Maarten H. Lequin

10.4k total citations
253 papers, 6.4k citations indexed

About

Maarten H. Lequin is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Maarten H. Lequin has authored 253 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 96 papers in Pediatrics, Perinatology and Child Health, 53 papers in Genetics and 46 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Maarten H. Lequin's work include Neonatal and fetal brain pathology (55 papers), Fetal and Pediatric Neurological Disorders (50 papers) and Craniofacial Disorders and Treatments (31 papers). Maarten H. Lequin is often cited by papers focused on Neonatal and fetal brain pathology (55 papers), Fetal and Pediatric Neurological Disorders (50 papers) and Craniofacial Disorders and Treatments (31 papers). Maarten H. Lequin collaborates with scholars based in Netherlands, United States and United Kingdom. Maarten H. Lequin's co-authors include Paul Govaert, Harm A.W.M. Tiddens, Jeroen Dudink, Wim C.J. Hop, Pim A. de Jong, Simon G. F. Robben, I.F.M. de Coo, Marie‐Lise C. van Veelen, Rick R. van Rijn and Yasutaka Nakano and has published in prestigious journals such as The Lancet, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Maarten H. Lequin

240 papers receiving 6.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maarten H. Lequin Netherlands 41 2.0k 1.6k 1.1k 1.1k 1.0k 253 6.4k
W.K. Chong United Kingdom 50 1.5k 0.7× 791 0.5× 833 0.7× 903 0.8× 1.1k 1.1× 140 6.4k
Andrea Rossi Italy 47 2.1k 1.1× 1.0k 0.6× 706 0.6× 1.3k 1.2× 2.3k 2.2× 404 8.4k
Daniela Prayer Austria 51 3.6k 1.8× 1.2k 0.7× 534 0.5× 1.6k 1.5× 722 0.7× 353 9.7k
Richard A. Prayson United States 54 2.0k 1.0× 1.1k 0.7× 619 0.5× 1.4k 1.3× 1.9k 1.8× 424 11.2k
Susan Blasér Canada 49 1.4k 0.7× 622 0.4× 763 0.7× 1.4k 1.3× 2.4k 2.3× 268 7.9k
Peter G. J. Nikkels Netherlands 45 2.1k 1.1× 925 0.6× 677 0.6× 903 0.8× 902 0.9× 218 5.8k
Noriko Salamon United States 44 1.1k 0.6× 1.0k 0.6× 406 0.4× 754 0.7× 527 0.5× 270 7.0k
Dennis Shaw United States 40 871 0.4× 467 0.3× 1.3k 1.1× 660 0.6× 1.4k 1.4× 164 5.3k
Françis Brunelle France 62 2.0k 1.0× 1.8k 1.1× 1.5k 1.3× 4.1k 3.8× 1.5k 1.5× 319 12.6k
Cathérine Garel France 43 3.1k 1.6× 624 0.4× 524 0.5× 1.3k 1.2× 639 0.6× 212 6.0k

Countries citing papers authored by Maarten H. Lequin

Since Specialization
Citations

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

Fields of papers citing papers by Maarten H. Lequin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maarten H. Lequin. 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 Maarten H. Lequin. The network helps show where Maarten H. Lequin may publish in the future.

