Michel Tchan

3.1k total citations
76 papers, 1.1k citations indexed

About

Michel Tchan is a scholar working on Physiology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Michel Tchan has authored 76 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Physiology, 31 papers in Molecular Biology and 21 papers in Clinical Biochemistry. Recurrent topics in Michel Tchan's work include Lysosomal Storage Disorders Research (28 papers), Metabolism and Genetic Disorders (21 papers) and Glycogen Storage Diseases and Myoclonus (14 papers). Michel Tchan is often cited by papers focused on Lysosomal Storage Disorders Research (28 papers), Metabolism and Genetic Disorders (21 papers) and Glycogen Storage Diseases and Myoclonus (14 papers). Michel Tchan collaborates with scholars based in Australia, United Kingdom and United States. Michel Tchan's co-authors include Rebecca Kozor, David Sillence, James Moon, Stuart M. Grieve, Christian Hamilton‐Craig, Gemma A. Figtree, Tarekegn Geberhiwot, Richard P. Steeds, Derralynn Hughes and Fraser M. Callaghan and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Michel Tchan

70 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michel Tchan Australia 19 478 418 249 248 216 76 1.1k
Agnieszka Jurecka Poland 21 649 1.4× 405 1.0× 180 0.7× 446 1.8× 35 0.2× 63 1.2k
Julian Raiman Canada 24 738 1.5× 559 1.3× 334 1.3× 331 1.3× 41 0.2× 58 1.5k
Elisabetta Pasquini Italy 23 232 0.5× 589 1.4× 698 2.8× 83 0.3× 57 0.3× 59 1.4k
Carolina Fischinger Moura de Souza Brazil 19 427 0.9× 507 1.2× 362 1.5× 170 0.7× 15 0.1× 110 1.2k
Anupam Chakrapani United Kingdom 19 466 1.0× 546 1.3× 628 2.5× 104 0.4× 34 0.2× 57 1.2k
Hilary Vallance Canada 18 221 0.5× 519 1.2× 469 1.9× 95 0.4× 43 0.2× 65 1.0k
Cristina Brinckmann Oliveira Netto Brazil 20 465 1.0× 289 0.7× 76 0.3× 159 0.6× 24 0.1× 50 902
Alberto Ponzone Italy 15 850 1.8× 546 1.3× 631 2.5× 353 1.4× 42 0.2× 34 1.8k
Simona Fecarotta Italy 17 299 0.6× 207 0.5× 75 0.3× 165 0.7× 23 0.1× 41 775
Sarah C. Grünert Germany 22 333 0.7× 716 1.7× 726 2.9× 81 0.3× 40 0.2× 86 1.6k

Countries citing papers authored by Michel Tchan

Since Specialization
Citations

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

Fields of papers citing papers by Michel Tchan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michel Tchan. 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 Michel Tchan. The network helps show where Michel Tchan may publish in the future.

