Keri Boyette

Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease

Priya S. Kishnani, Tzu‐Po Chuang, Deeksha Bali et al. · Human Molecular Genetics · 2009 · 70 citations

Life Sciences, Genetics, Molecular Genetics +17

Identification of differentially expressed microRNAs in human hepatocellular adenoma associated with type I glycogen storage disease: a potential utility as biomarkers

Li-Ya Chiu, Priya S. Kishnani, Tzu‐Po Chuang et al. · Journal of Gastroenterology · 2013 · 51 citations

Life Sciences, Molecular Biology, Molecular Medicine +16

Molecular analysis of the AGL gene: Identification of 25 novel mutations and evidence of genetic heterogeneity in patients with Glycogen Storage Disease Type III

Jennifer Goldstein, Stephanie Austin, Keri Boyette et al. · Genetics in Medicine · 2010 · 51 citations

Life Sciences, Genetics, Molecular Genetics +10

Echocardiographic manifestations of Glycogen Storage Disease III: Increase in wall thickness and left ventricular mass over time

Shawyntee M. Vertilus, Stephanie Austin, Kimberly S. Foster et al. · Genetics in Medicine · 2010 · 49 citations · Full text

Medicine, Cardiology, Internal Medicine +12

Common mutation in the PHKA2 gene with variable phenotype in patients with liver phosphorylase b kinase deficiency

Samira Achouitar, Jennifer Goldstein, Miski Mohamed et al. · Molecular Genetics and Metabolism · 2011 · 23 citations

Life Sciences, Genetics, Molecular Genetics +13