Dries Dobbelaere

3.1k total citations
42 papers, 1.3k citations indexed

About

Dries Dobbelaere is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Dries Dobbelaere has authored 42 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Clinical Biochemistry, 22 papers in Molecular Biology and 10 papers in Physiology. Recurrent topics in Dries Dobbelaere's work include Metabolism and Genetic Disorders (29 papers), Mitochondrial Function and Pathology (12 papers) and Neonatal Health and Biochemistry (8 papers). Dries Dobbelaere is often cited by papers focused on Metabolism and Genetic Disorders (29 papers), Mitochondrial Function and Pathology (12 papers) and Neonatal Health and Biochemistry (8 papers). Dries Dobbelaere collaborates with scholars based in France, United States and Switzerland. Dries Dobbelaere's co-authors include Marshall Summar, Saul W. Brusilow, Brendan Lee, Jòseph Vamecq, Anne‐Frédérique Dessein, Monique Fontaine, Karine Mention-Mulliez, Karine Mention, Marie Joncquel-Chevalier Curt and Claire Douillard and has published in prestigious journals such as Circulation, Neurology and Analytical Biochemistry.

In The Last Decade

Dries Dobbelaere

42 papers receiving 1.3k citations

Peers

Dries Dobbelaere

PHYSI

SURGE

EDM

Janneke G. Langendonk Netherlands

N. G. G. M. Abeling Netherlands

Henk Overmars Netherlands

Areeg El‐Gharbawy United States

H. Schmidt Germany

B F Kase Norway

Deborah Marsden United States

Isabel Ibarra‐González Mexico

Jacques Letarte Canada

Jaume Campistol Spain

Janneke G. Langendonk Netherlands

Dries Dobbelaere

504 ×1.1

727 ×1.6

561 ×2.3

PHYSI

276 ×1.2

SURGE

359 ×1.8

EDM

Citations per year, relative to Dries Dobbelaere Dries Dobbelaere (= 1×) peers Janneke G. Langendonk

Countries citing papers authored by Dries Dobbelaere

Since Specialization

Citations

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

Fields of papers citing papers by Dries Dobbelaere

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dries Dobbelaere

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

Paquot, Adrien, Gustavo Soto Ares, Anne‐Frédérique Dessein, et al.. (2024). Findings from the individualized management of a patient with Acyl-CoA Oxidase-1 (ACOX1) deficiency: A bedside-to-bench-to-bedside strategy. Molecular Genetics and Metabolism. 143(3). 108581–108581. 2 indexed citations

Grzych, Guillaume, Sylvie Deheul, Dries Dobbelaere, et al.. (2023). Comparison of biomarker for diagnosis of nitrous oxide abuse: challenge of cobalamin metabolic parameters, a retrospective study. Journal of Neurology. 270(4). 2237–2245. 17 indexed citations

Douillard, Claire, et al.. (2022). A case of pink urine associated with abdominal pain crisis. Annales de biologie clinique. 80(4). 389–392. 1 indexed citations

Posset, Roland, Sven F. Garbade, Nikolas Boy, et al.. (2019). Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—A successful strategy for clinical research of rare diseases. Journal of Inherited Metabolic Disease. 42(1). 93–106. 25 indexed citations

Germain, Nicolas, Anne‐Frédérique Dessein, Dries Dobbelaere, et al.. (2019). First-line Screening of OXPHOS Deficiencies Using Microscale Oxygraphy in Human Skin Fibroblasts: A Preliminary Study. International Journal of Medical Sciences. 16(7). 931–938. 7 indexed citations

Fontaine, Monique, Anne‐Frédérique Dessein, Karine Mention-Mulliez, et al.. (2018). Fluxomic assay-assisted diagnosis orientation in a cohort of 11 patients with myopathic form of CPT2 deficiency. Molecular Genetics and Metabolism. 123(4). 441–448. 11 indexed citations

