Vincent Marion

2.4k total citations
42 papers, 1.5k citations indexed

About

Vincent Marion is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Vincent Marion has authored 42 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 18 papers in Molecular Biology and 7 papers in Hematology. Recurrent topics in Vincent Marion's work include Genetic and Kidney Cyst Diseases (19 papers), Genetic Syndromes and Imprinting (15 papers) and Hedgehog Signaling Pathway Studies (6 papers). Vincent Marion is often cited by papers focused on Genetic and Kidney Cyst Diseases (19 papers), Genetic Syndromes and Imprinting (15 papers) and Hedgehog Signaling Pathway Studies (6 papers). Vincent Marion collaborates with scholars based in France, Netherlands and Germany. Vincent Marion's co-authors include Hélène Dollfus, Corinne Stoetzel, Rogier M. Bertina, Frits R. Rosendaal, Fanny Stutzmann, Elisabeth Flori, Nadia Messaddeq, Jeroen Eikenboom, Cathy Obringer and M. Durand and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Vincent Marion

41 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vincent Marion France 22 876 853 206 140 125 42 1.5k
Robert W. A. M. Kuijpers Netherlands 22 278 0.3× 369 0.4× 476 2.3× 45 0.3× 99 0.8× 64 1.7k
Daniel N. Duong United States 8 68 0.1× 590 0.7× 323 1.6× 236 1.7× 75 0.6× 10 1.2k
Ela Shai Israel 18 124 0.1× 499 0.6× 178 0.9× 25 0.2× 75 0.6× 37 933
Olav Klingenberg Norway 18 89 0.1× 511 0.6× 93 0.5× 210 1.5× 91 0.7× 42 900
Gary Elliott United States 16 233 0.3× 930 1.1× 135 0.7× 94 0.7× 239 1.9× 22 1.8k
Gaynor Miller United Kingdom 15 77 0.1× 380 0.4× 142 0.7× 86 0.6× 34 0.3× 20 700
Richard A. Flavell United States 7 445 0.5× 531 0.6× 65 0.3× 57 0.4× 261 2.1× 8 1.4k
Eyal Reinstein Israel 16 359 0.4× 1.0k 1.2× 32 0.2× 161 1.1× 82 0.7× 41 1.5k
Yuning Xiong United States 21 166 0.2× 726 0.9× 163 0.8× 53 0.4× 91 0.7× 31 1.2k
Pierre Boisseau France 19 161 0.2× 811 1.0× 486 2.4× 40 0.3× 68 0.5× 52 1.8k

