Pascal Papillier

1.6k total citations
39 papers, 1.2k citations indexed

About

Pascal Papillier is a scholar working on Public Health, Environmental and Occupational Health, Molecular Biology and Health, Toxicology and Mutagenesis. According to data from OpenAlex, Pascal Papillier has authored 39 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Public Health, Environmental and Occupational Health, 13 papers in Molecular Biology and 9 papers in Health, Toxicology and Mutagenesis. Recurrent topics in Pascal Papillier's work include Reproductive Biology and Fertility (27 papers), Effects and risks of endocrine disrupting chemicals (9 papers) and Sperm and Testicular Function (8 papers). Pascal Papillier is often cited by papers focused on Reproductive Biology and Fertility (27 papers), Effects and risks of endocrine disrupting chemicals (9 papers) and Sperm and Testicular Function (8 papers). Pascal Papillier collaborates with scholars based in France, Russia and Morocco. Pascal Papillier's co-authors include Svetlana Uzbekova, C. Perreau, Pascal Mermillod, Rozenn Dalbiès‐Tran, Sophie Pennetier, Aurore Thélie, Virginie Maillard, Sébastien Elis, Philippe Monget and Alice Desmarchais and has published in prestigious journals such as Scientific Reports, Environmental Pollution and International Journal of Molecular Sciences.

In The Last Decade

Pascal Papillier

39 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pascal Papillier France 19 788 472 384 283 199 39 1.2k
Sébastien Elis France 26 458 0.6× 389 0.8× 278 0.7× 318 1.1× 275 1.4× 54 1.4k
Waleed F. A. Marei Egypt 19 769 1.0× 269 0.6× 488 1.3× 194 0.7× 364 1.8× 61 1.3k
P. S. P. Gupta India 19 958 1.2× 247 0.5× 679 1.8× 251 0.9× 372 1.9× 79 1.3k
Ahmed Z. Balboula United States 21 443 0.6× 403 0.9× 264 0.7× 186 0.7× 189 0.9× 57 1.1k
Weihua Du China 23 955 1.2× 541 1.1× 611 1.6× 249 0.9× 134 0.7× 70 1.5k
Rozenn Dalbiès‐Tran France 24 1.4k 1.8× 706 1.5× 773 2.0× 493 1.7× 459 2.3× 42 1.9k
F. Cillo Italy 14 512 0.6× 392 0.8× 226 0.6× 219 0.8× 87 0.4× 22 810
Carolyn M. Komar United States 15 296 0.4× 275 0.6× 209 0.5× 234 0.8× 289 1.5× 21 874
Katarzyna Knapczyk‐Stwora Poland 16 248 0.3× 233 0.5× 209 0.5× 153 0.5× 162 0.8× 59 730
Laura A. Favetta Canada 19 520 0.7× 398 0.8× 220 0.6× 289 1.0× 82 0.4× 60 1.1k

Countries citing papers authored by Pascal Papillier

Since Specialization
Citations

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

Fields of papers citing papers by Pascal Papillier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pascal Papillier

