Ghazanfar Ali

Publications by Year

Research Areas

Skin and Cellular Biology Research, Hair Growth and Disorders, Genetics and Neurodevelopmental Disorders, RNA regulation and disease, Wnt/β-catenin signaling in development and cancer

Most-Cited Works

• → Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability(2012)229 cited
• → Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39(2009)120 cited
• → Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability(2011)88 cited
• → Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non‐syndromic hearing impairment(2004)78 cited
• → Green synthesis and characterization of tin dioxide nanoparticles for photocatalytic and antimicrobial studies(2020)75 cited
• → Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment(2010)71 cited
• → Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability(2014)71 cited
• → A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis(2007)70 cited
• → Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene(2006)60 cited
• → Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability(2018)58 cited