Nagasamy Soumittra

Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India.

Vedam L. Ramprasad, Ronnie George, Nagasamy Soumittra et al. · PubMed · 2008 · 102 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

<i>CERKL</i>Mutations Cause an Autosomal Recessive Cone-Rod Dystrophy with Inner Retinopathy

Tomás S. Alemán, Nagasamy Soumittra, Artur V. Cideciyan et al. · Investigative Ophthalmology & Visual Science · 2009 · 89 citations

Medicine, Genetics, Vision Science +17

BRCA1, BRCA2 and CHEK2 (1100 del C) germline mutations in hereditary breast and ovarian cancer families in South India.

Thangarajan Rajkumar, Nagasamy Soumittra, Nirmala Karunakaran Nancy et al. · PubMed · 2003 · 51 citations

Life Sciences, Genetics, Molecular Genetics +17

Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families

Srilekha Sundaramurthy, Tharigopala Arokiasamy, Natarajan N. Srikrupa et al. · PLoS ONE · 2015 · 39 citations · Full text

Medicine, Genetics, Ophthalmology +17

Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy

Nagasamy Soumittra, Sampath K. Loganathan, Dharanija Madhavan et al. · Journal of Human Genetics · 2014 · 37 citations

Medicine, Genetics, Molecular Biology +17