Emmanuelle Viré

3.5k total citations · 1 hit paper
20 papers, 2.6k citations indexed

About

Emmanuelle Viré is a scholar working on Molecular Biology, Neurology and Neurology. According to data from OpenAlex, Emmanuelle Viré has authored 20 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 3 papers in Neurology and 3 papers in Neurology. Recurrent topics in Emmanuelle Viré's work include Epigenetics and DNA Methylation (8 papers), Prion Diseases and Protein Misfolding (6 papers) and RNA Research and Splicing (4 papers). Emmanuelle Viré is often cited by papers focused on Epigenetics and DNA Methylation (8 papers), Prion Diseases and Protein Misfolding (6 papers) and RNA Research and Splicing (4 papers). Emmanuelle Viré collaborates with scholars based in United Kingdom, United States and Spain. Emmanuelle Viré's co-authors include François Fuks, Luciano Di Croce, Lluís Morey, Manel Esteller, Mario F. Fraga, Loı̈c Blanchon, Aleyde Van Eynde, David Bernard, Céline Mirjolet and Rachel Deplus and has published in prestigious journals such as Nature, Nature Communications and The EMBO Journal.

In The Last Decade

Emmanuelle Viré

20 papers receiving 2.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The Polycomb group protein EZH2 directly controls DNA methylation

2005 1.7k citations Emmanuelle Viré, Carmen Brenner et al. Nature profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Emmanuelle Viré United Kingdom	13	2.2k	544	288	255	205	20	2.6k
Carmen Brenner Belgium	9	2.1k 0.9×	440 0.8×	302 1.0×	224 0.9×	132 0.6×	10	2.4k
Giuseppe Zardo Italy	21	2.3k 1.0×	1.1k 2.1×	252 0.9×	272 1.1×	212 1.0×	38	2.8k
Luke B. Hesson Australia	29	2.4k 1.1×	494 0.9×	284 1.0×	402 1.6×	101 0.5×	66	3.0k
Manuel Rodríguez‐Paredes Germany	18	1.5k 0.7×	381 0.7×	229 0.8×	290 1.1×	175 0.9×	24	2.1k
Ashley Lau United States	8	2.8k 1.2×	710 1.3×	277 1.0×	299 1.2×	148 0.7×	10	3.2k
Matteo Cesaroni United States	23	2.2k 1.0×	606 1.1×	186 0.6×	314 1.2×	137 0.7×	45	2.7k
Karl Agger Denmark	19	3.9k 1.8×	484 0.9×	551 1.9×	328 1.3×	191 0.9×	25	4.4k
Rachel Deplus Belgium	14	3.1k 1.4×	522 1.0×	571 2.0×	256 1.0×	169 0.8×	18	3.6k
Touati Benoukraf Singapore	23	1.5k 0.7×	487 0.9×	196 0.7×	285 1.1×	88 0.4×	47	2.0k
Fides D. Lay United States	16	1.8k 0.8×	374 0.7×	306 1.1×	122 0.5×	100 0.5×	20	2.1k

Countries citing papers authored by Emmanuelle Viré

Since Specialization

Citations

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

Fields of papers citing papers by Emmanuelle Viré

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanuelle Viré

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

All Works

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20 of 20 papers shown

1.

Jones, Emma, Elizabeth Hill, Jacqueline M. Linehan, et al.. (2023). Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6. Neurobiology of Disease. 190. 106363–106363. 3 indexed citations

2.

Shireby, Gemma, Yasuo Miki, Emmanuelle Viré, et al.. (2022). Epigenetic age acceleration is associated with oligodendrocyte proportions in MSA and control brain tissue. Neuropathology and Applied Neurobiology. 49(1). e12872–e12872. 9 indexed citations

3.

Kroll, François, Athanasios Dimitriadis, Tracy Campbell, et al.. (2022). Prion protein gene mutation detection using long-read Nanopore sequencing. Scientific Reports. 12(1). 8284–8284. 6 indexed citations

4.

Viré, Emmanuelle & Simon Mead. (2022). Gene expression and epigenetic markers of prion diseases. Cell and Tissue Research. 392(1). 285–294. 5 indexed citations

5.

