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A Case for Returning to Multiplex Families for Further Understanding the Heritability of Schizophrenia: A Psychiatrist's Perspective
Author(s) -
Lynn E. DeLisi
Publication year - 2016
Publication title -
complex psychiatry
Language(s) - English
Resource type - Journals
eISSN - 2673-3005
pISSN - 2673-298X
DOI - 10.1159/000442820
Subject(s) - schizophrenia (object oriented programming) , perspective (graphical) , mechanism (biology) , heritability , mental illness , psychology , psychiatry , multiplex , genetics , biology , mental health , computer science , philosophy , epistemology , artificial intelligence
The genetic mechanism for schizophrenia still remains unknown despite decades of research. A tremendous amount of investigator time and effort has gone into ascertainment of clinical samples for genetic studies over the years. Most recently, a large international effort of unprecedented collaboration has occurred to combine data worldwide in pursuit of uncovering the relevant genetic risk factors. However, in the process, the use of multiplex families to understand the genetics has waned, and it has been presumed that large resources of unrelated patients and controls are more efficient to find risk alleles than families. This commentary is a call to return to the use of this largely abandoned resource for further understanding the underlying biological mechanism of this serious mental illness.

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