Ghazanfar Ali

Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor et al. · The American Journal of Human Genetics · 2012 · 228 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

Julie M. Schultz, Shaheen N. Khan, Zubair M. Ahmed et al. · The American Journal of Human Genetics · 2009 · 120 citations · Full text

Genetics, Audiology, Pathology +9

Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

Muhammad Rafiq, Andreas W. Kuß, Lucia Puettmann et al. · The American Journal of Human Genetics · 2011 · 88 citations · Full text

Genome Instability, Mendelian Disorder, Alpha 1,2-Mannosidase Gene +7

Low prevalence of Connexin 26 (<i>GJB2</i>) variants in Pakistani families with autosomal recessive non‐syndromic hearing impairment

RLP Santos, Muhammad Wajid, TL Pham et al. · Clinical Genetics · 2004 · 78 citations · Full text

Green synthesis and characterization of tin dioxide nanoparticles for photocatalytic and antimicrobial studies

Sirajul Haq, Wajid Rehman, Muhammad Waseem et al. · Materials Research Express · 2020 · 75 citations · Full text

Engineering, Metal Nanoparticles, Inorganic Photochemistry +18