrome in Indian Asian patients with oculocutaneous albinism K Arcot Sadagopan, R Kathirvel, RB Keep, P Sundaresan, H Huang, ... Ophthalmic Genetics 38 (2), 194-196 , 2017 2017 Citations: 5
Molecular genetic analysis and diagnosis of albinism patients in India K Renugadevi, AK Sil, P Vijayalakshmi, P Sundaresan JSM Genet Genomics 4 , 2017 2017 Citations: 1
Molecular Genetic Testing for Carrier-Prenatal Diagnosis and Computational Analysis of Oculocutaneous Albinism Type 1 K Renugadevi, J Mary, V Perumalsamy, S Seshadri, S Jagadeesh, ... J Genet Disor Genet Rep 3, 2 , 2014 2014 Citations: 5
Prenatal Molecular Diagnosis of Fetal Sample R Kathirvel, V Perumalsamy, AM John, S Rajaiah, S Jagadeesh, ... Investigative Ophthalmology & Visual Science 53 (14), 1579-1579 , 2012 2012
Genetic Carrier Screening for Oculocutaneous Albinism in India P Sundaresan, R Kathirvel, V Perumalsamy Investigative Ophthalmology & Visual Science 53 (14), 1560-1560 , 2012 2012 Citations: 1
Novel Mutations in MC1R Gene: First Evidence for OCA Type II Disease in Indian Population R Kathirvel, SA Kumar, V Perumalsamy, S Periasamy Investigative Ophthalmology & Visual Science 52 (14), 3299-3299 , 2011 2011
Spectrum of candidate gene mutations associated with Indian familial oculocutaneous and ocular albinism K Renugadevi, AK Sil, V Perumalsamy, P Sundaresan Molecular Vision 16, 1514 , 2010 2010 Citations: 20
Spectrum of Candidate Genes Mutation Associated with Indian Familial Oculocutaneous Albinism Patients P Sundaresan, K Renugadevi, AK Sil, P Vijayalakshmi Investigative Ophthalmology & Visual Science 51 (13), 2605-2605 , 2010 2010
Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II. K Renugadevi, AK Sil, V Perumalsamy, P Sundaresan Human Genetics 125 (3), 340-340 , 2009 2009 Citations: 3
MOST CITED SCHOLAR PUBLICATIONS
Spectrum of candidate gene mutations associated with Indian familial oculocutaneous and ocular albinism K Renugadevi, AK Sil, V Perumalsamy, P Sundaresan Molecular Vision 16, 1514 , 2010 2010 Citations: 20
Cutaneous freckling: Possible new clinical marker for the diagnosis of Hermansky-Pudlak syndrome in Indian Asian patients with oculocutaneous albinism K Arcot Sadagopan, R Kathirvel, RB Keep, P Sundaresan, H Huang, ... Ophthalmic Genetics 38 (2), 194-196 , 2017 2017 Citations: 5
Molecular Genetic Testing for Carrier-Prenatal Diagnosis and Computational Analysis of Oculocutaneous Albinism Type 1 K Renugadevi, J Mary, V Perumalsamy, S Seshadri, S Jagadeesh, ... J Genet Disor Genet Rep 3, 2 , 2014 2014 Citations: 5
Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II. K Renugadevi, AK Sil, V Perumalsamy, P Sundaresan Human Genetics 125 (3), 340-340 , 2009 2009 Citations: 3
Molecular genetic analysis and diagnosis of albinism patients in India K Renugadevi, AK Sil, P Vijayalakshmi, P Sundaresan JSM Genet Genomics 4 , 2017 2017 Citations: 1
Genetic Carrier Screening for Oculocutaneous Albinism in India P Sundaresan, R Kathirvel, V Perumalsamy Investigative Ophthalmology & Visual Science 53 (14), 1560-1560 , 2012 2012 Citations: 1
Prenatal Molecular Diagnosis of Fetal Sample R Kathirvel, V Perumalsamy, AM John, S Rajaiah, S Jagadeesh, ... Investigative Ophthalmology & Visual Science 53 (14), 1579-1579 , 2012 2012
Novel Mutations in MC1R Gene: First Evidence for OCA Type II Disease in Indian Population R Kathirvel, SA Kumar, V Perumalsamy, S Periasamy Investigative Ophthalmology & Visual Science 52 (14), 3299-3299 , 2011 2011
Spectrum of Candidate Genes Mutation Associated with Indian Familial Oculocutaneous Albinism Patients P Sundaresan, K Renugadevi, AK Sil, P Vijayalakshmi Investigative Ophthalmology & Visual Science 51 (13), 2605-2605 , 2010 2010
