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

<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 · 88 citations

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

Breast Oncology, Base Deletion, Cancer Pathology +16

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

Ocular Disease, Genetics, Genetic Epidemiology +19

A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration.

Manir Ali, Vedam L. Ramprasad, Nagasamy Soumittra et al. · PubMed · 2008 · 37 citations