Marc D’Hooghe

2.4k total citations
18 papers, 580 citations indexed

About

Marc D’Hooghe is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Marc D’Hooghe has authored 18 papers receiving a total of 580 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 3 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Marc D’Hooghe's work include RNA regulation and disease (3 papers), Mitochondrial Function and Pathology (2 papers) and Porphyrin Metabolism and Disorders (2 papers). Marc D’Hooghe is often cited by papers focused on RNA regulation and disease (3 papers), Mitochondrial Function and Pathology (2 papers) and Porphyrin Metabolism and Disorders (2 papers). Marc D’Hooghe collaborates with scholars based in Belgium, United States and Netherlands. Marc D’Hooghe's co-authors include Marjo S. van der Knaap, Linda De Meırleır, Lieven Lagae, Berten Ceulemans, Rudy Van Coster, Stephanie Z. Ruyle, Albee Messing, Sakkubai Naidu, Anna Jansen and Alyssa Reddy and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Marc D’Hooghe

17 papers receiving 567 citations

Peers

Countries citing papers authored by Marc D’Hooghe

Since Specialization

Citations

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

Fields of papers citing papers by Marc D’Hooghe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc D’Hooghe. 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 Marc D’Hooghe. The network helps show where Marc D’Hooghe may publish in the future.

Co-authorship network of co-authors of Marc D’Hooghe

This figure shows the co-authorship network connecting the top 25 collaborators of Marc D’Hooghe. A scholar is included among the top collaborators of Marc D’Hooghe 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 Marc D’Hooghe. Marc D’Hooghe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Title	Journal	Authors	Indexed citations
1	Harlequin syndrome in a pediatric population: a case series	Acta Neurologica Belgica	Filip Roelens, Marc D’Hooghe et al.	1
2	Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1	European Journal of Human Genetics	Katrien Stouffs, Emmanuel Scalais et al.	25
3	A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy	Brain	Cas Simons, David A. Dyment et al.	59
4	Autosomal recessive cerebellar ataxia of adult onset due to STUB1 Mutations	Neurology	Chantal Depondt, Simona Donatello et al.	28
5	X-Linked Sideroblastic Anemia and Ataxia		Soumeya Bekri, Marc D’Hooghe et al.	5
6	Variant Ataxia Telangiectasia: Clinical and Molecular Findings and Evaluation of Radiosensitive Phenotypes in a Patient and Relatives	NeuroMolecular Medicine	Kathleen Claes, Julie Depuydt et al.	28
7	Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction	PLoS ONE	Benedetta Izzi, Inge François et al.	19
8	Characteristics of Early MRI in Children and Adolescents with Vanishing White Matter	Neuropediatrics	Marjan E. Steenweg, Frederik Barkhof et al.	27
9	X-linked sideroblastic anemia and ataxia: A new family with identification of a fourth ABCB7 gene mutation	European Journal of Paediatric Neurology	Marc D’Hooghe, Dominik Selleslag et al.	31
10	Treatment and long term outcome in West syndrome: The clinical reality. A multicentre follow up study	Seizure	Lieven Lagae, Hélène Verhelst et al.	69
11	Fetal MRI of the placenta in extreme early onset IUGR	Prenatal Diagnosis	Kenneth Coenegrachts, Marc D’Hooghe et al.	2
12	The FIFA/F-MARC update on doping	British Journal of Sports Medicine	Jiří Dvořák, Marc D’Hooghe et al.	1
13	FIFA’s approach to doping in football	British Journal of Sports Medicine	Jiří Dvořák, Toni Graf-Baumann et al.	12
14	Steroids in intractable childhood epilepsy: Clinical experience and review of the literature	Seizure	Paul Boon, Berten Ceulemans et al.	76
15	Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease	Annals of Neurology	Rong Li, Toby Johnson et al.	183
16	Differential organ involvement in peroxisomal disorders	Journal of Inherited Metabolic Disease	Frank Roels, Marianne Depreter et al.	0
17	Classical Friedreich’s Ataxia and Its Genotype	European Neurology	J. J. Martin, L. Martin et al.	1
18	Unilateral internuclear ophthalmoplegia and ipsiversive torsional nystagmus	Journal of Neurology	I. Dehaene, Jan Casselman et al.	13

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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