Vanessa Besson

888 total citations
15 papers, 683 citations indexed

About

Vanessa Besson is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Vanessa Besson has authored 15 papers receiving a total of 683 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Surgery. Recurrent topics in Vanessa Besson's work include Congenital heart defects research (4 papers), Mesenchymal stem cell research (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Vanessa Besson is often cited by papers focused on Congenital heart defects research (4 papers), Mesenchymal stem cell research (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Vanessa Besson collaborates with scholars based in France, Netherlands and United Kingdom. Vanessa Besson's co-authors include David Sassoon, Giovanna Marazzi, Alice Pannérec, Edgar R. Gomes, Ara Parlakian, Bruno Cadot, Kathryn J. Mitchell, Yann Hérault, Arnaud Duchon and Véronique Brault and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Cell Biology and Circulation Research.

In The Last Decade

Vanessa Besson

14 papers receiving 680 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vanessa Besson France	10	523	228	206	154	91	15	683
Jiayin Yang China	11	998 1.9×	311 1.4×	126 0.6×	259 1.7×	98 1.1×	26	1.2k
Laura Menéndez United States	10	759 1.5×	145 0.6×	87 0.4×	122 0.8×	46 0.5×	12	995
Jana Juhásová Czechia	16	370 0.7×	144 0.6×	99 0.5×	95 0.6×	30 0.3×	52	700
Sara Benedetti United Kingdom	12	485 0.9×	227 1.0×	123 0.6×	71 0.5×	62 0.7×	25	639
Courtney S. Young United States	12	862 1.6×	152 0.7×	126 0.6×	216 1.4×	116 1.3×	20	991
Lina Kassar-Duchossoy France	7	878 1.7×	240 1.1×	168 0.8×	142 0.9×	93 1.0×	9	999
Sylvia Merkert Germany	16	848 1.6×	224 1.0×	64 0.3×	100 0.6×	97 1.1×	36	1.0k
Elicia Estrella United States	15	678 1.3×	83 0.4×	148 0.7×	158 1.0×	93 1.0×	28	922
M. Coletta Italy	10	637 1.2×	338 1.5×	221 1.1×	118 0.8×	66 0.7×	14	819
Kathleen Church United States	9	625 1.2×	187 0.8×	327 1.6×	252 1.6×	64 0.7×	25	831

Countries citing papers authored by Vanessa Besson

Since Specialization

Citations

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

Fields of papers citing papers by Vanessa Besson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vanessa Besson

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

All Works

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15 of 15 papers shown

Tanaka, Karo, Vanessa Besson, Manon Rivagorda, et al.. (2022). Paternally expressed gene 3 (Pw1/Peg3) promotes sexual dimorphism in metabolism and behavior. PLoS Genetics. 18(1). e1010003–e1010003. 8 indexed citations

Pannérec, Alice, Barbara Gayraud-Morel, David Ollitrault, et al.. (2018). Inhibition of the Activin Receptor Type-2B Pathway Restores Regenerative Capacity in Satellite Cell-Depleted Skeletal Muscle. Frontiers in Physiology. 9. 515–515. 9 indexed citations

Sojoodi, Mozhdeh, Karo Tanaka, Yves Heremans, et al.. (2016). The zinc finger transcription factor PW1/PEG3 restrains murine beta cell cycling. Diabetologia. 59(7). 1474–1479. 6 indexed citations

Hoareau‐Coudert, Bénédicte, Nathalie Mougenot, Virginie Monceau, et al.. (2016). 0074 : Resident PW1+ progenitor cells participate in vascular remodeling during pulmonary arterial hypertension. Archives of Cardiovascular Diseases Supplements. 8(3). 247–247.

Hoareau‐Coudert, Bénédicte, Nathalie Mougenot, Virginie Monceau, et al.. (2016). Resident PW1 ⁺ Progenitor Cells Participate in Vascular Remodeling During Pulmonary Arterial Hypertension. Circulation Research. 118(5). 822–833. 33 indexed citations

Besson, Vanessa, et al.. (2016). A Novel Mutant Allele of Pw1/Peg3 Does Not Affect Maternal Behavior or Nursing Behavior. PLoS Genetics. 12(5). e1006053–e1006053. 21 indexed citations

Besson, Vanessa, Sergiy Kyryachenko, Peggy Janich, et al.. (2016). Expression Analysis of the Stem Cell Marker Pw1/Peg3 Reveals a CD34 Negative Progenitor Population in the Hair Follicle. Stem Cells. 35(4). 1015–1027. 8 indexed citations

Nadaud, Sophie, Virginie Monceau, Nathalie Mougenot, et al.. (2015). Lung Progenitor Cells Expressing PW1 Gene Participate in Vascular Remodeling During Pulmonary Arterial Hypertension. The FASEB Journal. 29(S1). 3 indexed citations

Pannérec, Alice, et al.. (2013). Defining skeletal muscle resident progenitors and their cell fate potentials. Development. 140(14). 2879–2891. 112 indexed citations

10.

Besson, Vanessa, Piera Smeriglio, Amélie Wegener, et al.. (2011). PW1 gene/paternally expressed gene 3 (PW1/Peg3) identifies multiple adult stem and progenitor cell populations. Proceedings of the National Academy of Sciences. 108(28). 11470–11475. 58 indexed citations

11.

Mitchell, Kathryn J., Alice Pannérec, Bruno Cadot, et al.. (2010). Identification and characterization of a non-satellite cell muscle resident progenitor during postnatal development. Nature Cell Biology. 12(3). 257–266. 326 indexed citations

12.

Duchon, Arnaud, Vanessa Besson, Patricia Lopes Pereira, Laetitia Magnol, & Yann Hérault. (2008). Inducing Segmental Aneuploid Mosaicism in the Mouse Through Targeted Asymmetric Sister Chromatid Event of Recombination. Genetics. 180(1). 51–59. 13 indexed citations

13.

Brault, Véronique, Vanessa Besson, Laetitia Magnol, Arnaud Duchon, & Yann Hérault. (2007). Cre/loxP-Mediated Chromosome Engineering of the Mouse Genome. Handbook of experimental pharmacology. 29–48. 39 indexed citations

14.

Besson, Vanessa, Véronique Brault, Arnaud Duchon, et al.. (2007). Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses. Human Molecular Genetics. 16(17). 2040–2052. 29 indexed citations

15.

Besson, Vanessa, Jean‐Charles Bizot, Nadia Messaddeq, et al.. (2005). Training and aging modulate the loss‐of‐balance phenotype observed in a new ENU‐induced allele of Otopetrin1. Biology of the Cell. 97(10). 787–798. 18 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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