Céline Vallot

3.2k total citations · 1 hit paper
35 papers, 1.7k citations indexed

About

Céline Vallot is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Céline Vallot has authored 35 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 12 papers in Cancer Research and 9 papers in Genetics. Recurrent topics in Céline Vallot's work include Single-cell and spatial transcriptomics (10 papers), Epigenetics and DNA Methylation (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Céline Vallot is often cited by papers focused on Single-cell and spatial transcriptomics (10 papers), Epigenetics and DNA Methylation (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Céline Vallot collaborates with scholars based in France, United States and United Kingdom. Céline Vallot's co-authors include Claire Rougeulle, Fabien Reyal, Adeline Durand, Christophe Huret, Annelise Bennaceur‐Griscelli, François Radvanyi, Justine Marsolier, Kevin Grosselin, Ahmed Dahmani and Elisabetta Marangoni and has published in prestigious journals such as Nature Communications, Nature Genetics and Nature reviews. Cancer.

In The Last Decade

Céline Vallot

33 papers receiving 1.7k 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.

High-throughput single-cell ChIP-seq identifies heterogeneity of chromatin states in breast cancer

2019 329 citations Kevin Grosselin, Adeline Durand et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Céline Vallot France	19	1.3k	494	334	267	164	35	1.7k
Silvana Debernardi United Kingdom	21	1.4k 1.1×	642 1.3×	256 0.8×	244 0.9×	127 0.8×	39	2.1k
Yuval Tabach Israel	20	1.6k 1.2×	460 0.9×	204 0.6×	479 1.8×	90 0.5×	49	2.1k
Rik G.H. Lindeboom Netherlands	19	1.5k 1.2×	365 0.7×	240 0.7×	285 1.1×	66 0.4×	26	1.9k
Dávid Szüts Hungary	23	1.4k 1.1×	515 1.0×	217 0.6×	428 1.6×	106 0.6×	56	1.7k
Christiaan Klijn Netherlands	20	1.2k 1.0×	407 0.8×	342 1.0×	813 3.0×	131 0.8×	30	1.8k
Qiu Wu China	16	2.2k 1.7×	714 1.4×	233 0.7×	363 1.4×	276 1.7×	57	2.7k
Mélanie Letexier France	12	1.3k 1.0×	432 0.9×	372 1.1×	304 1.1×	156 1.0×	17	2.0k
Roser Pinyol Spain	17	972 0.8×	376 0.8×	102 0.3×	274 1.0×	257 1.6×	24	1.8k
Mónica Álvarez‐Fernández Spain	22	1.4k 1.1×	282 0.6×	185 0.6×	529 2.0×	288 1.8×	30	1.9k
Ondřej Gojiš United Kingdom	11	1.2k 0.9×	298 0.6×	296 0.9×	279 1.0×	104 0.6×	18	1.6k

Countries citing papers authored by Céline Vallot

Since Specialization

Citations

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

Fields of papers citing papers by Céline Vallot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Céline Vallot

This figure shows the co-authorship network connecting the top 25 collaborators of Céline Vallot. A scholar is included among the top collaborators of Céline Vallot 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 Céline Vallot. Céline Vallot 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

Huret, Christophe, Laura Sourd, Ahmed Dahmani, et al.. (2025). Characterization of Drug-Tolerant Persister Cells in Triple-Negative Breast Cancer Identifies a Shared Persistence Program across Treatments and Patients. Cancer Research. 86(3). 802–817. 1 indexed citations

Lupien, Mathieu, et al.. (2024). Epigenomic heterogeneity as a source of tumour evolution. Nature reviews. Cancer. 25(1). 7–26. 20 indexed citations

Vert, Jean‐Philippe, et al.. (2023). A benchmark of computational pipelines for single-cell histone modification data. Genome biology. 24(1). 143–143. 5 indexed citations

Vallot, Céline. (2023). RNA barcoding: the catalyst for the single-cell revolution. Nature Reviews Genetics. 24(8). 491–491. 1 indexed citations

