Schizophrenia under the genomic lens: next generation sequencing of Western Australian families with schizophrenia

Status	Finished
Effective start/end date	1/01/14 → 31/12/16

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No association between common genetic variation in FOXP2 and language impairment in schizophrenia
McCarthy, N. S., Clark, M. L., Jablensky, A. & Badcock, J. C., Jan 2019, In: Psychiatry Research. 271, p. 590-597 8 p.
Research output: Contribution to journal › Article › peer-review
9 Citations (Scopus)
Assessment of Cognition and Personality as Potential Endophenotypes in the Western Australian Family Study of Schizophrenia
McCarthy, N. S., Badcock, J. C., Clark, M. L., Knowles, E. E. M., Cadby, G., Melton, P. E., Morgan, V. A., Blangero, J., Moses, E. K., Glahn, D. C. & Jablensky, A., 6 Jun 2018, In: Schizophrenia Bulletin. 44, 4, p. 908-921 14 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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12 Citations (Scopus)

305 Downloads (Pure)
Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity
Khan, F. F., Melton, P. E., McCarthy, N. S., Morar, B., Blangero, J., Moses, E. K. & Jablensky, A., Jul 2018, In: Schizophrenia Research. 197, p. 337-345 9 p.
Research output: Contribution to journal › Article › peer-review

Open Access
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14 Citations (Scopus)

488 Downloads (Pure)