Vincent Marion

2.5k citations

42 papers · 1.5k · h-index 22

Impact in

Genetics top 2%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
Internal Medicine top 5%
- Venous Thromboembolism Diagnosis and Management

Papers in

Genetics 25
- Genetic and Kidney Cyst Diseases 19
- Genetic Syndromes and Imprinting 12
Molecular Biology 13
- Hedgehog Signaling Pathway Studies 3
- Epigenetics and DNA Methylation 3

Co-authors: Hélène Dollfus (24 shared papers)Corinne Stoetzel (17 shared papers)Rogier M. Bertina (3 shared papers)Frits R. Rosendaal (3 shared papers)Fanny Stutzmann (2 shared papers)Elisabeth Flori (3 shared papers)Nadia Messaddeq (5 shared papers)Jeroen Eikenboom (4 shared papers)
Journals: Clinical Genetics (4 papers)Diabetes (3 papers)Journal of Thrombosis and Haemostasis (3 papers)PLoS ONE (2 papers)Ophthalmic Genetics (2 papers)
Partner nations: France Netherlands Germany

In The Last Decade

Vincent Marion

41 papers receiving 1.5k citations

Peers

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-authors

The 25 scholars most cited alongside Vincent Marion, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Vincent Marion Line = papers co-authored together Vincent Marion links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation Proceedings of the National Academy of Sciences ·Vincent Marion, Corinne Stoetzel, Dominique Schlicht, Nadia Messaddeq, Michael Koch, Elisabeth Flori, Jean Marc Danse, Jean‐Louis Mandel, Hélène Dollfus	2009	155
2	Retinal dystrophy in Bardet–Biedl syndrome and related syndromic ciliopathies Progress in Retinal and Eye Research ·Anaïs Mockel, Yaumara Perdomo, Fanny Stutzmann, J. Letsch, Vincent Marion, Hélène Dollfus	2011	113
3	Haplotypes of the EPCR gene, plasma sEPCR levels and the risk of deep venous thrombosis Journal of Thrombosis and Haemostasis ·Shirley Uitte de Willige, Vincent Marion, Frits R. Rosendaal, Hans L. Vos, Marieke C. Visser, Rogier M. Bertina	2004	108
4	Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18) Journal of Medical Genetics ·Sophie Scheidecker, Christelle Etard, Nathan W. Pierce, Véronique Geoffroy, Élise Schaefer, Jean Muller, Kirsley Chennen, Elisabeth Flori, Valérie Pelletier, Olivier Poch, Vincent Marion, Corinne Stoetzel, Uwe Strähle, Maxence V. Nachury, Hélène Dollfus	2013	104
5	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 ·Vincent Marion, Fanny Stutzmann, Marion Gérard, Charlie De Melo, Élise Schaefer, Aurélie Claussmann, Sophie Hellé, Valérie Delague, Eric H. Souied, Catherine Barrey, Alain Verloès, Corinne Stoetzel, Hélène Dollfus	2012	101
6	Bardet-Biedl Syndrome Clinical Journal of the American Society of Nephrology ·O. Imhoff, Vincent Marion, Corinne Stoetzel, M. Durand, Muriel Holder, Sabine Sigaudy, Pierre Sarda, Christian P. Hamel, Christian Brandt, Hélène Dollfus, Bruno Moulin	2010	92
7	von Willebrand factor and its propeptide: the influence of secretion and clearance on protein levels and the risk of venous thrombosis Journal of Thrombosis and Haemostasis ·A. Yaël Nossent, Vincent Marion, Nico H. van Tilburg, Frits R. Rosendaal, Rogier M. Bertina, Jan A. van Mourik, Jeroen Eikenboom	2006	76
8	Fibrinogen Aα Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension European Respiratory Journal ·J Suntharalingam, Kimberley Goldsmith, Vincent Marion, Lü Long, Carmen Treacy, Frank Dudbridge, Mark Toshner, (unknown), Jeroen Eikenboom, Nicholas W. Morrell	2007	72
9	BBS-Induced Ciliary Defect Enhances Adipogenesis, Causing Paradoxical Higher-Insulin Sensitivity, Glucose Usage, and Decreased Inflammatory Response Cell Metabolism ·Vincent Marion, Anaïs Mockel, Charlie De Melo, Cathy Obringer, Aurélie Claussmann, Alban Simon, Nadia Messaddeq, M. Durand, Luc Dupuis, Jean‐Philippe Loeffler, Peter King, (unknown), Nikolai Petrovsky, Corinne Stoetzel, Hélène Dollfus	2012	71
10	Homozygosity Mapping and Candidate Prioritization Identify Mutations, Missed by Whole-Exome Sequencing, in SMOC2, Causing Major Dental Developmental Defects The American Journal of Human Genetics ·Agnès Bloch‐Zupan, Xavier Jamet, Christelle Etard, Virginie Laugel, Jean Muller, Véronique Geoffroy, Jean-Pierre Strauss, Valérie Pelletier, Vincent Marion, Olivier Poch, Uwe Strähle, Corinne Stoetzel, Hélène Dollfus	2011	66
