Siu‐Li Yong

2.0k total citations · 1 hit paper
12 papers, 1.2k citations indexed

About

Siu‐Li Yong is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Siu‐Li Yong has authored 12 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Surgery and 5 papers in Molecular Biology. Recurrent topics in Siu‐Li Yong's work include Genetic Syndromes and Imprinting (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Siu‐Li Yong is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Siu‐Li Yong collaborates with scholars based in Canada, United States and Qatar. Siu‐Li Yong's co-authors include Jonathan Zonana, Roberta A Pagon, John M. Graham, John M. Opitz, R. Brian Lowry, Margot I. Van Allen, Barbara McGillivray, Susan Ritchie, J. Tapio Pantzar and Judith G. Hall and has published in prestigious journals such as Human Molecular Genetics, The Journal of Pediatrics and American Journal of Medical Genetics.

In The Last Decade

Siu‐Li Yong

12 papers receiving 1.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association

1981 610 citations Roberta A Pagon, John M. Graham et al. The Journal of Pediatrics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Siu‐Li Yong Canada	11	523	437	420	353	326	12	1.2k
Sabine Sigaudy France	21	217 0.4×	215 0.5×	205 0.5×	629 1.8×	535 1.6×	70	1.3k
Marie‐Louise Briard France	21	236 0.5×	221 0.5×	287 0.7×	630 1.8×	418 1.3×	55	1.4k
Susan Fernbach United States	15	426 0.8×	492 1.1×	370 0.9×	1.2k 3.5×	289 0.9×	20	2.1k
Conny M.A. van Ravenswaaij Netherlands	11	709 1.4×	574 1.3×	379 0.9×	628 1.8×	676 2.1×	13	1.5k
Charles W. McCluggage United States	13	215 0.4×	125 0.3×	96 0.2×	175 0.5×	190 0.6×	15	689
Johanna M. van Hagen Netherlands	17	263 0.5×	275 0.6×	195 0.5×	446 1.3×	322 1.0×	41	1.0k
Beate Albrecht Germany	23	126 0.2×	114 0.3×	214 0.5×	862 2.4×	1.0k 3.2×	45	1.7k
Louise C. Wilson United Kingdom	20	122 0.2×	88 0.2×	178 0.4×	629 1.8×	638 2.0×	46	1.2k
Sirpa Ala‐Mello Finland	17	140 0.3×	88 0.2×	187 0.4×	498 1.4×	468 1.4×	29	1.2k
Chia‐Cheng Hung Taiwan	19	165 0.3×	94 0.2×	81 0.2×	310 0.9×	181 0.6×	38	785

Countries citing papers authored by Siu‐Li Yong

Since Specialization

Citations

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

Fields of papers citing papers by Siu‐Li Yong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Siu‐Li Yong. 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 Siu‐Li Yong. The network helps show where Siu‐Li Yong may publish in the future.

Co-authorship network of co-authors of Siu‐Li Yong

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

Cohen, Ana S.A., Katelin N. Townsend, Christof Senger, et al.. (2014). Somatic mosaicism for the p.His1047Arg mutation in PIK3CA in a girl with mesenteric lipomatosis. American Journal of Medical Genetics Part A. 164(9). 2360–2364. 11 indexed citations

Peñaherrera, Maria S., Margot I. Van Allen, Siu‐Li Yong, et al.. (2010). Methylation profiling in individuals with Russell–Silver syndrome. American Journal of Medical Genetics Part A. 152A(2). 347–355. 29 indexed citations

Chijiwa, Chieko, Saadet Mercimek‐Mahmutoglu, Laura Stewart, et al.. (2010). Pseudohypoparathyroidism type 1a and the GNAS p.R231H mutation: Somatic mosaicism in a mother with two affected sons. American Journal of Medical Genetics Part A. 152A(11). 2784–2790. 12 indexed citations

Wang, Jia‐Chi, Brenda Lomax, Lesley Turner, et al.. (2009). Molecular breakpoint mapping of 6q11‐q14 interstitial deletions in seven patients. American Journal of Medical Genetics Part A. 149A(3). 372–379. 6 indexed citations

Wang, Jia‐Chi, Michelle Steinraths, Brenda Lomax, et al.. (2007). Craniosynostosis associated with distal 5q‐trisomy: Further evidence that extra copy of MSX2 gene leads to craniosynostosis. American Journal of Medical Genetics Part A. 143A(24). 2931–2936. 15 indexed citations

Dill, F. J., et al.. (2001). Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters. American Journal of Medical Genetics. 101(1). 65–69. 40 indexed citations

Choy, Francis Y.M., Chao Wei, Derek A. Applegarth, & Siu‐Li Yong. (1994). A new missense mutation in glucocerebrosidase exon 9 of a non Jewish Caucasian type 1 Gaucher disease patient. Human Molecular Genetics. 3(5). 821–823. 14 indexed citations

Allen, Margot I. Van, D. M. Juriloff, Muriel J. Harris, et al.. (1993). Evidence for multi‐site closure of the neural tube in humans. American Journal of Medical Genetics. 47(5). 723–743. 280 indexed citations

Allen, Margot I. Van, Giorgio Filippi, Jacqueline Siegel‐Bartelt, et al.. (1993). Clinical variability within Brachmann‐de Lange syndrome: A proposed classification system. American Journal of Medical Genetics. 47(7). 947–958. 63 indexed citations

10.

Gunasekaran, Thirumazhisai S., Eric Hassall, Urs P. Steinbrecher, & Siu‐Li Yong. (1992). Recurrence of extrahepatic biliary atresia in two half sibs. American Journal of Medical Genetics. 43(3). 592–594. 20 indexed citations

11.

Pagon, Roberta A, John M. Graham, Jonathan Zonana, & Siu‐Li Yong. (1981). Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association. The Journal of Pediatrics. 99(2). 223–227. 610 indexed citations breakdown →

12.

Lowry, R. Brian, Siu‐Li Yong, & John M. Opitz. (1980). Borderline normal intelligence in the Smith‐Lemli‐Opitz (RSH) syndrome. American Journal of Medical Genetics. 5(2). 137–143. 89 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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