Morgane Pertuit

505 total citations
16 papers, 247 citations indexed

About

Morgane Pertuit is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Neurology. According to data from OpenAlex, Morgane Pertuit has authored 16 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Endocrinology, Diabetes and Metabolism and 5 papers in Neurology. Recurrent topics in Morgane Pertuit's work include Growth Hormone and Insulin-like Growth Factors (5 papers), Neuroblastoma Research and Treatments (5 papers) and Pituitary Gland Disorders and Treatments (4 papers). Morgane Pertuit is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (5 papers), Neuroblastoma Research and Treatments (5 papers) and Pituitary Gland Disorders and Treatments (4 papers). Morgane Pertuit collaborates with scholars based in France, United States and Germany. Morgane Pertuit's co-authors include Anne Barlier, A Enjalbert, Corinne Gérard, Pauline Romanet, Ramahefarizo Rasolonjanahary, Karine Magalon, David Romano, Jean‐Vianney Barnier, David Taïeb and Marie‐Françoise Odou and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, PEDIATRICS and Endocrinology.

In The Last Decade

Morgane Pertuit

15 papers receiving 243 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Morgane Pertuit France	10	104	89	76	68	53	16	247
Samuel Backman Sweden	9	95 0.9×	43 0.5×	74 1.0×	70 1.0×	31 0.6×	11	177
Limor Drori-Herishanu United States	5	159 1.5×	105 1.2×	127 1.7×	33 0.5×	54 1.0×	6	292
Iikki Donner Finland	7	65 0.6×	108 1.2×	47 0.6×	70 1.0×	21 0.4×	14	245
Kornelia Hasse-Lazar Poland	10	220 2.1×	61 0.7×	77 1.0×	40 0.6×	71 1.3×	27	352
Jose Luis Monteserin Garcia Spain	8	122 1.2×	87 1.0×	104 1.4×	36 0.5×	76 1.4×	18	315
Xinming Zhou China	8	41 0.4×	108 1.2×	65 0.9×	89 1.3×	41 0.8×	19	291
Floor A.M. Duijkers Netherlands	9	46 0.4×	114 1.3×	41 0.5×	73 1.1×	18 0.3×	22	237
Léopoldine Bricaire France	10	76 0.7×	95 1.1×	41 0.5×	21 0.3×	67 1.3×	19	293
Serge Nolet Canada	13	117 1.1×	118 1.3×	141 1.9×	68 1.0×	15 0.3×	15	331
Araceli García‐Martínez Spain	10	110 1.1×	77 0.9×	62 0.8×	44 0.6×	69 1.3×	19	246

Countries citing papers authored by Morgane Pertuit

Since Specialization

Citations

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

Fields of papers citing papers by Morgane Pertuit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Morgane Pertuit

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

All Works

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16 of 16 papers shown

Romanet, Pauline, Anne Barlier, Thierry Brue, et al.. (2024). CSNK2B Mutation: A Rare Cause of IGHD. Clinical Endocrinology. 102(4). 421–426.

Gueorguieva, Iva, Morgane Pertuit, Rachel Reynaud, et al.. (2023). A novel TBX19 gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin. Frontiers in Endocrinology. 13. 1080649–1080649. 2 indexed citations

Romanet, Pauline, Amira Mohamed, Sophie Giraud, et al.. (2018). UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population. The Journal of Clinical Endocrinology & Metabolism. 104(3). 753–764. 39 indexed citations

Baumstarck, Karine, Dominique Figarella‐Branger, Morgane Pertuit, et al.. (2018). Psychological impact of von Hippel-Lindau genetic screening in patients with a previous history of hemangioblastoma of the central nervous system. Journal of Psychosocial Oncology. 36(5). 624–634. 5 indexed citations

Guérin, Carole, Alessio Impériale, Anne Barlier, et al.. (2017). Paraganglioma of the organ of Zuckerkandl associated with a somatic HIF2α mutation: A case report. Oncology Letters. 13(3). 1083–1086. 4 indexed citations

Ambrosetti, Damien, M. Durand, Jeanne Amiel, et al.. (2017). ALK-TPM3 rearrangement in adult renal cell carcinoma: Report of a new case showing loss of chromosome 3 and literature review. Cancer Genetics. 221. 31–37. 20 indexed citations

Cuny, Thomas, Martin Bidlingmaier, Céline Defilles, et al.. (2016). In vitro impact of pegvisomant on growth hormone-secreting pituitary adenoma cells. Endocrine Related Cancer. 23(7). 509–519. 8 indexed citations

Taïeb, David, Anne Barlier, Chunzhang Yang, et al.. (2015). Somatic gain-of-function HIF2A mutations in sporadic central nervous system hemangioblastomas. Journal of Neuro-Oncology. 126(3). 473–481. 14 indexed citations

Romanet, Pauline, Irène Netchine, Morgane Pertuit, et al.. (2015). Case Report of GNAS Epigenetic Defect Revealed by a Congenital Hypothyroidism. PEDIATRICS. 135(4). e1079–e1083. 21 indexed citations

10.

Blanchet, Elise M., S. Gabriel, Victoria Martucci, et al.. (2014). ¹⁸F‐FDG PET/CT as a predictor of hereditary head and neck paragangliomas. European Journal of Clinical Investigation. 44(3). 325–332. 26 indexed citations

11.

Jamilloux, Yvan, Judith Favier, Morgane Pertuit, et al.. (2013). A MEN1 syndrome with a paraganglioma. European Journal of Human Genetics. 22(2). 283–285. 21 indexed citations

12.

Blanchard, Marie‐Pierre, Morgane Pertuit, Sylvie Thirion, et al.. (2012). Ras and Rap1 govern spatiotemporal dynamic of activated ERK in pituitary living cells. Cellular Signalling. 24(12). 2237–2248. 10 indexed citations

13.

Pertuit, Morgane, et al.. (2011). The gsp Oncogene Disrupts Ras/ERK-Dependent Prolactin Gene Regulation in gsp Inducible Somatotroph Cell Line. Endocrinology. 152(4). 1234–1243. 7 indexed citations

14.

Pertuit, Morgane, Anne Barlier, A Enjalbert, & Corinne Gérard. (2009). Signalling Pathway Alterations in Pituitary Adenomas: Involvement of Gsα, cAMP and Mitogen‐Activated Protein Kinases. Journal of Neuroendocrinology. 21(11). 869–877. 26 indexed citations

15.

Romano, Diego, Karine Magalon, Morgane Pertuit, et al.. (2007). Conditional Overexpression of the Wild-Type Gsα as the gsp Oncogene Initiates Chronic Extracellularly Regulated Kinase 1/2 Activation and Hormone Hypersecretion in Pituitary Cell Lines. Endocrinology. 148(6). 2973–2983. 12 indexed citations

16.

Romano, David, Morgane Pertuit, Ramahefarizo Rasolonjanahary, et al.. (2006). Regulation of the RAP1/RAF-1/Extracellularly Regulated Kinase-1/2 Cascade and Prolactin Release by the Phosphoinositide 3-Kinase/AKT Pathway in Pituitary Cells. Endocrinology. 147(12). 6036–6045. 32 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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