Clement Chu

1.3k total citations
8 papers, 292 citations indexed

About

Clement Chu is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Clement Chu has authored 8 papers receiving a total of 292 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Clement Chu's work include Genomics and Rare Diseases (3 papers), DNA Repair Mechanisms (2 papers) and BRCA gene mutations in cancer (2 papers). Clement Chu is often cited by papers focused on Genomics and Rare Diseases (3 papers), DNA Repair Mechanisms (2 papers) and BRCA gene mutations in cancer (2 papers). Clement Chu collaborates with scholars based in United States, Germany and Israel. Clement Chu's co-authors include Irina Artsimovitch, Robert Landick, A. Simon Lynch, Ashley K. Tehranchi, Jacob E. Corn, James M. Berger, James L. Keck, Jue D. Wang, Dale Muzzey and Jared Maguire and has published in prestigious journals such as Science, PLoS ONE and Clinical Chemistry.

In The Last Decade

Clement Chu

8 papers receiving 280 citations

Peers

Clement Chu

GENET

MB

PPCH

ECOLO

PRM

Tatjana Jatsenko Estonia

David Ding United States

Haijun Zhu China

Naveen Kumar Nair India

Paolo Strigini Italy

Miriam Groß Germany

Christine Lüthi Switzerland

Dejiu Zhang China

Dilek Imanci France

T. P. Lin United States

Tatjana Jatsenko Estonia

Clement Chu

99 ×0.6

GENET

219 ×1.4

MB

106 ×2.0

PPCH

43 ×1.3

ECOLO

11 ×0.3

PRM

Citations per year, relative to Clement Chu Clement Chu (= 1×) peers Tatjana Jatsenko

Countries citing papers authored by Clement Chu

Since Specialization

Citations

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

Fields of papers citing papers by Clement Chu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clement Chu

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

All Works

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8 of 8 papers shown

1.

Welker, Noah C., et al.. (2020). High-throughput fetal fraction amplification increases analytical performance of noninvasive prenatal screening. Genetics in Medicine. 23(3). 443–450. 27 indexed citations

2.

Hogan, Gregory J., Valentina Vysotskaia, Kyle A. Beauchamp, et al.. (2018). Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification. Clinical Chemistry. 64(7). 1063–1073. 46 indexed citations

3.

Grauman, Peter, Lindsay Spurka, Irving E. Wang, et al.. (2018). Detecting clinically actionable variants in the 3′ exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogene. BMC Medical Genetics. 19(1). 176–176. 14 indexed citations

4.

Vysotskaia, Valentina, Gregory J. Hogan, Xin Wang, et al.. (2017). Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment. PeerJ. 5. e3046–e3046. 15 indexed citations

5.

Kang, Hyunseok P., Jared Maguire, Clement Chu, et al.. (2016). Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing. PeerJ. 4. e2162–e2162. 13 indexed citations

6.

Zielinski, Dina, Barak Markus, Mona A. Sheikh, et al.. (2014). OTX2 Duplication Is Implicated in Hemifacial Microsomia. PLoS ONE. 9(5). e96788–e96788. 35 indexed citations

7.

Tehranchi, Ashley K., Clement Chu, Jacob E. Corn, et al.. (2012). Binding Mechanism of Metal⋅NTP Substrates and Stringent-Response Alarmones to Bacterial DnaG-Type Primases. Structure. 20(9). 1478–1489. 56 indexed citations

8.

Artsimovitch, Irina, Clement Chu, A. Simon Lynch, & Robert Landick. (2003). A New Class of Bacterial RNA Polymerase Inhibitor Affects Nucleotide Addition. Science. 302(5645). 650–654. 86 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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