| Alterations of the CIB2 calcium-and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48 S Riazuddin, IA Belyantseva, APJ Giese, K Lee, AA Indzhykulian, ... Nature genetics 44 (11), 1265-1271, 2012 | 255 | 2012 |
| Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42 G Borck, AU Rehman, K Lee, HM Pogoda, N Kakar, S Von Ameln, ... The American Journal of Human Genetics 88 (2), 127-137, 2011 | 130 | 2011 |
| Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome ZM Ahmed, S Riazuddin, S Aye, RA Ali, H Venselaar, S Anwar, ... Human genetics 124, 215-223, 2008 | 108 | 2008 |
| Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86 AU Rehman, RLP Santos-Cortez, RJ Morell, MC Drummond, T Ito, K Lee, ... The American Journal of Human Genetics 94 (1), 144-152, 2014 | 96 | 2014 |
| Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p AU Rehman, K Gul, RJ Morell, K Lee, ZM Ahmed, S Riazuddin, RA Ali, ... Human genetics 130, 759-765, 2011 | 55 | 2011 |
| Autosomal-recessive hearing impairment due to rare missense variants within S1PR2 RLP Santos-Cortez, R Faridi, AU Rehman, K Lee, M Ansar, X Wang, ... The American Journal of Human Genetics 98 (2), 331-338, 2016 | 52 | 2016 |
| Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q MH Raza, R Amjad, S Riazuddin, D Drayna Human genetics 131, 311-313, 2012 | 24 | 2012 |
| Genetic variants of ADAM33 are associated with asthma susceptibility in the Punjabi population of Pakistan MF Sabar, MU Ghani, M Shahid, A Sumrin, A Ali, M Akram, MA Tariq, ... Journal of Asthma 53 (4), 341-348, 2016 | 23 | 2016 |
| University of Washington Center for Mendelian G AU Rehman, RL Santos-Cortez, RJ Morell, MC Drummond, T Ito, K Lee, ... Nickerson DA, Shendure J, Bamshad M, Riazuddin S, Billington N, Khan SN …, 2014 | 18 | 2014 |
| DFNB86, a novel autosomal recessive nonsyndromic deafness locus on chromosome 16p13. 3 RA Ali, AU Rehman, SN Khan, T Husnain, S Riazuddin, TB Friedman, ... Clinical genetics 81 (5), 498, 2012 | 13 | 2012 |
| BREAKTHROUGHS IN DISEASE PREVENTION AND TREATMENT M RAMEEZ, AU KHAN, R Ali CURRENT STUDIES IN HEALTH AND LIFE SCIENCES, 431, 2023 | | 2023 |
| Epigenetic and Genetic Factors Involved in Disease Diagnosis and Prognosis J Naveed, RA Ali, A Manan, SS Ali Pakistan J. Mol. Med 2 (2), 109-122, 2015 | | 2015 |
| Mesenchymal Stem Cells as a Potential Therapy for Cardiovascular Diseases: A Mini-review S Kalsoom, M Aslam, S Khurshid, RA Ali, R Gul Pakistan J. Mol. Med 2 (1), 39-47, 2015 | | 2015 |
| GENETIC BASIS OF SOUND TRANSDUCTION RA ALI University of the Punjab, Lahore, Pakistan, 2010 | | 2010 |
| Biologically active peptides from Aspergillus flavipes R Ali, KA Khan, A Ghaffar, ZH Zaidi Pakistan Journal of Scientific and Industrial Research (Pakistan) 30 (2), 1987 | | 1987 |
Thomas B. FriedmanNIDCD?NIHVerified email at nidcd.nih.gov
