The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations

Por Yan, Denise, Kannan-Sundhari, Abhiraami, Vishwanath, Subramanian, Qing, Jie, Mittal, Rahul, Kameswaran, Mohan, Liu, Xue Zhong
Publicado no Genet Test Mol Biomarkers (2015)

PDZD7-MYO7A complex identified in enriched stereocilia membranes

Por Morgan, Clive P, Krey, Jocelyn F, Grati, M'hamed, Zhao, Bo, Fallen, Shannon, Kannan-Sundhari, Abhiraami, Liu, Xue Zhong, Choi, Dongseok, Müller, Ulrich, Barr-Gillespie, Peter G
Publicado no eLife (2016)

MYO3A causes human dominant deafness and interacts with protocadherin 15-CD2 isoform

Por Grati, M’hamed, Yan, Denise, Raval, Manmeet H., Walsh, Tom, Ma, Qi, Chakchouk, Imen, Kannan-Sundhari, Abhiraami, Mittal, Rahul, Masmoudi, Saber, Blanton, Susan H., Tekin, Mustafa, King, Mary-Claire, Yengo, Christopher M., Liu, Xue Zhong
Publicado no Hum Mutat (2016)

Spectrum of DNA variants for nonsyndromic deafness in a large cohort from multiple continents

Por Yan, Denise, Tekin, Demet, Bademci, Guney, Foster, Joseph, Cengiz, F. Basak, Kannan-Sundhari, Abhiraami, Guo, Shengru, Mittal, Rahul, Zou, Bing, Grati, Mhamed, Kabahuma, Rosemary I., Kameswaran, Mohan, Lasisi, Taye J, Adedeji, Waheed A, Lasisi, Akeem O., Menendez, Ibis, Herrera, Marianna, Carranza, Claudia, Maroofian, Reza, Crosby, Andrew H., Bensaid, Mariem, Masmoudi, Saber, Behnam, Mahdiyeh, Mojarrad, Majid, Feng, Yong, Duman, Duygu, Mawla, Alex M., Nord, Alex S., Blanton, Susan H., Liu, Xuezhong, Tekin, Mustafa
Publicado no Hum Genet (2016)