Patrick Verloo

1.8k total citations
25 papers, 434 citations indexed

About

Patrick Verloo is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Patrick Verloo has authored 25 papers receiving a total of 434 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 7 papers in Genetics. Recurrent topics in Patrick Verloo's work include Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (6 papers) and Autoimmune Neurological Disorders and Treatments (4 papers). Patrick Verloo is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (6 papers) and Autoimmune Neurological Disorders and Treatments (4 papers). Patrick Verloo collaborates with scholars based in Belgium, Netherlands and United States. Patrick Verloo's co-authors include Hélène Verhelst, Rudy Van Coster, Sara Seneca, Linda De Meırleır, Joél Smet, Guillaume Sébire, Jan De Bleecker, Bruno Van Vlem, Jules G. Leroy and Johan Van Hove and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Neurology.

In The Last Decade

Patrick Verloo

24 papers receiving 427 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrick Verloo Belgium 11 273 108 60 56 48 25 434
Michela Ripolone Italy 13 349 1.3× 67 0.6× 43 0.7× 63 1.1× 74 1.5× 40 526
Tomohiro Kumada Japan 13 168 0.6× 97 0.9× 34 0.6× 46 0.8× 85 1.8× 44 398
Charlotte Thiels Germany 11 225 0.8× 40 0.4× 22 0.4× 46 0.8× 66 1.4× 25 399
Céline Bris France 13 355 1.3× 146 1.4× 18 0.3× 60 1.1× 90 1.9× 35 515
M. Tardieu France 11 217 0.8× 110 1.0× 31 0.5× 26 0.5× 118 2.5× 36 424
Elena Procopio Italy 16 407 1.5× 164 1.5× 63 1.1× 88 1.6× 165 3.4× 47 670
Mahesh Kamate India 11 142 0.5× 84 0.8× 66 1.1× 39 0.7× 149 3.1× 59 426
Jutta Gärtner Germany 14 366 1.3× 56 0.5× 29 0.5× 109 1.9× 60 1.3× 19 650
Anna Marcé‐Grau Spain 10 139 0.5× 52 0.5× 24 0.4× 48 0.9× 20 0.4× 19 284
Ewa Jamroz Poland 13 241 0.9× 69 0.6× 23 0.4× 139 2.5× 91 1.9× 52 529

Countries citing papers authored by Patrick Verloo

Since Specialization
Citations

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

Fields of papers citing papers by Patrick Verloo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Verloo

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick Verloo. A scholar is included among the top collaborators of Patrick Verloo 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 Patrick Verloo. Patrick Verloo 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.
Mendes, Marisa I., Nicole I. Wolf, Joëlle Rudinger‐Thirion, et al.. (2024). Simultaneous determination of cytosolic aminoacyl-tRNA synthetase activities by LC–MS/MS. Nucleic Acids Research. 52(22). e107–e107. 1 indexed citations
2.
Venegas, Eva, Simone A.G. Langeveld, Kirsten Ahring, et al.. (2024). Nutrient Status and Intakes of Adults with Phenylketonuria. Nutrients. 16(16). 2724–2724. 2 indexed citations
3.
Raes, Ann, et al.. (2024). Concomitant Treatment With Lumasiran and Nedosiran in a Child With Primary Hyperoxaluria Type 1. Kidney International Reports. 10(2). 620–621. 1 indexed citations
4.
Hoorens, Anne, Tassos Grammatikopoulos, Maesha Deheragoda, et al.. (2021). Two cases of DCDC2 ‐related neonatal sclerosing cholangitis with developmental delay and literature review. Clinical Genetics. 100(4). 447–452. 4 indexed citations
5.
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
6.
Schwahn, Bernd, T Scheffner, Hedwig Stepman, et al.. (2020). Cystathionine beta synthase deficiency and brain edema associated with methionine excess under betaine supplementation: Four new cases and a review of the evidence. JIMD Reports. 52(1). 3–10. 11 indexed citations
7.
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
8.
Verhelst, Hélène, Patrick Verloo, Annelies Dheedene, Bert Callewaert, & Björn Menten. (2017). NR4A2 causes an autism spectrum disorder. European Journal of Paediatric Neurology. 21. e49–e49. 2 indexed citations
9.
Fıçıcıoğlu, Can, Leona Serrano, Grace Han, et al.. (2015). Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell Loss. Investigative Ophthalmology & Visual Science. 56(13). 7875–7875. 28 indexed citations
10.
Vanakker, Olivier, Rudy Mercelis, Alexander F. Lipka, et al.. (2014). Lambert–Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplication. European Journal of Paediatric Neurology. 18(3). 439–443. 4 indexed citations
11.
Verloo, Patrick, et al.. (2011). Hashimoto encephalopathy and antibodies against dimethylargininase-1: A rare cause of cognitive decline in a pediatric Down's syndrome patient. Clinical Neurology and Neurosurgery. 113(8). 678–679. 8 indexed citations
12.
Jansen, Anna, Ann Oostra, Brigitte Desprechins, et al.. (2011). TUBA1A mutations. Neurology. 76(11). 988–992. 53 indexed citations
13.
Verhelst, Hélène, Patrick Verloo, Karlien Dhondt, et al.. (2010). Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster. European Journal of Paediatric Neurology. 15(2). 163–166. 26 indexed citations
14.
Roels, Frank, Patrick Verloo, François Eyskens, et al.. (2009). Mitochondrial mosaics in the liver of 3 infants with mtDNA defects. BMC Clinical Pathology. 9(1). 4–4. 12 indexed citations
15.
Biervliet, Stéphanie Van, Patrick Verloo, Myriam Van Winckel, et al.. (2009). Abdominal pain and vomiting as first sign of mitochondrial disease.. PubMed. 72(3). 365–8. 7 indexed citations
16.
Verloo, Patrick, et al.. (2007). Epilepsy starting 7 years after successful liver transplantation in a girl with argininosuccinate lyase deficiency: MRI and MRS findings. Journal of Inherited Metabolic Disease. 30. 85–85. 2 indexed citations
17.
Roels, Frank, Patrick Verloo, Sara Seneca, et al.. (2006). Mitochondrial mosaics in the liver of patients with Pearson and Alpers-Huttenlocher syndromes.. Ghent University Academic Bibliography (Ghent University). 29. 119–119.
18.
Velde, Saskia Vande, Patrick Verloo, Stéphanie Van Biervliet, & Eddy Robberecht. (2006). Heroin withdrawal leads to metabolic alkalosis in an infant with cystic fibrosis. European Journal of Pediatrics. 166(1). 75–76. 4 indexed citations
19.
Verloo, Patrick, Clemens H. M. Kocken, Annemarie Voorberg-van der Wel, et al.. (2004). Plasmodium falciparum-activated Chloride Channels Are Defective in Erythrocytes from Cystic Fibrosis Patients. Journal of Biological Chemistry. 279(11). 10316–10322. 64 indexed citations
20.
Coster, Rudy Van, Joél Smet, Linda De Meırleır, et al.. (2001). Blue Native Polyacrylamide Gel Electrophoresis: A Powerful Tool in Diagnosis of Oxidative Phosphorylation Defects. Pediatric Research. 50(5). 658–665. 116 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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