| 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 |
| Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families R Harripaul, N Vasli, A Mikhailov, MA Rafiq, K Mittal, C Windpassinger, ... Molecular psychiatry 23 (4), 973-984, 2018 | 175 | 2018 |
| 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 |
| A homozygous nonsense mutation in the human desmocollin-3 (DSC3) gene underlies hereditary hypotrichosis and recurrent skin vesicles M Ayub, S Basit, M Jelani, FU Rehman, M Iqbal, M Yasinzai, W Ahmad The American Journal of Human Genetics 85 (4), 515-520, 2009 | 95 | 2009 |
| 2. Antioxidants, its role in preventing free radicals and infectious diseases in human body M Suleman, A Khan, A Baqi, MS Kakar, M Ayub Pure and Applied Biology (PAB) 8 (1), 380-388, 2019 | 60 | 2019 |
| Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3) Z Azeem, M Jelani, G Naz, M Tariq, N Wasif, S Kamran-ul-Hassan Naqvi, ... Human genetics 123, 515-519, 2008 | 52 | 2008 |
| Genetics of human hereditary hearing impairment R Meena, M Ayub Journal of Ayub Medical College Abbottabad 29 (4), 671-676, 2017 | 40 | 2017 |
| Mutation Analysis of the ASPM Gene in 18 Pakistani Families With Autosomal Recessive Primary Microcephaly R Kousar, H Nawaz, M Khurshid, G Ali, SU Khan, H Mir, M Ayub, A Wali, ... Journal of child neurology 25 (6), 715-720, 2010 | 34 | 2010 |
| In vitro anticancer MCF-7, anti-inflammatory, and brine shrimp lethality assay (BSLA) and GC-MS analysis of whole plant butanol fraction of Rheum ribes (WBFRR) JK Achakzai, M Anwar Panezai, MA Kakar, AM Kakar, S Kakar, J Khan, ... BioMed research international 2019, 2019 | 31 | 2019 |
| Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families M Tariq, M Ayub, M Jelani, S Basit, G Naz, N Wasif, SI Raza, AK Naveed, ... British Journal of Dermatology 160 (5), 1006-1010, 2009 | 30 | 2009 |
| Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14. 11–q21. 32 A Wali, MS Chishti, M Ayub, M Yasinzai, Kafaitullah, G Ali, P John, ... Clinical genetics 72 (1), 23-29, 2007 | 30 | 2007 |
| Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan S Khan, R Habib, H Mir, G Naz, M Ayub, S Shafique, T Yamin, N Ali, ... Clinical and experimental dermatology 36 (6), 652-654, 2011 | 24 | 2011 |
| A novel 4-bp insertion mutation in EDA1 gene in a Pakistani family with X-linked hypohidrotic ectodermal dysplasia M Tariq, N Wasif, M Ayub, W Ahmad European Journal of Dermatology 17 (3), 209-212, 2007 | 20 | 2007 |
| A novel missense mutation in the ectodysplasin‐A (EDA) gene underlies X‐linked recessive nonsyndromic hypodontia M Ayub, F Ur‐Rehman, M Yasinzai, W Ahmad International journal of dermatology 49 (12), 1399-1402, 2010 | 19 | 2010 |
| 1. Phytochemicals and their role in curing fatal diseases: a review A Khan, M Suleman, S Abdul Baqi, M Ayub Pure and Applied Biology (PAB) 8 (1), 343-354, 2019 | 18 | 2019 |
| 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 |
| Biological screening of Hedera nepalensis B Ahmad, N Munir, S Bashir, S Azam, I Khan, M Ayub Journal of Medicinal Plants Research 6 (39), 5250-5257, 2012 | 15 | 2012 |
| Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families Z Azeem, N Wasif, S Basit, S Razak, RA Waheed, A Islam, M Ayub, ... The Journal of dermatology 38 (8), 755-760, 2011 | 14 | 2011 |
| Thalassemia patients from baluchistan in Pakistan are infected with multiple hepatitis B or C virus strains S Ahmed, M Ayub, M Naeem, FH Nazir, A Hussain, D Ghilzai, LO Magnius, ... The American journal of tropical medicine and hygiene 104 (4), 1569, 2021 | 13 | 2021 |
| Mutations in the lipase‐H gene causing autosomal recessive hypotrichosis and woolly hair S Mehmood, A Jan, D Muhammad, F Ahmad, H Mir, M Younus, G Ali, ... Australasian Journal of Dermatology 56 (3), e66-e70, 2015 | 13 | 2015 |
Sulman BasitAssistant Professor at the Department of Biochemistry and Molecular Medicine, College of MedicineVerified email at taibahu.edu.sa
