Carlo Marcelis

8.3k total citations
67 papers, 1.6k citations indexed

About

Carlo Marcelis is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Carlo Marcelis has authored 67 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 22 papers in Molecular Biology and 17 papers in Surgery. Recurrent topics in Carlo Marcelis's work include Genomic variations and chromosomal abnormalities (14 papers), Congenital gastrointestinal and neural anomalies (12 papers) and Esophageal and GI Pathology (10 papers). Carlo Marcelis is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Congenital gastrointestinal and neural anomalies (12 papers) and Esophageal and GI Pathology (10 papers). Carlo Marcelis collaborates with scholars based in Netherlands, United States and Germany. Carlo Marcelis's co-authors include Ivo de Blaauw, Han G. Brunner, Pieter A. Doevendans, Frans C. S. Ramaekers, Valerie L. R. M. Verstraeten, M. A. F. Kamps, Jos L. V. Broers, Arthur van den Wijngaard, Maurice A. M. Van Steensel and Frederik Houben and has published in prestigious journals such as Science, Nature Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Carlo Marcelis

66 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carlo Marcelis Netherlands 25 757 433 327 208 129 67 1.6k
Marja W. Wessels Netherlands 24 993 1.3× 735 1.7× 244 0.7× 467 2.2× 45 0.3× 64 2.1k
Ashwin Dalal India 20 651 0.9× 543 1.3× 132 0.4× 44 0.2× 104 0.8× 151 1.4k
Marie Legendre France 23 741 1.0× 583 1.3× 143 0.4× 37 0.2× 88 0.7× 82 1.6k
Angela F. Brady United Kingdom 18 845 1.1× 593 1.4× 139 0.4× 41 0.2× 50 0.4× 43 1.6k
Antonis Voutetakis United States 22 634 0.8× 605 1.4× 162 0.5× 105 0.5× 66 0.5× 57 1.3k
Peter Gustavsson Sweden 20 1.3k 1.7× 476 1.1× 97 0.3× 73 0.4× 34 0.3× 38 1.8k
Laurence Cuisset France 25 2.1k 2.7× 297 0.7× 232 0.7× 35 0.2× 162 1.3× 62 2.5k
Mara Giordano Italy 20 503 0.7× 371 0.9× 111 0.3× 61 0.3× 39 0.3× 83 1.3k
Nicolette S. den Hollander Netherlands 21 510 0.7× 499 1.2× 183 0.6× 82 0.4× 49 0.4× 43 1.6k
Vincent Marion France 22 853 1.1× 876 2.0× 125 0.4× 89 0.4× 22 0.2× 42 1.5k

Countries citing papers authored by Carlo Marcelis

Since Specialization
Citations

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

Fields of papers citing papers by Carlo Marcelis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carlo Marcelis

