Tracy Heung

1.4k total citations
29 papers, 415 citations indexed

About

Tracy Heung is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Tracy Heung has authored 29 papers receiving a total of 415 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 17 papers in Epidemiology and 13 papers in Genetics. Recurrent topics in Tracy Heung's work include Congenital heart defects research (22 papers), Congenital Heart Disease Studies (16 papers) and Coronary Artery Anomalies (10 papers). Tracy Heung is often cited by papers focused on Congenital heart defects research (22 papers), Congenital Heart Disease Studies (16 papers) and Coronary Artery Anomalies (10 papers). Tracy Heung collaborates with scholars based in Canada, United States and Netherlands. Tracy Heung's co-authors include Anne S. Bassett, Erik Boot, Eva W.C. Chow, Candice K. Silversides, Pranesh Chakraborty, Kristin D. Kernohan, Nancy J. Butcher, Dennis E. Bulman, Aoy Tomita‐Mitchell and Sarah Malecki and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genome Research and Human Molecular Genetics.

In The Last Decade

Tracy Heung

27 papers receiving 410 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tracy Heung Canada 10 290 194 133 116 58 29 415
Tadayuki Ayabe Japan 10 75 0.3× 37 0.2× 130 1.0× 19 0.2× 75 1.3× 24 384
Shio Jean Lin Taiwan 13 86 0.3× 103 0.5× 114 0.9× 33 0.3× 4 0.1× 25 418
So Hee Eun South Korea 8 119 0.4× 54 0.3× 66 0.5× 20 0.2× 9 0.2× 17 350
Jana Noeldeke Switzerland 7 122 0.4× 33 0.2× 15 0.1× 66 0.6× 180 3.1× 10 492
Hongyu Lu China 10 65 0.2× 70 0.4× 20 0.2× 27 0.2× 29 0.5× 28 290
Alessandra Carta Italy 10 40 0.1× 166 0.9× 31 0.2× 34 0.3× 235 4.1× 26 538
Robert M. Porsch Hong Kong 6 92 0.3× 39 0.2× 209 1.6× 17 0.1× 28 0.5× 7 344
Martin Chada Germany 11 60 0.2× 17 0.1× 28 0.2× 75 0.6× 32 0.6× 17 275
Gadintshware Gaoatswe Ireland 6 85 0.3× 86 0.4× 27 0.2× 24 0.2× 67 1.2× 7 408
Y.-L. Lo Taiwan 9 109 0.4× 36 0.2× 42 0.3× 183 1.6× 33 0.6× 11 577

Countries citing papers authored by Tracy Heung

Since Specialization
Citations

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

Fields of papers citing papers by Tracy Heung

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tracy Heung

This figure shows the co-authorship network connecting the top 25 collaborators of Tracy Heung. A scholar is included among the top collaborators of Tracy Heung 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 Tracy Heung. Tracy Heung 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.
Grippe, Talyta, Tracy Heung, Robert Chen, et al.. (2025). Dissecting the Phenotypic Spectrum and Complexity of Movement Disorders in 22q11.2 Deletion Syndrome. European Journal of Neurology. 32(6). e70256–e70256.
2.
Heung, Tracy, et al.. (2025). A non-fasting marker of metabolic syndrome in a high-risk population. The journal of nutrition health & aging. 29(7). 100573–100573. 3 indexed citations
3.
Heung, Tracy, et al.. (2025). Influence of Polygenic Risk on Height and BMI in Adults With a 22q11.2 Microdeletion. Journal of the Endocrine Society. 9(9). bvaf115–bvaf115. 1 indexed citations
4.
Dierckxsens, Nicolas, Erika Souche, Tracy Heung, et al.. (2024). Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndrome. Genome Research. 35(4). 786–797. 1 indexed citations
5.
Malecki, Sarah, Tracy Heung, Walter P. Wodchis, et al.. (2024). Young adults with a 22q11.2 microdeletion and the cost of aging with complexity in a population-based context. Genetics in Medicine. 26(5). 101088–101088. 7 indexed citations
6.
Heung, Tracy, et al.. (2023). Adult-onset obstructive sleep apnea and pediatric pharyngoplasty in 22q11.2 deletion syndrome. Sleep Medicine. 104. 49–55. 3 indexed citations
7.
Heung, Tracy, Bhooma Thiruvahindrapuram, Worrawat Engchuan, et al.. (2023). Polygenic risk for triglyceride levels in the presence of a high impact rare variant. BMC Medical Genomics. 16(1). 6 indexed citations
8.
Shirzadi, Zahra, Henk Mutsaerts, Erik Boot, et al.. (2022). Elevated regional cerebral blood flow in adults with 22q11.2 deletion syndrome. The World Journal of Biological Psychiatry. 24(3). 260–265.
9.
Reuter, Miriam S., Michael Zech, Maja Hempel, et al.. (2022). Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies. European Journal of Human Genetics. 30(5). 611–618. 3 indexed citations
10.
Mojarad, Bahareh A., Worrawat Engchuan, Brett Trost, et al.. (2022). Genome-wide tandem repeat expansions contribute to schizophrenia risk. Molecular Psychiatry. 27(9). 3692–3698. 22 indexed citations
11.
McGinn, Daniel E., T. Blaine Crowley, Tracy Heung, et al.. (2022). Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes. 13(10). 1800–1800. 2 indexed citations
12.
Heung, Tracy, et al.. (2022). Schizophrenia Risk Mediated by microRNA Target Genes Overlapped by Genome-Wide Rare Copy Number Variation in 22q11.2 Deletion Syndrome. Frontiers in Genetics. 13. 812183–812183. 9 indexed citations
13.
Fiksinski, Ania, Tracy Heung, Maria Corral, et al.. (2021). Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model. Psychological Medicine. 52(14). 3184–3192. 9 indexed citations
14.
Mojarad, Bahareh A., Yue Yin, Roozbeh Manshaei, et al.. (2021). Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia. Translational Psychiatry. 11(1). 84–84. 12 indexed citations
15.
Homans, Jelle F., Tracy Heung, Candice K. Silversides, et al.. (2020). The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis. The Spine Journal. 20(6). 956–963. 6 indexed citations
16.
Heung, Tracy, Sarah Malecki, Elemi Breetvelt, et al.. (2020). Impact of a 22q11.2 Microdeletion on Adult All-Cause Mortality in Tetralogy of Fallot Patients. Canadian Journal of Cardiology. 36(7). 1091–1097. 11 indexed citations
17.
Heung, Tracy, Sarah Malecki, Marcos Sanches, et al.. (2020). 22q11.2 microdeletion and increased risk for type 2 diabetes. EClinicalMedicine. 26. 100528–100528. 21 indexed citations
18.
Heung, Tracy, Enoch Ng, Sarah Malecki, et al.. (2019). All-cause mortality and survival in adults with 22q11.2 deletion syndrome. Genetics in Medicine. 21(10). 2328–2335. 36 indexed citations
19.
Boot, Erik, Nancy J. Butcher, Samantha Cooper, et al.. (2016). Obesity in adults with 22q11.2 deletion syndrome. Genetics in Medicine. 19(2). 204–208. 55 indexed citations
20.
Steel, Zachary, Robert C. Brooks, Tracy Heung, et al.. (2011). Psychosocial risk and protective factors for depression in the dialysis population: A systematic review and meta-regression analysis. Journal of Psychosomatic Research. 71(5). 300–310. 39 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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