Viré, Emmanuelle, Lee Darwent, Holger Hummerich, et al.. (2022). DNA methylation analysis of archival lymphoreticular tissues in Creutzfeldt–Jakob disease. Acta Neuropathologica. 144(4). 785–787. 2 indexed citations

6.

Campbell, Tracy, Tony Bélicard, Adam R. Smith, et al.. (2020). Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt–Jakob disease. Acta Neuropathologica. 140(6). 863–879. 16 indexed citations

7.

Norsworthy, Penny J., Andrew G.B. Thompson, Tze How Mok, et al.. (2020). A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis. Nature Communications. 11(1). 3960–3960. 25 indexed citations

8.

Bettencourt, Conceição, Yasuo Miki, Ignazio S. Piras, et al.. (2020). MOBP and HIP1 in multiple system atrophy: New α‐synuclein partners in glial cytoplasmic inclusions implicated in the disease pathogenesis. Neuropathology and Applied Neurobiology. 47(5). 640–652. 10 indexed citations

9.

Bettencourt, Conceição, Sandrine C. Foti, Yasuo Miki, et al.. (2019). White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy. Acta Neuropathologica. 139(1). 135–156. 33 indexed citations

10.

Amaral, Paulo, Tommaso Leonardi, Namshik Han, et al.. (2018). Genomic positional conservation identifies topological anchor point RNAs linked to developmental loci. Genome biology. 19(1). 32–32. 93 indexed citations

11.

Larrieu, Delphine, Emmanuelle Viré, Samuel C. Robson, et al.. (2018). Inhibition of the acetyltransferase NAT10 normalizes progeric and aging cells by rebalancing the Transportin-1 nuclear import pathway. Science Signaling. 11(537). 67 indexed citations

12.

Puddu, Fabio, Ilaria Guerini, Hengyao Niu, et al.. (2015). Synthetic viability genomic screening defines Sae2 function in DNA repair. The EMBO Journal. 34(11). 1509–1522. 36 indexed citations

13.

Viré, Emmanuelle, Christina Curtis, Verónica Dávalos, et al.. (2014). The Breast Cancer Oncogene EMSY Represses Transcription of Antimetastatic microRNA miR-31. Molecular Cell. 53(5). 806–818. 48 indexed citations

14.

Viré, Emmanuelle, Christina Curtis, Verónica Dávalos, et al.. (2014). The Breast Cancer Oncogene EMSY Represses Transcription of Antimetastatic microRNA miR-31. Molecular Cell. 54(1). 203–203. 6 indexed citations

15.

Xu, Hong, Jian Xian, Emmanuelle Viré, et al.. (2014). Up‐regulation of the interferon‐related genes in BRCA2 knockout epithelial cells. The Journal of Pathology. 234(3). 386–397. 21 indexed citations

16.

Hellebrekers, Debby M.E.I., Veerle Melotte, Emmanuelle Viré, et al.. (2007). Identification of Epigenetically Silenced Genes in Tumor Endothelial Cells. Cancer Research. 67(9). 4138–4148. 113 indexed citations

17.

Villa, Raffaella, Diego Pasini, Arantxa Gutiérrez, et al.. (2007). Role of the Polycomb Repressive Complex 2 in Acute Promyelocytic Leukemia. Cancer Cell. 11(6). 513–525. 191 indexed citations

18.

Hellebrekers, Debby M.E.I., Karolien Castermans, Emmanuelle Viré, et al.. (2006). Epigenetic Regulation of Tumor Endothelial Cell Anergy: Silencing of Intercellular Adhesion Molecule-1 by Histone Modifications. Cancer Research. 66(22). 10770–10777. 129 indexed citations

19.

Hellebrekers, Debby M.E.I., Kam-Wing Jair, Emmanuelle Viré, et al.. (2006). Angiostatic activity of DNA methyltransferase inhibitors. Molecular Cancer Therapeutics. 5(2). 467–475. 80 indexed citations

20.

Viré, Emmanuelle, Carmen Brenner, Rachel Deplus, et al.. (2005). The Polycomb group protein EZH2 directly controls DNA methylation. Nature. 439(7078). 871–874. 1676 indexed citations breakdown →

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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