Harold, D., Connolly, S., Riley, B. P., Kendler, K. S., McCarthy, S. E., McCombie, W. R., Richards, A., Owen, M. J., O'Donovan, M. C., Walters, J., Wellcome Trust Case Control Consortium 2, The Schizophrenia Working Group of the Psychiatric Genomics Consortium, Donohoe, G., Gill, M., Corvin, A. & Morris, D. W. (2019).
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
180(3), 223-231.
https://doi.org/10.1002/ajmg.b.32716