William Chia

7.1k total citations · 1 hit paper
90 papers, 5.9k citations indexed

About

William Chia is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, William Chia has authored 90 papers receiving a total of 5.9k indexed citations (citations by other indexed papers that have themselves been cited), including 83 papers in Molecular Biology, 34 papers in Cell Biology and 26 papers in Cellular and Molecular Neuroscience. Recurrent topics in William Chia's work include Developmental Biology and Gene Regulation (44 papers), Neurobiology and Insect Physiology Research (22 papers) and Hippo pathway signaling and YAP/TAZ (15 papers). William Chia is often cited by papers focused on Developmental Biology and Gene Regulation (44 papers), Neurobiology and Insect Physiology Research (22 papers) and Hippo pathway signaling and YAP/TAZ (15 papers). William Chia collaborates with scholars based in Singapore, United Kingdom and United States. William Chia's co-authors include Xiaohang Yang, Michael Zavortink, Xavier Morin, Richard Daneman, Fengwei Yu, Hongyan Wang, Yu Cai, J. John Holbrook, Tony Atkinson and Anthony R. Clarke and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

William Chia

90 papers receiving 5.8k citations

Hit Papers

A protein trap strategy t... 2001 2026 2009 2017 2001 200 400 600

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
William Chia 4.6k 2.2k 1.2k 640 529 90 5.9k
John Sondek 7.8k 1.7× 2.9k 1.3× 1.2k 1.0× 712 1.1× 534 1.0× 114 10.0k
David A. Zacharias 6.2k 1.3× 1.6k 0.7× 1.5k 1.2× 506 0.8× 221 0.4× 33 8.3k
David Drechsel 8.0k 1.7× 3.7k 1.6× 738 0.6× 458 0.7× 258 0.5× 49 10.1k
Nicholas J. Cowan 8.7k 1.9× 5.0k 2.2× 1.4k 1.1× 559 0.9× 659 1.2× 98 12.1k
Kenneth E. Prehoda 3.0k 0.7× 2.3k 1.0× 582 0.5× 189 0.3× 393 0.7× 60 4.2k
David J. Owen 7.0k 1.5× 5.4k 2.4× 661 0.5× 532 0.8× 267 0.5× 78 9.3k
Susan R. Wente 9.7k 2.1× 1.7k 0.8× 260 0.2× 781 1.2× 187 0.4× 106 11.0k
Takanari Inoue 3.9k 0.8× 1.7k 0.8× 1.0k 0.8× 313 0.5× 328 0.6× 81 5.5k
Sally A. Lewis 4.2k 0.9× 2.7k 1.2× 512 0.4× 302 0.5× 319 0.6× 43 5.4k
Jeffrey Field 4.8k 1.0× 1.6k 0.7× 494 0.4× 392 0.6× 132 0.2× 87 6.7k

Countries citing papers authored by William Chia

Since Specialization
Citations

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

Fields of papers citing papers by William Chia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William Chia

