Laurène Syx

1.1k total citations
10 papers, 588 citations indexed

About

Laurène Syx is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Laurène Syx has authored 10 papers receiving a total of 588 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Laurène Syx's work include Genomics and Chromatin Dynamics (7 papers), Epigenetics and DNA Methylation (5 papers) and Genetic Syndromes and Imprinting (2 papers). Laurène Syx is often cited by papers focused on Genomics and Chromatin Dynamics (7 papers), Epigenetics and DNA Methylation (5 papers) and Genetic Syndromes and Imprinting (2 papers). Laurène Syx collaborates with scholars based in France, United Kingdom and United States. Laurène Syx's 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 and has published in prestigious journals such as Cell, Nature Communications and PLoS ONE.

In The Last Decade

Laurène Syx

10 papers receiving 584 citations

Peers

Countries citing papers authored by Laurène Syx

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Laurène Syx

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

#	Work	Indexed citations
1	Temporal and regional X-linked gene reactivation in the mouse germline reveals site-specific retention of epigenetic silencing 2025 ·Nature Structural & Molecular Biology ·(unknown), Laurène Syx, Emmanuelle Beyne, Peggy Raynaud, Dina Zielinski, Aurélie Teissandier, Caroline Lee, Marius Walter, Nicolas Servant, Karim Chébli, Déborah Bourc’his, M. Azim Surani, Maud Borensztein	2
2	Locus specific epigenetic modalities of random allelic expression imbalance 2021 ·Nature Communications ·Lucile Marion‐Poll, (unknown), Dina Zielinski, (unknown), Mikaël Attia, Ava C. Carter, Laurène Syx, Howard Y. Chang, Anne-Valérie Gendrel, Édith Heard	11
3	The role of Xist ‐mediated Polycomb recruitment in the initiation of X‐chromosome inactivation 2019 ·EMBO Reports ·Aurélie Bousard, Ana Cláudia Raposo, Jan J Żylicz, Christel Picard, (unknown), Yanyan Qi, (unknown), Laurène Syx, Howard Y. Chang, Édith Heard, Simão Teixeira da Rocha	83
4	Kinetics of Xist -induced gene silencing can be predicted from combinations of epigenetic and genomic features 2019 ·Genome Research ·(unknown), Iris H. Jonkers, Laurène Syx, Ilona Dunkel, Julie Chaumeil, Christel Picard, (unknown), Chongjian Chen, John T. Lis, Édith Heard, Edda G. Schulz, Annalisa Marsico	38
5	The Implication of Early Chromatin Changes in X Chromosome Inactivation 2018 ·Cell ·Jan J Żylicz, Aurélie Bousard, Kristina Žumer, François Dossin, Eusra Mohammad, Simão Teixeira da Rocha, Björn Schwalb, Laurène Syx, Florent Dingli, Damarys Loew, Patrick Cramer, Édith Heard	183
6	Transcriptome Profiling of Single Mouse Oocytes 2018 ·Methods in molecular biology ·Maud Borensztein, Laurène Syx, Nicolas Servant, Édith Heard	3
7	Xist-dependent imprinted X inactivation and the early developmental consequences of its failure 2017 ·Nature Structural & Molecular Biology ·Maud Borensztein, Laurène Syx, Katia Ancelin, Patricia Diabangouaya, Christel Picard, Tao Liu, Junbin Liang, (unknown), Rafael Galupa, Nicolas Servant, Emmanuel Barillot, M. Azim Surani, Chongjian Chen, Édith Heard	116
8	Contribution of epigenetic landscapes and transcription factors to X-chromosome reactivation in the inner cell mass 2017 ·Nature Communications ·Maud Borensztein, Ikuhiro Okamoto, Laurène Syx, Guillaume Guilbaud, Christel Picard, Katia Ancelin, Rafael Galupa, Patricia Diabangouaya, Nicolas Servant, Emmanuel Barillot, M. Azim Surani, Mitinori Saitou, Chongjian Chen, Konstantinos Anastassiadis, Édith Heard	47
9	Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activation 2016 ·eLife ·Katia Ancelin, Laurène Syx, Maud Borensztein, Noémie Ranisavljevic, (unknown), Luis Briseño-Roa, Tao Liu, Eric Metzger, Nicolas Servant, Emmanuel Barillot, Chongjian Chen, Roland Schüle, Édith Heard	93
10	Combined Linkage and Association Studies Show that HLA Class II Variants Control Levels of Antibodies against Epstein-Barr Virus Antigens 2014 ·PLoS ONE ·Vincent Pedergnana, Laurène Syx, Aurélie Cobat, Julien Guergnon, Pauline Brice, Christophe Fermé, Patrice Carde, Olivier Hermine, Catherine Le Pendeven, Corinne Amiel, Yassine Taoufik, Alexandre Alcaïs, Ioannis Theodorou, Caroline Besson, Laurent Abel	12

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.

Explore authors with similar magnitude of impact