Marie Vincent

4.5k total citations
41 papers, 635 citations indexed

About

Marie Vincent is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Marie Vincent has authored 41 papers receiving a total of 635 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Genetics and 7 papers in Epidemiology. Recurrent topics in Marie Vincent's work include Biochemical and Molecular Research (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Marie Vincent is often cited by papers focused on Biochemical and Molecular Research (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Marie Vincent collaborates with scholars based in France, Belgium and United Kingdom. Marie Vincent's co-authors include Greet Van den Berghe, Jaak Jaeken, Bertrand Isidor, Françoise Van den Bergh, S. K. Wadman, F. A. Beemer, M. Durán, Peter de Cock, Sandrine Marie and Yannick Jacques and has published in prestigious journals such as Nature Communications, American Journal of Respiratory and Critical Care Medicine and Annals of Neurology.

In The Last Decade

Marie Vincent

40 papers receiving 620 citations

Peers

Countries citing papers authored by Marie Vincent

Since Specialization

Citations

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

Fields of papers citing papers by Marie Vincent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marie Vincent

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

#	Work	Indexed citations
1	A postzygotic GNA13 variant upregulates the RHOA/ROCK pathway and alters melanocyte function in a mosaic skin hypopigmentation syndrome 2025 ·Nature Communications ·(unknown), (unknown), Paul Kuentz, Rachida Tacine, Marie Vincent, S. Barbarot, Fanny Morice‐Picard, F. Boralévi, (unknown), J. Mazereeuw‐Hautier, Yannis Duffourd, Laurence Faivre, Arthur Sorlin, P. Vabres, Jérôme Delon	2
2	An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical Recommendations 2025 ·American Journal of Medical Genetics Part A ·(unknown), Nadine Holmes, Anne‐Sophie Denommé‐Pichon, Marie Vincent, (unknown), (unknown), Bertrand Isidor, Charlotte W. Ockeloen, Efterpi Pavlidou, Helen Stewart, Virginie J. M. Verhoeven, Athina Ververi, Abhijit Dixit, Ajoy Sarkar, (unknown), Evan Reid, Meena Balasubramanian	1
3	Expanding the Spectrum of Congenital Myopathy Linked to Variants in the MYBPC1 Gene 2024 ·Neurology Clinical Practice ·(unknown), Dong Li, (unknown), Armelle Magot, (unknown), Yann Péréon, Marie Vincent, Bertrand Isidor, Damien Sternberg, Elizabeth M. McCormick, Håkon Håkonarson, Sandra Mercier, Marni J. Falk	1
4	CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases 2023 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), (unknown), Laurence Faivre, Fiona Bruinsma, Marie Vincent, Marie‐Line Jacquemont, (unknown), David Geneviève, David J. Amor, Angela Morgan	6
5	Evolutionary conserved NSL complex/BRD4 axis controls transcription activation via histone acetylation 2020 ·Nature Communications ·(unknown), Bilal N. Sheikh, M. Felicia Basilicata, Marie Vincent, Mathilde Nizon, Cindy Colson, Matthew Bird, James E. Bradner, (unknown), Michael Boutros, Asifa Akhtar	20
6	Clinical, Histopathological, and Molecular Diagnostics in Lethal Lung Developmental Disorders 2019 ·American Journal of Respiratory and Critical Care Medicine ·Marie Vincent, Justyna A. Karolak, Gail Deutsch, Tomasz Gambin, Edwina J. Popek, Bertrand Isidor, Przemysław Szafrański, Cédric Le Caignec, Paweł Stankiewicz	44
7	Identification of Mutations in SDR9C7 in Three Patients with Autosomal Recessive Congenital Ichthyosis 2019 ·Acta Dermato Venereologica ·J. Mazereeuw‐Hautier, (unknown), Véronique Gaston, (unknown), Marie Vincent, H. Aubert, Fanny Morice‐Picard, Nathalie Jonca	4
