Anne Athias

5.0k total citations
83 papers, 4.2k citations indexed

About

Anne Athias is a scholar working on Molecular Biology, Surgery and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Anne Athias has authored 83 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 39 papers in Surgery and 16 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Anne Athias's work include Cholesterol and Lipid Metabolism (32 papers), Peroxisome Proliferator-Activated Receptors (15 papers) and Cancer, Lipids, and Metabolism (13 papers). Anne Athias is often cited by papers focused on Cholesterol and Lipid Metabolism (32 papers), Peroxisome Proliferator-Activated Receptors (15 papers) and Cancer, Lipids, and Metabolism (13 papers). Anne Athias collaborates with scholars based in France, United States and Netherlands. Anne Athias's co-authors include Philippe Gambert, Laurent Lagrost, Christian Lallemant, Éric Solary, David Masson, Gérard Lizard, Catherine Desrumaux, Ginette Bessède, Valérie Deckert and Dominique Delmas and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and PLoS ONE.

In The Last Decade

Anne Athias

82 papers receiving 4.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anne Athias France	39	2.0k	1.5k	922	582	515	83	4.2k
Charles L. Bisgaier United States	29	1.4k 0.7×	1.4k 1.0×	932 1.0×	394 0.7×	517 1.0×	57	4.4k
Papasani V. Subbaiah United States	38	1.8k 0.9×	1.4k 0.9×	951 1.0×	341 0.6×	492 1.0×	124	4.2k
Joan Carles Escolà‐Gil Spain	35	1.5k 0.8×	1.7k 1.2×	906 1.0×	485 0.8×	485 0.9×	151	4.1k
Jahangir Iqbal United States	40	1.9k 0.9×	1.4k 0.9×	936 1.0×	393 0.7×	691 1.3×	92	5.1k
P. Haydn Pritchard Canada	38	1.5k 0.7×	1.9k 1.3×	1.2k 1.4×	228 0.4×	335 0.7×	111	4.3k
Hideaki Kaneto Japan	36	1.7k 0.8×	1.3k 0.9×	1.3k 1.5×	445 0.8×	1.1k 2.1×	106	5.3k
B H Chung United States	31	1.1k 0.6×	1.1k 0.7×	1.1k 1.1×	298 0.5×	504 1.0×	52	3.4k
Ganesamoorthy Subbanagounder United States	27	1.8k 0.9×	1.3k 0.9×	714 0.8×	1.9k 3.2×	365 0.7×	29	5.2k
Bingbing Jiang United States	29	2.6k 1.3×	705 0.5×	701 0.8×	499 0.9×	1.4k 2.7×	42	4.9k
Elisabeth Teissier France	27	1.5k 0.7×	760 0.5×	276 0.3×	599 1.0×	434 0.8×	43	3.1k

Countries citing papers authored by Anne Athias

Since Specialization

Citations

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

Fields of papers citing papers by Anne Athias

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Athias

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

Paul, Catherine, Nadhir Yousfi, Jean‐Luc Boucher, et al.. (2015). TLR4/IFNγ pathways induce tumor regression via NOS II-dependent NO and ROS production in murine breast cancer models. OncoImmunology. 5(5). e1123369–e1123369. 24 indexed citations

Nury, Thomas, Joseph Gresti, Anne Athias, et al.. (2013). Determination of heavy metal content and lipid profiles in mussel extracts from two sites on the moroccan atlantic coast and evaluation of their biological activities on MIN6 pancreatic cells. Environmental Toxicology. 29(11). n/a–n/a. 1 indexed citations

Baarine, Mauhamad, Pierre Andreoletti, Anne Athias, et al.. (2012). Evidence of oxidative stress in very long chain fatty acid – Treated oligodendrocytes and potentialization of ROS production using RNA interference-directed knockdown of ABCD1 and ACOX1 peroxisomal proteins. Neuroscience. 213. 1–18. 92 indexed citations

Colin, Didier, Emeric Limagne, Sylvie Jeanningros, et al.. (2011). Endocytosis of Resveratrol via Lipid Rafts and Activation of Downstream Signaling Pathways in Cancer Cells. Cancer Prevention Research. 4(7). 1095–1106. 85 indexed citations

Zabala‐Letona, Amaia, Isabelle Niot, Fabienne Laugerette, et al.. (2011). CLA-Enriched Diet Containing t10,c12- CLA Alters Bile Acid Homeostasis and Increases the Risk of Cholelithiasis in Mice. Journal of Nutrition. 141(8). 1437–1444. 7 indexed citations

