Amy Y. Y. Chan

733 total citations
26 papers, 379 citations indexed

About

Amy Y. Y. Chan is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Amy Y. Y. Chan has authored 26 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 15 papers in Hematology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Amy Y. Y. Chan's work include Hemoglobinopathies and Related Disorders (19 papers), Iron Metabolism and Disorders (13 papers) and Blood groups and transfusion (6 papers). Amy Y. Y. Chan is often cited by papers focused on Hemoglobinopathies and Related Disorders (19 papers), Iron Metabolism and Disorders (13 papers) and Blood groups and transfusion (6 papers). Amy Y. Y. Chan collaborates with scholars based in Hong Kong, China and United States. Amy Y. Y. Chan's co-authors include Edmond S.K., David H.K. Chui, Li Chong Chan, Samuel S. Chong, C.C So, Wen Wang, Wendy N. Erber, John F. Prior, Ivy Ng and Charles R. Cantor and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Clinical Chemistry.

In The Last Decade

Amy Y. Y. Chan

26 papers receiving 364 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amy Y. Y. Chan Hong Kong 8 233 186 181 76 64 26 379
Rosalba Di Marzo Italy 10 251 1.1× 167 0.9× 66 0.4× 146 1.9× 21 0.3× 23 365
Nermeen Varawalla United Kingdom 5 448 1.9× 343 1.8× 116 0.6× 57 0.8× 22 0.3× 10 523
U. Sancken Germany 10 91 0.4× 77 0.4× 94 0.5× 99 1.3× 29 0.5× 18 368
Iswari Setianingsih Indonesia 9 238 1.0× 205 1.1× 74 0.4× 77 1.0× 14 0.2× 25 314
Manoussos N. Papadakis Greece 10 203 0.9× 139 0.7× 76 0.4× 105 1.4× 8 0.1× 22 301
C Hesketh United Kingdom 7 309 1.3× 236 1.3× 58 0.3× 121 1.6× 11 0.2× 7 432
Konstantinos Varvagiannis Greece 5 309 1.3× 243 1.3× 96 0.5× 75 1.0× 20 0.3× 11 373
A Metaxotou-Mavromati Greece 14 501 2.2× 388 2.1× 140 0.8× 90 1.2× 23 0.4× 28 549
Duantida Songdej Thailand 11 182 0.8× 166 0.9× 105 0.6× 73 1.0× 17 0.3× 51 357
Meihuan Chen China 8 155 0.7× 124 0.7× 70 0.4× 70 0.9× 12 0.2× 49 257

Countries citing papers authored by Amy Y. Y. Chan

Since Specialization
Citations

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

Fields of papers citing papers by Amy Y. Y. Chan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amy Y. Y. 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 Amy Y. Y. Chan. The network helps show where Amy Y. Y. Chan may publish in the future.

