Laurens Wiel

1.8k total citations
6 papers, 234 citations indexed

About

Laurens Wiel is a scholar working on Molecular Biology, Genetics and Virology. According to data from OpenAlex, Laurens Wiel has authored 6 papers receiving a total of 234 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 1 paper in Virology. Recurrent topics in Laurens Wiel's work include Genomics and Rare Diseases (5 papers), RNA and protein synthesis mechanisms (3 papers) and Genomics and Phylogenetic Studies (3 papers). Laurens Wiel is often cited by papers focused on Genomics and Rare Diseases (5 papers), RNA and protein synthesis mechanisms (3 papers) and Genomics and Phylogenetic Studies (3 papers). Laurens Wiel collaborates with scholars based in Netherlands, United Kingdom and United States. Laurens Wiel's co-authors include Christian Gilissen, Joris A. Veltman, Gerrit Vriend, Coos Baakman, Teunis J. P. van Dam, Robin van der Lee, Martijn A. Huynen, Hanka Venselaar, Han G. Brunner and Lisenka E.L.M. Vissers and has published in prestigious journals such as Nucleic Acids Research, The American Journal of Human Genetics and Clinical Chemistry.

In The Last Decade

Laurens Wiel

6 papers receiving 234 citations

Peers

Countries citing papers authored by Laurens Wiel

Since Specialization

Citations

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

Fields of papers citing papers by Laurens Wiel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurens Wiel

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

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	Mind the Gap: The Complete Human Genome Unlocks Benefits for Clinical Genomics 2022 ·Clinical Chemistry ·Daniel Seung Kim, Laurens Wiel, Euan A. Ashley	2
2	De novo mutation hotspots in homologous protein domains identify function-altering mutations in neurodevelopmental disorders 2022 ·The American Journal of Human Genetics ·Laurens Wiel, (unknown), Hanka Venselaar, Lisenka E.L.M. Vissers, Han G. Brunner, Rolph Pfundt, Gerrit Vriend, Joris A. Veltman, Christian Gilissen	7
3	MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains 2019 ·Human Mutation ·Laurens Wiel, Coos Baakman, (unknown), Joris A. Veltman, Gerrit Vriend, Christian Gilissen	115
4	Aggregation of population‐based genetic variation over protein domain homologues and its potential use in genetic diagnostics 2017 ·Human Mutation ·Laurens Wiel, Hanka Venselaar, Joris A. Veltman, Gert Vriend, Christian Gilissen	20
5	Spatial Clustering of de Novo Missense Mutations Identifies Candidate Neurodevelopmental Disorder-Associated Genes 2017 ·The American Journal of Human Genetics ·Stefan H. Lelieveld, Laurens Wiel, Hanka Venselaar, Rolph Pfundt, Gerrit Vriend, Joris A. Veltman, Han G. Brunner, Lisenka E.L.M. Vissers, Christian Gilissen	46
6	Genome-scale detection of positive selection in nine primates predicts human-virus evolutionary conflicts 2017 ·Nucleic Acids Research ·Robin van der Lee, Laurens Wiel, Teunis J. P. van Dam, Martijn A. Huynen	44

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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