Anna Wai-Fun Cheng - Concepedia

Author

Anna Wai-Fun Cheng

Chinese University of Hong Kong ORCID

Also Known As

A Cheng, A. Cheng, Anna Cheng, Anna W. F. Cheng, Anna Wai Fun Cheng, Anna Wai-Fun Cheng, Wai-Fun Cheng

Publications

629

Citations

H-Index

Concepts

All Affiliations

Chinese University of Hong Kong Prince of Wales Hospital University of Cambridge

About

Anna Wai-Fun Cheng is an author at Chinese University of Hong Kong specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	86
2	Molecular Biology	2	2	42
3	Biochemistry	1	1	19
4	Biology	1	1	25
5	Microbiology	1	1	19

Anna Wai-Fun Cheng

Publications

518

Citations

H-Index

Page 1

	Year	Citations
Phenotypic Features, Androgen Receptor Binding, and Mutational Analysis in 278 Clinical Cases Reported as Androgen Insensitivity Syndrome<sup>1</sup> S. Faisal Ahmed, Anna Wai-Fun Cheng, L. Dovey, The Journal of Clinical Endocrinology & Metabolism	2000	315
Assessment of the gonadotrophin-gonadal axis in androgen insensitivity syndrome S. Faisal Ahmed, Anna Wai-Fun Cheng, Ieuan A. Hughes Archives of Disease in Childhood	1999	117
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome Ching‐Wan Lam, Yuet‐Ping Yuen, Anna Wai-Fun Cheng, Clinica Chimica Acta Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseMissense Mutation Leu72pro	2005	29
Novel Donor Splice Site Mutation of ABCG5 Gene in Sitosterolemia Ching‐Wan Lam, Anna Wai-Fun Cheng, Sui-Fan Tong, Molecular Genetics and Metabolism BiologyGenetic DisorderGeneticsMolecular GeneticsGenomics	2002	25
DNA-Based Diagnosis of Isolated Sulfite Oxidase Deficiency by Denaturing High-Performance Liquid Chromatography Ching‐Wan Lam, Chi Kong Li, Chi-Kong Lai, Molecular Genetics and Metabolism BiochemistryDna-based DiagnosisHigh-performance Liquid ChromatographyBioanalysisAnalytical Chemistry	2002	19
Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b Yuet‐Ping Yuen, Anna Wai-Fun Cheng, Sui-Fan Tong, Molecular Genetics and Metabolism G6pt1 GeneMendelian DisorderGenetic DisorderMedicineGenetics	2002	13

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