Arnaud Vanlander

2.0k citations

31 papers · 673 indexed · h-index 15

Impact in

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Developmental Neuroscience top 10%
- Anesthesia and Neurotoxicity Research

Papers in ⓘ

Molecular Biology 22
- Mitochondrial Function and Pathology 18
- RNA and protein synthesis mechanisms 4
- RNA modifications and cancer 4
- ATP Synthase and ATPases Research 3
- Biochemical and Molecular Research 3
- Genomics and Phylogenetic Studies 2
Clinical Biochemistry 12
- Metabolism and Genetic Disorders 12

Co-authors: Rudy Van Coster (20 shared papers)Joél Smet (20 shared papers)Boél De Paepe (10 shared papers)Sara Seneca (14 shared papers)Linda De Meırleır (5 shared papers)Willy Lissens (5 shared papers)Michal Minczuk (3 shared papers)Christopher A. Powell (3 shared papers)
Journals: Journal of Inherited Metabolic Disease (2 papers)Orphanet Journal of Rare Diseases (1 paper)Human Molecular Genetics (1 paper)European Journal of Human Genetics (1 paper)Phytotherapy Research (1 paper)
Partner nations: Belgium United States Germany

In The Last Decade

Arnaud Vanlander

31 papers receiving 667 citations

Peers

Countries citing papers authored by Arnaud Vanlander

Since Specialization

Citations

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

Fields of papers citing papers by Arnaud Vanlander

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Arnaud Vanlander, 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 Arnaud Vanlander Line = papers co-authored together Arnaud Vanlander 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 31 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy Human Molecular Genetics ·Nikhita Bolar, Arnaud Vanlander, Claudia Wilbrecht, Nathalie Van der Aa, Joél Smet, Boél De Paepe, Geert Vandeweyer, R. Frank Kooy, François Eyskens, Elien De Latter, Gwenda Delanghe, Paul Govaert, Jules G. Leroy, Bart Loeys, Roland Lill, Lut Van Laer, Rudy Van Coster	2013	90
2	Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Annelies Peeters, Abhijit Babaji Shinde, Ruud Dirkx, Joél Smet, Katrien De Bock, Marc Espeel, Ilse Vanhorebeek, Arnaud Vanlander, Rudy Van Coster, Peter Carmeliet, Marc Fransen, Paul P. Van Veldhoven, Myriam Baes	2014	64
3	Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q Anesthesiology ·Arnaud Vanlander, Juergen G. Okun, Annick De Jaeger, Joél Smet, Elien De Latter, Boél De Paepe, G. Dacremont, Birgitte Wuyts, Bert Vanheel, Peter De Paepe, Philippe G. Jorens, Niels Van Regenmortel, Rudy Van Coster	2014	61
4	Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder Journal of Medical Genetics ·Curtis R. Coughlin, Gunter Scharer, Marisa W. Friederich, Hung‐Chun Yu, Elizabeth A. Geiger, Geralyn Creadon‐Swindell, Abigail E. Collins, Arnaud Vanlander, Rudy Van Coster, Christopher A. Powell, Michael A. Swanson, Michal Minczuk, Johan L.K. Van Hove, Tamim H. Shaikh	2015	55
5	Two Siblings with Homozygous Pathogenic Splice-Site Variant in Mitochondrial Asparaginyl-tRNA Synthetase (NARS2) Human Mutation ·Arnaud Vanlander, Björn Menten, Joél Smet, Linda De Meırleır, Tom Sante, Boél De Paepe, Sara Seneca, Sarah F. Pearce, Christopher A. Powell, Sarah Vergult, Alex Michotte, Elien De Latter, Lies Vantomme, Michal Minczuk, Rudy Van Coster	2014	43
6	Mutation of the iron‐sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy Journal of Inherited Metabolic Disease ·François‐Guillaume Debray, Claudia Stümpfig, Arnaud Vanlander, Vinciane Dideberg, Claire Josse, Jean‐Hubert Caberg, François Boemer, Vincent Bours, René Stevens, Sara Seneca, Joél Smet, Roland Lill, Rudy Van Coster	2015	38
7	TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism Journal of Inherited Metabolic Disease ·Elizabeth Jennions, Carola Hedberg‐Oldfors, Anna‐Karin Berglund, Gittan Kollberg, Carl‐Johan Törnhage, Erik A. Eklund, Anders Oldfors, Patrick Verloo, Arnaud Vanlander, Linda De Meırleır, Sara Seneca, Fredrik Sterky, Niklas Darín	2019	36
8	New insights into the phenotype of FARS2 deficiency Molecular Genetics and Metabolism ·Elise Vantroys, Austin Larson, Marisa W. Friederich, Kaz M. Knight, Michael A. Swanson, Christopher A. Powell, Joél Smet, Sarah Vergult, Boél De Paepe, Sara Seneca, Herbert Roeyers, Björn Menten, Michal Minczuk, Arnaud Vanlander, Johan Van Hove, Rudy Van Coster	2017	35
9	Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench? European Journal of Human Genetics ·Sara Seneca, Kim Vancampenhout, Rudy Van Coster, Joél Smet, Willy Lissens, Arnaud Vanlander, Boél De Paepe, An I. Jonckheere, Katrien Stouffs, Linda De Meırleır	2014	31
10	Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome Acta Anaesthesiologica Scandinavica ·Arnaud Vanlander, Philippe G. Jorens, Joél Smet, Boél De Paepe, Walter Verbrugghe, Gert G. Van den Eynden, Françoise Meire, Patrick Pauwels, Nathalie Van der Aa, Sara Seneca, Willy Lissens, Jürgen G. Okun, Rudy Van Coster	2012	24
