Ken‐Shiung Chen

1.0k total citations
15 papers, 749 citations indexed

About

Ken‐Shiung Chen is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ken‐Shiung Chen has authored 15 papers receiving a total of 749 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ken‐Shiung Chen's work include Genetic Syndromes and Imprinting (4 papers), Neurogenetic and Muscular Disorders Research (4 papers) and RNA regulation and disease (3 papers). Ken‐Shiung Chen is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Neurogenetic and Muscular Disorders Research (4 papers) and RNA regulation and disease (3 papers). Ken‐Shiung Chen collaborates with scholars based in United States, Singapore and Taiwan. Ken‐Shiung Chen's co-authors include Lorraine Potocki, Thearith Koeuth, James R. Lupski, James R. Lupski, Prasad Manian, Qi Zhao, Yuchio Yanagawa, S.K. Alex Law, Takayoshi Masuoka and Shiro Konishi and has published in prestigious journals such as Nature Genetics, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

Ken‐Shiung Chen

15 papers receiving 733 citations

Peers

Countries citing papers authored by Ken‐Shiung Chen

Since Specialization

Citations

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

Fields of papers citing papers by Ken‐Shiung Chen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ken‐Shiung Chen. 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 Ken‐Shiung Chen. The network helps show where Ken‐Shiung Chen may publish in the future.

Co-authorship network of co-authors of Ken‐Shiung Chen

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Rasd1 Modulates the Coactivator Function of NonO in the Cyclic AMP Pathway 2011 ·PLoS ONE ·(unknown), (unknown), (unknown), Ken‐Shiung Chen	13
2	Rasd1 interacts with Ear2 (Nr2f6) to regulate renin transcription 2011 ·BMC Molecular Biology ·(unknown), (unknown), Ken‐Shiung Chen	14
3	UBE3A regulates MC1R expression: a link to hypopigmentation in Angelman syndrome 2011 ·Pigment Cell & Melanoma Research ·(unknown), Ken‐Shiung Chen	13
4	NMDA receptor activation enhances inhibitory GABAergic transmission onto hippocampal pyramidal neurons via presynaptic and postsynaptic mechanisms 2011 ·Journal of Neurophysiology ·(unknown), Takayoshi Masuoka, (unknown), Ken‐Shiung Chen, Yuchio Yanagawa, S.K. Alex Law, Shiro Konishi	56
5	Genome-wide gene expression profiling of the Angelman syndrome mice with Ube3a mutation 2010 ·European Journal of Human Genetics ·(unknown), Ken‐Shiung Chen	19
6	Genetic Studies of Prader-Willi Patients Provide Evidence for Conservation of Genomic Architecture in Proximal Chromosome 15q 2010 ·Annals of Human Genetics ·Aihua Hou, Shuan‐Pei Lin, (unknown), (unknown), Hsiang‐Yu Lin, (unknown), Chi‐Yu Huang, (unknown), Chih‐Kuang Chuang, Ken‐Shiung Chen	1
7	Mouse imprinting defect mutations that model Angelman syndrome 2006 ·genesis ·Mei‐Yi Wu, Ken‐Shiung Chen, Jan Bressler, Aihua Hou, Ting‐Fen Tsai, Arthur L. Beaudet	23
8	Fliih, a Gelsolin-Related Cytoskeletal Regulator Essential for Early Mammalian Embryonic Development 2002 ·Molecular and Cellular Biology ·Hugh D. Campbell, (unknown), Ian S. McLennan, Leise A. Berven, Michael F. Crouch, (unknown), (unknown), (unknown), Ken‐Shiung Chen, James R. Lupski, Birgit Ledermann, Ian G. Young, Klaus I. Matthaei	75
9	Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome 2001 ·Human Genetics ·(unknown), Manju Ghosh, Saima Riazuddin, Sadaf Naz, Shaheen Khan, Zubair M. Ahmed, Sheikh Riazuddin, Yong Liang, P.S.N. Menon, Tenesha N. Smith, Ann C. M. Smith, Ken‐Shiung Chen, James R. Lupski, Edward R. Wilcox, Lorraine Potocki, Thomas B. Friedman	94
10	Subunit 3 of the COP9 Signal Transduction Complex Is Conserved from Plants to Humans and Maps within the Smith–Magenis Syndrome Critical Region in 17p11.2 1999 ·Genomics ·Lorraine Potocki, Ken‐Shiung Chen, James R. Lupski	24
11	DNA Rearrangements on Both Homologues of Chromosome 17 in a Mildly Delayed Individual with a Family History of Autosomal Dominant Carpal Tunnel Syndrome 1999 ·The American Journal of Human Genetics ·Lorraine Potocki, Ken‐Shiung Chen, Thearith Koeuth, James M. Killian, Susan T. Iannaccone, Stuart K. Shapira, Catherine D. Kashork, Aimee S. Spikes, Lisa G. Shaffer, James R. Lupski	49
12	Prenatal Diagnosis of Charcot‐Marie‐Tooth Disease Type 1A 1999 ·Annals of the New York Academy of Sciences ·Catherine D. Kashork, Ken‐Shiung Chen, James R. Lupski, Lisa G. Shaffer	3
13	Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome 1997 ·Nature Genetics ·Ken‐Shiung Chen, Prasad Manian, Thearith Koeuth, Lorraine Potocki, Qi Zhao, (unknown), (unknown), James R. Lupski	296
14	The Smith-Magenis syndrome [del(17)p11.2]: Clinical review and molecular advances 1996 ·Mental Retardation and Developmental Disabilities Research Reviews ·Ken‐Shiung Chen, Lorraine Potocki, James R. Lupski	47
15	Smith‐Magenis syndrome deletion: A case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization 1995 ·American Journal of Medical Genetics ·Ramesh C. Juyal, Frank Greenberg, (unknown), James R. Lupski, Barbara J. Trask, Ger van den Engh, Elizabeth A. Lindsay, (unknown), Ken‐Shiung Chen, Antonio Baldini, Lisa G. Shaffer, Pragna I. Patel	22

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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