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

All Works

20 of 20 papers shown
1.
Desmarchais, Alice, Svetlana Uzbekova, Pascal Papillier, et al.. (2024). Metabolic status is a key factor influencing proteomic changes in ewe granulosa cells induced by chronic BPS exposure. BMC Genomics. 25(1). 1095–1095. 1 indexed citations
2.
Demattei, Marie-Véronique, Pascal Papillier, Anaïs Vitorino Carvalho, et al.. (2024). Characterization of oviduct epithelial spheroids for the study of embryo–maternal communication in cattle. Theriogenology. 217. 113–126. 5 indexed citations
3.
Wu, Luyao, Marie Bousquet, Alice Desmarchais, et al.. (2023). Cumulative and potential synergistic effects of seven different bisphenols on human granulosa cells in vitro?. Environmental Pollution. 330. 121818–121818. 18 indexed citations
4.
Carvalho, Anaïs Vitorino, Pascal Papillier, Béatrice Mandon‐Pepin, et al.. (2023). Bisphenol A and bisphenol S both disrupt ovine granulosa cell steroidogenesis but through different molecular pathways. Journal of Ovarian Research. 16(1). 30–30. 22 indexed citations
5.
Cadoret, Véronique, Pascal Papillier, Alice Desmarchais, et al.. (2022). Bisphenol S Impairs Oestradiol Secretion during In Vitro Basal Folliculogenesis in a Mono-Ovulatory Species Model. Toxics. 10(8). 437–437. 7 indexed citations
6.
Lière, Philippe, Antoine Pianos, Alice Desmarchais, et al.. (2022). Bisphenol S Alters the Steroidome in the Preovulatory Follicle, Oviduct Fluid and Plasma in Ewes With Contrasted Metabolic Status. Frontiers in Endocrinology. 13. 892213–892213. 17 indexed citations
7.
Desmarchais, Alice, Juliette Cognié, Pascal Papillier, et al.. (2021). Chronic low BPS exposure through diet impairs in vitro embryo production parameters according to metabolic status in the ewe. Ecotoxicology and Environmental Safety. 229. 113096–113096. 15 indexed citations
8.
Boulanger, Laurent, Nathalie Daniel, Véronique Cadoret, et al.. (2020). Investigating the role of BCAR4 in ovarian physiology and female fertility by genome editing in rabbit. Scientific Reports. 10(1). 4992–4992. 7 indexed citations
9.
Desmarchais, Alice, et al.. (2020). Bisphenol A and S impaired ovine granulosa cell steroidogenesis. Reproduction. 159(5). 571–583. 39 indexed citations
10.
Fouchécourt, Sophie, Sébastien Elis, Charlotte Lécureuil, et al.. (2019). An evolutionary approach to recover genes predominantly expressed in the testes of the zebrafish, chicken and mouse. BMC Evolutionary Biology. 19(1). 137–137. 10 indexed citations
11.
Monniaux, Danielle, Carine Genêt, Virginie Maillard, et al.. (2019). Prenatal programming by testosterone of follicular theca cell functions in ovary. Cellular and Molecular Life Sciences. 77(6). 1177–1196. 16 indexed citations
12.
Thélie, Aurore, et al.. (2012). An oocyte‐preferential histone mRNA stem‐loop‐binding protein like is expressed in several mammalian species. Molecular Reproduction and Development. 79(6). 380–391. 11 indexed citations
13.
14.
Perreau, C., Pascal Papillier, Joëlle Dupont, et al.. (2010). Effect of PUFA on embryo cryoresistance, gene expression and AMPKα phosphorylation in IVF-derived bovine embryos. Prostaglandins & Other Lipid Mediators. 93(1-2). 30–36. 48 indexed citations
15.
Thélie, Aurore, Pascal Papillier, C. Perreau, et al.. (2009). Regulation of bovine oocyte‐specific transcripts during in vitro oocyte maturation and after maternal–embryonic transition analyzed using a transcriptomic approach. Molecular Reproduction and Development. 76(8). 773–782. 20 indexed citations
16.
Mermillod, Pascal, Rozenn Dalbiès‐Tran, Svetlana Uzbekova, et al.. (2008). Factors Affecting Oocyte Quality: Who is Driving the Follicle?. Reproduction in Domestic Animals. 43(s2). 393–400. 67 indexed citations
17.
Thélie, Aurore, Pascal Papillier, Sophie Pennetier, et al.. (2007). Differential regulation of abundance and deadenylation of maternal transcripts during bovine oocyte maturation in vitro and in vivo. BMC Developmental Biology. 7(1). 125–125. 90 indexed citations
18.
Uzbekova, Svetlana, Yannick Arlot‐Bonnemains, Joëlle Dupont, et al.. (2007). Spatio-Temporal Expression Patterns of Aurora Kinases A, B, and C and Cytoplasmic Polyadenylation-Element-Binding Protein in Bovine Oocytes During Meiotic Maturation1. Biology of Reproduction. 78(2). 218–233. 67 indexed citations
19.
Dalbiès‐Tran, Rozenn, Pascal Papillier, Sophie Pennetier, Svetlana Uzbekova, & Philippe Monget. (2005). Bovine mater‐like NALP9 is an oocyte marker gene. Molecular Reproduction and Development. 71(4). 414–421. 34 indexed citations
20.
Pennetier, Sophie, Svetlana Uzbekova, C. Perreau, et al.. (2004). Spatio-Temporal Expression of the Germ Cell Marker Genes MATER, ZAR1, GDF9, BMP15,andVASA in Adult Bovine Tissues, Oocytes, and Preimplantation Embryos1. Biology of Reproduction. 71(4). 1359–1366. 136 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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