Author

B. A. Pannebakker

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Evolutionary Biology· 3

Signature Assays, Organisms & Methods

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Organism:Drosophila· 3 Approach:statistical model· 2 Research Focus:chromatin & epigenetic regulation· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1

Frequent Co-Authors

D. M. Shuker· 2 shared L. van de Zande· 2 shared N. Cook· 2 shared D. J. Parker· 1 shared E. Geuverink· 1 shared E. Tauber· 1 shared F. Turner· 1 shared J. van den Heuvel· 1 shared

Activity by Year

2019-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersEvolutionary Biology

D. M. Shuker

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3 papers

Recent·Most cited

A single QTL with large effect is associated with female functional virginity in an asexual parasitoid wasp

W.-J. Ma, B. A. Pannebakker, X. Li, E. Geuverink, S. Y. Anvar, P. Veltsos, T. Schwander, L. van de Zande, L. W. Beukeboom

The paper identifies a single QTL with large effect associated with female functional virginity in an asexual parasitoid wasp through QTL mapping and candidate gene analysis.

bioRxiv · Nov 5, 2020Evolutionary Biology

Genomics of sex allocation in the parasitoid wasp Nasonia vitripennis

B. A. Pannebakker, N. Cook, J. van den Heuvel, L. van de Zande, D. M. Shuker

The paper conducts a genome-wide association study to identify genetic loci associated with sex ratio variation in Nasonia vitripennis, finding 18 linked SNPs and shared genetic basis with clutch size.

bioRxiv · Mar 18, 2020Evolutionary Biology

Genome-wide disruption of DNA methylation by 5-aza-2’-deoxycytidine in a parasitoid wasp

N. Cook, D. J. Parker, F. Turner, E. Tauber, B. A. Pannebakker, D. M. Shuker

This paper demonstrates that 5-aza-dC disrupts DNA methylation genome-wide in Nasonia vitripennis, leading to both hypo- and hyper-methylation with context- and sequence-specific effects.

bioRxiv · May 12, 2019 · PreprintEvolutionary Biology