Bart van Lier
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Kidney Cyst Diseases
- Molecular Biology top 10%
- Congenital heart defects research
- RNA modifications and cancer
- Epigenetics and DNA Methylation
Papers in
- Genetics 6
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 2
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- Genetic factors in colorectal cancer 1
- Co-authors
- Alexander Hoischen (2 shared papers)Marloes Steehouwer (2 shared papers)Joris A. Veltman (2 shared papers)Christian Gilissen (2 shared papers)Peer Arts (2 shared papers)Han G. Brunner (2 shared papers)Joep de Ligt (1 shared paper)Marisol del Rosario (1 shared paper)
- Journals
- Nature Genetics (3 papers)Clinical Chemistry (2 papers)Clinical Genetics (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- NetherlandsUnited KingdomPortugal
In The Last Decade
Bart van Lier
7 papers receiving 1.6k citations
Bart van Lier's Hit Papers
Peers
Comparison fields: 5 of 75
- Genetics 1.1k
- Molecular Biology 772
- Cancer Research 151
- Genetics 105
- Hematology 84
Countries citing papers authored by Bart van Lier
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
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-authors
The 25 scholars most cited alongside Bart van Lier, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | A de novo paradigm for mental retardation Hit paper breakdown → | 2010 | 680 |
| 2 | 2010 | 387 | |
| 3 | 2010 | 236 | |
| 4 | 2011 | 212 | |
| 5 | 2013 | 81 | |
| 6 | 2016 | 44 | |
| 7 | 2014 | 25 |
About Bart van Lier
Bart van Lier is a scholar working on Genetics, Genetics, Pathology and Forensic Medicine, Immunology and Molecular Biology, having authored 7 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (2 papers), RNA modifications and cancer (1 paper), Genomics and Phylogenetic Studies (1 paper), Immunodeficiency and Autoimmune Disorders (1 paper), Epigenetics and DNA Methylation (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (1.1k citations), Molecular Biology (772 citations), Cancer Research (151 citations), Genetics (105 citations) and Hematology (84 citations). Bart van Lier has collaborated with scholars based in Netherlands, United Kingdom and Portugal. Frequent co-authors include Alexander Hoischen, Marloes Steehouwer, Joris A. Veltman, Christian Gilissen, Peer Arts, Han G. Brunner, Joep de Ligt, Marisol del Rosario, Bregje W.M. van Bon and Petra de Vries. Their work appears in journals such as Nature Genetics, Clinical Chemistry, Clinical Genetics and The American Journal of Human Genetics.
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.