Foot-and-mouth disease: overview of motives of disease spread and efficacy of available vaccines

Por Saeed, Ali, Kanwal, Sehrish, Arshad, Memoona, Ali, Muhammad, Shaikh, Rehan Sadiq, Abubakar, Muhammad
Publicado no J Anim Sci Technol (2015)

A New Locus for Nonsyndromic Deafness DFNB51 Maps to Chromosome 11p13-p12

Por Shaikh, Rehan Sadiq, Ramzan, Khushnooda, Nazli, Sabiha, Sattar, Sameera, Khan, Shaheen N., Riazuddin, Saima, Ahmed, Zubair M., Friedman, Thomas B., Riazuddin, Sheikh
Publicado em 2005

Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy

Por Shaikh, Rehan S, Reuter, Peggy, Sisk, Robert A, Kausar, Tasleem, Shahzad, Mohsin, Maqsood, Muhammad I, Yousif, Ateeq, Ali, Muhammad, Riazuddin, Saima, Wissinger, Bernd, Ahmed, Zubair M
Publicado no Eur J Hum Genet (2015)

Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani population

Por Yousaf, Sairah, Shahzad, Mohsin, Tasleem, Kausar, Sheikh, Shakeel A., Tariq, Nabeela, Shabbir, Asra S., Ali, Muhammad, Waryah, Ali M., Shaikh, Rehan S., Riazuddin, Saima, Ahmed, Zubair M.
Publicado no Pigment Cell Melanoma Res (2015)

Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population

Por Jaworek, Thomas J, Kausar, Tasleem, Bell, Shannon M, Tariq, Nabeela, Maqsood, Muhammad Imran, Sohail, Asma, Ali, Muhmmmad, Iqbal, Furhan, Rasool, Shafqat, Riazuddin, Saima, Shaikh, Rehan S, Ahmed, Zubair M
Publicado em 2012

Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population

Por Shahzad, Mohsin, Yousaf, Sairah, Waryah, Yar M., Gul, Hadia, Kausar, Tasleem, Tariq, Nabeela, Mahmood, Umair, Ali, Muhammad, Khan, Muzammil A., Waryah, Ali M., Shaikh, Rehan S., Riazuddin, Saima, Ahmed, Zubair M.
Publicado no Sci Rep (2017)

Identification and functional characterization of natural human melanocortin 1 receptor (MC1R) mutant alleles in Pakistani population

Por Shahzad, Mohsin, Sires Campos, Julia, Tariq, Nabeela, Herraiz Serrano, Cecilia, Yousaf, Rizwan, Jiménez-Cervantes, Celia, Yousaf, Sairah, Waryah, Yar M., Dad, Haseeb A., Blue, Elizabeth M., Sobreira, Nara, López-Giráldez, Francesc, Kausar, Tasleem, Ali, Muhammad, Waryah, Ali M., Riazuddin, Saima, Shaikh, Rehan S., García-Borrón, José Carlos, Ahmed, Zubair M.
Publicado no Pigment Cell Melanoma Res (2015)

Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

Por Borck, Guntram, Rehman, Atteeq Ur, Lee, Kwanghyuk, Pogoda, Hans-Martin, Kakar, Naseebullah, von Ameln, Simon, Grillet, Nicolas, Hildebrand, Michael S., Ahmed, Zubair M., Nürnberg, Gudrun, Ansar, Muhammad, Basit, Sulman, Javed, Qamar, Morell, Robert J., Nasreen, Nabilah, Shearer, A. Eliot, Ahmad, Adeel, Kahrizi, Kimia, Shaikh, Rehan S., Ali, Rana A., Khan, Shaheen N., Goebel, Ingrid, Meyer, Nicole C., Kimberling, William J., Webster, Jennifer A., Stephan, Dietrich A., Schiller, Martin R., Bahlo, Melanie, Najmabadi, Hossein, Gillespie, Peter G., Nürnberg, Peter, Wollnik, Bernd, Riazuddin, Saima, Smith, Richard J.H., Ahmad, Wasim, Müller, Ulrich, Hammerschmidt, Matthias, Friedman, Thomas B., Riazuddin, Sheikh, Leal, Suzanne M., Ahmad, Jamil, Kubisch, Christian
Publicado em 2011