Arnaud Vanlander

2.0k total citations
31 papers, 673 citations indexed

About

Arnaud Vanlander is a scholar working on Molecular Biology, Clinical Biochemistry and Epidemiology. According to data from OpenAlex, Arnaud Vanlander has authored 31 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 4 papers in Epidemiology. Recurrent topics in Arnaud Vanlander's work include Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (12 papers) and RNA modifications and cancer (4 papers). Arnaud Vanlander is often cited by papers focused on Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (12 papers) and RNA modifications and cancer (4 papers). Arnaud Vanlander collaborates with scholars based in Belgium, United States and Germany. Arnaud Vanlander's co-authors include Rudy Van Coster, Joél Smet, Boél De Paepe, Sara Seneca, Linda De Meırleır, Willy Lissens, Christopher A. Powell, Michal Minczuk, Roland Lill and Björn Menten and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Anesthesiology.

In The Last Decade

Arnaud Vanlander

31 papers receiving 667 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Arnaud Vanlander Belgium	15	458	181	80	68	62	31	673
Emma Footitt United Kingdom	17	387 0.8×	412 2.3×	16 0.2×	78 1.1×	42 0.7×	29	735
Martin Magner Czechia	17	493 1.1×	287 1.6×	11 0.1×	103 1.5×	37 0.6×	64	892
M. P. Champion United Kingdom	14	299 0.7×	317 1.8×	4 0.1×	63 0.9×	42 0.7×	17	728
Mohammed Almannai Saudi Arabia	17	597 1.3×	381 2.1×	13 0.2×	137 2.0×	44 0.7×	43	935
S. Ohara Japan	16	288 0.6×	146 0.8×	28 0.3×	20 0.3×	123 2.0×	52	1.0k
François‐Guillaume Debray Belgium	14	305 0.7×	211 1.2×	34 0.4×	84 1.2×	23 0.4×	26	507
B. Mousson France	14	494 1.1×	406 2.2×	15 0.2×	33 0.5×	47 0.8×	38	606
Susan Winter United States	19	442 1.0×	525 2.9×	17 0.2×	156 2.3×	20 0.3×	31	859
J. M. Saudubray France	12	392 0.9×	518 2.9×	46 0.6×	50 0.7×	21 0.3×	26	660
Mónica Garcı́a-Castro Spain	13	209 0.5×	15 0.1×	14 0.2×	22 0.3×	30 0.5×	24	453

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-authorship network of co-authors of Arnaud Vanlander

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

Gansemans, Yannick, Joél Smet, Xavier Verhelst, et al.. (2025). Mitochondrial dysfunction characterises the multigenerational effects of maternal obesity on MASLD. JHEP Reports. 7(6). 101404–101404. 1 indexed citations

Hoste, Levi, Agnieszka Prytula-Ebels, Ruth De Bruyne, et al.. (2023). Comparison of SARS-CoV-2 seroconversion in children with chronic diseases with healthy children and adults during the first waves of the COVID-19 pandemic. Frontiers in Pediatrics. 11. 1210181–1210181. 1 indexed citations

Tang, Maoxing, Annekatrien Boel, Mina Popovic, et al.. (2022). Human germline nuclear transfer to overcome mitochondrial disease and failed fertilization after ICSI. Journal of Assisted Reproduction and Genetics. 39(3). 609–618. 17 indexed citations

Hedberg‐Oldfors, Carola, Anna‐Karin Berglund, Gittan Kollberg, et al.. (2019). TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism. Journal of Inherited Metabolic Disease. 42(5). 898–908. 36 indexed citations

Selim, Laila, Rudy Van Coster, Ahmed S. Hassan, et al.. (2018). Mitochondrial Neurogastrointestinal Encephalopathy: Clinical, Biochemical and Molecular Study in Three Egyptian Patients.. PubMed. 27(2). 193–205. 2 indexed citations

Smet, Joél, Arnaud Vanlander, Sarah Vergult, et al.. (2018). 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. 13(1). 80–80. 14 indexed citations

Hemelsoet, Dimitri, Arnaud Vanlander, Joél Smet, et al.. (2018). Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in MTFMT. Neurology Genetics. 4(6). e298–e298. 5 indexed citations

Vanlander, Arnaud & Rudy Van Coster. (2018). Clinical and genetic aspects of defects in the mitochondrial iron–sulfur cluster synthesis pathway. JBIC Journal of Biological Inorganic Chemistry. 23(4). 495–506. 17 indexed citations

Larson, Austin, Marisa W. Friederich, Michael A. Swanson, et al.. (2017). New insights into the phenotype of FARS2 deficiency. Molecular Genetics and Metabolism. 122(4). 172–181. 35 indexed citations

10.

Vandecasteele, Stefaan J., Sara Seneca, Joél Smet, et al.. (2017). Tigecycline-induced inhibition of mitochondrial DNA translation may cause lethal mitochondrial dysfunction in humans. Clinical Microbiology and Infection. 24(4). 431.e1–431.e3. 15 indexed citations

11.

Vanlander, Arnaud, Laura Muiño Mosquera, Joseph Panzer, et al.. (2016). Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses. Mitochondrion. 27. 32–38. 10 indexed citations

12.

Vanlander, Arnaud, Björn Menten, Joél Smet, et al.. (2014). Two Siblings with Homozygous Pathogenic Splice-Site Variant in Mitochondrial Asparaginyl-tRNA Synthetase (NARS2). Human Mutation. 36(2). 222–231. 43 indexed citations

13.

Peeters, Annelies, Joél Smet, Katrien De Bock, et al.. (2014). Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1853(2). 285–298. 64 indexed citations

14.

Spits, Claudia, Katrien Stouffs, An I. Jonckheere, et al.. (2014). A Bumpy Ride on the Diagnostic Bench of Massive Parallel Sequencing, the Case of the Mitochondrial Genome. PLoS ONE. 9(11). e112950–e112950. 13 indexed citations

15.

Vanlander, Arnaud, Annick De Jaeger, Joél Smet, et al.. (2014). Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q. Anesthesiology. 122(2). 343–352. 61 indexed citations

16.

Seneca, Sara, Rudy Van Coster, Joél Smet, et al.. (2014). Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?. European Journal of Human Genetics. 23(1). 41–48. 31 indexed citations

17.

Praeter, Claudine De, Arnaud Vanlander, Piet Vanhaesebrouck, et al.. (2014). Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisions. European Journal of Pediatrics. 174(2). 267–270. 7 indexed citations

18.

Bolar, Nikhita, Arnaud Vanlander, Nathalie Van der Aa, et al.. (2013). Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy. Human Molecular Genetics. 22(13). 2590–2602. 90 indexed citations

19.

Paepe, Boél De, Joél Smet, Arnaud Vanlander, et al.. (2012). Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defects. Pediatric Research. 72(3). 232–240. 13 indexed citations

20.

Vanlander, Arnaud, et al.. (2010). Propranolol as a Novel Treatment for Congenital Visceral Haemangioma. Neonatology. 98(3). 229–231. 8 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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