Co-authorship network of co-authors of Amy Y. Y. Chan

This figure shows the co-authorship network connecting the top 25 collaborators of Amy Y. Y. Chan. A scholar is included among the top collaborators of Amy Y. Y. 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 Amy Y. Y. Chan. Amy Y. Y. 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
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Chan, Amy Y. Y., et al.. (2014). Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing. Journal of Clinical Pathology. 68(1). 69–72. 2 indexed citations
3.
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Chan, Amy Y. Y., et al.. (2011). Hb A2Hong Kong – A Novel δ-Globin Variant in a Chinese Family Masks the Diagnosis of β-Thalassemia Trait. Hemoglobin. 35(2). 162–165. 12 indexed citations
5.
So, C.C, et al.. (2010). Haemoglobin Bonn in a Chinese family as a cause of spurious hypoxaemia measured by pulse oximetry. Journal of Clinical Pathology. 63(10). 947–949. 1 indexed citations
6.
So, C.C, et al.. (2009). Detection and characterisation of β-globin gene cluster deletions in Chinese using multiplex ligation-dependent probe amplification. Journal of Clinical Pathology. 62(12). 1107–1111. 18 indexed citations
7.
Lee, Acw, et al.. (2008). DOUBLE HETEROZYGOSITY FOR Hb NEW YORK [β113 GTG→GAG; VAL→GLU] AND β°-THALASSEMIA MUTATIONS MANIFESTS AS A THALASSEMIA TRAIT. Pediatric Hematology and Oncology. 25(3). 227–231. 3 indexed citations
8.
Chan, Amy Y. Y., et al.. (2006). A laboratory strategy for genotyping haemoglobin H disease in the Chinese. Journal of Clinical Pathology. 60(8). 931–934. 26 indexed citations
9.
S.K., Edmond, et al.. (2006). Molecular Diagnosis of a Case of Hb Phnom Penh [α117(GH5)Phe-I1e-α118(H1)Thr (α1)]. Hemoglobin. 30(3). 397–399. 5 indexed citations
10.
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Ding, Chunming, Rossa W. K. Chiu, Tze Kin Lau, et al.. (2004). MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. Proceedings of the National Academy of Sciences. 101(29). 10762–10767. 148 indexed citations
12.
S.K., Edmond, Amy Y. Y. Chan, & Acw Lee. (2004). Molecular Characterization of Hb Val de Marne [α133(H16)Ser→Arg; AGC→AGA; (α2)] in a Chinese Family. Hemoglobin. 28(3). 213–216. 2 indexed citations
13.
Wang, Wen, Edmond S.K., Amy Y. Y. Chan, et al.. (2003). Single-Tube Multiplex-PCR Screen for Anti-3.7 and Anti-4.2 α-Globin Gene Triplications. Clinical Chemistry. 49(10). 1679–1682. 81 indexed citations
14.
Wang, Wen, Edmond S.K., Amy Y. Y. Chan, David H.K. Chui, & Samuel S. Chong. (2003). Multiple Minisequencing Screen for Seven Southeast Asian Nondeletional α-Thalassemia Mutations. Clinical Chemistry. 49(5). 800–803. 7 indexed citations
15.
Chan, Amy Y. Y., Edmond S.K., Wing‐Yan Au, Eudora Y. Chow, & Li Chong Chan. (2002). DETECTION OF A SMALL NOVEL DELETION IN THEα-GLOBIN GENE AND TYPE II −α3.7DELETION BY HETERODUPLEX FORMATION. Hemoglobin. 26(3). 311–316. 1 indexed citations
16.
S.K., Edmond, et al.. (2002). Low affinity and unstable hemoglobin variant caused by AAC-->ATC (Asn-->Ile) mutation at codon 108 of the beta-globin gene.. PubMed. 87(5). 553–4. 2 indexed citations
17.
Chan, Amy Y. Y., et al.. (2002). Hb KODAIRA II: A HIGH OXYGEN AFFINITY VARIANT WITH A NOVEL MUTATION IN THEβ-GLOBIN GENE AND PHENOTYPIC IDENTITY TO Hb KODAIRA. Hemoglobin. 26(2). 205–207. 1 indexed citations
18.
S.K., Edmond, Amy Y. Y. Chan, E. K. W. Chiu, & Sy Ha. (2001). Haemoglobin H disease due to (- -SEA) α-globin gene deletion and α2-codon 30 (ΔGAG) mutation: a family study. Clinical & Laboratory Haematology. 23(5). 325–327. 4 indexed citations
19.
Au, WY, Amy Y. Y. Chan, L.C. Chan, et al.. (2001). Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family. Clinical & Laboratory Haematology. 23(1). 53–55. 1 indexed citations
20.
Sabu, K. K., Sy Ha, Amy Y. Y. Chan, et al.. (2000). Two Novel β-Thalassemia Alleles in the Chinese: the IVS-II-2 (−T) and Nucleotide +8 (C→T) β-Globin Gene Mutations. Hemoglobin. 24(4). 327–332. 10 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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