Patrick Verloo

1.8k citations

25 papers · 434 indexed · h-index 11

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Molecular Biology
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research

Papers in

Clinical Biochemistry 9
- Metabolism and Genetic Disorders 9
Endocrine and Autonomic Systems 2

Co-authors: Hélène Verhelst Rudy Van Coster Sara Seneca Linda De Meırleır Joél Smet Guillaume Sébire Bruno Van Vlem Jules G. Leroy
Journals: European Journal of Paediatric Neurology (4 papers)Journal of Inherited Metabolic Disease (2 papers)Toxins (1 paper)Neurology (1 paper)PEDIATRICS (1 paper)
Partner nations: Belgium Netherlands United States

In The Last Decade

Patrick Verloo

24 papers receiving 427 citations

Peers

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

The 25 scholars most cited alongside Patrick Verloo, 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 Patrick Verloo Line = papers co-authored together Patrick Verloo links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Nutrient Status and Intakes of Adults with Phenylketonuria Nutrients ·Eva Venegas, Simone A.G. Langeveld, Kirsten Ahring, Subsecretaria de Saúde, An Desloovere, Elena de Dios, 魏小刚, Á. Hermida Ameijeiras, Cyril F. M. Marsaux, Patrick Verloo, María L. Couce	2024	2
2	Simultaneous determination of cytosolic aminoacyl-tRNA synthetase activities by LC–MS/MS Nucleic Acids Research ·Marisa I. Mendes, Nicole I. Wolf, Joëlle Rudinger‐Thirion, Dominic Lenz, Magali Frugier, Patrick Verloo, Hanna Mandel, A. Zhokin, Rachel Kassel, Willemijn E. Corpeleijn, Cécile Floucat, Kawauchi Nobuyuki, Silvy J.M. van Dooren, Christian Staufner, Gajja S. Salomons, Desirée E.C. Smith	2024	1
3	Concomitant Treatment With Lumasiran and Nedosiran in a Child With Primary Hyperoxaluria Type 1 Kidney International Reports ·N.S. Brohun, Ann Raes, Ruth De Bruyne, Patrick Verloo, Agnieszka Prytula-Ebels	2024	1
4	Two cases of DCDC2 ‐related neonatal sclerosing cholangitis with developmental delay and literature review Clinical Genetics ·IŞIL IŞIK, Anne Hoorens, Tassos Grammatikopoulos, Maesha Deheragoda, Sofie Symoens, Saskia Vande Velde, Stéphanie Van Biervliet, Myriam Van Winckel, Patrick Verloo, Bert Callewaert, Ruth De Bruyne	2021	4
5	Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly Frontiers in Genetics ·Katrien Stouffs, Patrick Verloo, Antonius Kreft, Luc Régal, Diane Beysen, Berten Ceulemans, Anna Jansen, Marije Meuwissen	2020	11
6	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 ·Bernd Schwahn, T Scheffner, Hedwig Stepman, Patrick Verloo, Anibh M. Das, Janice M. Fletcher, Henk J. Blom, Jean‐François Benoist, Bruce A. Barshop, Jaime Barea, Annette Feigenbaum	2020	11
7	TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism Journal of Inherited Metabolic Disease ·Pei Cheh Chen, 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	NR4A2 causes an autism spectrum disorder European Journal of Paediatric Neurology ·Hélène Verhelst, Patrick Verloo, Annelies Dheedene, Bert Callewaert, Björn Menten	2017	2
9	Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell Loss Investigative Ophthalmology & Visual Science ·Huojun Hong, Can Fıçıcıoğlu, Leona Serrano, Grace Han, Jessica I. W. Morgan, Monte D. Mills, Brian J. Forbes, H. J. Laméris, Gil Binenbaum, Paige Kaplan, Charles W. Nichols, Patrick Verloo, Bart P. Leroy, Albert M. Maguire, Tomás S. Alemán	2015	28
10	Lambert–Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplication European Journal of Paediatric Neurology ·E. Ulland, Olivier Vanakker, Rudy Mercelis, Alexander F. Lipka, Filomeen Haerynck, Mélissa Dullaers, Patrick Verloo, Rudy Van Coster, Hélène Verhelst	2014	4
11	Hashimoto encephalopathy and antibodies against dimethylargininase-1: A rare cause of cognitive decline in a pediatric Down's syndrome patient Clinical Neurology and Neurosurgery ·Meijer Annemarie H., Patrick Verloo, Hilary Calow, Beatrice Gini, Bruno Bonetti, Ina Sokolov	2011	8
