Concepedia

Author

Bing-Zhi Yang

Baylor University Medical Center

Also Known As

B Z Yang, B. Yang, B. Z. Yang, B.Z. Yang, Bing-Zhi Yang, Bingzhi Yang

19

Publications

605

Citations

14

H-Index

39

Concepts

All Affiliations

Baylor University Medical CenterDuke Medical CenterInsermDuke University HospitalRadboud University Nijmegen
BY

About

Bing-Zhi Yang is an author at Baylor University Medical Center specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

10

10

349

2

Natural Sciences

2

2

160

3

Biochemistry

2

2

121

4

Health Sciences

1

1

32

5

Cell Biology

1

1

20

Bing-Zhi Yang

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15

Publications

595

Citations

14

H-Index

YearCitations

Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe disease

A. G. A. Bijvoet, Esther H. M. van de Kamp, Marian A. Kroos,

Human Molecular Genetics

1998

139

Molecular cloning and nucleotide sequence of cDNA encoding human muscle glycogen debranching enzyme.

Bing-Zhi Yang, J.H. Ding, Jan J. Enghild,

Journal of Biological Chemistry

1992

89

Assignment of the human glycogen debrancher gene to chromosome 1p21

Teresa L. Yang‐Feng, Keqin Zheng, Jingwei Yu,

Genomics

1992

71

Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA)

Fanny Mochel, F. Sedel, Adeline Vanderver,

Brain

2009

42

Carnitine/Acylcarnitine Translocase Deficiency (Neonatal Phenotype): Successful Prenatal and Postmortem Diagnosis Associated with a Novel Mutation in a Single Family

Bing-Zhi Yang, Jason M. Mallory, Diane S. Roe,

Molecular Genetics and Metabolism

2001

36

Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts

Diane S. Roe, Bing-Zhi Yang, Christine Vianey‐Saban,

Molecular Genetics and Metabolism

2005

32

Identification of Four Novel Mutations in Patients with Carnitine Palmitoyltransferase II (CPT II) Deficiency

Bing-Zhi Yang, Jia-Huan Ding, Tracy Dewese,

Molecular Genetics and Metabolism

1998

28

Definitive prenatal diagnosis for type III glycogen storage disease.

Bing-Zhi Yang, Jia-Huan Ding, Benjamin Brown,

PubMed

1990

27

A Novel Mutation Identified in Carnitine Palmitoyltransferase II Deficiency

Bing-Zhi Yang, Jia-Huan Ding, Diane S. Roe,

Molecular Genetics and Metabolism

1998

26

Elevated CSF <i>N</i> -acetylaspartylglutamate in patients with free sialic acid storage diseases

Fanny Mochel, Udo F. H. Engelke, Julie Barritault,

Neurology

2010

24

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