Mutation of SPATA7 in a family with autosomal recessive early-onset retinitis pigmentosa

Por Kannabiran, Chitra, Palavalli, Lakshmi, Jalali, Subhadra
Publicado em 2012

Genetic Analysis of Indian Families with Autosomal Recessive Retinitis Pigmentosa by Homozygosity Screening

Por Singh, Hardeep Pal, Jalali, Subhadra, Narayanan, Raja, Kannabiran, Chitra
Publicado em 2009

Late occurrence of granular dystrophy in bilateral keratoconus: Penetrating keratoplasty and long-term follow-up

Por Rathi, Varsha M, Vemuganti, Geeta K, Sangwan, Virender S, Kannabiran, Chitra
Publicado em 2011

Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa

Por Kannabiran, Chitra, Singh, Hardeep, Sahini, Nishika, Jalali, Subhadra, Mohan, Gayathri
Publicado em 2012

A missense mutation in LIM2 causes autosomal recessive congenital cataract

Por Ponnam, Surya Prakash G., Ramesha, Kekunnaya, Tejwani, Sushma, Matalia, Jyoti, Kannabiran, Chitra
Publicado em 2008

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract

Por Ponnam, Surya Prakash G, Ramesha, Kekunnaya, Tejwani, Sushma, Ramamurthy, Balasubramanya, Kannabiran, Chitra
Publicado em 2007

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract

Por Ponnam, Surya Prakash G, Ramesha, Kekunnaya, Tejwani, Sushma, Ramamurthy, Balasubramanya, Kannabiran, Chitra
Publicado em 2009

Mutational screening of Indian families with hereditary congenital cataract

Por Ponnam, Surya Prakash Goud, Ramesha, Kekkunaya, Matalia, Jyoti, Tejwani, Sushma, Ramamurthy, Balasubramanya, Kannabiran, Chitra
Publicado em 2013

A cataract-causing connexin 50 mutant is mislocalized to the ER due to loss of the fourth transmembrane domain and cytoplasmic domain()

Por Somaraju Chalasani, Madhavi Latha, Muppirala, Madhavi, G. Ponnam, Surya Prakash, Kannabiran, Chitra, Swarup, Ghanshyam
Publicado em 2012

Human βA3/A1-crystallin splicing mutation causes cataracts by activating the unfolded protein response and inducing apoptosis in differentiating lens fiber cells

Por Ma, Zhiwei, Yao, Wenliang, Chan, Chi Chao, Kannabiran, Chitra, Wawrousek, Eric, Hejtmancik, J. Fielding
Publicado no Biochim Biophys Acta (2016)

Immunophenotypes of macular corneal dystrophy in India and correlation with mutations in CHST6

Por Sultana, Afia, Klintworth, Gordon K., Thonar, Eugene J-M.A., Vemuganti, Geeta K., Kannabiran, Chitra
Publicado em 2009

Bilateral granular dystrophy: A clinicopathogenetic correlation after alcohol assisted debridement with phototherapeutic keratectomy

Por Sati, Alok, Ramappa, Muralidhar, Sharma, Neeraja, Chaurasia, Sunita, Vemuganti, Geeta K., Kannabiran, Chitra, Garg, Prashant
Publicado no Med J Armed Forces India (2015)

Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

Por Jiao, Xiaodong, Sultana, Afia, Garg, Prashant, Ramamurthy, Balasubramanya, Vemuganti, Geeta K, Gangopadhyay, Nibaran, Hejtmancik, J Fielding, Kannabiran, Chitra
Publicado em 2007

RB1 gene mutations in retinoblastoma and its clinical correlation

Por Ali, Mohammad Javed, Parsam, Vidya Latha, Honavar, Santosh G., Kannabiran, Chitra, Vemuganti, Geeta K., Reddy, Vijay Anand P.
Publicado em 2010

Premature Truncation of a Novel Protein, RD3, Exhibiting Subnuclear Localization Is Associated with Retinal Degeneration

Por Friedman, James S. , Chang, Bo , Kannabiran, Chitra , Chakarova, Christina , Singh, Hardeep P. , Jalali, Subhadra , Hawes, Norman L. , Branham, Kari , Othman, Mohammad , Filippova, Elena , Thompson, Debra A. , Webster, Andrew R. , Andréasson, Sten , Jacobson, Samuel G. , Bhattacharya, Shomi S. , Heckenlively, John R. , Swaroop, Anand 
Publicado em 2006

Trans-ethnic study confirmed independent associations of HLA-A*02:06 and HLA-B*44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complications

Por Ueta, Mayumi, Kannabiran, Chitra, Wakamatsu, Tais Hitomi, Kim, Mee Kum, Yoon, Kyung-Chul, Seo, Kyoung Yul, Joo, Choun-Ki, Sangwan, Virender, Rathi, Varsha, Basu, Sayan, Shamaila, Almas, Lee, Hyo Seok, Yoon, Sangchul, Sotozono, Chie, Gomes, José Álvaro Pereira, Tokunaga, Katsushi, Kinoshita, Shigeru
Publicado em 2014

NMNAT1 mutations cause Leber congenital amaurosis

Por Falk, Marni J, Zhang, Qi, Nakamaru-Ogiso, Eiko, Kannabiran, Chitra, Fonseca-Kelly, Zoe, Chakarova, Christina, Audo, Isabelle, Mackay, Donna S, Zeitz, Christina, Borman, Arundhati Dev, Staniszewska, Magdalena, Shukla, Rachna, Palavalli, Lakshmi, Mohand-Said, Saddek, Waseem, Naushin H, Jalali, Subhadra, Perin, Juan C, Place, Emily, Ostrovsky, Julian, Xiao, Rui, Bhattacharya, Shomi S, Consugar, Mark, Webster, Andrew R, Sahel, José-Alain, Moore, Anthony T, Berson, Eliot L, Liu, Qin, Gai, Xiaowu, Pierce, Eric A.
Publicado em 2012