Bing-Zhi Yang

Los Angeles County Department of Health Services — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

14h-index605citations19works0.02yr avg
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Research Topics

Metabolism and Genetic Disorders(12), Glycogen Storage Diseases and Myoclonus(5), Mitochondrial Function and Pathology(4), Peroxisome Proliferator-Activated Receptors(4), Genetics and Neurodevelopmental Disorders(3)

Publications19 total

Tunnel Lining Design for a Strike Slip Fault Rupture on Westside Purple Line Extension Project–Section 2
Lifelines 2022·2022· 2 cited
Investigation of the clinical features and therapeutic methods for the management of inflammatory lacrimal punctum diseases
Tropical Journal of Pharmaceutical Research·2017· 1 citedOpen Access
Elevated CSF <i>N</i> -acetylaspartylglutamate in patients with free sialic acid storage diseases
Neurology·2010· 24 citedOpen Access
Free sialic acid storage disease without sialuria
Annals of Neurology·2009· 22 citedOpen Access
Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA)
Brain·2009· 42 citedOpen Access
Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts
Molecular Genetics and Metabolism·2005· 32 cited
Characterization of the bidirectional promoter region between the human genes encoding VLCAD and PSD-95
Genomics·2003· 20 cited
Carnitine/Acylcarnitine Translocase Deficiency (Neonatal Phenotype): Successful Prenatal and Postmortem Diagnosis Associated with a Novel Mutation in a Single Family
Molecular Genetics and Metabolism·2001· 36 cited
Identification of a Novel Mutation in Patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency
Molecular Genetics and Metabolism·2000· 15 cited
Identification of Two Novel Mutations in the Hypoglycemic Phenotype of Very Long Chain Acyl-CoA Dehydrogenase Deficiency
Biochemical and Biophysical Research Communications·1999· 7 cited
Identification of Four Novel Mutations in Patients with Carnitine Palmitoyltransferase II (CPT II) Deficiency
Molecular Genetics and Metabolism·1998· 28 cited
A Novel Mutation Identified in Carnitine Palmitoyltransferase II Deficiency
Molecular Genetics and Metabolism·1998· 26 cited
Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe disease
Human Molecular Genetics·1998· 139 citedOpen Access
Improved Detection of the G1528C Mutation in LCHAD Deficiency
Biochemical and Molecular Medicine·1996· 10 cited
LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY: THE MAJOR DISEASE-CAUSING MUTATION AND DIAGNOSIS. 851
Pediatric Research·1996Open Access
Assignment of the human glycogen debrancher gene to chromosome 1p21
Genomics·1992· 71 cited
Molecular cloning and nucleotide sequence of cDNA encoding human muscle glycogen debranching enzyme.
Journal of Biological Chemistry·1992· 89 citedOpen Access
Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.
PubMed·1992· 14 cited
Definitive prenatal diagnosis for type III glycogen storage disease.
PubMed·1990· 27 cited

Frequent Co-authors

Jia-Huan Ding(11), Charles R. Roe(10), Diane S. Roe(5), Fanny Mochel(3), Udo F. H. Engelke(3), Julie Barritault(3), Raphael Schiffmann(3), Ron A. Wevers(3), Adeline Vanderver(2), David R. Adams(2), Christine R. Kaneski(2), F.W. Verheijen(2), Marjan Huizing(2), M. Brivet(2), Lawrence Sweetman(2), Tracy Dewese(2), Guocheng He(2), Jeff Wilkinson(2), Donald W. Day(2), Nathan H. McNeill(2)