Luc Régal

2.2k total citations
33 papers, 689 citations indexed

About

Luc Régal is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Luc Régal has authored 33 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Clinical Biochemistry. Recurrent topics in Luc Régal's work include Metabolism and Genetic Disorders (7 papers), Lysosomal Storage Disorders Research (6 papers) and Mitochondrial Function and Pathology (5 papers). Luc Régal is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Lysosomal Storage Disorders Research (6 papers) and Mitochondrial Function and Pathology (5 papers). Luc Régal collaborates with scholars based in Belgium, Netherlands and United States. Luc Régal's co-authors include Linda De Meırleır, John W.M. Creemers, Jaak Jaeken, Johanna M. P. van den Hout, Ans T. van der Ploeg, Katrien Jansen, Petra Tilkin, Simon Verheijden, Ludo Vanopdenbosch and Myriam Baes and has published in prestigious journals such as Journal of Clinical Oncology, Brain and Neurology.

In The Last Decade

Luc Régal

33 papers receiving 678 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luc Régal Belgium 15 336 195 131 119 117 33 689
Natalia Martín United States 13 372 1.1× 117 0.6× 74 0.6× 59 0.5× 160 1.4× 17 794
Meghan S. Soustek United States 12 480 1.4× 214 1.1× 131 1.0× 30 0.3× 83 0.7× 13 714
Ginat Narkis Israel 14 528 1.6× 62 0.3× 107 0.8× 72 0.6× 127 1.1× 23 836
Sebahattin Çırak Germany 20 538 1.6× 157 0.8× 142 1.1× 119 1.0× 170 1.5× 62 943
Carola Hedberg‐Oldfors Sweden 15 335 1.0× 83 0.4× 40 0.3× 74 0.6× 152 1.3× 42 570
Bernhard Weschke Germany 13 547 1.6× 164 0.8× 60 0.5× 96 0.8× 152 1.3× 23 985
Edoardo Malfatti France 19 867 2.6× 134 0.7× 94 0.7× 78 0.7× 158 1.4× 89 1.1k
Stefania Assereto Italy 17 563 1.7× 105 0.5× 138 1.1× 24 0.2× 149 1.3× 24 791
Josef Ekstein United States 12 407 1.2× 104 0.5× 122 0.9× 48 0.4× 193 1.6× 27 851
Annette Bley Germany 14 500 1.5× 349 1.8× 79 0.6× 47 0.4× 78 0.7× 29 816

Countries citing papers authored by Luc Régal

Since Specialization
Citations

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

Fields of papers citing papers by Luc Régal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luc Régal

