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 · 343 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

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

Gert Matthijs, Els Schollen, Cecilia Bjursell et al. · Human Mutation · 2000 · 163 citations

Life Sciences, Genetics, Molecular Genetics +9

Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden

Mohamed Abouelhoda, Nisha Patel, Hanan E. Shamseldin et al. · Genetics in Medicine · 2016 · 111 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

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 · 102 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Variation in DNAH1 may contribute to primary ciliary dyskinesia

Faiqa Imtiaz, Rabab Allam, Khushnooda Ramzan et al. · BMC Medical Genetics · 2015 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16