This figure shows the co-authorship network connecting the top 25 collaborators of William Chia. A scholar is included among the top collaborators of William Chia 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 William Chia. William Chia 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.
Udolph, Gerald, Murni Tio, Wanru Fang, et al.. (2009). On the roles of Notch, Delta, kuzbanian, and inscuteable during the development of Drosophila embryonic neuroblast lineages. Developmental Biology. 336(2). 156–168. 19 indexed citations
2.
Chia, William, et al.. (2008). Klumpfuss is involved in the determination of sensory organ precursors in Drosophila. Developmental Biology. 324(2). 177–191. 13 indexed citations
3.
Wang, Cheng, Ruifeng Lu, Xuezhi Ouyang, et al.. (2007). DrosophilaOverexpressing Parkin R275W Mutant Exhibits Dopaminergic Neuron Degeneration and Mitochondrial Abnormalities. Journal of Neuroscience. 27(32). 8563–8570. 97 indexed citations
4.
Wasser, Martin, et al.. (2007). EAST and Chromator control the destruction and remodeling of muscles during Drosophila metamorphosis. Developmental Biology. 307(2). 380–393. 25 indexed citations
5.
Wang, Hongyan, Yingshi Ouyang, W. Gregory Somers, William Chia, & Bingwei Lu. (2007). Polo inhibits progenitor self-renewal and regulates Numb asymmetry by phosphorylating Pon. Nature. 449(7158). 96–100. 147 indexed citations
6.
Buescher, Marita, Murni Tio, Guy Tear, et al.. (2006). Functions of the segment polarity genes midline and H15 in Drosophila melanogaster neurogenesis. Developmental Biology. 292(2). 418–429. 17 indexed citations
7.
Babu, Kavita, Sami Bahri, Luke Alphey, & William Chia. (2005). Bifocal and PP1 interaction regulates targeting of the R-cell growth cone in Drosophila. Developmental Biology. 288(2). 372–386. 9 indexed citations
8.
Wei, Shu‐Yi, Luis M. Escudero, Fengwei Yu, et al.. (2005). Echinoid Is a Component of Adherens Junctions That Cooperates with DE-Cadherin to Mediate Cell Adhesion. Developmental Cell. 8(4). 493–504. 146 indexed citations
9.
Wang, Hongyan, et al.. (2005). Ric-8 controls Drosophila neural progenitor asymmetric division by regulating heterotrimeric G proteins. Nature Cell Biology. 7(11). 1091–1098. 106 indexed citations
10.
Conder, Ryan, Hong Yu, Michael G. Ricos, et al.. (2004). dPak is required for integrity of the leading edge cytoskeleton during Drosophila dorsal closure but does not signal through the JNK cascade. Developmental Biology. 276(2). 378–390. 26 indexed citations
11.
Buescher, Marita, et al.. (2004). Drosophila T Box Proteins Break the Symmetry of Hedgehog-Dependent Activation of wingless. Current Biology. 14(19). 1694–1702. 36 indexed citations
13.
Tuxworth, Richard I. & William Chia. (2003). Asymmetric Cell Division. Molecular Cell. 11(2). 288–289. 4 indexed citations
14.
Udolph, Gerald, et al.. (2002). Inscuteable‐independent apicobasally oriented asymmetric divisions in the Drosophila embryonic CNS. EMBO Reports. 3(7). 660–665. 8 indexed citations
15.
Morin, Xavier, Richard Daneman, Michael Zavortink, & William Chia. (2001). A protein trap strategy to detect GFP-tagged proteins expressed from their endogenous loci in Drosophila. Proceedings of the National Academy of Sciences. 98(26). 15050–15055. 653 indexed citations breakdown →
16.
Bahri, Sami, William Chia, & Xiaohang Yang. (2001). Characterization and mutant analysis of the Drosophila sema 5c gene. Developmental Dynamics. 221(3). 322–330. 18 indexed citations
17.
Murugasu-Oei, B., Rohini Balakrishnan, Xiaohang Yang, William Chia, & Verônica Rodrigues. (1996). Mutations in masquerade, a novel serine-protease-like molecule, affect axonal guidance and taste behavior in Drosophila. Mechanisms of Development. 57(1). 91–101. 15 indexed citations
18.
Chia, William, et al.. (1992). Apical secretion and association of the Drosophila yellow gene product with developing larval cuticle structures during embryogenesis. Molecular and General Genetics MGG. 235(2-3). 397–405. 37 indexed citations
19.
Martin, Mark O., et al.. (1989). Regulatory elements involved in the tissue-specific expression of the yellow gene of Drosophila. Molecular and General Genetics MGG. 218(1). 118–126. 60 indexed citations
20.
Howes, G., Mark J. O’Connor, & William Chia. (1988). On the specificity and effects on transcription of P-element insertions at theyellowlocus ofDrosophila melanogaster. Nucleic Acids Research. 16(7). 3039–3052. 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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