Nasim Bekheirnia

Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene

Mir Reza Bekheirnia, Nasim Bekheirnia, Matthew N. Bainbridge et al. · Genetics in Medicine · 2016 · 99 citations · Full text

Medicine, Genetics, Molecular Genetics +17

DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

Alexandria T.M. Blackburn, Nasim Bekheirnia, Vanessa C. Uma et al. · Genetics in Medicine · 2019 · 37 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Characterization of the renal phenotype in <i>RMND1</i>‐related mitochondrial disease

Brian J. Shayota, Nhon T. Le, Nasim Bekheirnia et al. · Molecular Genetics & Genomic Medicine · 2019 · 19 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

Maimuna Sali Paul, Sydney L. Michener, Hongling Pan et al. · The American Journal of Human Genetics · 2024 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract Diseases

Nasim Bekheirnia, Kevin E. Glinton, Linda Rossetti et al. · Kidney360 · 2020 · 12 citations · Full text

Medicine, Genetics, Nephrology +17