Yan-Wo Chan

552 total citations
21 papers, 264 citations indexed

About

Yan-Wo Chan is a scholar working on Molecular Biology, Rheumatology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Yan-Wo Chan has authored 21 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Rheumatology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Yan-Wo Chan's work include Porphyrin Metabolism and Disorders (7 papers), Metabolism and Genetic Disorders (4 papers) and Heme Oxygenase-1 and Carbon Monoxide (3 papers). Yan-Wo Chan is often cited by papers focused on Porphyrin Metabolism and Disorders (7 papers), Metabolism and Genetic Disorders (4 papers) and Heme Oxygenase-1 and Carbon Monoxide (3 papers). Yan-Wo Chan collaborates with scholars based in Hong Kong, China and United States. Yan-Wo Chan's co-authors include Sui-Fan Tong, Ching‐Wan Lam, Chi-Kong Lai, Anna Wai-Fun Cheng, Ching‐Wan Lam, Wing‐Tat Poon, Chloe Miu Mak, Han‐Chih Hencher Lee, Chi‐Chung Shek and Gensy M.W. Tong and has published in prestigious journals such as Kidney International, Clinical Chemistry and American Journal of Kidney Diseases.

In The Last Decade

Yan-Wo Chan

21 papers receiving 259 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Yan-Wo Chan Hong Kong 13 115 48 47 45 40 21 264
Núria Matías Spain 8 233 2.0× 46 1.0× 48 1.0× 14 0.3× 14 0.3× 12 562
Oates Ja United States 12 114 1.0× 41 0.9× 16 0.3× 52 1.2× 21 0.5× 30 449
H. Niederhoff Germany 10 135 1.2× 25 0.5× 118 2.5× 21 0.5× 26 0.7× 44 304
Jinfei Yang China 13 206 1.8× 8 0.2× 39 0.8× 39 0.9× 25 0.6× 26 462
Yunfei Yan China 5 95 0.8× 13 0.3× 84 1.8× 101 2.2× 17 0.4× 10 345
M. Szczepanska-Konkel United States 10 191 1.7× 48 1.0× 24 0.5× 54 1.2× 52 1.3× 16 406
Hua-feng Liu China 12 136 1.2× 19 0.4× 22 0.5× 21 0.5× 10 0.3× 22 338
İlhan Yaylım Türkiye 13 173 1.5× 40 0.8× 10 0.2× 44 1.0× 29 0.7× 59 438
Susana Núñez Spain 9 188 1.6× 17 0.4× 28 0.6× 12 0.3× 9 0.2× 17 481
Xiujin Shen China 10 246 2.1× 9 0.2× 32 0.7× 56 1.2× 16 0.4× 17 419

Countries citing papers authored by Yan-Wo Chan

Since Specialization
Citations

This map shows the geographic impact of Yan-Wo Chan's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Yan-Wo Chan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yan-Wo Chan more than expected).

Fields of papers citing papers by Yan-Wo Chan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yan-Wo Chan. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Yan-Wo Chan. The network helps show where Yan-Wo Chan may publish in the future.

Co-authorship network of co-authors of Yan-Wo Chan

This figure shows the co-authorship network connecting the top 25 collaborators of Yan-Wo Chan. A scholar is included among the top collaborators of Yan-Wo Chan based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Yan-Wo Chan. Yan-Wo Chan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Mak, Chloe Miu, et al.. (2011). Young-Onset Parkinsonism in a Hong Kong Chinese Man With Adult-Onset Hallervorden–Spatz Syndrome. International Journal of Neuroscience. 121(4). 224–227. 17 indexed citations
2.
3.
Lam, Ching‐Wan, et al.. (2010). Circulating fluorocytes at the first attack of acute intermittent porphyria: A missing link in the pathogenesis. Clinica Chimica Acta. 412(1-2). 208–212. 3 indexed citations
4.
Kwok, Ka‐li, et al.. (2009). Maternally inherited Leigh syndrome: an unusual cause of infantile apnea. Sleep And Breathing. 14(2). 161–165. 4 indexed citations
5.
6.
Mak, Chloe Miu, C. W. Lam, Tak-Shing Siu, et al.. (2009). Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese. Molecular Genetics and Metabolism. 99(4). 431–433. 17 indexed citations
7.
Lai, Chi-Kong, Wing‐Tat Poon, & Yan-Wo Chan. (2006). Hidden Aconite Poisoning: Identification of Yunaconitine and Related Aconitum Alkaloids in Urine by Liquid Chromatography-Tandem Mass Spectrometry. Journal of Analytical Toxicology. 30(7). 426–433. 22 indexed citations
8.
Lam, Ching‐Wan, et al.. (2005). Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome. Clinica Chimica Acta. 364(1-2). 256–259. 20 indexed citations
9.
Lam, C W, et al.. (2005). Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria. Kidney International. 69(1). 123–128. 19 indexed citations
10.
Lai, Chi-Kong, Gensy M.W. Tong, Ping-Nam Wong, et al.. (2004). Novel mutations of the AGXT gene causing primary hyperoxaluria type 1. Journal of Nephrology. 17(3). 436–440. 17 indexed citations
11.
Chan, Angel On-Kei, Ching‐Wan Lam, Sui-Fan Tong, et al.. (2004). Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity. Clinica Chimica Acta. 351(1-2). 155–159. 7 indexed citations
12.
Lam, Ching‐Wan, Angel On-Kei Chan, Chi-Kong Lai, et al.. (2004). A novel mutation, Y255X, of the ARSB gene in a Chinese family with mucopolysaccharidosis type VI.. PubMed. 117(12). 1850–2. 5 indexed citations
13.
Lam, Ching‐Wan, et al.. (2003). Ethnic-specific splicing mutation of the carnitine-acylcarnitine translocase gene in a Chinese neonate presenting with sudden unexpected death.. PubMed. 116(7). 1110–2. 12 indexed citations
14.
Lam, Ching‐Wan, Chi Kong Li, Chi-Kong Lai, et al.. (2002). DNA-Based Diagnosis of Isolated Sulfite Oxidase Deficiency by Denaturing High-Performance Liquid Chromatography. Molecular Genetics and Metabolism. 75(1). 91–95. 15 indexed citations
15.
Lam, Ching‐Wan, Anna Wai-Fun Cheng, Sui-Fan Tong, & Yan-Wo Chan. (2002). Novel Donor Splice Site Mutation of ABCG5 Gene in Sitosterolemia. Molecular Genetics and Metabolism. 75(2). 178–180. 22 indexed citations
16.
Cheng, Anna Wai-Fun, et al.. (2002). Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b. Molecular Genetics and Metabolism. 77(3). 249–251. 9 indexed citations
17.
Lam, Ching‐Wan, Priscilla M.K. Poon, Sui-Fan Tong, et al.. (2001). Novel Mutation and Polymorphisms of the HMBS Gene Detected by Denaturing HPLC. Clinical Chemistry. 47(2). 343–346. 12 indexed citations
18.
Lam, Ching‐Wan, Kwun Nam Hui, Priscilla M.K. Poon, et al.. (2001). Novel splicing mutation of the PPOX gene (IVS10+1G→A) detected by denaturing high-performance liquid chromatography. Clinica Chimica Acta. 305(1-2). 197–200. 4 indexed citations
19.
Lam, Ching‐Wan, et al.. (2001). Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor. American Journal of Kidney Diseases. 38(6). 1307–1310. 18 indexed citations
20.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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