Alicia Chan

1.3k total citations
25 papers, 800 citations indexed

About

Alicia Chan is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Alicia Chan has authored 25 papers receiving a total of 800 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 6 papers in Physiology. Recurrent topics in Alicia Chan's work include Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (5 papers) and Lysosomal Storage Disorders Research (4 papers). Alicia Chan is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (5 papers) and Lysosomal Storage Disorders Research (4 papers). Alicia Chan collaborates with scholars based in Canada, United States and United Kingdom. Alicia Chan's co-authors include Salvatore DiMauro, Valeria Tiranti, Paolo Gasparini, Rossella Parini, Vamsi K. Mootha, Renè Massimiliano Marsano, Claudia Donnini, Carlo Viscomi, Agnès Rötig and Antonella Spinazzola and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Environmental Science & Technology.

In The Last Decade

Alicia Chan

21 papers receiving 781 citations

Peers

Alicia Chan

PHYSI

EPIDE

François Eyskens Belgium

Jozef Hertecant United Arab Emirates

Ksenija Fumić Croatia

Robin Casey Canada

Chike Bellarmine Item Austria

Shlomo Almashanu Israel

Dimitar Gavrilov United States

Zuhair N. Al‐Hassnan Saudi Arabia

Janine Reunert Germany

Yonglan Huang China

François Eyskens Belgium

Alicia Chan

462 ×0.9

331 ×1.0

158 ×0.8

PHYSI

43 ×0.4

55 ×0.7

EPIDE

Citations per year, relative to Alicia Chan Alicia Chan (= 1×) peers François Eyskens

Countries citing papers authored by Alicia Chan

Since Specialization

Citations

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

Fields of papers citing papers by Alicia Chan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alicia Chan

This figure shows the co-authorship network connecting the top 25 collaborators of Alicia Chan. A scholar is included among the top collaborators of Alicia 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 Alicia Chan. Alicia Chan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Perez, Jeffrey Paulo H., Alicia Chan, J. Frederick W. Mosselmans, & Liane G. Benning. (2025). Coexisting Phosphate Controls Arsenate Speciation and Partitioning during Fe(II)-Catalyzed Ferrihydrite Transformation. ACS Earth and Space Chemistry. 9(6). 1642–1653.

Chan, Alicia, et al.. (2024). Clinical and biochemical phenotypes, genotypes, and long-term outcomes of individuals with galactosemia type I from a single metabolic genetics center in Alberta. Molecular Genetics and Metabolism Reports. 38. 101055–101055.

Yadav, Pooja, P. J. Nolan, Kate M. Campbell, et al.. (2023). Nitrate-Stimulated Release of Naturally Occurring Sedimentary Uranium. Environmental Science & Technology. 57(10). 4354–4366. 17 indexed citations

Chan, Alicia, et al.. (2023). First report of type 2 diabetes mellitus in an adult with 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency. Endocrinology Diabetes and Metabolism Case Reports. 2023(1).

Athey, Taryn, et al.. (2022). Outcomes of mitochondrial long chain fatty acid oxidation and carnitine defects from a single center metabolic genetics clinic. Orphanet Journal of Rare Diseases. 17(1). 360–360. 4 indexed citations

Al‐Mossawi, Hussein, Chris Worth, Patrícia Maria Abreu Machado, et al.. (2021). A first in disease phase 2A trial of granulocyte monocyte colony stimulating factor neutralisation for axial spondyloarthritis (NAMASTE study). Clinical and Experimental Rheumatology. 39(5). 1161–1161.

Tingley, Kylie, Michal Inbar‐Feigenberg, John J. Mitchell, et al.. (2021). Establishing a core outcome set for mucopolysaccharidoses (MPS) in children: study protocol for a rapid literature review, candidate outcomes survey, and Delphi surveys. Trials. 22(1). 816–816. 2 indexed citations

Revel‐Vilk, Shoshana, Michal Becker‐Cohen, Tama Dinur, et al.. (2021). Upgrading the evidence for the use of ambroxol in Gaucher disease and GBA related Parkinson: Investigator initiated registry based on real life data. American Journal of Hematology. 96(5). 545–551. 33 indexed citations

Ferreira, Patrick, Alicia Chan, & Barry Wolf. (2017). Irreversibility of Symptoms with Biotin Therapy in an Adult with Profound Biotinidase Deficiency. JIMD Reports. 36. 117–120. 19 indexed citations

10.

Olpin, S. E., Brage Storstein Andresen, Aneal Khan, et al.. (2017). Fibroblast Fatty-Acid Oxidation Flux Assays Stratify Risk in Newborns with Presumptive-Positive Results on Screening for Very-Long Chain Acyl-CoA Dehydrogenase Deficiency. International Journal of Neonatal Screening. 3(1). 2–2. 5 indexed citations

11.

Mercimek‐Mahmutoglu, Saadet, Gajja S. Salomons, & Alicia Chan. (2014). Case Study for the Evaluation of Current Treatment Recommendations of Guanidinoacetate Methyltransferase Deficiency: Ineffectiveness of Sodium Benzoate. Pediatric Neurology. 51(1). 133–137. 11 indexed citations

12.

Liao, Xiaoping, Fred Y Peng, Fiona Bamforth, et al.. (2014). Mitochondriome and Cholangiocellular Carcinoma. PLoS ONE. 9(8). e104694–e104694. 10 indexed citations

13.

Armour, Christine M., et al.. (2013). A Patient With an Inborn Error of Vitamin B12 Metabolism (cblF) Detected by Newborn Screening. PEDIATRICS. 132(1). e257–e261. 15 indexed citations

14.

Cave, Dominic, et al.. (2011). Mitochondrial DNA Depletion Syndrome-An Unusual Reason for Interstage Attrition after the Modified Stage 1 Norwood Operation. Congenital Heart Disease. 8(1). E20–E23. 6 indexed citations

15.

Greenberg, Cheryl R., Louise A. Dilling, Gilbert R. Thompson, et al.. (2009). The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations. Molecular Genetics and Metabolism. 96(4). 201–207. 59 indexed citations

16.

Quintero‐Rivera, Fabiola, Alicia Chan, Diana Donovan, James F. Gusella, & Azra H. Ligon. (2007). Disruption of a synaptotagmin (SYT14) associated with neurodevelopmental abnormalities. American Journal of Medical Genetics Part A. 143A(6). 558–563. 16 indexed citations

17.

Choi, Hong Y., Emma Waddington, Teddy Chan, et al.. (2006). Correction of Apolipoprotein A-I-mediated Lipid Efflux and High Density Lipoprotein Particle Formation in Human Niemann-Pick Type C Disease Fibroblasts. Journal of Biological Chemistry. 281(48). 37081–37090. 36 indexed citations

18.

Spinazzola, Antonella, Carlo Viscomi, Erika Fernández‐Vizarra, et al.. (2006). MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion. Nature Genetics. 38(5). 570–575. 330 indexed citations

19.

Huntsman, Richard J., D. Barry Sinclair, Ravi Bhargava, & Alicia Chan. (2005). Atypical Presentations of Leigh Syndrome: A Case Series and Review. Pediatric Neurology. 32(5). 334–340. 50 indexed citations

20.

Mistry, Pramod K., Sandra Sirrs, Alicia Chan, et al.. (2002). Pulmonary hypertension in type 1 Gaucher’s disease: genetic and epigenetic determinants of phenotype and response to therapy. Molecular Genetics and Metabolism. 77(1-2). 91–98. 126 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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