Vinciane Dideberg

1.5k total citations
24 papers, 537 citations indexed

About

Vinciane Dideberg is a scholar working on Molecular Biology, Cognitive Neuroscience and Genetics. According to data from OpenAlex, Vinciane Dideberg has authored 24 papers receiving a total of 537 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Cognitive Neuroscience and 5 papers in Genetics. Recurrent topics in Vinciane Dideberg's work include Functional Brain Connectivity Studies (5 papers), Neural and Behavioral Psychology Studies (4 papers) and Attention Deficit Hyperactivity Disorder (3 papers). Vinciane Dideberg is often cited by papers focused on Functional Brain Connectivity Studies (5 papers), Neural and Behavioral Psychology Studies (4 papers) and Attention Deficit Hyperactivity Disorder (3 papers). Vinciane Dideberg collaborates with scholars based in Belgium, Netherlands and United Kingdom. Vinciane Dideberg's co-authors include Vincent Bours, Jacques Bélaïche, Édouard Louis, Séverine Vermeire, A. Van Gossum, François Boemer, Jean‐Hubert Caberg, Denis Franchimont, Paul Rutgeerts and Cécile Libioulle and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Scientific Reports.

In The Last Decade

Vinciane Dideberg

22 papers receiving 517 citations

Peers

Countries citing papers authored by Vinciane Dideberg

Since Specialization

Citations

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

Fields of papers citing papers by Vinciane Dideberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vinciane Dideberg

