Ali Amar

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract

Amelie T. van der Ven, Dervla M. Connaughton, Hadas Ityel et al. · Journal of the American Society of Nephrology · 2018 · 202 citations

In silico analysis of SIGMAR1 variant (rs4879809) segregating in a consanguineous Pakistani family showing amyotrophic lateral sclerosis without frontotemporal lobar dementia

Muhammad Ikram Ullah, Arsalan Ahmad, Syed Irfan Raza et al. · Neurogenetics · 2015 · 43 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Silico Analysis +12

Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis

Ali Amar, Amar J. Majmundar, Ihsan Ullah et al. · Human Genetics · 2019 · 43 citations · Full text

TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic Syndrome

Lina L. Kampf, Ronen Schneider, Lea Gerstner et al. · Journal of the American Society of Nephrology · 2019 · 41 citations · Full text

Association of FcγRIIa Polymorphism with Clinical Outcome of Dengue Infection: First Insight from Pakistan

Saima Naz Mohsin, Saqib Mahmood, Ali Amar et al. · American Journal of Tropical Medicine and Hygiene · 2015 · 35 citations · Full text