Françoise Chapon

5.4k total citations · 1 hit paper
82 papers, 2.9k citations indexed

About

Françoise Chapon is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Françoise Chapon has authored 82 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 25 papers in Neurology and 14 papers in Genetics. Recurrent topics in Françoise Chapon's work include Glioma Diagnosis and Treatment (12 papers), Vascular Malformations Diagnosis and Treatment (9 papers) and Mitochondrial Function and Pathology (9 papers). Françoise Chapon is often cited by papers focused on Glioma Diagnosis and Treatment (12 papers), Vascular Malformations Diagnosis and Treatment (9 papers) and Mitochondrial Function and Pathology (9 papers). Françoise Chapon collaborates with scholars based in France, United States and United Kingdom. Françoise Chapon's co-authors include Elisabeth Tournier‐Lasserve, Gwénola Boulday, Anne Joutel, Elisabetta Dejana, Luigi Maddaluno, Noemi Rudini, Valérie Domenga, Michaelle Cécillon, Nicole Battail and Swann Gaulis and has published in prestigious journals such as Nature, New England Journal of Medicine and Journal of Clinical Investigation.

In The Last Decade

Françoise Chapon

80 papers receiving 2.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

EndMT contributes to the onset and progression of cerebral cavernous malformations

2013 368 citations Luigi Maddaluno, Noemi Rudini et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Françoise Chapon France	26	1.2k	1.1k	447	351	312	82	2.9k
Marie‐Magdeleine Ruchoux France	24	726 0.6×	873 0.8×	300 0.7×	339 1.0×	255 0.8×	36	1.9k
Markus Bergmann Germany	27	1.1k 0.9×	988 0.9×	706 1.6×	316 0.9×	574 1.8×	88	3.8k
Yun Yuan China	27	630 0.5×	1.8k 1.7×	277 0.6×	730 2.1×	247 0.8×	272	3.0k
Maria Teresa Giordana Italy	28	934 0.8×	855 0.8×	780 1.7×	366 1.0×	483 1.5×	65	2.6k
Minna Pöyhönen Finland	31	2.3k 2.0×	865 0.8×	216 0.5×	287 0.8×	445 1.4×	76	3.7k
Paola Cavalla Italy	30	844 0.7×	996 0.9×	658 1.5×	328 0.9×	469 1.5×	83	3.1k
Cyril Goizet France	35	762 0.6×	1.7k 1.6×	735 1.6×	1.1k 3.2×	517 1.7×	133	4.0k
Yoshiaki Kumon Japan	33	1.1k 0.9×	634 0.6×	208 0.5×	429 1.2×	555 1.8×	122	3.0k
James A. Trofatter United States	25	1.8k 1.5×	1.5k 1.4×	154 0.3×	885 2.5×	286 0.9×	54	3.7k
Fanxia Shen United States	29	807 0.7×	1.1k 1.1×	392 0.9×	294 0.8×	621 2.0×	56	2.9k

Countries citing papers authored by Françoise Chapon

Since Specialization

Citations

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

Fields of papers citing papers by Françoise Chapon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Françoise Chapon

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

Vadrot, Nathalie, Flavie Ader, Maryline Moulin, et al.. (2023). Abnormal Cellular Phenotypes Induced by Three TMPO/LAP2 Variants Identified in Men with Cardiomyopathies. Cells. 12(2). 337–337. 4 indexed citations

Schaeffer, S., et al.. (2017). A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP (neuropathy, ataxia, and retinitis pigmentosa) syndrome. Biochemical and Biophysical Research Communications. 494(1-2). 133–137. 23 indexed citations

Riant, Florence, Françoise Bergametti, H.-D. Fournier, et al.. (2013). <b><i>CCM3</i></b> Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple Meningiomas. Molecular Syndromology. 4(4). 165–172. 69 indexed citations

