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 — A (Enhanced Table)

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

Name	h						Papers	Cites
Marc D’Hooghe Belgium	12	337	123	103	95	65	18	580
Hanna Mierzewska Poland	15	444 1.3×	40 0.3×	42 0.4×	105 1.1×	61 0.9×	57	728
Saadet Mercimek‐Andrews Canada	13	276 0.8×	63 0.5×	95 0.9×	77 0.8×	20 0.3×	52	623
Gretchen Golas United States	16	345 1.0×	145 1.2×	54 0.5×	199 2.1×	40 0.6×	21	869
Shruti Bagla United States	11	262 0.8×	77 0.6×	32 0.3×	83 0.9×	30 0.5×	19	449
Kei Shioda Japan	14	274 0.8×	27 0.2×	40 0.4×	74 0.8×	81 1.2×	25	517
Annette Bley Germany	14	500 1.5×	42 0.3×	37 0.4×	51 0.5×	97 1.5×	29	816
Caterina Carbonell Spain	7	115 0.3×	120 1.0×	44 0.4×	137 1.4×	64 1.0×	12	420
Yoshio Morimatsu Japan	15	391 1.2×	30 0.2×	76 0.7×	181 1.9×	59 0.9×	28	605
Elena I. Ilina Germany	9	184 0.5×	70 0.6×	22 0.2×	123 1.3×	26 0.4×	13	340
Michelle Demos Canada	13	270 0.8×	64 0.5×	31 0.3×	97 1.0×	16 0.2×	23	482

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

Roelens, Filip, et al.. (2021). Harlequin syndrome in a pediatric population: a case series. Acta Neurologica Belgica. 121(3). 625–631. 1 indexed citations

Stouffs, Katrien, Emmanuel Scalais, Marc D’Hooghe, et al.. (2018). Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1. European Journal of Human Genetics. 26(8). 1132–1142. 25 indexed citations

Simons, Cas, David A. Dyment, Stephen J. Bent, et al.. (2017). A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy. Brain. 140(12). 3105–3111. 59 indexed citations

Depondt, Chantal, Simona Donatello, Nicolas Simonis, et al.. (2014). Autosomal recessive cerebellar ataxia of adult onset due to STUB1 Mutations. Neurology. 82(19). 1749–1750. 28 indexed citations

Bekri, Soumeya, Marc D’Hooghe, & Pieter Vermeersch. (2014). X-Linked Sideroblastic Anemia and Ataxia. 5 indexed citations

Claes, Kathleen, Julie Depuydt, A. Malcolm R. Taylor, et al.. (2013). Variant Ataxia Telangiectasia: Clinical and Molecular Findings and Evaluation of Radiosensitive Phenotypes in a Patient and Relatives. NeuroMolecular Medicine. 15(3). 447–457. 28 indexed citations

Izzi, Benedetta, Inge François, Veerle Labarque, et al.. (2012). Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction. PLoS ONE. 7(6). e38579–e38579. 19 indexed citations

Steenweg, Marjan E., Frederik Barkhof, Marc D’Hooghe, et al.. (2012). Characteristics of Early MRI in Children and Adolescents with Vanishing White Matter. Neuropediatrics. 43(1). 22–26. 27 indexed citations

D’Hooghe, Marc, Dominik Selleslag, Geert Mortier, et al.. (2012). X-linked sideroblastic anemia and ataxia: A new family with identification of a fourth ABCB7 gene mutation. European Journal of Paediatric Neurology. 16(6). 730–735. 31 indexed citations

10.

Lagae, Lieven, Hélène Verhelst, Berten Ceulemans, et al.. (2010). Treatment and long term outcome in West syndrome: The clinical reality. A multicentre follow up study. Seizure. 19(3). 159–164. 69 indexed citations

11.

Coenegrachts, Kenneth, et al.. (2010). Fetal MRI of the placenta in extreme early onset IUGR. Prenatal Diagnosis. 30(4). 384–386. 2 indexed citations

12.

Dvořák, Jiří, et al.. (2006). The FIFA/F-MARC update on doping. British Journal of Sports Medicine. 40(suppl 1). i2–i2. 1 indexed citations

13.

Dvořák, Jiří, et al.. (2006). FIFA’s approach to doping in football. British Journal of Sports Medicine. 40(suppl 1). i3–i12. 12 indexed citations

14.

Boon, Paul, Berten Ceulemans, Marc D’Hooghe, et al.. (2005). Steroids in intractable childhood epilepsy: Clinical experience and review of the literature. Seizure. 14(6). 412–421. 76 indexed citations

15.

Li, Rong, Toby Johnson, Gajja S. Salomons, et al.. (2005). Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease. Annals of Neurology. 57(3). 310–326. 183 indexed citations

16.

Roels, Frank, Marianne Depreter, M. Girós, et al.. (2002). Differential organ involvement in peroxisomal disorders. Journal of Inherited Metabolic Disease. 25. 99–99.

17.

Martin, J. J., L. Martin, A. Löfgren, et al.. (1999). Classical Friedreich’s Ataxia and Its Genotype. European Neurology. 42(2). 109–115. 1 indexed citations

18.

Dehaene, I., Jan Casselman, Marc D’Hooghe, & Michel Van Zandijcke. (1996). Unilateral internuclear ophthalmoplegia and ipsiversive torsional nystagmus. Journal of Neurology. 243(6). 461–464. 13 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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