Author

Monique van der Voet

Radboud University NijmegenORCID 0000-0002-8829-1767Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Research Focus:gene regulatory network inference· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Organism:Drosophila· 1 Organism:human· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Annette SchenckiD· 2 shared Barbara FrankeiD· 2 shared Marieke KleiniD· 2 shared Alejandro Arias VásqueziD· 1 shared Anders Dupont BørglumiD· 1 shared Anna Castells‐NobauiD· 1 shared Anne van Rens· 1 shared Benjamin Harich· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetics

Annette SchenckORCID

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3 papers

Recent·Most cited

BioinformaticsbioRxivPreprintOct 14, 2022

Herb-paths, a network and statistical model to explore health-beneficial effects of herbs and herbal constituents

Monique van der Voet, Zhiyi Xu, Lotte M. van Rijnberk…·Eefje S. Poppelaars

Herb-paths integrates herb and compound effects to predict health-beneficial associations and validate them using Panax notoginseng and its extract.

DOI 10.1101/2022.10.14.512228

statistical model

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GeneticsAmerican Journal of PsychiatryPeer-reviewedFeb 12, 2020

Intellectual Disability-related genes increase ADHD risk and locomotor activity in Drosophila

Marieke Klein, Euginia L. Singgih, Anne van Rens…·Barbara Franke

This study identifies ADHD risk genes by linking ID-related genes to ADHD through common variants and validates their role in Drosophila behavior.

29 citations

Drosophilastatistical model

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GeneticsbioRxivPreprintSep 16, 2019

From rare Copy Number Variations to biological processes in ADHD

Benjamin Harich, Monique van der Voet, Marieke Klein…·Barbara Franke

This study identifies high-priority ADHD candidate genes by integrating rare CNV data with bioinformatics methods and finds shared genes with common variants.

1 citation

humanwhole-genome sequencing

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