8	297 Identification of mutations in SDR9C7 in three patients with autosomal recessive congenital ichthyosis 2019 ·Journal of Investigative Dermatology ·J. Mazereeuw‐Hautier, (unknown), Hélène Texier, Marie Vincent, H. Aubert, Fanny Morice‐Picard, Nathalie Jonca	1
9	Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes 2019 ·Molecular Medicine ·Anaïs Begemann, Mario A. Acuña, Markus Zweier, Marie Vincent, Katharina Steindl, Ruxandra Bachmann‐Gagescu, Annette Hackenberg, Lucia Abela, Barbara Plecko, (unknown), Alessandra Baumer, Kazuhiro Yamakawa, Yushi Inoue, Reza Asadollahi, Heinrich Sticht, Hanns Ulrich Zeilhofer, Anita Rauch	39
10	New splicing pathogenic variant in EBP causing extreme familial variability of Conradi–Hünermann–Happle Syndrome 2018 ·European Journal of Human Genetics ·Mathilde Pacault, Marie Vincent, Thomas Besnard, Caroline Kannengiesser, Claire Bénéteau, S. Barbarot, Xénia Latypova, (unknown), Antonin Lamazière, Norbert Winer, Madeleine Joubert, Stéphane Bezieau, Bertrand Isidor, Sandra Mercier, Mathilde Nizon, Stéphanie Leclerc‐Mercier, S. Hadj‐Rabia, Fabienne Dufernez	5
11	A de novo 2q37.2 deletion encompassing AGAP1 and SH3BP4 in a patient with autism and intellectual disability 2018 ·European Journal of Medical Genetics ·Mathilde Pacault, Mathilde Nizon, Olivier Pichon, Marie Vincent, Cédric Le Caignec, Bertrand Isidor	11
12	Radiographic presentation of musculoskeletal involvement in Werner syndrome (adult progeria) 2016 ·Diagnostic and Interventional Imaging ·A. David, Marie Vincent, (unknown), S. Barbarot, (unknown), Bertrand Isidor, Éric Frampas	9
13	Isolated and syndromic brachydactylies: Diagnostic value of hand X-rays 2015 ·Diagnostic and Interventional Imaging ·(unknown), (unknown), Marie Vincent, M.P. Quéré, (unknown), Éric Frampas, (unknown), A. David	13
14	Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome 2014 ·Genetics in Medicine ·Élise Schaefer, Corinne Collet, David Geneviève, Marie Vincent, Dietmar Lohmann, Elodie Sanchez, (unknown), Marie‐Madeleine Eliot, Gudrun Nürnberg, Maria-Rita Passos-Bueno, Dagmar Wieczorek, Lionel Van Maldergem, Bérénice Doray	42
15	Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability 2013 ·European Journal of Human Genetics ·Marie Vincent, Corinne Collet, Alain Verloès, Laëtitia Lambert, Christian Herlin, Catherine Blanchet, Elodie Sanchez, Séverine Drunat, Jacqueline Vigneron, Jean Laplanche, Jacques Puechberty, Pierre Sarda, David Geneviève	15
16	Mutation of a Nuclear Respiratory Factor 2 Binding Site in the 5′ Untranslated Region of the ADSL Gene in Three Patients with Adenylosuccinate Lyase Deficiency 2002 ·The American Journal of Human Genetics ·Sandrine Marie, Valérie Race, Marie‐Cécile Nassogne, Marie Vincent, Greet Van den Berghe	18
17	A mutation in the 5'UTR of the ADSL gene in a patient with adenylosuccinate lyase deficiency 1999 ·Cellular & Molecular Biology Letters ·Sandrine Marie, Valérie Race, Marie‐Cécile Nassogne, Marie Vincent, Greet Van den Berghe	3
18	Mutation analysis in adenylosuccinate lyase deficiency: Eight novel mutations in the re-evaluated full ADSL coding sequence 1999 ·Human Mutation ·Sandrine Marie, Harry Cuppens, (unknown), Martine Jaspers, (unknown), (unknown), Eric Legius, Marie Vincent, (unknown), J.J. Cassiman, Georges Berghe	42
19	Stimulation by Glycerate 2,3-Bisphosphate: A Common Property of Cytosolic Purine 5′-Nucleotidase in Various Tissues 1989 ·Advances in experimental medicine and biology ·Françoise Bontemps, Marie Vincent, Françoise Van den Bergh, Geert van Waeg, Greet Van den Berghe	1
20	Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis 1988 ·European Journal of Pediatrics ·Jaak Jaeken, S. K. Wadman, M. Durán, (unknown), F. A. Beemer, (unknown), (unknown), Peter de Cock, Françoise Van den Bergh, Marie Vincent, Greet Van den Berghe	103

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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