Bonnie Anne Salbert

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

Santhosh Girirajan, Jill A. Rosenfeld, Gregory M. Cooper et al. · Nature Genetics · 2010 · 669 citations · Full text

Developmental Biology, Two-hit Model, Genetics +8

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

Daniel Moreno‐De‐Luca, Jennifer G. Mullé, Erin B. Kaminsky et al. · The American Journal of Human Genetics · 2010 · 331 citations · Full text

Characteristics and outcomes of cardiomyopathy in children with Duchenne or Becker muscular dystrophy: A comparative study from the Pediatric Cardiomyopathy Registry

David Connuck, Lynn A. Sleeper, Steven D. Colan et al. · American Heart Journal · 2008 · 228 citations · Full text

Cardiomyopathy, Pediatric Heart Disease, Becker Muscular Dystrophy +6

Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: A study from the Pediatric Cardiomyopathy Registry

James D. Wilkinson, April M. Lowe, Bonnie Anne Salbert et al. · American Heart Journal · 2012 · 182 citations

Cardiomyopathy, Heart Failure, Cardiovascular Disease +7

Characterization of seizures associated with biotinidase deficiency

Bonnie Anne Salbert, John M. Pellock, Barry Wolf · Neurology · 1993 · 72 citations

Electrolyte Disorder, Molecular Neuroscience, Neurophysiology +12