Co-authorship network of co-authors of Maarten H. Lequin

This figure shows the co-authorship network connecting the top 25 collaborators of Maarten H. Lequin. A scholar is included among the top collaborators of Maarten H. Lequin 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 Maarten H. Lequin. Maarten H. Lequin 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
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Hofstede, Floris C., Hanneke A. Haijes, Klaske D. Lichtenbelt, et al.. (2024). Timing of cerebral damage in molybdenum cofactor deficiency: A meta-analysis of case reports. Genetics in Medicine Open. 2. 101853–101853. 2 indexed citations
4.
Löbel, Ulrike, Martin Catala, Felice D’Arco, et al.. (2024). Pituitary Gland Duplication Syndrome: An International Imaging Analysis. American Journal of Neuroradiology. 46(4). 808–814.
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Baarsen, Kirsten M. van, Shivaram Avula, Sebastian Toescu, et al.. (2024). Neuroimaging of postoperative pediatric cerebellar mutism syndrome: a systematic review. Neuro-Oncology Advances. 7(1). vdae212–vdae212.
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Dankbaar, Jan Willem, Pieter Wesseling, Sabine Plasschaert, et al.. (2024). T2-FLAIR Mismatch: An Imaging Biomarker for Children’sMYB/MYBL1–Altered Diffuse Astrocytoma or Angiocentric Glioma. American Journal of Neuroradiology. 45(6). 747–752. 3 indexed citations
7.
Groenendaal, Floris, et al.. (2023). Cranial MRI beyond the Neonatal Period and Neurodevelopmental Outcomes in Neonatal Encephalopathy Due to Perinatal Asphyxia: A Systematic Review. Journal of Clinical Medicine. 12(24). 7526–7526. 1 indexed citations
8.
Lequin, Maarten H., Floris Groenendaal, Jeroen Dudink, & Paul Govaert. (2023). Susceptibility weighted imaging can be a sensitive sequence to detect brain damage in neonates with kernicterus: a case report. BMC Neurology. 23(1). 104–104. 2 indexed citations
9.
Garel, Cathérine, Z. Leibovitz, Stéphanie Valence, et al.. (2023). Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation. American Journal of Neuroradiology. 44(3). 334–340.
10.
Voorman, Jeanine M., Marjolijn Ketelaar, Petra van Schie, et al.. (2021). Prognostic value of brain abnormalities for cognitive functioning in cerebral palsy: A prospective cohort study. European Journal of Paediatric Neurology. 32. 56–65. 6 indexed citations
11.
Annink, Kim V., Niek E. van der Aa, Jeroen Dudink, et al.. (2020). Introduction of Ultra-High-Field MR Imaging in Infants: Preparations and Feasibility. American Journal of Neuroradiology. 41(8). 1532–1537. 14 indexed citations
12.
Maier, Oliver, Holger Rehmann, Maarten H. Lequin, et al.. (2018). Identification of a Loss-of-Function Mutation in the Context of Glutaminase Deficiency and Neonatal Epileptic Encephalopathy. JAMA Neurology. 76(3). 342–342. 34 indexed citations
13.
Çizmeci, Mehmet Nevzat, Maarten H. Lequin, Klaske D. Lichtenbelt, et al.. (2018). Characteristic MR Imaging Findings of the Neonatal Brain in RASopathies. American Journal of Neuroradiology. 39(6). 1146–1152. 14 indexed citations
14.
Schot, Rachel, A. Jeannette M. Hoogeboom, Carsten R. Lincke, et al.. (2018). Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis. European Journal of Medical Genetics. 61(12). 783–789. 7 indexed citations
15.
Twigg, Stephen R.F., Jacqueline A.C. Goos, A. Jeannette M. Hoogeboom, et al.. (2015). Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability. The American Journal of Human Genetics. 97(3). 378–388. 43 indexed citations
16.
Raets, Marlou M. A., Jeroen Dudink, Charles Raybaud, et al.. (2014). Brain vein disorders in newborn infants. Developmental Medicine & Child Neurology. 57(3). 229–240. 19 indexed citations
17.
Nout, Erik, Irene M.J. Mathijssen, Jacques J. N. M. van der Meulen, et al.. (2010). Internal carotid dissection after Le Fort III distraction in Apert syndrome: A case report. Journal of Cranio-Maxillofacial Surgery. 38(7). 529–533. 14 indexed citations
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Rijn, Rick R. van, Maarten H. Lequin, & Hans Henrik Thodberg. (2009). Automatic determination of Greulich and Pyle bone age in healthy Dutch children. Pediatric Radiology. 39(6). 591–597. 80 indexed citations
19.
Loeve, Martine, Maarten H. Lequin, Marleen de Bruijne, et al.. (2008). Volumetric ultra low dose expiratory computed tomography scans could be sufficient to monitor CF lung disease. Journal of Cystic Fibrosis. 7. S59–S59. 1 indexed citations
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Dewit, Olivier, I.F.M. de Coo, Elly Verbeek, et al.. (2005). Brain abnormalities in a case of malonyl-CoA decarboxylase deficiency. Molecular Genetics and Metabolism. 87(2). 102–106. 28 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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