Ching‐Wan Lam

2.8k total citations
84 papers, 1.9k citations indexed

About

Ching‐Wan Lam is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Ching‐Wan Lam has authored 84 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 17 papers in Genetics. Recurrent topics in Ching‐Wan Lam's work include Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (10 papers) and Porphyrin Metabolism and Disorders (8 papers). Ching‐Wan Lam is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (10 papers) and Porphyrin Metabolism and Disorders (8 papers). Ching‐Wan Lam collaborates with scholars based in Hong Kong, China and United States. Ching‐Wan Lam's co-authors include Chloe Miu Mak, Chun Yiu Law, Albert Yan‐Wo Chan, Lisa Chan, Yuk Ming Dennis Lo, Anthony T.�C. Chan, Philip J. Johnson, Sing-Fai Leung, Dolly P. Huang and Han‐Chih Hencher Lee and has published in prestigious journals such as Analytical Chemistry, Chemical Communications and Annals of Neurology.

In The Last Decade

Ching‐Wan Lam

82 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ching‐Wan Lam Hong Kong 23 744 262 258 247 204 84 1.9k
Paul Jordan United States 26 481 0.6× 75 0.3× 210 0.8× 312 1.3× 295 1.4× 90 2.2k
Min Dong United States 26 973 1.3× 51 0.2× 198 0.8× 260 1.1× 177 0.9× 104 2.3k
Rudolf Oehler Austria 28 744 1.0× 92 0.4× 103 0.4× 330 1.3× 132 0.6× 81 2.3k
Kondala R. Atkuri United States 13 731 1.0× 94 0.4× 94 0.4× 167 0.7× 121 0.6× 18 1.7k
Krzysztof Zwierz Poland 22 585 0.8× 65 0.2× 61 0.2× 139 0.6× 131 0.6× 159 1.8k
Hyun Ju Yoo South Korea 29 1.2k 1.6× 38 0.1× 129 0.5× 175 0.7× 298 1.5× 111 2.5k
Yuji Moriwaki Japan 27 758 1.0× 216 0.8× 149 0.6× 93 0.4× 403 2.0× 112 2.3k
Barbara Marzocchi Italy 20 586 0.8× 213 0.8× 71 0.3× 63 0.3× 207 1.0× 47 1.6k
Annalisa Castagna Italy 32 1.3k 1.8× 43 0.2× 109 0.4× 143 0.6× 166 0.8× 100 3.2k
Beata Kośmider United States 28 1.0k 1.4× 60 0.2× 73 0.3× 181 0.7× 236 1.2× 64 2.2k

Countries citing papers authored by Ching‐Wan Lam

Since Specialization
Citations

This map shows the geographic impact of Ching‐Wan Lam'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 Ching‐Wan Lam with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ching‐Wan Lam more than expected).

Fields of papers citing papers by Ching‐Wan Lam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ching‐Wan Lam. 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 Ching‐Wan Lam. The network helps show where Ching‐Wan Lam may publish in the future.

Co-authorship network of co-authors of Ching‐Wan Lam

This figure shows the co-authorship network connecting the top 25 collaborators of Ching‐Wan Lam. A scholar is included among the top collaborators of Ching‐Wan Lam 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 Ching‐Wan Lam. Ching‐Wan Lam 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.
Law, Chun Yiu, et al.. (2023). Allan-Herndon-Dudley syndrome in Hong Kong: Implication for newborn screening. Clinica Chimica Acta. 551. 117621–117621. 2 indexed citations
2.
Lam, Ching‐Wan, et al.. (2021). Postzygotic inactivating mutation of KIF13A located at chromosome 6p22.3 in a patient with a novel mosaic neuroectodermal syndrome. Journal of Human Genetics. 66(8). 825–829. 3 indexed citations
4.
Cheng, Yu-Hong, et al.. (2019). Plasmonic gold nanoparticles as multifaceted probe for tissue imaging. Chemical Communications. 55(19). 2761–2764. 16 indexed citations
5.
To, Kelvin Kai‐Wang, Kim-Chung Lee, Samson S. Y. Wong, et al.. (2016). Lipid metabolites as potential diagnostic and prognostic biomarkers for acute community acquired pneumonia. Diagnostic Microbiology and Infectious Disease. 85(2). 249–254. 44 indexed citations
6.
Lam, Ching‐Wan, Ka Sing Wong, Howan Leung, & Chun Yiu Law. (2016). Limb girdle myasthenia with digenic RAPSN and a novel disease gene AK9 mutations. European Journal of Human Genetics. 25(2). 192–199. 17 indexed citations
7.
Lam, Ching‐Wan, Chloe Miu Mak, Elizabeth T. Lau, et al.. (2016). MOESM1 of Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong. Figshare. 1 indexed citations
8.
Lam, Ching‐Wan, et al.. (2015). Unmasking a novel disease gene NEO1 associated with autism spectrum disorders by a hemizygous deletion on chromosome 15 and a functional polymorphism. Behavioural Brain Research. 300. 135–142. 10 indexed citations
9.
Lam, Ching‐Wan, Chun Yiu Law, Chi-Kong Lai, et al.. (2014). NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome. Clinica Chimica Acta. 440. 201–204. 5 indexed citations
10.
Lam, Ching‐Wan & Chloe Miu Mak. (2013). Allele dropout caused by a non-primer-site SNV affecting PCR amplification — A call for next-generation primer design algorithm. Clinica Chimica Acta. 421. 208–212. 21 indexed citations
11.
Lee, Han‐Chih Hencher, Chi-Kong Lai, Tak-Shing Siu, et al.. (2011). Non-invasive urinary screening for aromatic l-amino acid decarboxylase deficiency in high-prevalence areas: A pilot study. Clinica Chimica Acta. 413(1-2). 126–130. 18 indexed citations
12.
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
13.
Lee, Han‐Chih Hencher, Chi-Kong Lai, Tak-Shing Siu, et al.. (2010). Role of Postmortem Genetic Testing Demonstrated in a Case of Glutaric Aciduria Type II. Diagnostic Molecular Pathology. 19(3). 184–186. 9 indexed citations
14.
Chang, Hsiu‐Hao, et al.. (2009). Glycogen Storage Disease Type Ib: The First Case in Taiwan. Pediatrics & Neonatology. 50(3). 125–128. 3 indexed citations
15.
Mak, Chloe Miu, Yok‐Lam Kwong, Ching‐Wan Lam, et al.. (2007). Identification of a novelTTRGly67Glu mutant and the first case series of familial transthyretin amyloidosis in Hong Kong Chinese. Amyloid. 14(4). 293–297. 10 indexed citations
16.
Lam, Ching‐Wan, et al.. (2005). Ketoconazole Induced Torsades de Pointes Without Concomitant Use of QT Interval‐Prolonging Drug. Journal of Cardiovascular Electrophysiology. 16(12). 1375–1377. 16 indexed citations
17.
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
18.
Lam, Ching‐Wan, et al.. (2004). Diagnostic value of pleural fluid adenosine deaminase activity in tuberculous pleurisy. Clinica Chimica Acta. 341(1-2). 101–107. 60 indexed citations
19.
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
20.
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

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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