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Department of Biomedicine

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Rajkumar, A. P., Christensen, J. H., Mattheisen, M., Jacobsen, I., Bache, I., Pallesen, J., Grove, J., Qvist, P., Mcquillin, A., Gurling, H. M., Tümer, Z., Mors, O. & Børglum, A. D. (2015). Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder. Bipolar Disorders (English Edition, Online), 17(2), 205-211. https://doi.org/10.1111/bdi.12239

Rajkumar, A. P., Qvist, P., Lazarus, R., Lescai, F., Ju, J., Nyegaard, M., Mors, O., Børglum, A. D., Li, Q. & Christensen, J. H. (2015). Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq. BMC Genomics, 16, 548. https://doi.org/10.1186/s12864-015-1767-y

Børglum, A., Mors, O., Nyegaard, M., Christensen, J. H., Qvist, P., Rajkumar, A. P. & Wegener, G. (2013). Heterozygous mouse with an inactivated brd1 allele and uses in psychiatry. (Patent No. PCT/EP2013/069524). https://patents.google.com/patent/WO2014044777A1/it

Qvist, P., Huertas, P., Jimeno, S., Nyegaard, M., Hassan, M. J., Jackson, S. P. & Børglum, A. (2011). CtIP Mutations Cause Seckel and Jawad Syndromes. PLoS Genetics, 7(10), e1002310. https://doi.org/10.1371/journal.pgen.1002310

Displaying results 61 to 64 out of 64

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Revised 11.09.2025

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Per Qvist