Bart van Lier

2.1k total citations · 1 hit paper
3 papers, 745 citations indexed

About

Bart van Lier is a scholar working on Genetics, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Bart van Lier has authored 3 papers receiving a total of 745 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 0 papers in Infectious Diseases. Recurrent topics in Bart van Lier's work include Genetics and Neurodevelopmental Disorders (2 papers), Genomics and Rare Diseases (2 papers) and RNA modifications and cancer (1 paper). Bart van Lier is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Genomics and Rare Diseases (2 papers) and RNA modifications and cancer (1 paper). Bart van Lier collaborates with scholars based in Netherlands. Bart van Lier's co-authors include Alexander Hoischen, Han G. Brunner, Peer Arts, Marloes Steehouwer, Christian Gilissen, Joris A. Veltman, Bregje W.M. van Bon, Petra de Vries, Irene M. Janssen and Lisenka E.L.M. Vissers and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Clinical Chemistry.

In The Last Decade

Bart van Lier

3 papers receiving 730 citations

Hit Papers

A de novo paradigm for mental retardation 2010 2026 2015 2020 2010 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bart van Lier Netherlands 3 545 403 83 63 56 3 745
Nienke Wieskamp Netherlands 7 531 1.0× 477 1.2× 84 1.0× 53 0.8× 77 1.4× 7 858
Pamela Magini Italy 16 349 0.6× 347 0.9× 119 1.4× 42 0.7× 27 0.5× 38 717
Eva Pipiras France 15 424 0.8× 475 1.2× 80 1.0× 30 0.5× 42 0.8× 26 744
Daniel A. Peiffer United States 14 466 0.9× 554 1.4× 135 1.6× 44 0.7× 31 0.6× 19 926
Véronique Geoffroy France 12 510 0.9× 559 1.4× 70 0.8× 43 0.7× 64 1.1× 17 775
Martine Doco‐Fenzy France 15 302 0.6× 349 0.9× 59 0.7× 28 0.4× 47 0.8× 29 690
Julien Thévenon France 15 474 0.9× 450 1.1× 41 0.5× 25 0.4× 78 1.4× 51 798
Bruce J. Herron United States 14 472 0.9× 739 1.8× 48 0.6× 31 0.5× 86 1.5× 29 1.1k
Jiong Yan United States 15 487 0.9× 650 1.6× 56 0.7× 31 0.5× 76 1.4× 27 1.0k
Dominique Martin‐Coignard France 14 424 0.8× 522 1.3× 41 0.5× 29 0.5× 53 0.9× 22 817

Countries citing papers authored by Bart van Lier

Since Specialization
Citations

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

Fields of papers citing papers by Bart van Lier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bart van Lier

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

All Works

3 of 3 papers shown
1.
Bosgoed, Ermanno, Bart van Lier, Erik‐Jan Kamsteeg, et al.. (2014). Translating Sanger-Based Routine DNA Diagnostics into Generic Massive Parallel Ion Semiconductor Sequencing. Clinical Chemistry. 61(1). 154–162. 22 indexed citations
2.
Gilissen, Christian, Heleen H. Arts, Alexander Hoischen, et al.. (2010). Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome. The American Journal of Human Genetics. 87(3). 418–423. 197 indexed citations
3.
Vissers, Lisenka E.L.M., Joep de Ligt, Christian Gilissen, et al.. (2010). A de novo paradigm for mental retardation. Nature Genetics. 42(12). 1109–1112. 526 indexed citations breakdown →

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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