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

Por Ramprasad, Vedam Lakshmi, George, Ronnie, Soumittra, Nagasamy, Sharmila, Ferdinamarie, Vijaya, Lingam, Kumaramanickavel, Govindasamy
Publicado em 2008

Molecular profiling of complete congenital stationary night blindness: A pilot study on an Indian cohort

Por Malaichamy, Sivasankar, Sen, Parveen, Sachidanandam, Ramya, Arokiasamy, Tharigopala, Lancelot, Marie Elise, Audo, Isabelle, Zeitz, Christina, Soumittra, Nagasamy
Publicado em 2014

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

Por Srilekha, Sundaramurthy, Arokiasamy, Tharigopala, Srikrupa, Natarajan N., Umashankar, Vetrivel, Meenakshi, Swaminathan, Sen, Parveen, Kapur, Suman, Soumittra, Nagasamy
Publicado no PLoS One (2015)

Molecular genetics analysis of hereditary breast and ovarian cancer patients in India

Por Soumittra, Nagasamy, Meenakumari, Balaiah, Parija, Tithi, Sridevi, Veluswami, Nancy, Karunakaran N, Swaminathan, Rajaraman, Rajalekshmy, Kamalalayam R, Majhi, Urmila, Rajkumar, Thangarajan
Publicado em 2009

Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis

Por Ramprasad, Vedam Lakshmi, Soumittra, Nagasamy, Nancarrow, Derek, Sen, Parveen, McKibbin, Martin, Williams, Grange A, Arokiasamy, Tharigopala, Lakshmipathy, Praveena, Inglehearn, Chris F, Kumaramanickavel, Govindasamy
Publicado em 2008

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

Por Ali, Manir, Ramprasad, Vedam Lakshmi, Soumittra, Nagasamy, Mohamed, Moin D., Jafri, Hussain, Rashid, Yasmin, Danciger, Michael, McKibbin, Martin, Kumaramanickavel, Govindasamy, Inglehearn, Chris F.
Publicado em 2008