Co-authorship network of co-authors of Michel Tchan

This figure shows the co-authorship network connecting the top 25 collaborators of Michel Tchan. A scholar is included among the top collaborators of Michel Tchan 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 Michel Tchan. Michel Tchan 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.
Stevanovski, Igor, Sanjog R. Chintalaphani, Pak Leng Cheong, et al.. (2025). Targeted Long‐Read Sequencing as a Single Assay Improves the Diagnosis of Spastic‐Ataxia Disorders. Annals of Clinical and Translational Neurology. 12(4). 832–841. 3 indexed citations
2.
3.
Moussa, Yvonne E., et al.. (2024). A Case Series of Disproportionate Elevations of Cardiac Troponin and Macrotroponin in Fabry Disease. SHILAP Revista de lepidopterología. 12. 1 indexed citations
4.
Nicholls, Kathy, Charles Denaro, Michel Tchan, et al.. (2024). Fabry‐specific treatment in Australia: time to align eligibility criteria with international best practices. Internal Medicine Journal. 54(6). 882–890.
5.
Thompson, Susan, Arthavan Selvanathan, Cathryn M. Lewis, et al.. (2023). Treatment of HMG-CoA Lyase Deficiency—Longitudinal Data on Clinical and Nutritional Management of 10 Australian Cases. Nutrients. 15(3). 531–531. 3 indexed citations
6.
Tchan, Michel, Sophie Devery, Rupendra Shrestha, et al.. (2023). Informing a value care model: lessons from an integrated adult neurogenomics clinic. Internal Medicine Journal. 53(12). 2198–2207. 3 indexed citations
7.
Williams, Laura, Andrew Lockhart, Kishore R. Kumar, et al.. (2023). ATP1A3 related disease manifesting as rapid onset dystonia-parkinsonism with prominent myoclonus and exaggerated startle. Parkinsonism & Related Disorders. 117. 105864–105864.
8.
Trivedi, S., et al.. (2022). Electrocardiographic Characteristics and Their Correlation with Echocardiographic Alterations in Fabry Disease. Journal of Cardiovascular Development and Disease. 9(1). 11–11. 4 indexed citations
9.
Mallawaarachchi, Amali, Ben Lundie, Yvonne Hort, et al.. (2021). Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing. European Journal of Human Genetics. 29(5). 760–770. 30 indexed citations
10.
Aung-Htut, May T., et al.. (2020). Novel Mutations Found in Individuals with Adult-Onset Pompe Disease. Genes. 11(2). 135–135. 7 indexed citations
11.
Boyd, Anita, Charles Denaro, Norman Sadick, et al.. (2020). Basal Segmental Longitudinal Strain: A Marker of Subclinical Myocardial Involvement in Anderson-Fabry Disease. Journal of the American Society of Echocardiography. 34(4). 405–413.e2. 14 indexed citations
12.
Aung-Htut, May T., Michel Tchan, R. Johnsen, et al.. (2020). Splice modulating antisense oligonucleotides restore some acid-alpha-glucosidase activity in cells derived from patients with late-onset Pompe disease. Scientific Reports. 10(1). 6702–6702. 6 indexed citations
13.
Tchan, Michel. (2018). Hyperammonemia and lactic acidosis in adults: Differential diagnoses with a focus on inborn errors of metabolism. Reviews in Endocrine and Metabolic Disorders. 19(1). 69–79. 8 indexed citations
14.
Tchan, Michel, Judy Savige, Chirag Patel, et al.. (2015). KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetic Testing for Diagnosis. Seminars in Nephrology. 35(6). 545–549.e2. 6 indexed citations
15.
Patel, Chirag, Michel Tchan, Judy Savige, et al.. (2015). KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetics and Genetic Counseling. Seminars in Nephrology. 35(6). 550–556.e1. 3 indexed citations
16.
Tchan, Michel, et al.. (2014). Cognitive and Psychological Functioning in Fabry Disease. Archives of Clinical Neuropsychology. 29(7). 642–650. 29 indexed citations
17.
Tchan, Michel, Mary T. Westbrook, Gisela Wilcox, et al.. (2013). The Management of Pregnancy in Maple Syrup Urine Disease: Experience with Two Patients. JIMD Reports. 10. 113–117. 13 indexed citations
18.
Boyd, Anita, Michel Tchan, David Sillence, et al.. (2013). Left Atrial Enlargement and Reduced Atrial Compliance Occurs Early in Fabry Cardiomyopathy. Journal of the American Society of Echocardiography. 26(12). 1415–1423. 50 indexed citations
19.
Riley, Lisa G., Minal Menezes, Joëlle Rudinger‐Thirion, et al.. (2013). Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia. Orphanet Journal of Rare Diseases. 8(1). 193–193. 40 indexed citations
20.
Tchan, Michel & D. Sillence. (2011). Fabry disease and Factor V Leiden: a potent vascular risk combination. Internal Medicine Journal. 41(5). 422–426. 4 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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