Laurène Syx
- Genetics top 10%
- Genetic Syndromes and Imprinting 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetics and Neurodevelopmental Disorders 2
-
- Genomics and Chromatin Dynamics 7
- Epigenetics and DNA Methylation 5
- RNA modifications and cancer 1
- Single-cell and spatial transcriptomics 1
- CRISPR and Genetic Engineering 1
- Co-authors
- Édith HeardAurélie BousardJan J ŻyliczSimão Teixeira da RochaChongjian ChenChristel PicardMaud BorenszteinEmmanuel Barillot
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Laurène Syx
10 papers receiving 584 citations
Peers
Comparison fields: 5 of 51
- Genetics 258
- Cancer Research 134
- Molecular Biology 510
- Aging 7
- Immunology 36
Countries citing papers authored by Laurène Syx
This map shows the geographic impact of Laurène Syx'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 Laurène Syx with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laurène Syx more than expected).
Fields of papers citing papers by Laurène Syx
This network shows the impact of papers produced by Laurène Syx. 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 Laurène Syx. The network helps show where Laurène Syx may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Laurène Syx, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 2 | |
| 2 | 2021 | 11 | |
| 3 | 2019 | 83 | |
| 4 | 2019 | 38 | |
| 5 | 2018 | 183 | |
| 6 | 2018 | 3 | |
| 7 | 2017 | 116 | |
| 8 | 2017 | 47 | |
| 9 | 2016 | 93 | |
| 10 | 2014 | 12 |
About Laurène Syx
Laurène Syx is a scholar working on Genetics, Molecular Biology and Cancer Research, having authored 10 papers that have together received 588 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (7 papers), Epigenetics and DNA Methylation (5 papers), Genetic Syndromes and Imprinting (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), RNA modifications and cancer (1 paper), Single-cell and spatial transcriptomics (1 paper) and CRISPR and Genetic Engineering (1 paper). The work is most often cited by research in Genetics (258 citations), Cancer Research (134 citations) and Molecular Biology (510 citations). Laurène Syx has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Édith Heard, Aurélie Bousard, Jan J Żylicz, Simão Teixeira da Rocha, Chongjian Chen, Christel Picard, Maud Borensztein, Emmanuel Barillot, Nicolas Servant and Katia Ancelin. Their work appears in journals such as Cell, Nature Communications and PLoS ONE.
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.