2011
DOI: 10.4314/ajpsy.v14i2.1
|View full text |Cite
|
Sign up to set email alerts
|

Genetics of schizophrenia: communicating scientific findings in the clinical setting

Abstract: The expected identification of susceptibility genes for psychiatric disorders may bring new opportunities and expectations from patients and families for the clinical translation of research findings in psychiatric genetics. In this article information is provided about familial risk of schizophrenia with the theory behind individualizing risk of recurrence highlighted. Recent new findings regarding the new genetic frontier, Copy Number Variations (CNV), are summarized and the genetic architecture of familial … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
5
0
1

Year Published

2017
2017
2022
2022

Publication Types

Select...
3
1

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(6 citation statements)
references
References 19 publications
0
5
0
1
Order By: Relevance
“…This clear pathway from research to practice is at the heart of D&I via the inclusion of multiple stakeholders (parents, children patients, and clinicians). Similarly, Roos [142] discussed the role of genomics, recurrent risk, and family history in clinical care for schizophrenia, as did Vortsman and colleagues [143] when discussing the implementation of pharmacotherapy into the clinical care of autism spectrum disorder. Finally, Hendershot [141] offered a rare discussion of when and how to implement genomic information (i.e., pharmacogenomics) into evidence-based practice guidelines for alcohol use disorder and that there is a need for efficient, not just effective, translation.…”
Section: Part 1: Emphasizing Linear Translational Frameworkmentioning
confidence: 99%
See 1 more Smart Citation
“…This clear pathway from research to practice is at the heart of D&I via the inclusion of multiple stakeholders (parents, children patients, and clinicians). Similarly, Roos [142] discussed the role of genomics, recurrent risk, and family history in clinical care for schizophrenia, as did Vortsman and colleagues [143] when discussing the implementation of pharmacotherapy into the clinical care of autism spectrum disorder. Finally, Hendershot [141] offered a rare discussion of when and how to implement genomic information (i.e., pharmacogenomics) into evidence-based practice guidelines for alcohol use disorder and that there is a need for efficient, not just effective, translation.…”
Section: Part 1: Emphasizing Linear Translational Frameworkmentioning
confidence: 99%
“…The research on translating the genetic epidemiology of psychiatric disorders [5, 6, 126, 139, 140, 142, 155] is scarce. Occasionally, the translation of both genetic epidemiology and molecular genomics are discussed together [75, 153, 156, 157].…”
Section: Part 2: Relying On Molecular Genomic Informationmentioning
confidence: 99%
“…We administered the positive and negative syndrome scale (PANSS) to measure severity of psychotic symptoms. These scales have been widely used locally in genetics and treatment studies [ 3 , 19 22 ]. The Camberwell assessment of needs scale (CAN) was used to measure met and unmet needs [ 23 ].…”
Section: Main Textmentioning
confidence: 99%
“…Due to the complexity of psychiatric disorders PGC is among the most challenging topics encountered in clinical practice. Professional education is needed to better prepare psychiatrists to provide PGC in a manner that will assist patients and families to better understand the genetics of schizophrenia ( 5 ).…”
Section: Introductionmentioning
confidence: 99%