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Article

Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia.

Annals of human genetics - 1 Mar 2018

Al Eissa Mariam M, Fiorentino Alessia, Sharp Sally I, O'Brien Niamh L, Wolfe Kate, Giaroli Giovanni, Curtis David, Bass Nicholas J, McQuillin Andrew

Abstract excerpt

Schizophrenia (SCZ) is a severe, highly heritable psychiatric disorder. Elucidation of the genetic architecture of the disorder will facilitate greater understanding of the altered underlying neurobiological mechanisms. The aim of this study was to identify likely aetiological variants in subjects affected with SCZ. Exome sequence data from a SCZ cas-control sample from Sweden was analysed for likely aetiological...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 29148569
DOI: 10.1111/ahg.12226
PMCID: PMC5813151

Genes

ULK1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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