Vallot, Céline. (2022). Epigenomic tumor evolution under the spotlight: the promises of single-cell approaches. Comptes Rendus Biologies. 345(1). 11–16. 1 indexed citations

Marsolier, Justine, Adeline Durand, Anne-Marie Lyne, et al.. (2022). H3K27me3 conditions chemotolerance in triple-negative breast cancer. Nature Genetics. 54(4). 459–468. 80 indexed citations

Marsolier, Justine, et al.. (2020). Interactive analysis of single-cell epigenomic landscapes with ChromSCape. Nature Communications. 11(1). 5702–5702. 16 indexed citations

Grosselin, Kevin, Adeline Durand, Justine Marsolier, et al.. (2019). High-throughput single-cell ChIP-seq identifies heterogeneity of chromatin states in breast cancer. Nature Genetics. 51(6). 1060–1066. 329 indexed citations breakdown →

Vallot, Céline & Claire Rougeulle. (2016). Single-cell Visualization of Chromosome Transcriptional Territories by RNA-paint. BIO-PROTOCOL. 6(17). 2 indexed citations

10.

Vallot, Céline, Sébastien Briois, Marion Aguirrebengoa, et al.. (2015). A vlincRNA participates in senescence maintenance by relieving H2AZ-mediated repression at the INK4 locus. Nature Communications. 6(1). 5971–5971. 48 indexed citations

11.

Vallot, Céline, Jean‐François Ouimette, M. Makhlouf, et al.. (2015). Erosion of X Chromosome Inactivation in Human Pluripotent Cells Initiates with XACT Coating and Depends on a Specific Heterochromatin Landscape. Cell stem cell. 16(5). 533–546. 102 indexed citations

12.

Vallot, Céline, et al.. (2014). PRC2-independent chromatin compaction and transcriptional repression in cancer. Oncogene. 34(6). 741–751. 7 indexed citations

13.

Vallot, Céline, Christophe Huret, Yann Lesecque, et al.. (2013). XACT, a long noncoding transcript coating the active X chromosome in human pluripotent cells. Nature Genetics. 45(3). 239–241. 105 indexed citations

14.

Vallot, Céline & Claire Rougeulle. (2013). Inactivation du chromosome X chez l’humain. médecine/sciences. 29(2). 223–225. 4 indexed citations

15.

Vallot, Céline & Claire Rougeulle. (2013). Long non-coding RNAs and human X-chromosome regulation. RNA Biology. 10(8). 1262–1265. 9 indexed citations

16.

Trésallet, Christophe, Antoine Brouquet, Catherine Julié, et al.. (2011). Evaluation of predictive models in daily practice for the identification of patients with Lynch syndrome. International Journal of Cancer. 130(6). 1367–1377. 18 indexed citations

17.

Vallot, Céline, Nicolas Stransky, Isabelle Bernard‐Pierrot, et al.. (2010). A Novel Epigenetic Phenotype Associated With the Most Aggressive Pathway of Bladder Tumor Progression. JNCI Journal of the National Cancer Institute. 103(1). 47–60. 59 indexed citations

18.

Estecio, Marcos R., Juan Gallegos, Céline Vallot, et al.. (2010). Genome architecture marked by retrotransposons modulates predisposition to DNA methylation in cancer. Genome Research. 20(10). 1369–1382. 67 indexed citations

19.

Bernard‐Pierrot, Isabelle, Nadège Gruel, Nicolas Stransky, et al.. (2008). Characterization of the Recurrent 8p11-12 Amplicon Identifies PPAPDC1B, a Phosphatase Protein, as a New Therapeutic Target in Breast Cancer. Cancer Research. 68(17). 7165–7175. 73 indexed citations

20.

Julié, Catherine, Christophe Trésallet, Antoine Brouquet, et al.. (2008). Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based ApproachVersusMolecular Screening. The American Journal of Gastroenterology. 103(11). 2825–2835. 89 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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