Iram Anjum

Comprehensive Mutational Screening in a Cohort of Danish Families with Hereditary Congenital Cataract

Lars Hestbjerg Hansen, Annemette Mikkelsen, Peter Nu ̈rnberg et al. · Investigative Ophthalmology & Visual Science · 2009 · 106 citations · Full text

Life Sciences, Genetics, Ophthalmology +14

Genetic heterogeneity in Pakistani microcephaly families

Muhammad Sajid Hussain, Syeda Marriam Bakhtiar, Muhammad Farooq et al. · Clinical Genetics · 2012 · 54 citations

Life Sciences, Genetics, Molecular Genetics +14

Effect of UV Irradiation (A and C) on Casuarina equisetifolia-Mediated Biosynthesis and Characterization of Antimicrobial and Anticancer Activity of Biocompatible Zinc Oxide Nanoparticles

Amna Komal Khan, Sullivan Renouard, Samantha Drouet et al. · Pharmaceutics · 2021 · 43 citations · Full text

Life Sciences, Botany, Plant Sciences +16

An update of pathogenic variants in <i>ASPM</i>, <i>WDR62, CDK5RAP2</i>,<i> STIL, CENPJ,</i> and<i> CEP135</i> underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

Sajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia et al. · Molecular Genetics & Genomic Medicine · 2020 · 35 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family.

Iram Anjum, Hans Eiberg, Shahid Mahmood Baig et al. · PubMed · 2010 · 26 citations

Medicine, Genetics, Ophthalmology +17