Asuri N. Prasad

Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder

Ajay P. Sharma, Cheryl R. Greenberg, Asuri N. Prasad et al. · Pediatric Nephrology · 2007 · 111 citations

Medicine, Inherited Metabolic Disease, Hematology +2

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype

Chitra Prasad, Asuri N. Prasad, Bernard N. Chodirker et al. · Clinical Genetics · 2000 · 100 citations

Outcome of the First 3-Years of a DNA-Based Neonatal Screening Program for Glutaric Acidemia Type 1 in Manitoba and Northwestern Ontario, Canada

Cheryl R. Greenberg, Asuri N. Prasad, Louise A. Dilling et al. · Molecular Genetics and Metabolism · 2002 · 78 citations

Newborn Screening, Neonatology, First 3-Years +6

Heterozygous De Novo UBTF Gain-of-Function Variant Is Associated with Neurodegeneration in Childhood

Simon Edvardson, Claudia M. Nicolae, Pankaj B. Agrawal et al. · The American Journal of Human Genetics · 2017 · 53 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +7

Hepatic Carnitine Palmitoyl Transferase 1 (CPT1 A) Deficiency in North American Hutterites (Canadian and American): Evidence for a Founder Effect and Results of a Pilot Study on a DNA-Based Newborn Screening Program

C. Prasad, John P. Johnson, Jean‐Paul Bonnefont et al. · Molecular Genetics and Metabolism · 2001 · 50 citations

Genetic Testing, Hepatology, Cpt1 A +9