Medhat Naim

PKD1 Duplicated regions limit clinical Utility of Whole Exome Sequencing for Genetic Diagnosis of Autosomal Dominant Polycystic Kidney Disease

Hamad Ali, Fahd Al‐Mulla, Naser Hussain et al. · Scientific Reports · 2019 · 82 citations · Full text

Medicine, Molecular Genetics, Nephrology +17

A novel PKD1 variant demonstrates a disease-modifying role in trans with a truncating PKD1 mutation in patients with Autosomal Dominant Polycystic Kidney Disease

Hamad Ali, Naser Hussain, Medhat Naim et al. · BMC Nephrology · 2015 · 32 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Global analysis of urinary extracellular vesicle small RNAs in autosomal dominant polycystic kidney disease

Hamad Ali, Md. Zubbair Malik, Mohamed Abu‐Farha et al. · The Journal of Gene Medicine · 2024 · 22 citations · Full text

Medicine, Molecular Biology, Nephrology +17

The genetic landscape of autosomal dominant polycystic kidney disease in Kuwait

Hamad Ali, Medhat Naim, Sarah R. Senum et al. · Clinical Kidney Journal · 2022 · 13 citations · Full text

Medicine, Genetics, Molecular Genetics +16