Stefaan Scheers

516 total citations
8 papers, 352 citations indexed

About

Stefaan Scheers is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Stefaan Scheers has authored 8 papers receiving a total of 352 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Stefaan Scheers's work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Chromosomal and Genetic Variations (3 papers). Stefaan Scheers is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Chromosomal and Genetic Variations (3 papers). Stefaan Scheers collaborates with scholars based in Belgium, France and United States. Stefaan Scheers's co-authors include Rob van Luijk, J. Wauters, R. Frank Kooy, Edwin Reyniers, Liesbeth Rooms, Berten Ceulemans, Yolande van Bever, Jenneke van den Ende, Annick Laridon and Winnie Courtens and has published in prestigious journals such as Human Mutation, European Journal of Human Genetics and Cytogenetic and Genome Research.

In The Last Decade

Stefaan Scheers

8 papers receiving 332 citations

Peers

Stefaan Scheers

GENET

MB

PPCH

PS

PMH

Rob van Luijk Belgium

Eve Õiglane‐Shlik Estonia

Devin M. Cox United States

Viola Doccini Italy

Fernanda T. Bellucco Brazil

Lucia Pucci Italy

Irina Stefanova Germany

Natalie Trump United Kingdom

Simone C. Yendle Australia

Chelsea Lowther Canada

Rob van Luijk Belgium

Stefaan Scheers

276 ×1.0

GENET

153 ×1.0

MB

90 ×1.0

PPCH

66 ×1.0

PS

61 ×1.0

PMH

Citations per year, relative to Stefaan Scheers Stefaan Scheers (= 1×) peers Rob van Luijk

Countries citing papers authored by Stefaan Scheers

Since Specialization

Citations

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

Fields of papers citing papers by Stefaan Scheers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefaan Scheers

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Dijck, Anke Van, Ilse M. van der Werf, Edwin Reyniers, et al.. (2015). Five patients with a chromosome 1q21.1 triplication show macrocephaly, increased weight and facial similarities. European Journal of Medical Genetics. 58(10). 503–508. 21 indexed citations

2.

Winnepenninckx, Birgitta, Cheryl Longman, Ronald S. Murray, et al.. (2007). The molecular basis of the folate-sensitive fragile site FRA11A at 11q13. Cytogenetic and Genome Research. 119(1-2). 9–14. 20 indexed citations

3.

Suls, Arvid, Kristl G. Claeys, D. Goossens, et al.. (2006). Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients. Human Mutation. 27(9). 914–920. 90 indexed citations

4.

Rooms, Liesbeth, Edwin Reyniers, Stefaan Scheers, et al.. (2006). TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions. European Journal of Human Genetics. 14(10). 1090–1096. 34 indexed citations

5.

Courtens, Winnie, Wim Wuyts, Stefaan Scheers, et al.. (2006). A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review. European Journal of Medical Genetics. 49(5). 402–413. 8 indexed citations

6.

Bever, Yolande van, Liesbeth Rooms, Annick Laridon, et al.. (2005). Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype. American Journal of Medical Genetics Part A. 135A(1). 91–95. 49 indexed citations

7.

Rooms, Liesbeth, Edwin Reyniers, Wim Wuyts, et al.. (2005). Multiplex ligation‐dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics. Clinical Genetics. 69(1). 58–64. 51 indexed citations

8.

Rooms, Liesbeth, Edwin Reyniers, Rob van Luijk, et al.. (2003). Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA). Human Mutation. 23(1). 17–21. 79 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.

Explore authors with similar magnitude of impact