Countries citing papers authored by Vincent Marion

Since Specialization
Citations

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

Fields of papers citing papers by Vincent Marion

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vincent Marion

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

All Works

20 of 20 papers shown
1.
Obringer, Cathy, Corinne Stoetzel, Michel J. Roux, et al.. (2019). In vivo phenotypic and molecular characterization of retinal degeneration in mouse models of three ciliopathies. Experimental Eye Research. 186. 107721–107721. 7 indexed citations
2.
Zacchia, Miriam, Giovanna Capolongo, Francesco Trepiccione, & Vincent Marion. (2017). Impact of Local and Systemic Factors on Kidney Dysfunction in Bardet-Biedl Syndrome. Kidney & Blood Pressure Research. 42(5). 784–793. 9 indexed citations
3.
Scheidecker, Sophie, Christelle Etard, Laurence Haren, et al.. (2015). Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy. The American Journal of Human Genetics. 96(4). 666–674. 50 indexed citations
4.
Cognard, Noëlle, Cathy Obringer, Corinne Stoetzel, et al.. (2015). Comparing the Bbs10 complete knockout phenotype with a specific renal epithelial knockout one highlights the link between renal defects and systemic inactivation in mice. PubMed. 4(1). 10–10. 25 indexed citations
5.
Chennupati, Ramesh, Vincent Marion, Ben Janssen, et al.. (2014). Endothelial Arginine Resynthesis Contributes to the Maintenance of Vasomotor Function in Male Diabetic Mice. PLoS ONE. 9(7). e102264–e102264. 9 indexed citations
6.
Visser, Marlieke, Rick van Minkelen, Vincent Marion, et al.. (2013). Genome‐wide linkage scan in affected sibling pairs identifies novel susceptibility region for venous thromboembolism: Genetics In Familial Thrombosis study. Journal of Thrombosis and Haemostasis. 11(8). 1474–1484. 14 indexed citations
7.
Eschbach, Judith, Jérôme Sinniger, Jamal Bouitbir, et al.. (2013). Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age. Neurobiology of Disease. 58. 220–230. 41 indexed citations
8.
Marion, Vincent, Fanny Stutzmann, Marion Gérard, et al.. (2012). Exome sequencing identifies mutations in LZTFL1, a BBSome and smoothened trafficking regulator, in a family with Bardet–Biedl syndrome with situs inversus and insertional polydactyly. Journal of Medical Genetics. 49(5). 317–321. 101 indexed citations
9.
Marion, Vincent, Cathy Obringer, Nadia Messaddeq, et al.. (2012). BBS-Induced Ciliary Defect Enhances Adipogenesis, Causing Paradoxical Higher-Insulin Sensitivity, Glucose Usage, and Decreased Inflammatory Response. Cell Metabolism. 16(3). 363–377. 71 indexed citations
10.
Aliferis, Konstantinos A., Corinne Stoetzel, Valérie Pelletier, et al.. (2011). A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype. Ophthalmic Genetics. 32(4). 250–255. 14 indexed citations
11.
Marion, Vincent, Paul van Dijk, Patrick Lindsey, et al.. (2011). Arginine Deficiency Causes Runting in the Suckling Period by Selectively Activating the Stress Kinase GCN2. Journal of Biological Chemistry. 286(11). 8866–8874. 11 indexed citations
12.
Stutzmann, Fanny, et al.. (2011). Retinal dystrophy in Bardet–Biedl syndrome and related syndromic ciliopathies. Progress in Retinal and Eye Research. 30(4). 258–274. 113 indexed citations
13.
Kremer, Stéphane, Corinne Stoetzel, D Christmann, et al.. (2011). Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary cilia. Clinical Genetics. 80(6). 523–531. 30 indexed citations
14.
Stoetzel, Corinne, Laura Liebermann, Vincent Marion, et al.. (2010). Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral Ectopia Lentis. Ophthalmic Genetics. 31(1). 47–51. 29 indexed citations
15.
Marion, Vincent, Corinne Stoetzel, M. Durand, et al.. (2010). Bardet-Biedl Syndrome. Clinical Journal of the American Society of Nephrology. 6(1). 22–29. 91 indexed citations
16.
Suntharalingam, J, Kimberley Goldsmith, Vincent Marion, et al.. (2007). Fibrinogen Aα Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension. European Respiratory Journal. 31(4). 736–741. 72 indexed citations
17.
Eikenboom, Jeroen, et al.. (2006). Acquired von Willebrand syndrome: Diagnostic problems and therapeutic options. American Journal of Hematology. 82(1). 55–58. 15 indexed citations
18.
Willige, Shirley Uitte de, Vincent Marion, Frits R. Rosendaal, et al.. (2004). Haplotypes of the EPCR gene, plasma sEPCR levels and the risk of deep venous thrombosis. Journal of Thrombosis and Haemostasis. 2(8). 1305–1310. 108 indexed citations
19.
Malo, J., et al.. (2001). Primary Myelodysplasia: Management and Outcome at 3 Years in 45 Patients Age 65 and Older. Journal of the American Geriatrics Society. 49(10). 1358–1360. 2 indexed citations
20.
Marion, Vincent, et al.. (1996). Intérêt de la cytométrie en flux dans la détection des auto-anticorps anti-érythrocytaires. Transfusion Clinique et Biologique. 3(2). 99–107. 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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