Posset, Roland, Sven F. Garbade, Nikolas Boy, et al.. (2018). Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—a successful strategy for clinical research of rare diseases. Journal of Inherited Metabolic Disease. 3 indexed citations

Dessein, Anne‐Frédérique, Monique Fontaine, Marie Joncquel-Chevalier Curt, et al.. (2017). Fluxomic evidence for impaired contribution of short-chain acyl-CoA dehydrogenase to mitochondrial palmitate β-oxidation in symptomatic patients with ACADS gene susceptibility variants. Clinica Chimica Acta. 471. 101–106. 10 indexed citations

Roland, Dominique, Gilbert Briand, Jòseph Vamecq, et al.. (2017). Coupled brain and urine spectroscopy - in vivo metabolomic characterization of HMG-CoA lyase deficiency in 5 patients. Molecular Genetics and Metabolism. 121(2). 111–118. 11 indexed citations

10.

Posset, Roland, Ángeles García‐Cazorla, Vassili Valayannopoulos, et al.. (2016). Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders. Journal of Inherited Metabolic Disease. 39(5). 661–672. 49 indexed citations

11.

Béghin, Laurent, Stéphanie Coopman, Manuel Schiff, et al.. (2016). Doubling diet fat on sugar ratio in children with mitochondrial OXPHOS disorders: Effects of a randomized trial on resting energy expenditure, diet induced thermogenesis and body composition. Clinical Nutrition. 35(6). 1414–1422. 2 indexed citations

12.

Curt, Marie Joncquel-Chevalier, Monique Fontaine, Anne‐Frédérique Dessein, et al.. (2015). Creatine biosynthesis and transport in health and disease. Biochimie. 119. 146–165. 166 indexed citations

13.

Jardri, Renaud, Agna A. Bartels‐Velthuis, Martin Debbané, et al.. (2014). From Phenomenology to Neurophysiological Understanding of Hallucinations in Children and Adolescents. Schizophrenia Bulletin. 40(Suppl_4). S221–S232. 63 indexed citations

14.

Dobbelaere, Dries, et al.. (2014). Results from a Nationwide Cohort Temporary Utilization Authorization (ATU) Survey of Patients in France Treated with Pheburane® (Sodium Phenylbutyrate) Taste-Masked Granules. Pediatric Drugs. 16(5). 407–415. 11 indexed citations

15.

Héron, Bénédicte, Vassili Valayannopoulos, Julien Baruteau, et al.. (2012). Miglustat therapy in the French cohort of paediatric patients with Niemann-Pick disease type C. Orphanet Journal of Rare Diseases. 7(1). 36–36. 64 indexed citations

16.

Douillard, Claire, Karine Mention, Dries Dobbelaere, et al.. (2012). Hypoglycaemia related to inherited metabolic diseases in adults. Orphanet Journal of Rare Diseases. 7(1). 26–26. 35 indexed citations

17.

Davit–Spraul, Anne, Monique Piraud, Dries Dobbelaere, et al.. (2011). Liver glycogen storage diseases due to phosphorylase system deficiencies: Diagnosis thanks to non invasive blood enzymatic and molecular studies. Molecular Genetics and Metabolism. 104(1-2). 137–143. 42 indexed citations

18.

Dessein, Anne‐Frédérique, Monique Fontaine, Brage Storstein Andresen, et al.. (2010). A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report. Orphanet Journal of Rare Diseases. 5(1). 26–26. 15 indexed citations

19.

Dessein, Anne‐Frédérique, Monique Fontaine, Dries Dobbelaere, et al.. (2009). Deuterated palmitate-driven acylcarnitine formation by whole-blood samples for a rapid diagnostic exploration of mitochondrial fatty acid oxidation disorders. Clinica Chimica Acta. 406(1-2). 23–26. 14 indexed citations

20.

Gitiaux, Cyril, Emmanuel Roze, Kiyoka Kinugawa, et al.. (2008). Spectrum of movement disorders associated with glutaric aciduria type 1: A study of 16 patients. Movement Disorders. 23(16). 2392–2397. 45 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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