Publications

For citations and H index, see this scholar profile.

2019

 

 

Henriksson, J. et al., 2019. Genome-wide CRISPR screens in T helper cells reveal pervasive cross-talk between activation and differentiation. Cell.

 

2018

Arvidsson, G., Henriksson, J. & Sander, B., 2018. Mixed-species RNAseq analysis of human lymphoma cells adhering to mouse stromal cells identifies a core gene set that is also differentially expressed in the lymph node microenvironment of mantle cell lymphoma and chronic lymphocytic leukemia patients. Haematologica.

Hagai, T. et al., 2018. Gene expression variability across cells and species shapes innate immunity. Nature, 563(7730), pp.197–202.

Miragaia, R.J. et al., 2018. Single-cell RNA-sequencing resolves self-antigen expression during mTEC development. Scientific reports, 8(1), p.685.

Pramanik, J. et al., 2018. Genome-wide analyses reveal the IRE1a-XBP1 pathway promotes T helper cell differentiation by resolving secretory stress and accelerating proliferation. Genome medicine, 10(1), p.76.

Severo, M.S. et al., 2018. Unbiased classification of mosquito blood cells by single-cell genomics and high-content imaging. Proceedings of the National Academy of Sciences of the United States of America, 115(32), pp.E7568–E7577.

Vento-Tormo, R. et al., 2018. Single-cell reconstruction of the early maternal–fetal interface in humans. Nature, 563(7731), pp.347–353.

2016

Kolodziejczyk, A.A. et al., 2015. Single Cell RNA-Sequencing of Pluripotent States Unlocks Modular Transcriptional Variation. Cell stem cell, 17(4), pp.471–485.

Mahani, A., Henriksson, J. & Wright, A.P.H., 2013. Origins of Myc proteins–using intrinsic protein disorder to trace distant relatives. PloS one, 8(9), p.e75057.

2015

Dahlman, I. et al., 2015. The fat cell epigenetic signature in post-obese women is characterized by global hypomethylation and differential DNA methylation of adipogenesis genes. International journal of obesity, 39(6), pp.910–919.

Hench, J. et al., 2015. The Homeobox Genes of Caenorhabditis elegans and Insights into Their Spatio-Temporal Expression Dynamics during Embryogenesis. PloS one, 10(5), p.e0126947.

2013

Arczewska, K.D. et al., 2013. Active transcriptomic and proteomic reprogramming in the C. elegans nucleotide excision repair mutant xpa-1. Nucleic acids research, 41(10), pp.5368–5381.

Henriksson, J., Piasecki, B.P., et al., 2013. Finding ciliary genes: a computational approach. Methods in enzymology, 525, pp.327–350.

Henriksson, J., Hench, J., et al., 2013. Endrov: an integrated platform for image analysis. Nature methods, 10(6), pp.454–456.

Xue-Franzén, Y. et al., 2013. Distinct roles of the Gcn5 histone acetyltransferase revealed during transient stress-induced reprogramming of the genome. BMC genomics, 14, p.479.

2010

Henriksson, J., Lundh, T. & Wennberg, B., 2010. A model of sympatric speciation through reinforcement. Kinetic and Related Models, 3(1), pp.143–163.

Xue-Franzén, Y. et al., 2010. Genome-wide characterisation of the Gcn5 histone acetyltransferase in budding yeast during stress adaptation reveals evolutionarily conserved and diverged roles. BMC genomics, 11(1), p.200.

2009

Bratic, I. et al., 2009. Mitochondrial DNA level, but not active replicase, is essential for Caenorhabditis elegans development. Nucleic acids research, 37(6), pp.1817–1828.

Hench, J. et al., 2009. Spatio-temporal reference model of Caenorhabditis elegans embryogenesis with cell contact maps. Developmental biology, 333(1), pp.1–13.