Alison Yeung

3.5k total citations
19 papers, 385 citations indexed

About

Alison Yeung is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Alison Yeung has authored 19 papers receiving a total of 385 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Alison Yeung's work include Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (6 papers) and Chromosomal and Genetic Variations (3 papers). Alison Yeung is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (6 papers) and Chromosomal and Genetic Variations (3 papers). Alison Yeung collaborates with scholars based in Australia, United States and New Zealand. Alison Yeung's co-authors include Zornitza Stark, David J. Amor, Tiong Yang Tan, Sebastian Lunke, Susan M. White, Clara Gaff, Natalie Thorne, Trent Burgess, Ingrid E. Scheffer and Howard R. Slater and has published in prestigious journals such as Gene, BJOG An International Journal of Obstetrics & Gynaecology and Genetics in Medicine.

In The Last Decade

Alison Yeung

19 papers receiving 372 citations

Peers

Alison Yeung

GENET

PPCH

SURGE

Ho‐Ming Luk China

Frédérique Tihy Canada

Julie Scuffins United States

Christèle du Souich Canada

Sawona Biswas United States

Cristina Molinatto Italy

Layla Shahmirzadi United States

Mélanie Fradin France

Nina B. Gold United States

Amal Hashem Saudi Arabia

Ho‐Ming Luk China

Alison Yeung

267 ×0.9

GENET

249 ×1.9

100 ×1.4

PPCH

24 ×0.6

50 ×1.4

SURGE

Citations per year, relative to Alison Yeung Alison Yeung (= 1×) peers Ho‐Ming Luk

Countries citing papers authored by Alison Yeung

Since Specialization

Citations

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

Fields of papers citing papers by Alison Yeung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alison Yeung

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

All Works

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19 of 19 papers shown

Downie, Lilian, David J. Amor, John Christodoulou, et al.. (2024). Gene selection for genomic newborn screening: Moving toward consensus?. Genetics in Medicine. 26(5). 101077–101077. 21 indexed citations

Fennell, Andrew, Samuel F. Berkovic, Carolyn Ellaway, et al.. (2022). The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome. American Journal of Medical Genetics Part A. 188(12). 3432–3447. 12 indexed citations

Goranitis, Ilias, You Wu, Sebastian Lunke, et al.. (2022). Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and children. Genetics in Medicine. 24(5). 1037–1044. 30 indexed citations

Yeung, Alison, et al.. (2020). Inspiring Collaboration and Engagement. 2 indexed citations

Tan, Natalie B., Rachel Stapleton, Zornitza Stark, et al.. (2020). Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review. Molecular Genetics & Genomic Medicine. 8(11). e1508–e1508. 44 indexed citations

Hopkins, Sam, Susan A. Brooks, & Alison Yeung. (2020). Mentoring to Empower Researchers. 2 indexed citations

Tan, Tiong Yang, Sebastian Lunke, Belinda Chong, et al.. (2019). A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis. European Journal of Human Genetics. 27(12). 1791–1799. 35 indexed citations

Yiu, Eppie M., Alison Yeung, Jeremy L. Freeman, et al.. (2019). Hyperinsulinaemic hypoglycaemia: A rare association of vanishing white matter disease. JIMD Reports. 51(1). 11–16. 5 indexed citations

Lunke, Sebastian, Zornitza Stark, Alison Yeung, et al.. (2018). Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders. European Journal of Human Genetics. 26(5). 644–651. 83 indexed citations

10.

Johnston, JM, et al.. (2018). Hong Kong domestic health spending: financial years 1989/90 to 2014/15.. PubMed. 24 Suppl 8(1). 1–24. 1 indexed citations

11.

Stark, Zornitza, Harriet Dashnow, Sebastian Lunke, et al.. (2017). A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data. European Journal of Human Genetics. 25(11). 1268–1272. 13 indexed citations

12.

Yeung, Alison, et al.. (2017). Cervicofacial subcutaneous emphysema: a clinical case and review of the literature.. PubMed. 64(3). 68–71. 9 indexed citations

13.

Stark, Zornitza, Trent Burgess, Alison Yeung, et al.. (2015). SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia. American Journal of Medical Genetics Part A. 167(10). 2319–2326. 18 indexed citations

14.

Yeung, Alison, et al.. (2013). Neonatal presentation of chromosome 9q33.2–q34.3 duplication. Gene. 527(2). 541–544. 1 indexed citations

15.

Ganesamoorthy, Devika, George McGillivray, F Norris, et al.. (2013). Meeting the challenge of interpreting high‐resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?. BJOG An International Journal of Obstetrics & Gynaecology. 120(5). 594–606. 29 indexed citations

16.

Bilodeau, Elizabeth Ann, et al.. (2012). Sporadic Burkitt lymphoma of the jaw: case report and review of the literature.. PubMed. 43(4). 333–6. 2 indexed citations

17.

Yeung, Alison, et al.. (2009). Pallister–Killian syndrome caused by mosaicism for a supernumerary ring chromosome 12p. American Journal of Medical Genetics Part A. 149A(3). 505–509. 20 indexed citations

18.

Yeung, Alison, Damien L. Bruno, Ingrid E. Scheffer, et al.. (2009). 4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment. European Journal of Medical Genetics. 52(6). 440–442. 49 indexed citations

19.

Yeung, Alison, David J. Amor, & Ravi Savarirayan. (2009). Familial upper eyelid coloboma with ipsilateral anterior hairline abnormality: Two new reports of MOTA syndrome. American Journal of Medical Genetics Part A. 149A(4). 767–769. 9 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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