Rob van Luijk

473 total citations
9 papers, 345 citations indexed

About

Rob van Luijk is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Rob van Luijk has authored 9 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Rob van Luijk's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (3 papers). Rob van Luijk is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (3 papers). Rob van Luijk collaborates with scholars based in Belgium, India and France. Rob van Luijk's co-authors include J. Wauters, Stefaan Scheers, R. Frank Kooy, Liesbeth Rooms, Edwin Reyniers, 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

Rob van Luijk

9 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rob van Luijk Belgium 8 276 153 90 66 61 9 345
Stefaan Scheers Belgium 8 282 1.0× 153 1.0× 94 1.0× 68 1.0× 61 1.0× 8 352
Devin M. Cox United States 7 238 0.9× 164 1.1× 60 0.7× 21 0.3× 18 0.3× 9 299
Eve Õiglane‐Shlik Estonia 10 185 0.7× 177 1.2× 76 0.8× 16 0.2× 32 0.5× 17 320
Fernanda T. Bellucco Brazil 9 140 0.5× 107 0.7× 43 0.5× 56 0.8× 21 0.3× 24 233
Viola Doccini Italy 9 182 0.7× 109 0.7× 108 1.2× 25 0.4× 92 1.5× 10 317
Irina Stefanova Germany 6 129 0.5× 68 0.4× 42 0.5× 12 0.2× 43 0.7× 10 204
Jin Szatkiewicz United States 11 220 0.8× 125 0.8× 22 0.2× 29 0.4× 20 0.3× 30 321
Chelsea Lowther Canada 8 245 0.9× 191 1.2× 34 0.4× 16 0.2× 14 0.2× 8 330
Lucia Pucci Italy 11 210 0.8× 143 0.9× 54 0.6× 25 0.4× 18 0.3× 21 286
Simone C. Yendle Australia 6 308 1.1× 132 0.9× 42 0.5× 10 0.2× 200 3.3× 6 426

Countries citing papers authored by Rob van Luijk

Since Specialization
Citations

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

Fields of papers citing papers by Rob van Luijk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rob van Luijk. 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 Rob van Luijk. The network helps show where Rob van Luijk may publish in the future.

Co-authorship network of co-authors of Rob van Luijk

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

All Works

9 of 9 papers shown
1.
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
2.
Courtens, Winnie, J. Wauters, Marek Wojciechowski, et al.. (2007). A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review. Clinical Dysmorphology. 16(4). 231–239. 5 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, et al.. (2003). Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation. Annales de Génétique. 47(1). 53–59. 9 indexed citations
9.
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.

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