Egyszerű nézet

dc.contributor.author Réthelyi János
dc.contributor.author Benkovits Judit
dc.contributor.author Bitter István
dc.date.accessioned 2014-12-09T14:42:49Z
dc.date.available 2014-12-09T14:42:49Z
dc.date.issued 2013
dc.identifier 84890144483
dc.identifier.citation pagination=2424-2437; journalVolume=37; journalIssueNumber=10 Pt 1; journalTitle=NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/712
dc.identifier.uri doi:10.1016/j.neubiorev.2013.04.010
dc.description.abstract Genetic research targeting schizophrenia has undergone tremendous development during recent years. Supported by recently developed high-throughput genotyping technologies, both rare and common genetic variants have been identified that show consistent association with schizophrenia. These results have been replicated by independent studies and refined in meta-analyses. The genetic variation uncovered consists of common alleles, i.e. single nucleotide polymorphisms (SNPs) conveying small effects (odds ratios below 1.1) on disease risk. The source of rare variants is copy number variations (CNVs), only detectable in a small proportion of patients (3-5% for all known CNVs) with schizophrenia, furthermore extremely rare de novo mutations captured by next generation sequencing, the most recent technological advancement in the field. Despite these findings, the search for the genetic architecture underlying schizophrenia continues since these variants explain only a small proportion of the overall phenotypic variance. Gene-environment interactions provide a compelling model for resolving this paradox and interpreting the risk factors of schizophrenia. Epidemiologically proven risk factors, such as prenatal infection, obstetric complications, urbanicity, cannabis, and trauma have been demonstrated to interact with genetic risk, giving rise to higher prevalence rates or more severe symptomatology in individuals with direct or indirect genetic predisposition for schizophrenia. Further research will have to explain how the different forms of genetic variation interact and how environmental factors modulate their effects. Moreover, the challenging question lying ahead of us is how genetic and environmental factors translate to molecular disease pathways. New approaches, including animal studies and in vitro disease modeling, as well as innovative real-world environment assessment methods, will help to understand the complex etiology of schizophrenia.
dc.relation.ispartof urn:issn:0149-7634
dc.title Genes and environments in schizophrenia: The different pieces of a manifold puzzle
dc.type Journal Article
dc.date.updated 2014-12-09T14:40:52Z
dc.language.rfc3066 en
dc.identifier.mtmt 2363901
dc.identifier.wos 000330490100011
dc.identifier.pubmed 23628741
dc.contributor.department SE/ÁOK/K/Pszichiátriai és Pszichoterápiás Klinika
dc.contributor.institution Semmelweis Egyetem


Kapcsolódó fájlok:

A fájl jelenleg csak egyetemi IP címről érhető el.

Megtekintés/Megnyitás

Ez a rekord az alábbi gyűjteményekben szerepel:

Egyszerű nézet