11	Human germline nuclear transfer to overcome mitochondrial disease and failed fertilization after ICSI Journal of Assisted Reproduction and Genetics ·Maoxing Tang, Annekatrien Boel, Noemi Castelluccio, A Cardona Barberán, A Christodoulaki, Bieke Bekaert, Mina Popovic, Frauke Vanden Meerschaut, Petra De Sutter, Björn Menten, Sofie Symoens, Arnaud Vanlander, Dominic Stoop, Paul Coucke, Björn Heindryckx	2022	17
12	Clinical and genetic aspects of defects in the mitochondrial iron–sulfur cluster synthesis pathway JBIC Journal of Biological Inorganic Chemistry ·Arnaud Vanlander, Rudy Van Coster	2018	17
13	Tigecycline-induced inhibition of mitochondrial DNA translation may cause lethal mitochondrial dysfunction in humans Clinical Microbiology and Infection ·Stefaan J. Vandecasteele, Sara Seneca, Joél Smet, Marijke Reynders, J. De Ceulaer, Arnaud Vanlander, Rudy Van Coster	2017	15
14	Effect of Resveratrol on Cultured Skin Fibroblasts from Patients with Oxidative Phosphorylation Defects Phytotherapy Research ·Boél De Paepe, Katrien Vandemeulebroecke, Joél Smet, Arnaud Vanlander, Sara Seneca, Willy Lissens, Johan L. Van Hove, Ellen Deschepper, Paz Briones, Rudy Van Coster	2013	15
15	Severe hepatopathy and neurological deterioration after start of valproate treatment in a 6-year-old child with mitochondrial tryptophanyl-tRNA synthetase deficiency Orphanet Journal of Rare Diseases ·Elise Vantroys, Joél Smet, Arnaud Vanlander, Sarah Vergult, Ruth De Bruyne, Frank Roels, Hedwig Stepman, Herbert Roeyers, Björn Menten, Rudy Van Coster	2018	14
16	Diagnostic utility of small fiber analysis in skin biopsies from children with chronic pain Muscle & Nerve ·Jonas Görlach, Daniel Amsel, Heike Kölbel, Michelle Grzybowsky, Frank Rutsch, Hannah Schlierbach, Arnaud Vanlander, Esther Pogatzki‐Zahn, Kathrin Habig, S Garkisch, Verena Müller, Thorsten Fritz, Andreas Ziegler, Andreas Hahn, Heidrun H. Krämer, Rudy Van Coster, Anne Schänzer	2019	14
17	Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defects Pediatric Research ·Boél De Paepe, Joél Smet, Arnaud Vanlander, Sara Seneca, Willy Lissens, Linda De Meırleır, Mado Vandewoestyne, Dieter Deforce, Richard J. Rodenburg, Rudy Van Coster	2012	13
18	A Bumpy Ride on the Diagnostic Bench of Massive Parallel Sequencing, the Case of the Mitochondrial Genome PLoS ONE ·Kim Vancampenhout, Ben Caljon, Claudia Spits, Katrien Stouffs, An I. Jonckheere, Linda De Meırleır, Willy Lissens, Arnaud Vanlander, Joél Smet, Boél De Paepe, Rudy Van Coster, Sara Seneca	2014	13
19	Forearm Deoxyhemoglobin and Deoxymyoglobin (Deoxy[Hb + Mb]) Measured by Near-Infrared Spectroscopy (NIRS) Using a Handgrip Test in Mitochondrial Myopathy Applied Spectroscopy ·Bert Celie, Jan Boone, Joél Smet, Arnaud Vanlander, Jan De Bleecker, Rudy N. Van Coster, Jan Bourgois	2015	13
20	Severe congenital neutropenia with neurological impairment due to a homozygous VPS45 p.E238K mutation: A case report suggesting a genotype–phenotype correlation American Journal of Medical Genetics Part A ·Ilse Meerschaut, Victoria Bordon, Catharina Dhooge, Patricia Delbeke, Arnaud Vanlander, Anthony Simon, Christoph Klein, R. Frank Kooy, Raz Somech, Bert Callewaert	2015	11

About Arnaud Vanlander

Arnaud Vanlander is a scholar working on Molecular Biology, Clinical Biochemistry, Epidemiology, Genetics and Cellular and Molecular Neuroscience, having authored 31 papers that have together received 673 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (12 papers), RNA and protein synthesis mechanisms (4 papers), RNA modifications and cancer (4 papers), ATP Synthase and ATPases Research (3 papers), Metalloenzymes and iron-sulfur proteins (3 papers), Biochemical and Molecular Research (3 papers) and Genomics and Phylogenetic Studies (2 papers). The work is most often cited by research in Clinical Biochemistry (181 citations), Developmental Neuroscience (46 citations), Anesthesiology and Pain Medicine (43 citations), Molecular Biology (458 citations) and Critical Care and Intensive Care Medicine (30 citations). Arnaud Vanlander has collaborated with scholars based in Belgium, United States and Germany. Frequent co-authors include Rudy Van Coster, Joél Smet, Boél De Paepe, Sara Seneca, Linda De Meırleır, Willy Lissens, Michal Minczuk, Christopher A. Powell, Roland Lill and Björn Menten. Their work appears in journals such as Journal of Inherited Metabolic Disease, Orphanet Journal of Rare Diseases, Human Molecular Genetics, European Journal of Human Genetics and Phytotherapy Research.

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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