Annick Pierce

1.4k total citations
15 papers, 1.1k citations indexed

About

Annick Pierce is a scholar working on Molecular Biology, Nutrition and Dietetics and Surgery. According to data from OpenAlex, Annick Pierce has authored 15 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Nutrition and Dietetics and 3 papers in Surgery. Recurrent topics in Annick Pierce's work include Infant Nutrition and Health (8 papers), Glycosylation and Glycoproteins Research (5 papers) and RNA modifications and cancer (3 papers). Annick Pierce is often cited by papers focused on Infant Nutrition and Health (8 papers), Glycosylation and Glycoproteins Research (5 papers) and RNA modifications and cancer (3 papers). Annick Pierce collaborates with scholars based in France and Mexico. Annick Pierce's co-authors include Laurence Fénart, Gérard Torpier, Bénédicte Dehouck, Roméo Cecchelli, Marie‐Pierre Dehouck, Monique Benaı̈ssa, Joël Mazurier, Geneviève Spik, Pierrette Mäes and Didier Colavizza and has published in prestigious journals such as The Journal of Cell Biology, PLoS ONE and European Journal of Biochemistry.

In The Last Decade

Annick Pierce

15 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Annick Pierce France	13	467	397	203	147	139	15	1.1k
Lotta Gustafsson Sweden	21	677 1.4×	416 1.0×	430 2.1×	100 0.7×	91 0.7×	38	1.5k
Sophie Thenet France	20	817 1.7×	124 0.3×	139 0.7×	83 0.6×	158 1.1×	44	1.2k
Penny L. Jeffery Australia	16	392 0.8×	263 0.7×	171 0.8×	154 1.0×	253 1.8×	35	1.1k
Sonja Aits Sweden	13	681 1.5×	119 0.3×	60 0.3×	146 1.0×	145 1.0×	16	1.3k
Jeremy A. Goettel United States	20	788 1.7×	191 0.5×	254 1.3×	581 4.0×	129 0.9×	50	1.8k
Sandra E. Reznik United States	21	400 0.9×	59 0.1×	100 0.5×	181 1.2×	136 1.0×	76	1.2k
Jian‐Ning Liu China	19	453 1.0×	74 0.2×	91 0.4×	83 0.6×	89 0.6×	79	1.1k
Chantal Augeron France	15	688 1.5×	141 0.4×	210 1.0×	148 1.0×	65 0.5×	18	1.2k
Hiroko Takeuchi Japan	23	405 0.9×	178 0.4×	163 0.8×	540 3.7×	233 1.7×	57	1.6k
Christian Brix Folsted Andersen Denmark	17	993 2.1×	95 0.2×	133 0.7×	114 0.8×	169 1.2×	28	1.7k

Countries citing papers authored by Annick Pierce

Since Specialization

Citations

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

Fields of papers citing papers by Annick Pierce

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annick Pierce

This figure shows the co-authorship network connecting the top 25 collaborators of Annick Pierce. A scholar is included among the top collaborators of Annick Pierce 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 Annick Pierce. Annick Pierce 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:

15 of 15 papers shown

Pierce, Annick, et al.. (2017). OGT: a short overview of an enzyme standing out from usual glycosyltransferases. Biochemical Society Transactions. 45(2). 365–370. 32 indexed citations

Hoedt, Esthelle, Karima Chaoui, Isabelle Huvent, et al.. (2014). SILAC-Based Proteomic Profiling of the Human MDA-MB-231 Metastatic Breast Cancer Cell Line in Response to the Two Antitumoral Lactoferrin Isoforms: The Secreted Lactoferrin and the Intracellular Delta-Lactoferrin. PLoS ONE. 9(8). e104563–e104563. 14 indexed citations

Vercoutter‐Edouart, Anne‐Sophie, Ikram El Yazidi‐Belkoura, Céline Guinez, et al.. (2014). Detection and identification of O ‐GlcNAcylated proteins by proteomic approaches. PROTEOMICS. 15(5-6). 1039–1050. 30 indexed citations

Hoedt, Esthelle, Stephan Hardivillé, Christophe Mariller, et al.. (2010). Discrimination and evaluation of lactoferrin and delta-lactoferrin gene expression levels in cancer cells and under inflammatory stimuli using TaqMan real-time PCR. BioMetals. 23(3). 441–452. 18 indexed citations

Pierce, Annick, Dominique Legrand, & Joël Mazurier. (2009). La lactoferrine : une protéine multifonctionnelle. médecine/sciences. 25(4). 361–369. 48 indexed citations

Mariller, Christophe, et al.. (2008). Proteomic approach to the identification of novel delta-lactoferrin target genes: Characterization of DcpS, an mRNA scavenger decapping enzyme. Biochimie. 91(1). 109–122. 19 indexed citations

Benaı̈ssa, Monique, Jean‐Philippe Peyrat, Louis Hornez, et al.. (2004). Expression and prognostic value of lactoferrin mRNA isoforms in human breast cancer. International Journal of Cancer. 114(2). 299–306. 49 indexed citations

Mariller, Christophe, Monique Benaı̈ssa, Edith Browaeys, et al.. (2004). Expression of delta-lactoferrin induces cell cycle arrest. BioMetals. 17(3). 325–329. 23 indexed citations

Fillebeen, Carine, Marie‐Magdeleine Ruchoux, Valérie Mitchell, et al.. (2001). Lactoferrin is synthesized by activated microglia in the human substantia nigra and its synthesis by the human microglial CHME cell line is upregulated by tumor necrosis factor α or 1-methyl-4-phenylpyridinium treatment. Molecular Brain Research. 96(1-2). 103–113. 74 indexed citations

10.

Dehouck, Bénédicte, Laurence Fénart, Marie‐Pierre Dehouck, et al.. (1997). A New Function for the LDL Receptor: Transcytosis of LDL across the Blood–Brain Barrier. The Journal of Cell Biology. 138(4). 877–889. 453 indexed citations

11.

Lamkhioued, Bouchaïb, Abdelilah S. Gounni, Valérie Gruart, et al.. (1995). Human eosinophils express a receptor for secretory component. Role in secretory IgA‐dependent activation. European Journal of Immunology. 25(1). 117–125. 94 indexed citations

12.

Pierce, Annick, et al.. (1994). Expression of the lactotransferrin receptor during the differentiation process of the megakaryocyte Dami cell line. Biology of the Cell. 82(2-3). 149–159. 12 indexed citations

13.

Pierce, Annick, et al.. (1993). Transcriptional induction of β‐galactoside α‐2,6‐sialyltransferase in rat fibroblast by dexamethasone. European Journal of Biochemistry. 211(1-2). 135–140. 25 indexed citations

14.

Pierce, Annick, Didier Colavizza, Monique Benaı̈ssa, et al.. (1991). Molecular cloning and sequence analysis of bovine lactotransferrin. European Journal of Biochemistry. 196(1). 177–184. 205 indexed citations

15.

Damonneville, Martine, Claude Auriault, Claudie Verwaerde, et al.. (1986). Induction of a Protective Immune IgE Response in Rats by Injection of Defined Antigens of Schistosomulum-Released Products: Immunochemical Properties of the Target Antigens. International Archives of Allergy and Immunology. 79(3). 320–328. 10 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.

Explore authors with similar magnitude of impact