Betty Y.L. Hsu - Concepedia

Author

Betty Y.L. Hsu

Also Known As

B Hsu, B Y Hsu, B. Y. Hsu, B. Y.-L. Hsu, Betty Y L Hsu, Betty Y. L. HSU, Betty Y. L. Hsu, Betty Y.L Hsu, Betty Y.L. HSU, Betty Y.L. Hsu

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Children's Hospital of Philadelphia University of Pennsylvania Philadelphia University Hospital for Sick Children Royal Children's Hospital

About

Betty Y.L. Hsu is an author at Children's Hospital of Philadelphia specializing in medicine, physiology, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	727
2	Biochemistry	6	6	425
3	Health Sciences	4	4	317
4	Natural Sciences	2	2	234
5	Biomolecular Engineering	1	1	14

Betty Y.L. Hsu

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene Charles A. Stanley, Yen K. Lieu, Betty Y.L. Hsu, New England Journal of Medicine	1998	670
Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators. Charles A. Stanley, Jun Fang, K Kutyna, Diabetes Hyperinsulinism/hyperammonemia SyndromeGeneticsMolecular BiologyMolecular GeneticsDisease Gene Identification	2000	171
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome Betty Y.L. Hsu, Andrea Kelly, Paul Thornton, The Journal of Pediatrics Metabolic SyndromeElectrolyte DisorderMetabolic DisorderHyperinsulinism/hyperammonemia SyndromePhysiology	2001	140
Hyperinsulinism/Hyperammonemia Syndrome in Children with Regulatory Mutations in the Inhibitory Guanosine Triphosphate-Binding Domain of Glutamate Dehydrogenase1 Courtney MacMullen, Jie Fang, Betty Y.L. Hsu, The Journal of Clinical Endocrinology & Metabolism	2001	140
Fasting Hypoketotic Coma in a Child with Deficiency of Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Geoffrey N. Thompson, Betty Y.L. Hsu, James Pitt, New England Journal of Medicine Metabolic DisorderPathologyMitochondrial OxidationOxidative StressMetabolic Syndrome	1997	90
Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations Jie Fang, Betty Y.L. Hsu, Courtney MacMullen, Biochemical Journal	2002	79
Effects of a GTP-insensitive Mutation of Glutamate Dehydrogenase on Insulin Secretion in Transgenic Mice* Changhong Li, Andrea Matter, Andrea Kelly, Journal of Biological Chemistry GeneticsInsulin SignalingMetabolic SyndromeGlutamate DehydrogenaseBiochemical Genetics	2006	67
Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency Stephen D. Cederbaum, Samantha Koo-McCoy, Ingrid Tein, Molecular Genetics and Metabolism Inherited Metabolic DiseasePhysiologyPrimary Carnitine DeficiencyMembrane BiologyLong-term Follow	2002	66
Sudden neonatal death in carnitine transporter deficiency Piero Rinaldo, Charles A. Stanley, Betty Y.L. Hsu, The Journal of Pediatrics	1997	63
Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations Jie Fang, Betty Y.L. Hsu, Courtney MacMullen, Biochemical Journal GeneticsMolecular BiologyMolecular GeneticsRedox BiologyOxidative Stress	2002	63

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