Faiqa Imtiaz

Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture

Nabil Enattah, Tine G.K. Jensen, Mette Ødegaard Nielsen et al. · The American Journal of Human Genetics · 2008 · 336 citations · Full text

Biology, Independent Introduction, Medicine +11

Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)

Gert Matthijs, Els Schollen, Cecilia Bjursell et al. · Human Mutation · 2000 · 159 citations

Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden

Mohamed Abouelhoda, Turki M. Sobahy, Mohamed El-Kalioby et al. · Genetics in Medicine · 2016 · 106 citations · Full text

Global Health, Genetics, Genetic Epidemiology +10

The T/G−13915 variant upstream of the lactase gene ( <i>LCT</i> ) is the founder allele of lactase persistence in an urban Saudi population

Faiqa Imtiaz, Erkki Savilahti, Annikki Sarnesto et al. · Journal of Medical Genetics · 2007 · 101 citations · Full text

Variation in DNAH1 may contribute to primary ciliary dyskinesia

Faiqa Imtiaz, Rabab Allam, Khushnooda Ramzan et al. · BMC Medical Genetics · 2015 · 84 citations · Full text