This figure shows the co-authorship network connecting the top 25 collaborators of Luc Régal. A scholar is included among the top collaborators of Luc Régal 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 Luc Régal. Luc Régal 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.
2.
Rocco, A., Sara Seneca, Luc Régal, et al.. (2023). Sustained OMA1-mediated integrated stress response is beneficial for spastic ataxia type 5. Brain. 147(3). 1043–1056. 7 indexed citations
3.
Ebberink, Merel S., Jos P.N. Ruiter, Sabine A. Fuchs, et al.. (2022). Thermo‐sensitive mitochondrial trifunctional protein deficiency presenting with episodic myopathy. Journal of Inherited Metabolic Disease. 45(4). 819–831. 2 indexed citations
4.
Stouffs, Katrien, Patrick Verloo, Luc Régal, et al.. (2020). Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly. Frontiers in Genetics. 11. 26–26. 11 indexed citations
5.
Scalais, Emmanuel, Patricia Borde, Luc Régal, et al.. (2019). Parenteral hydroxocobalamin dose intensification in five patients with different types of early onset intracellular cobalamin defects: Clinical and biochemical responses. JIMD Reports. 49(1). 70–79. 9 indexed citations
6.
Aarsen, Femke K., Iris Plug, Luc Régal, et al.. (2018). Classic infantile Pompe patients approaching adulthood: a cohort study on consequences for the brain. Developmental Medicine & Child Neurology. 60(6). 579–586. 83 indexed citations
7.
Capelle, Carine I. van, Ingrid M.E. Frohn-Mulder, Laurens P. Koopman, et al.. (2018). Cardiac outcome in classic infantile Pompe disease after 13 years of treatment with recombinant human acid alpha-glucosidase. International Journal of Cardiology. 269. 104–110. 23 indexed citations
8.
Régal, Luc, Isabelle Maystadt, Nicol C. Voermans, et al.. (2017). PREPL deficiency: delineation of the phenotype and development of a functional blood assay. Genetics in Medicine. 20(1). 109–118. 24 indexed citations
9.
Régal, Luc, Peter M. van Hasselt, François Foulquier, et al.. (2014). ALG11-CDG: Three novel mutations and further characterization of the phenotype. Molecular Genetics and Metabolism Reports. 2. 16–19. 14 indexed citations
10.
Schaballie, Heidi, Marleen Renard, Christiane Vermylen, et al.. (2013). Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome. European Journal of Pediatrics. 172(5). 613–622. 14 indexed citations
11.
Morawski, Markus, Tünde Juhász, Ulrike Zeitschel, et al.. (2013). Cellular and ultra structural evidence for cytoskeletal localization of prolyl endopeptidase-like protein in neurons. Neuroscience. 242. 128–139. 12 indexed citations
12.
Steenweg, Marjan E., Adeline Vanderver, Berten Ceulemans, et al.. (2012). Novel Infantile-Onset Leukoencephalopathy With High Lactate Level and Slow Improvement. Archives of Neurology. 69(6). 718–22. 9 indexed citations
13.
Régal, Luc, Halil İbrahim Aydın, Hilde Van Esch, et al.. (2012). Two novel deletions in hypotonia–cystinuria syndrome. Molecular Genetics and Metabolism. 107(3). 614–616. 12 indexed citations
14.
Rymen, Daisy, Liesbeth Keldermans, Valérie Race, et al.. (2012). COG5-CDG: expanding the clinical spectrum. Orphanet Journal of Rare Diseases. 7(1). 94–94. 33 indexed citations
15.
Régal, Luc, Christine Wittevrongel, Chantal Thys, et al.. (2012). NPC1 defect results in abnormal platelet formation and function: studies in Niemann–Pick disease type C1 patients and zebrafish. Human Molecular Genetics. 22(1). 61–73. 29 indexed citations
16.
Boonen, Kurt, Luc Régal, Jaak Jaeken, & John W.M. Creemers. (2011). PREPL, a Prolyl Endopeptidase-Like Enzyme by Name Only? – Lessons from Patients. CNS & Neurological Disorders - Drug Targets. 10(3). 355–360. 15 indexed citations
17.
Meyts, Isabelle, Katrien Jansen, Marleen Renard, et al.. (2010). Neuromyelitis optica-IgG(+) optic neuritis associated with celiac disease and dysgammaglobulinemia: A role for tacrolimus?. European Journal of Paediatric Neurology. 15(3). 265–267. 14 indexed citations
18.
Régal, Luc, Merel S. Ebberink, Nathalie Goemans, et al.. (2010). Mutations in PEX10 are a cause of autosomal recessive ataxia. Annals of Neurology. 68(2). 259–263. 56 indexed citations
19.
Régal, Luc, Ludo Vanopdenbosch, Petra Tilkin, et al.. (2006). The G93C Mutation in Superoxide Dismutase 1. Archives of Neurology. 63(2). 262–262. 65 indexed citations
20.
Régal, Luc, Philippe Demaerel, & Bénédicte Dubois. (2005). Cerebral Syphilitic Gumma in a Human Immunodeficiency Virus–Positive Patient. Archives of Neurology. 62(8). 1310–1310. 14 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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