Publications

This section features research publications authored by our team.

Copy number variant risk loci for schizophrenia converge on the BDNF pathway – Ehrhart, F., Silva, A., Amelsvoort, T. van, von Scheibler, E., Evelo, C., & Linden, D. E. J., The World Journal of Biological Psychiatry, 2024.
Title of Your Paper 2 – Authors, Journal/Conference, Year
Title of Your Paper 3 – Authors, Journal/Conference, Year

External research articles

A selection of key studies that inform and support our research.

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects – Marshall, C.R., Howrigan, D.P., Merico, D., Thiruvahindrapuram, B., Wu, W., Greer, D.S., Antaki, D., Shetty, A., Holmans, P.A., Pinto, D. and Gujral, M., Nature genetics, 2017.
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia – Kirov, G., Grozeva, D., Norton, N., Ivanov, D., Mantripragada, K.K., Holmans, P., International Schizophrenia Consortium, Wellcome Trust Case Control Consortium, Craddock, N., Owen, M.J. and O’Donovan, M.C., Human molecular genetics, 2009.
Large recurrent microdeletions associated with schizophrenia – Stefansson, H., Rujescu, D., Cichon, S., Pietiläinen, O.P., Ingason, A., Steinberg, S., Fossdal, R., Sigurdsson, E., Sigmundsson, T., Buizer-Voskamp, J.E. and Hansen, T., Nature, 2008.