This figure shows the co-authorship network connecting the top 25 collaborators of Vinciane Dideberg. A scholar is included among the top collaborators of Vinciane Dideberg 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 Vinciane Dideberg. Vinciane Dideberg 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	Association between executive functions and COMT Val108/158Met polymorphism among healthy younger and older adults: A preliminary study 2024 ·PLoS ONE ·Zoltán Apa, (unknown), Vinciane Dideberg, Fabienne Collette	0
2	Newborn screening of duchenne muscular dystrophy specifically targeting deletions amenable to exon-skipping therapy 2021 ·Scientific Reports ·(unknown), Jean‐Hubert Caberg, Vinciane Dideberg, Tamara Dangouloff, Johan T. den Dunnen, Vincent Bours, Laurent Servais, François Boemer	13
3	Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases: Belgian Guidelines for Human Genetics Centers 2021 ·JMIR Medical Informatics ·(unknown), (unknown), Vinciane Dideberg, Kathleen Claes, Sofie Symoens, Wim Coucke, Valérie Benoît, (unknown), Martine De Rycke, Sara Seneca, Lut Van Laer, Wim Wuyts, Anniek Corveleyn, (unknown), (unknown), Françoise Wilkin, Marie Ravoet, (unknown), (unknown), (unknown)	0
4	Newborn screening for SMA in Southern Belgium 2019 ·Neuromuscular Disorders ·François Boemer, Jean‐Hubert Caberg, Vinciane Dideberg, (unknown), Vincent Bours, Mickaël Hiligsmann, Tamara Dangouloff, Laurent Servais	57
5	[(S)un (M)ay (A)rise on SMA : the hope of a region without spinal muscular atrophy]. 2019 ·PubMed ·François Boemer, Jean‐Hubert Caberg, Vinciane Dideberg, (unknown), Sandrine Marie, Lionel Marcélis, Vincent Bours, Tamara Dangouloff, Laurent Servais	6
6	A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseases 2017 ·Scientific Reports ·François Boemer, Corinne Fasquelle, (unknown), Claire Josse, Vinciane Dideberg, Karin Segers, (unknown), (unknown), (unknown), Vincent Bours	29
7	Modulating effect of COMT Val158Met polymorphism on interference resolution during a working memory task 2015 ·Brain and Cognition ·Mathieu Jaspar, Vinciane Dideberg, Vincent Bours, Pierre Maquet, Fabienne Collette	10
8	Mutation of the iron‐sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy 2015 ·Journal of Inherited Metabolic Disease ·François‐Guillaume Debray, (unknown), Arnaud Vanlander, Vinciane Dideberg, Claire Josse, Jean‐Hubert Caberg, François Boemer, Vincent Bours, René Stevens, Sara Seneca, Joél Smet, Roland Lill, Rudy Van Coster	38
9	Influence of COMT Genotype on Antero-posterior Cortical Functional Connectivity Underlying Interference Resolution 2014 ·Cerebral Cortex ·Mathieu Jaspar, (unknown), Vinciane Dideberg, Vincent Bours, Pierre Maquet, Fabienne Collette	11
10	Modulating effect of COMT genotype on the brain regions underlying proactive control process during inhibition 2013 ·Cortex ·Mathieu Jaspar, Sarah Genon, Vincenzo Muto, Christelle Meyer, (unknown), Vinciane Dideberg, Vincent Bours, Éric Salmon, Pierre Maquet, Fabienne Collette	28
11	Genetic Diagnosis of Duchenne and Becker Muscular Dystrophy using Multiplex Ligation-Dependent Probe Amplification in Rwandan Patients 2013 ·Journal of Tropical Pediatrics ·Annette Uwineza, (unknown), (unknown), (unknown), (unknown), (unknown), Vinciane Dideberg, Vincent Bours, Léon Mutesa	8
12	Altered White Matter Architecture in BDNF Met Carriers 2013 ·PLoS ONE ·Erik Ziegler, (unknown), (unknown), Vincenzo Muto, (unknown), Johan Stender, Evelyne Balteau, Vinciane Dideberg, Vincent Bours, Pierre Maquet, Christophe Phillips	16
13	Concurrent Synaptic and Systems Memory Consolidation during Sleep 2013 ·Journal of Neuroscience ·(unknown), (unknown), Jessica Schrouff, Vincenzo Muto, Vinciane Dideberg, Evelyne Balteau, Christian Degueldre, Christophe Phillips, A. Luxen, Fabienne Collette, Vincent Bours, Pierre Maquet	23
14	Evidence of association between interferon regulatory factor 5 gene polymorphisms and asthma 2012 ·Gene ·(unknown), Matthew Rose‐Zerilli, Gerard H. Koppelman, Johanna K. Sandling, John W. Holloway, Dirkje S. Postma, Stephen T. Holgate, Vincent Bours, Ann‐Christine Syvänen, Vinciane Dideberg	15
15	IL28B polymorphism and the control of hepatitis C virus infection: ready for clinical use? 2011 ·PubMed ·Hans Orlent, Hendrik Reynaert, Stefan Bourgeois, Vinciane Dideberg, Michael Adler, Isabelle Colle, Stéphane De Maeght, Wim Laleman, P. Michielsen, Christophe Moreno, (unknown), Peter Stärkel, Jean Delwaide	1
16	An insertion deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases 2007 ·Human Molecular Genetics ·Vinciane Dideberg, Guðrún Kristjánsdóttir, Lili Milani, Cécile Libioulle, Snævar Sigurðsson, Édouard Louis, (unknown), Séverine Vermeire, Paul Rutgeerts, Jacques Bélaïche, Denis Franchimont, A. Van Gossum, Vincent Bours, A-C Syvänen	138
17	Lymphotoxin alpha gene in Crohn's disease patients: absence of implication in the response to infliximab in a large cohort study 2006 ·Pharmacogenetics and Genomics ·Vinciane Dideberg, Édouard Louis, Frédéric Farnir, (unknown), Séverine Vermeire, Paul Rutgeerts, Martine De Vos, A. Van Gossum, Jacques Bélaïche, Vincent Bours	22
18	The TNF/ADAM 17 system: implication of an ADAM 17 haplotype in the clinical response to infliximab in Crohn's disease 2006 ·Pharmacogenetics and Genomics ·Vinciane Dideberg, Emilie Théâtre, Frédéric Farnir, Séverine Vermeire, Paul Rutgeerts, Martine De Vos, Jacques Bélaïche, Denis Franchimont, A. Van Gossum, Édouard Louis, Vincent Bours	34
19	Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test? 2001 ·European Journal of Human Genetics ·Alain Verloès, Y. Gillerot, Lionel Van Maldergem, Roland Schoos, Christian Herens, Mauricette Jamar, Vinciane Dideberg, (unknown), L Koulischer	37
20	GOMBO syndrome: Another ?pseudorecessive? disorder due to a cryptic translocation 2000 ·American Journal of Medical Genetics ·Alain Verloès, (unknown), Mauricette Jamar, Vinciane Dideberg, Christian Herens	12

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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