Laforêt, Pascal, Benjamin Granger, Dalil Hamroun, et al.. (2013). The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease. Revue Neurologique. 169(8-9). 595–602. 39 indexed citations

Read, Marie‐Hélène, et al.. (2012). Blood metabolite data in response to maximal exercise in healthy subjects. Clinical Physiology and Functional Imaging. 32(4). 274–281. 9 indexed citations

Boulday, Gwénola, Noemi Rudini, Luigi Maddaluno, et al.. (2011). Developmental timing of CCM2 loss influences cerebral cavernous malformations in mice. The Journal of Experimental Medicine. 208(9). 1835–1847. 104 indexed citations

Labauge, Pierre, Fabrice Parker, Françoise Chapon, & Elisabeth Tournier‐Lasserve. (2008). Cavernomes du système nerveux central. 31(1). 1–7. 1 indexed citations

Palm, Thomas, Francesco Scaravilli, Marie‐Magdeleine Ruchoux, et al.. (2007). Trisomy 19 ependymoma, a newly recognized genetico-histological association, including clear cell ependymoma. Molecular Cancer. 6(1). 47–47. 26 indexed citations

Clarot, F., et al.. (2006). Lethal paradoxical cerebral vein thrombosis due to suspicious anticoagulant rodenticide intoxication with chlorophacinone. Forensic Science International. 166(2-3). 85–90. 10 indexed citations

10.

Lechevalier, B, et al.. (2005). [Perry and Purdy's syndrome (familial and fatal parkinsonism with hypoventilation and athymhormia)].. PubMed. 189(3). 481–90; discussion 490. 11 indexed citations

11.

Bourdon, Violaine, et al.. (2003). Chromosome imbalances in oligodendroglial tumors detected by comparative genomic hybridization. Annales de Génétique. 47(2). 105–111. 10 indexed citations

12.

Rocher, Anne B., Françoise Chapon, Xavier Blaizot, Jean‐Claude Baron, & Chantal Chavoix. (2003). Resting-state brain glucose utilization as measured by PET is directly related to regional synaptophysin levels: a study in baboons. NeuroImage. 20(3). 1894–1898. 152 indexed citations

13.

Ruchoux, M M, Francesco Scaravilli, Françoise Chapon, et al.. (2003). CDKN2A, CDKN2B and p14 ^ARF are frequently and differentially methylated in ependymal tumours. Neuropathology and Applied Neurobiology. 29(6). 574–583. 46 indexed citations

14.

Derlon, Jean-Michel, Françoise Chapon, Karim Bénali, et al.. (2000). Non-invasive grading of oligodendrogliomas: correlations between in vivo metabolic pattern and histopathology. European Journal of Nuclear Medicine and Molecular Imaging. 27(7). 778–787. 76 indexed citations

15.

Joutel, Anne, F. Andreux, Swann Gaulis, et al.. (2000). The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients. Journal of Clinical Investigation. 105(5). 597–605. 447 indexed citations

16.

Macro, Margaret, Isabelle André‐Schmutz, E. Comby, et al.. (1999). IgE Multiple Myeloma. Leukemia & lymphoma. 32(5-6). 597–603. 22 indexed citations

17.

Xiang, Fengqing, et al.. (1999). A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21. Neuromuscular Disorders. 9(5). 308–312. 18 indexed citations

18.

Reznik, Yves, et al.. (1997). Pituitary apoplexy of a gonadotroph adenoma following gonadotrophin releasing hormone agonist therapy for prostatic cancer. Journal of Endocrinological Investigation. 20(9). 566–568. 25 indexed citations

19.

Sayette, Vincent de La, et al.. (1991). Meningioma of the third ventricle. Neuroradiology. 33(4). 354–356. 11 indexed citations

20.

Chapon, Françoise, et al.. (1989). [Familial myopathy with "cytoplasmic body" (or "spheroid") type inclusions, disclosed by respiratory insufficiency].. PubMed. 145(6-7). 460–5. 27 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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