S.W. Cheung

1.4k total citations
7 papers, 235 citations indexed

About

S.W. Cheung is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, S.W. Cheung has authored 7 papers receiving a total of 235 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Plant Science. Recurrent topics in S.W. Cheung's work include Genomic variations and chromosomal abnormalities (5 papers), Congenital heart defects research (4 papers) and Chromosomal and Genetic Variations (4 papers). S.W. Cheung is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Congenital heart defects research (4 papers) and Chromosomal and Genetic Variations (4 papers). S.W. Cheung collaborates with scholars based in United States, Denmark and Netherlands. S.W. Cheung's co-authors include James R. Lupski, Paweł Stankiewicz, Chad A. Shaw, Daryl A. Scott, Margaret Wat, Chester Brown, Ankita Patel, Christine M. Eng, Tomasz Gambin and Seema R. Lalani and has published in prestigious journals such as The American Journal of Human Genetics, Fertility and Sterility and Journal of Medical Genetics.

In The Last Decade

S.W. Cheung

7 papers receiving 221 citations

Peers

Countries citing papers authored by S.W. Cheung

Since Specialization

Citations

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

Fields of papers citing papers by S.W. Cheung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S.W. Cheung. 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 S.W. Cheung. The network helps show where S.W. Cheung may publish in the future.

Co-authorship network of co-authors of S.W. Cheung

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes 2014 ·The American Journal of Human Genetics ·Claudia M.B. Carvalho, Shivakumar Vasanth, Marwan Shinawi, (unknown), Melissa B. Ramocki, Chester Brown, Jesper Graakjær, Anne‐Bine Skytte, Angela Maria Vianna‐Morgante, Ana Cristina Victorino Krepischi, Gayle Patel, (unknown), Kyrieckos A. Aleck, Cynthia Lim, S.W. Cheung, Carla Rosenberg, Nicholas Katsanis, James R. Lupski	39
2	Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing 2013 ·European Journal of Human Genetics ·Joanna Wiszniewska, Weimin Bi, Chad A. Shaw, Paweł Stankiewicz, Sung‐Hae Kang, Amber N. Pursley, Seema R. Lalani, Patricia Hixson, Tomasz Gambin, (unknown), Hans-Georg O. Bock, Maria Descartes, Frank J. Probst, Fernando Scaglia, Arthur L. Beaudet, James R. Lupski, Christine M. Eng, S.W. Cheung, Carlos A. Bacino, Ankita Patel	77
3	Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia 2011 ·Journal of Medical Genetics ·Margaret Wat, Danielle Veenma, Jacob S. Hogue, Ashley M. Holder, (unknown), (unknown), Neil A. Hanchard, (unknown), Caraciolo J. Fernandes, Anthony E. Johnson, Kevin P. Lally, Anne Slavotinek, Olivier Danhaive, T Schaible, S.W. Cheung, Katherine A. Rauen, Vijay S. Tonk, Dick Tibboel, Annelies de Klein, Daryl A. Scott	65
4	Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond–Blackfan anaemia 2010 ·Journal of Medical Genetics ·Margaret Wat, (unknown), Wojciech Wiszniewski, Trevor Resnick, Patricia I. Bader, Elizabeth Roeder, Debra Freedenberg, Chester Brown, (unknown), S.W. Cheung, Daryl A. Scott	28
5	Application of metaphase HR‐CGH and targeted chromosomal microarray analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features 2008 ·American Journal of Medical Genetics Part A ·Beata Nowakowska, Paweł Stankiewicz, Ewa Obersztyn, Zhishuo Ou, Jessica Shu Nan Li, A. Craig Chinault, Marta Smyk, Katarzyna Borg, Tadeusz Mazurczak, S.W. Cheung, Ewa Bocian	12
6	Jumping 22q11.21 Translocation: Clinical Consequences and Counseling in an Oligospermic but Otherwise Healthy Adult Male 2005 ·Fertility and Sterility ·Sallie McAdoo, (unknown), L.I. Lipshultz, Joe Leigh Simpson, (unknown), S.W. Cheung	1
7	The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3 2003 ·Cytogenetic and Genome Research ·Paweł Stankiewicz, S.W. Cheung, Chad A. Shaw, Reza Saleki, Krisztián Szigeti, James R. Lupski	13

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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