Chiara Auwerx

716 total citations
16 papers, 226 citations indexed

About

Chiara Auwerx is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Chiara Auwerx has authored 16 papers receiving a total of 226 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Chiara Auwerx's work include Genetic Associations and Epidemiology (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (3 papers). Chiara Auwerx is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (3 papers). Chiara Auwerx collaborates with scholars based in Switzerland, Estonia and United Kingdom. Chiara Auwerx's co-authors include Zoltán Kutalik, Marie C. Sadler, Alexandre Reymond, Eleonora Porcu, Andres Metspalu, Kaido Lepik, Reedik Mägi, Diogo M. Ribeiro, Toshiko Tanaka and Olivier Delaneau and has published in prestigious journals such as Nature Communications, The American Journal of Human Genetics and Genome biology.

In The Last Decade

Chiara Auwerx

15 papers receiving 225 citations

Peers

Chiara Auwerx

GENET

PPCH

PHYSI

Katarzyna A. Ellsworth United States

Graciela Moya Argentina

Nasim Monfared Canada

Mukesh Tanwar India

Ajay Jajodia India

Tao Qiu China

Lester Hui United States

Said Al‐Yahyaee Oman

Barbka Repič Lampret Slovenia

Mauricio De Castro United States

Katarzyna A. Ellsworth United States

Chiara Auwerx

124 ×1.0

GENET

106 ×0.9

20 ×0.6

PPCH

27 ×1.2

PHYSI

45 ×2.6

Citations per year, relative to Chiara Auwerx Chiara Auwerx (= 1×) peers Katarzyna A. Ellsworth

Countries citing papers authored by Chiara Auwerx

Since Specialization

Citations

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

Fields of papers citing papers by Chiara Auwerx

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Auwerx

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

All Works

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16 of 16 papers shown

Sadler, Marie C., et al.. (2025). Leveraging large-scale biobank EHRs to enhance pharmacogenetics of cardiometabolic disease medications. Nature Communications. 16(1). 2913–2913. 2 indexed citations

Graaf, Adriaan van der, et al.. (2025). MR-link-2: pleiotropy robust cis Mendelian randomization validated in three independent reference datasets of causality. Nature Communications. 16(1). 6112–6112.

Sadler, Marie C., et al.. (2024). Breaking down causes, consequences, and mediating effects of telomere length variation on human health. Genome biology. 25(1). 125–125. 6 indexed citations

Auwerx, Chiara, et al.. (2024). Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVs. The American Journal of Human Genetics. 111(11). 2347–2361. 1 indexed citations

Auwerx, Chiara, Zoltán Kutalik, & Alexandre Reymond. (2024). The pleiotropic spectrum of proximal 16p11.2 CNVs. The American Journal of Human Genetics. 111(11). 2309–2346. 1 indexed citations

Auwerx, Chiara, Marie C. Sadler, C. Clark, et al.. (2024). Rare copy-number variants as modulators of common disease susceptibility. Genome Medicine. 16(1). 5–5. 15 indexed citations

Auwerx, Chiara, Marie C. Sadler, Adriaan van der Graaf, et al.. (2023). The impact of 22q11.2 copy-number variants on human traits in the general population. The American Journal of Human Genetics. 110(2). 300–313. 4 indexed citations

Hanßen, Ruth, Chiara Auwerx, Marie C. Sadler, et al.. (2023). Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease. Cell Reports Medicine. 4(8). 101155–101155. 14 indexed citations

Sadler, Marie C., Chiara Auwerx, Patrick Deelen, & Zoltán Kutalik. (2023). Multi-layered genetic approaches to identify approved drug targets. Cell Genomics. 3(7). 100341–100341. 13 indexed citations

10.

Auwerx, Chiara, et al.. (2023). Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations. eLife. 12. 17 indexed citations

11.

Auwerx, Chiara, Marie C. Sadler, Alexandre Reymond, & Zoltán Kutalik. (2022). From pharmacogenetics to pharmaco-omics: Milestones and future directions. Human Genetics and Genomics Advances. 3(2). 100100–100100. 25 indexed citations

12.

Lepamets, Maarja, Chiara Auwerx, Margit Nõukas, et al.. (2022). Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations. Human Genetics and Genomics Advances. 3(4). 100133–100133. 5 indexed citations

13.

Sadler, Marie C., Chiara Auwerx, Kaido Lepik, Eleonora Porcu, & Zoltán Kutalik. (2022). Quantifying the role of transcript levels in mediating DNA methylation effects on complex traits and diseases. Nature Communications. 13(1). 7559–7559. 14 indexed citations

14.

Auwerx, Chiara, Maarja Lepamets, Marie C. Sadler, et al.. (2022). The individual and global impact of copy-number variants on complex human traits. The American Journal of Human Genetics. 109(4). 647–668. 35 indexed citations

15.

Porcu, Eleonora, Marie C. Sadler, Kaido Lepik, et al.. (2021). Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome. Nature Communications. 12(1). 5647–5647. 63 indexed citations

16.

Mounier, Ninon, Chiara Auwerx, Eirini Marouli, et al.. (2021). Composite trait Mendelian randomization reveals distinct metabolic and lifestyle consequences of differences in body shape. Communications Biology. 4(1). 1064–1064. 11 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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