Fareeha Zulfiqar

Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene

Qingjiong Zhang, Fareeha Zulfiqar, Xueshan Xiao et al. · Human Genetics · 2007 · 119 citations

Life Sciences, Genetics, Molecular Genetics +9

Mutation spectrum of<i>MYO7A</i>and evaluation of a novel nonsyndromic deafness<i>DFNB2</i>allele with residual function

Saima Riazuddin, Sabiha Nazli, Zubair M. Ahmed et al. · Human Mutation · 2008 · 106 citations

Life Sciences, Genetics, Molecular Genetics +15

Mutations in βB3-Crystallin Associated with Autosomal Recessive Cataract in Two Pakistani Families

Sheikh Riazuddin, Afshan Yasmeen, Wenliang Yao et al. · Investigative Ophthalmology & Visual Science · 2005 · 96 citations

Life Sciences, Genetics, Molecular Genetics +14

Mutation of ATF6 causes autosomal recessive achromatopsia

Muhammad Ansar, Regie Lyn P. Santos‐Cortez, Muhammad Arif Nadeem Saqib et al. · Human Genetics · 2015 · 84 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family

Mounira Hmani‐Aifa, Z. Benzina, Fareeha Zulfiqar et al. · European Journal of Human Genetics · 2008 · 62 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6