F. Conte-Auriol

825 total citations
14 papers, 591 citations indexed

About

F. Conte-Auriol is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, F. Conte-Auriol has authored 14 papers receiving a total of 591 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Rheumatology. Recurrent topics in F. Conte-Auriol's work include Genetic Syndromes and Imprinting (4 papers), Protein Kinase Regulation and GTPase Signaling (2 papers) and Bone health and treatments (2 papers). F. Conte-Auriol is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Protein Kinase Regulation and GTPase Signaling (2 papers) and Bone health and treatments (2 papers). F. Conte-Auriol collaborates with scholars based in France, Mexico and United States. F. Conte-Auriol's co-authors include Jean‐Pierre Salles, Isabelle Gennero, Sara Laurencin‐Dalicieux, M. Tauber, G Brunel, Fabienne Briand‐Mésange, Philippe Kémoun, Jean‐Christophe Farges, Higinio Arzate and A. Sampath Narayanan and has published in prestigious journals such as Journal of Clinical Investigation, Molecular and Cellular Biology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

F. Conte-Auriol

14 papers receiving 575 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. Conte-Auriol France	10	311	140	134	113	111	14	591
Lisa Stadmeyer United States	12	737 2.4×	136 1.0×	57 0.4×	17 0.2×	79 0.7×	14	1.1k
Satoko Sunamura Japan	9	589 1.9×	39 0.3×	58 0.4×	17 0.2×	50 0.5×	11	858
Faiza Afzal United States	7	448 1.4×	88 0.6×	49 0.4×	21 0.2×	58 0.5×	10	733
Nina Zippel Germany	9	259 0.8×	31 0.2×	78 0.6×	25 0.2×	90 0.8×	18	504
Mari Nakagawa Japan	7	263 0.8×	22 0.2×	26 0.2×	21 0.2×	77 0.7×	12	570
Monique Fangradt Germany	8	140 0.5×	64 0.5×	98 0.7×	10 0.1×	65 0.6×	9	451
Anja Buchheiser Germany	9	183 0.6×	35 0.3×	196 1.5×	18 0.2×	160 1.4×	15	541
Kristine D. Estrada United States	8	269 0.9×	94 0.7×	35 0.3×	22 0.2×	56 0.5×	10	441
Claudia Geißler Germany	10	329 1.1×	38 0.3×	86 0.6×	14 0.1×	69 0.6×	14	503
T Arnett United Kingdom	7	260 0.8×	49 0.3×	53 0.4×	9 0.1×	54 0.5×	15	522

Countries citing papers authored by F. Conte-Auriol

Since Specialization

Citations

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

Fields of papers citing papers by F. Conte-Auriol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. Conte-Auriol. 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 F. Conte-Auriol. The network helps show where F. Conte-Auriol may publish in the future.

Co-authorship network of co-authors of F. Conte-Auriol

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

14 of 14 papers shown

Gennero, Isabelle, F. Conte-Auriol, & Jean‐Pierre Salles. (2017). Laboratory diagnosis of hypophosphatasia. Archives de Pédiatrie. 24(5). 5S57–5S60. 10 indexed citations

Salles, Jean‐Pierre, Philippe Khau Van Kien, F. Conte-Auriol, et al.. (2015). Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and FBN1 Genotype. Journal of Bone and Mineral Research. 30(8). 1369–1376. 29 indexed citations

Cadoudal, Thomas, Marie Buléon, Coralie Sengenès, et al.. (2014). Impairment of adipose tissue in Prader–Willi syndrome rescued by growth hormone treatment. International Journal of Obesity. 38(9). 1234–1240. 28 indexed citations

Salles, Jean‐Pierre, Sara Laurencin‐Dalicieux, F. Conte-Auriol, Fabienne Briand‐Mésange, & Isabelle Gennero. (2012). Bone defects in LPA receptor genetically modified mice. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1831(1). 93–98. 12 indexed citations

Gennero, Isabelle, Sara Laurencin‐Dalicieux, F. Conte-Auriol, et al.. (2011). Absence of the lysophosphatidic acid receptor LPA1 results in abnormal bone development and decreased bone mass. Bone. 49(3). 395–403. 61 indexed citations

Édouard, Thomas, Jean-Philippe Combier, Sophie Bel-Vialar, et al.. (2010). Functional Effects of PTPN11 (SHP2) Mutations Causing LEOPARD Syndrome on Epidermal Growth Factor-Induced Phosphoinositide 3-Kinase/AKT/Glycogen Synthase Kinase 3β Signaling. Molecular and Cellular Biology. 30(10). 2498–2507. 70 indexed citations

Touvier, Thierry, F. Conte-Auriol, Olivier Briand, et al.. (2009). LEPROT and LEPROTL1 cooperatively decrease hepatic growth hormone action in mice. Journal of Clinical Investigation. 119(12). 3830–3838. 39 indexed citations

Édouard, Thomas, Patrick Raynal, Armelle Yart, et al.. (2008). Nouveaux mécanismes moléculaires impliqués dans l’insensibilité à l’hormone de croissance. Archives de Pédiatrie. 15(2). 179–188. 3 indexed citations

Feigerlová, Eva, Gwénaëlle Diene, F. Conte-Auriol, et al.. (2008). Hyperghrelinemia Precedes Obesity in Prader-Willi Syndrome. The Journal of Clinical Endocrinology & Metabolism. 93(7). 2800–2805. 104 indexed citations

10.

Kémoun, Philippe, Sara Laurencin‐Dalicieux, Jean‐Christophe Farges, et al.. (2007). Human dental follicle cells acquire cementoblast features under stimulation by BMP-2/-7 and enamel matrix derivatives (EMD) in vitro. Cell and Tissue Research. 329(2). 283–294. 186 indexed citations

11.

Kémoun, Philippe, Sara Laurencin‐Dalicieux, Frédéric Vaysse, et al.. (2007). Localization of STRO-1, BMP-2/-3/-7, BMP receptors and phosphorylated Smad-1 during the formation of mouse periodontium. Tissue and Cell. 39(4). 257–266. 42 indexed citations

12.

Salles, Jean‐Pierre, et al.. (2007). Bone mineral density assessment in patients with Pader–Willi syndrome. Bone. 40(6). S75–S75. 1 indexed citations

13.

Salles, Jean‐Pierre, P. Moulin, Fabienne Briand‐Mésange, et al.. (2005). FGF 23 et phosphatémie. Immuno-analyse & Biologie Spécialisée. 20(3). 136–143. 1 indexed citations

14.

Gennero, Isabelle, P. Moulin, Thomas Édouard, et al.. (2004). Métabolisme minéral osseux: données récentes et perspectives relatives à l’ostéogenèse. Archives de Pédiatrie. 11(12). 1473–1483. 5 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