This figure shows the co-authorship network connecting the top 25 collaborators of Carlo Marcelis. A scholar is included among the top collaborators of Carlo Marcelis 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 Carlo Marcelis. Carlo Marcelis 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
1.
Dingemans, Alexander J.M., Sandra Jansen, Jeroen van Reeuwijk, et al.. (2024). Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals. Nature Medicine. 30(7). 1994–2003. 4 indexed citations
2.
Boer, Elke de, Carlo Marcelis, Kornelia Neveling, et al.. (2023). A complex structural variant near SOX3 causes X-linked split-hand/foot malformation. Human Genetics and Genomics Advances. 4(3). 100200–100200. 1 indexed citations
3.
Sticht, Heinrich, François Lecoquierre, Alice Goldenberg, et al.. (2022). Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy. European Journal of Human Genetics. 31(3). 345–352. 4 indexed citations
4.
Evertz, Reinder, Arco J. Teske, Carlo Marcelis, et al.. (2020). Arrhythmogenic Right Ventricular Cardiomyopathy in a Pediatric Patient. SHILAP Revista de lepidopterología. 2(6). 919–924. 2 indexed citations
5.
Chavali, Pavithra L., Lovorka Stojic, Luke W. Meredith, et al.. (2017). Neurodevelopmental protein Musashi-1 interacts with the Zika genome and promotes viral replication. Science. 357(6346). 83–88. 117 indexed citations
6.
Cramer, G. Etienne, Jeannette Bakker, Michelle Michels, et al.. (2017). High T2-weighted signal intensity for risk prediction of sudden cardiac death in hypertrophic cardiomyopathy. International journal of cardiac imaging. 34(1). 113–120. 21 indexed citations
7.
Wijers, Charlotte H. W., Ivo de Blaauw, Carlo Marcelis, et al.. (2016). Previous miscarriages andGLI2are associated with anorectal malformations in offspring. Human Reproduction. 32(2). 299–306. 9 indexed citations
8.
Ockeloen, Charlotte W., Jan M. Cobben, Carlo Marcelis, & David A. Koolen. (2013). A rare complex malformation of the hand in split hand foot malformation type 3 (SHFM3). Clinical Dysmorphology. 22(3). 106–108. 1 indexed citations
9.
Feitz, Wout, et al.. (2013). “This bicycle gives me a headache”, a congenital anomaly. BMC Research Notes. 6(1). 412–412. 12 indexed citations
10.
Marcelis, Carlo & Arjan Pm de Brouwer. (2012). Feingold Syndrome 1. 2 indexed citations
11.
Silfhout, Anneke T. Vulto‐van, et al.. (2012). Two patients with intellectual disability, overlapping facial features, and overlapping deletions in 6p25.1p24.3. Clinical Dysmorphology. 22(1). 18–21. 7 indexed citations
12.
Houben, Frederik, Winnok H. De Vos, Ingrid P.C. Krapels, et al.. (2012). Cytoplasmic localization of PML particles in laminopathies. Histochemistry and Cell Biology. 139(1). 119–134. 21 indexed citations
13.
Hoyweghen, Ine Van, et al.. (2011). Constructing “best interests”: Genetic testing of children in families with hypertrophic cardiomyopathy. American Journal of Medical Genetics Part A. 155(8). 1930–1938. 23 indexed citations
14.
Marcelis, Carlo, Ivo de Blaauw, & Han G. Brunner. (2011). Chromosomal anomalies in the etiology of anorectal malformations: A review. American Journal of Medical Genetics Part A. 155(11). 2692–2704. 37 indexed citations
15.
Dijk, Fleur S. van, Ariana Kariminejad, Carlo Marcelis, et al.. (2010). Complete COL1A1 allele deletions in osteogenesis imperfecta. Genetics in Medicine. 12(11). 736–741. 33 indexed citations
16.
Marcelis, Carlo, et al.. (2009). A Feingold syndrome case with previously undescribed features and a new mutation.. PubMed. 20(3). 261–7. 1 indexed citations
17.
Backx, Liesbeth, Jean‐Pierre Fryns, Carlo Marcelis, et al.. (2008). Haploinsufficiency of the gene Quaking (QKI) is associated with the 6q terminal deletion syndrome. European Journal of Human Genetics. 17. 136. 7 indexed citations
18.
Bongers, Ernie M.H.F., Ilse J. de Wijs, Carlo Marcelis, Lies H. Hoefsloot, & Nine V.A.M. Knoers. (2008). Identification of entire LMX1B gene deletions in nail patella syndrome: evidence for haploinsufficiency as the main pathogenic mechanism underlying dominant inheritance in man. European Journal of Human Genetics. 16(10). 1240–1244. 29 indexed citations
19.
Emans, Pieter J., G. Kootstra, Carlo Marcelis, Emile A. M. Beuls, & Ernst van Heurn. (2005). The Currarino triad: the variable expression. Journal of Pediatric Surgery. 40(8). 1238–1242. 48 indexed citations
20.
Marcelis, Carlo, H.W.H.M. van der Putten, Carli Tops, Ludy Lutgens, & Ute Moog. (2001). Chemotherapy resistant ovarian cancer in carriers of an hMSH2 mutation?. Familial Cancer. 1(2). 109–111. 18 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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