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F129EXOME SEQUENCING WITH SUBSEQUENT MULTI-TIER ANALYSES IN A LARGE COHORT OF MULTIPLY AFFECTED FAMILIES PROVIDES NEW INSIGHT INTO SCHIZOPHRENIA.

Authors :
Koller, Anna
Greve, Carola
Kaurani, Lalit
Klockmeier, Konrad
Degenhardt, Frauke C.
Maaser, Anna
Forstner, Andreas J.
Thiele, Holger
Maier, Wolfgang
Schwab, Sibylle
Reif, Andreas
Nöthen, Markus M.
Rujescu, Dan
Rietschel, Marcella
Degenhardt, Franziska
Source :
European Neuropsychopharmacology. 2019 Supplement4, Vol. 29, pS1180-S1181. 2p.
Publication Year :
2019

Abstract

Highlights from the article: To prioritize the implicated genes for the follow-up analyses, large publicly available and inhouse WES datasets (> 3.000 SCZ patients) were analysed for additional pathogenic mutations in the newly identified candidate genes. In a subsequent multi-tier approach, we combined the WES data with gene expression data derived from brain tissues (both from publicly available datasets and our own inhouse SCZ brain samples), and complex protein-protein-interaction analyses. Additionally, the PPI analysis showed that both brain expressed genes, SMARCC1 and MECP2, were tightly connected with previously reported SCZ candidate genes.

Details

Language :
English
ISSN :
0924977X
Volume :
29
Database :
Academic Search Index
Journal :
European Neuropsychopharmacology
Publication Type :
Academic Journal
Accession number :
137723741
Full Text :
https://doi.org/10.1016/j.euroneuro.2018.08.209