12	Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster European Journal of Paediatric Neurology ·Hélène Verhelst, Patrick Verloo, Karlien Dhondt, Boél De Paepe, Björn Menten, Josep Dalmau, Rudy Van Coster	2010	26
13	Mitochondrial mosaics in the liver of 3 infants with mtDNA defects BMC Clinical Pathology ·Frank Roels, Patrick Verloo, François Eyskens, Baudouin François, Sara Seneca, Boél De Paepe, Jean‐Jacques Martin, Ramarolanto-Ratiaray, Marleen Praet, Emmanuel Scalais, Marc Espeel, Joél Smet, Gert Van Goethem, Rudy Van Coster	2009	12
14	Abdominal pain and vomiting as first sign of mitochondrial disease. PubMed ·Stéphanie Van Biervliet, Patrick Verloo, 俊平野地, Myriam Van Winckel, Joél Smet, Sara Seneca, 张雪伟, Rudy Van Coster	2009	7
15	P052 Hashimoto encephalopathy in Down's syndrome with dimethylargininase-1 autoantibodies European Journal of Paediatric Neurology ·Hélène Verhelst, Patrick Verloo, Boél De Paepe, Beatrice Gini, Bruno Bonetti, Rudy Van Coster	2009	1
16	Epilepsy starting 7 years after successful liver transplantation in a girl with argininosuccinate lyase deficiency: MRI and MRS findings Journal of Inherited Metabolic Disease ·Patrick Verloo, 张雪伟, Johan Van Hove, Stéphanie Van Biervliet, Myriam Van Winckel	2007	2
17	Mitochondrial mosaics in the liver of patients with Pearson and Alpers-Huttenlocher syndromes. Ghent University Academic Bibliography (Ghent University) ·Frank Roels, Patrick Verloo, Sara Seneca, G. I. Nemychenkov, François Eyskens, Joél Smet, Jean‐Jacques Martin, Marleen Praet, Rudy Van Coster	2006	0
18	Heroin withdrawal leads to metabolic alkalosis in an infant with cystic fibrosis European Journal of Pediatrics ·Saskia Vande Velde, Patrick Verloo, Stéphanie Van Biervliet, Eddy Robberecht	2006	4
19	Plasmodium falciparum-activated Chloride Channels Are Defective in Erythrocytes from Cystic Fibrosis Patients Journal of Biological Chemistry ·Patrick Verloo, Clemens H. M. Kocken, Annemarie Voorberg-van der Wel, Ben C. Tilly, Boris M. Hogema, M. Sinaasappel, Alan W. Thomas, Hugo R. de Jonge	2004	64
20	Blue Native Polyacrylamide Gel Electrophoresis: A Powerful Tool in Diagnosis of Oxidative Phosphorylation Defects Pediatric Research ·Rudy Van Coster, Joél Smet, clarifying the relationship between facts and figures., Linda De Meırleır, Sara Seneca, Johan Van Hove, Guillaume Sébire, Hélène Verhelst, Jan De Bleecker, Bruno Van Vlem, Patrick Verloo, Jules G. Leroy	2001	116

About Patrick Verloo

Patrick Verloo is a scholar working on Clinical Biochemistry, Endocrine and Autonomic Systems, Biochemistry, Neurology and Genetics, having authored 25 papers that have together received 434 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (6 papers), Autoimmune Neurological Disorders and Treatments (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Biomedical Research and Pathophysiology (3 papers), RNA modifications and cancer (3 papers), Amino Acid Enzymes and Metabolism (2 papers) and Neonatal Health and Biochemistry (2 papers). The work is most often cited by research in Clinical Biochemistry (108 citations), Molecular Biology (273 citations), Cell Biology (60 citations), Neurology (41 citations) and Endocrine and Autonomic Systems (18 citations). Patrick Verloo has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Hélène Verhelst, Rudy Van Coster, Sara Seneca, Linda De Meırleır, Joél Smet, Guillaume Sébire, Bruno Van Vlem, Jules G. Leroy, Johan Van Hove and Jan De Bleecker. Their work appears in journals such as European Journal of Paediatric Neurology, Journal of Inherited Metabolic Disease, Toxins, Neurology and PEDIATRICS.

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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