11	Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy The American Journal of Human Genetics ·Sophie Scheidecker, Christelle Etard, Laurence Haren, Corinne Stoetzel, Sarah Hull, Gavin Arno, Vincent Plagnol, Séverine Drunat, Sandrine Passemard, Annick Toutain, Cathy Obringer, Mériam Koob, Véronique Geoffroy, Vincent Marion, Uwe Strähle, Pia Østergaard, Alain Verloès, Andreas Merdes, Anthony T. Moore, Hélène Dollfus	2015	51
12	Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age Neurobiology of Disease ·Judith Eschbach, Jérôme Sinniger, Jamal Bouitbir, Anissa Fergani, Anna-Isabel Schlagowski, Joffrey Zoll, Bernard Gény, Frédérique René, Yves Larmet, Vincent Marion, Robert H. Baloh, Matthew B. Harms, Michael E. Shy, Nadia Messadeq, Patrick Weydt, Jean‐Philippe Loeffler, Albert C. Ludolph, Luc Dupuis	2013	44
13	Bardet–Biedl syndrome highlights the major role of the primary cilium in efficient water reabsorption Kidney International ·Vincent Marion, Dominique Schlicht, Anaïs Mockel, Sophie Caillard, O. Imhoff, Corinne Stoetzel, Paul van Dijk, Christian Brandt, Bruno Moulin, Hélène Dollfus	2011	44
14	Pharmacological Modulation of the Retinal Unfolded Protein Response in Bardet-Biedl Syndrome Reduces Apoptosis and Preserves Light Detection Ability Journal of Biological Chemistry ·Anaïs Mockel, Cathy Obringer, Theodorus B. M. Hakvoort, Mathias W. Seeliger, Wouter H. Lamers, Corinne Stoetzel, Hélène Dollfus, Vincent Marion	2012	41
15	Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary cilia Clinical Genetics ·V Bennouna-Greene, Stéphane Kremer, Corinne Stoetzel, D Christmann, C. Schuster, M. Durand, Alain Verloès, Sabine Sigaudy, Muriel Holder‐Espinasse, Julien Godet, Christian Brandt, Vincent Marion, A. Danion, J-L Dietemann, Hélène Dollfus	2011	35
16	Mesoaxial polydactyly is a major feature in Bardet–Biedl syndrome patients with LZTFL1 (BBS17) mutations Clinical Genetics ·Élise Schaefer, Julia Lauer, M. Durand, V. Pelletier, Cathy Obringer, Aurélie Claussmann, Jean Braun, Claire Redin, Chester A. Mathis, Jean Muller, Catherine Schmidt‐Mutter, Elisabeth Flori, Vincent Marion, Corinne Stoetzel, Hélène Dollfus	2013	30
17	Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral Ectopia Lentis Ophthalmic Genetics ·V. Bennouna Greene, Corinne Stoetzel, V. Pelletier, Y. Perdomo-Trujillo, Laura Liebermann, Vincent Marion, H. De Korvin, Cathérine Boileau, Jean‐Louis Dufier, Hélène Dollfus	2010	29
18	Olfaction evaluation and correlation with brain atrophy in Bardet‐Biedl syndrome Clinical Genetics ·Jean Braun, Vincent Noblet, M. Durand, Sophie Scheidecker, Anna Zinetti‐Bertschy, Jack Foucher, Vincent Marion, Jean Muller, S. Riehm, Hélène Dollfus, Stéphane Kremer	2014	28
19	Confirmation of TFAP2A gene involvement in branchio‐oculo‐facial syndrome (BOFS) and report of temporal bone anomalies American Journal of Medical Genetics Part A ·Corinne Stoetzel, S. Riehm, V. Bennouna Greene, V. Pelletier, Jacqueline Vigneron, Bruno Leheup, Vincent Marion, Sophie Hellé, Jean-Marc Danse, Christelle Thibault-Carpentier, Luc Moulinier, F. Veillon, Hélène Dollfus	2009	26
20	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 ·Noëlle Cognard, M. Julia Scerbo, Cathy Obringer, Xiangxiang Yu, Fanny Costa, Elodie Haser, Dane Le, Corinne Stoetzel, Michel J. Roux, Bruno Moulin, Hélène Dollfus, Vincent Marion	2015	25

About Vincent Marion

Vincent Marion is a scholar working on Genetics, Molecular Biology, Hematology, Surgery and Pathology and Forensic Medicine, having authored 42 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (19 papers), Genetic Syndromes and Imprinting (12 papers), Biomedical Research and Pathophysiology (3 papers), Hedgehog Signaling Pathway Studies (3 papers), Epigenetics and DNA Methylation (3 papers), Blood Coagulation and Thrombosis Mechanisms (3 papers), Amino Acid Enzymes and Metabolism (2 papers) and Microtubule and mitosis dynamics (2 papers). The work is most often cited by research in Genetics (855 citations), Internal Medicine (83 citations), Hematology (180 citations), Molecular Biology (736 citations) and Cell Biology (120 citations). Vincent Marion has collaborated with scholars based in France, Netherlands and Germany. Frequent 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. Their work appears in journals such as Clinical Genetics, Diabetes, Journal of Thrombosis and Haemostasis, PLoS ONE and Ophthalmic Genetics.

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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