Ahmed N. Mohammad

Type 1 sialidosis presenting with ataxia, seizures and myoclonus with no visual involvement

Ahmed N. Mohammad, Katelyn A. Bruno, Stacy M. Hines et al. · Molecular Genetics and Metabolism Reports · 2018 · 22 citations · Full text

Protein molecular modeling techniques investigating novel <i><scp>TAB</scp>2</i> variant R347X causing cardiomyopathy and congenital heart defects in multigenerational family

Thomas R. Caulfield, John E. Richter, Emily Brown et al. · Molecular Genetics & Genomic Medicine · 2018 · 21 citations · Full text

Protein informatics combined with multiple data sources enriches the clinical characterization of novel <i><scp>TRPV</scp>4</i> variant causing an intermediate skeletal dysplasia

Stephanie L. Hines, John E. Richter, Ahmed N. Mohammad et al. · Molecular Genetics & Genomic Medicine · 2019 · 12 citations · Full text

Integrative data fusion for comprehensive assessment of a novel <i>CHEK2</i> variant using combined genomics, imaging, and functional–structural assessments <i>via</i> protein informatics

Stephanie L. Hines, Ahmed N. Mohammad, Jessica L. Jackson et al. · Molecular Omics · 2018 · 10 citations

Combined Genomics, Engineering, Molecular Biology +18