Katsogiannou, Maria, Charbel El Boustany, Florian Gackière, et al.. (2009). Caveolae Contribute to the Apoptosis Resistance Induced by the α1A-Adrenoceptor in Androgen-Independent Prostate Cancer Cells. PLoS ONE. 4(9). e7068–e7068. 12 indexed citations

Gautier, Thomas, Alexis Klein, Valérie Deckert, et al.. (2008). Effect of Plasma Phospholipid Transfer Protein Deficiency on Lethal Endotoxemia in Mice. Journal of Biological Chemistry. 283(27). 18702–18710. 55 indexed citations

Masson, David, Rui Xiao, Jean-Paul Paı̈s de Barros, et al.. (2008). Activation of the constitutive androstane receptor decreases HDL in wild-type and human apoA-I transgenic mice. Journal of Lipid Research. 49(8). 1682–1691. 36 indexed citations

Ingueneau, Cécile, Uyen Huynh‐Do, Bertrand Marcheix, et al.. (2008). TRPC1 is regulated by caveolin‐1 and is involved in oxidized LDL‐induced apoptosis of vascular smooth muscle cells. Journal of Cellular and Molecular Medicine. 13(8b). 1620–1631. 47 indexed citations

10.

Perségol, L., Matthieu Foissac, Laurent Lagrost, et al.. (2007). HDL particles from type 1 diabetic patients are unable to reverse the inhibitory effect of oxidised LDL on endothelium-dependent vasorelaxation. Diabetologia. 50(11). 2384–2387. 45 indexed citations

11.

Prunet, C., Jean‐Michel Petit, Anne Athias, et al.. (2005). High circulating levels of 7β- and 7α-hydroxycholesterol and presence of apoptotic and oxidative markers in arterial lesions of normocholesterolemic atherosclerotic patients undergoing endarterectomy. Pathologie Biologie. 54(1). 22–32. 29 indexed citations

12.

Berthier, Arnaud, Stéphanie Lemaire‐Ewing, C. Prunet, et al.. (2004). Involvement of a calcium-dependent dephosphorylation of BAD associated with the localization of Trpc-1 within lipid rafts in 7-ketocholesterol-induced THP-1 cell apoptosis. Cell Death and Differentiation. 11(8). 897–905. 141 indexed citations

13.

Masson, David, Bart Staels, Thomas Gautier, et al.. (2004). Cholesteryl ester transfer protein modulates the effect of liver X receptor agonists on cholesterol transport and excretion in the mouse. Journal of Lipid Research. 45(3). 543–550. 43 indexed citations

14.

Monier, Serge, Mohammad Samadi, Céline Prunet, et al.. (2003). Impairment of the cytotoxic and oxidative activities of 7β-hydroxycholesterol and 7-ketocholesterol by esterification with oleate. Biochemical and Biophysical Research Communications. 303(3). 814–824. 70 indexed citations

15.

Bettaı̈eb, Ali, Anne Athias, Ginette Bessède, et al.. (2001). Ceramide generation occurring during 7β-hydroxycholesterol- and 7-ketocholesterol-induced apoptosis is caspase independent and is not required to trigger cell death. Cell Death and Differentiation. 8(1). 83–99. 63 indexed citations

16.

Perségol, L., et al.. (2000). Co-incubation of native and oxidized low-density lipoproteins: potentiation of relaxation impairment. European Journal of Pharmacology. 406(3). 429–437. 8 indexed citations

17.

Couderc, Rémy, et al.. (1997). Effects of Human Low-Density Lipoproteins on Superoxide Production by Formyl-Methionyl-Leucyl-Phenylalanine Activated Polymorphonuclear Leukocytes. Clinical Chemistry and Laboratory Medicine (CCLM). 35(2). 73–80. 4 indexed citations

18.

Gandjini, Hassan, Philippe Gambert, Anne Athias, et al.. (1994). Composition and immunoreactivity of serum low density lipoproteins (LDL) before and after LDL-apheresis on dextran sulfate-cellulose columns. Transfusion Science. 15(3). 289–297. 2 indexed citations

19.

Gambert, Philippe, et al.. (1988). Direct quantitation of serum high density lipoprotein subfractions separated by gradient gel electrophoresis. Clinica Chimica Acta. 172(2-3). 183–190. 34 indexed citations

20.

Gambert, Philippe, Christian Lallemant, Jean Luc André, et al.. (1981). Cholesterol content of serum lipoprotein fractions in children maintained on chronic hemodialysis. Clinica Chimica Acta. 110(2-3). 295–300. 3 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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