Yuet‐Ping Yuen - Concepedia

Author

Yuet‐Ping Yuen

Prince of Wales Hospital ORCID

Also Known As

Gao Yuan, Yuet-Ping Yuen, Yuet-ping Liz Yuen, Yuet-ping Yuen, YuetPing Yuen, Yuet‐Ping Yuen

Publications

353

Citations

H-Index

Concepts

All Affiliations

Prince of Wales Hospital Chinese University of Hong Kong Queen Mary Hospital University of Hong Kong Tuen Mun Hospital

About

Yuet‐Ping Yuen is an author at Prince of Wales Hospital specializing in medicine, genetics, and inherited metabolic disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	201
2	Public Health	1	1	37
3	Social Sciences	1	1	22
4	Biochemistry	1	1	19
5	Child Development	1	1	22

Yuet‐Ping Yuen

Publications

299

Citations

H-Index

Page 1

	Year	Citations
Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants Chloe Miu Mak, Ching‐Wan Lam, Nai-chung Fong, Journal of Human Genetics Disease SusceptibilityMolecular VirologyPathogenesisViral PathogenesisGenetic Epidemiology	2011	37
Analysis of inborn errors of metabolism: disease spectrum for expanded newborn screening in Hong Kong. Han‐Chih Hencher Lee, Chloe Miu Mak, Ching‐Wan Lam, PubMed	2011	36
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 mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor Ching‐Wan Lam, Yuet‐Ping Yuen, Chi-Kong Lai, American Journal of Kidney Diseases Chinese PatientUrologyMendelian DisorderKidney TransplantPrimary Hyperoxaluria	2001	23
Non-invasive urinary screening for aromatic l-amino acid decarboxylase deficiency in high-prevalence areas: A pilot study Han‐Chih Hencher Lee, Chi-Kong Lai, Kin-Cheong Eric Yau, Clinica Chimica Acta Pilot StudyUrological ResearchUrologyVoiding DysfunctionInherited Metabolic Disease	2011	22
<i><scp>BRAT</scp>1</i> encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures Ingrid E. Scheffer, Katja Boysen, Amy Schneider, Developmental Medicine & Child Neurology Pediatric HydrocephalusNeurological DisorderGeneticsDisease Gene IdentificationSocial Sciences	2019	22
Novel mutations of the AGXT gene causing primary hyperoxaluria type 1 Yuet‐Ping Yuen, Chi-Kong Lai, Gensy M.W. Tong, Journal of Nephrology	2004	20
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
Molecular basis of von Hippel-Lindau syndrome in Chinese patients. Wai‐Kwan Siu, Ching-Wan Lam, Chloe Miu Mak, PubMed	2011	17
Potential Effects of NPC1L1 Polymorphisms in Protecting against Clinical Disease in a Chinese Family with Sitosterolaemia Miao Hu, Yuet‐Ping Yuen, Jeffrey SS Kwok, Journal of Atherosclerosis and Thrombosis	2014	15

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