Investigation of the role of TCF4 rare sequence variants in schizophrenia.

doi:10.1002/ajmg.b.32318

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Article

Investigation of the role of TCF4 rare sequence variants in schizophrenia.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Jul 2015

Basmanav F Buket, Forstner Andreas J, Fier Heide, Herms Stefan, Meier Sandra, Degenhardt Franziska, Hoffmann Per, Barth Sandra, Fricker Nadine, Strohmaier Jana, Witt Stephanie H, Ludwig Michael, Schmael Christine, Moebus Susanne, Maier Wolfgang, Mössner Rainald, Rujescu Dan, Rietschel Marcella, Lange Christoph, Nöthen Markus M, Cichon Sven

Abstract excerpt

Transcription factor 4 (TCF4) is one of the most robust of all reported schizophrenia risk loci and is supported by several genetic and functional lines of evidence. While numerous studies have implicated common genetic variation at TCF4 in schizophrenia risk, the role of rare, small-sized variants at this locus-such as single nucleotide variants and short indels which are below the resolution of chip-based...

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Identifiers

PMID: 26010163
DOI: 10.1002/ajmg.b.32318

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TCF4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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