Investigation of the role ofTCF4rare sequence variants in schizophrenia-Reference-Cited by-同舟云学术

Investigation of the role ofTCF4rare sequence variants in schizophrenia

Published:2015-05-22 Issue:5 Volume:168 Page:354-362
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Basmanav F. Buket¹²,Forstner Andreas J.¹²,Fier Heide¹²³,Herms Stefan²⁴,Meier Sandra⁵⁶,Degenhardt Franziska¹²,Hoffmann Per¹²⁴⁷,Barth Sandra¹²,Fricker Nadine¹²,Strohmaier Jana⁵,Witt Stephanie H.⁵,Ludwig Michael⁸,Schmael Christine¹⁵,Moebus Susanne⁹,Maier Wolfgang¹⁰,Mössner Rainald¹⁰¹¹,Rujescu Dan¹²,Rietschel Marcella⁵,Lange Christoph³¹³¹⁴,Nöthen Markus M.¹²,Cichon Sven¹²⁴⁷

Affiliation:

1. Institute of Human Genetics; University of Bonn; Bonn Germany

2. Department of Genomics; Life and Brain Center; Bonn Germany

3. Department of Genomic Mathematics; University of Bonn; Bonn Germany

4. Division of Medical Genetics, University Hospital Basel and Department of Biomedicine; University of Basel; Basel Switzerland

5. Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health; Medical Faculty Mannheim/Heidelberg University; Mannheim Germany

6. National Center for Register-Based Research; Aarhus University; Aarhus Denmark

7. Institute of Neuroscience and Medicine INM-1; Research Center Juelich; Juelich Germany

8. Department of Clinical Chemistry and Clinical Pharmacology; University of Bonn; Bonn Germany

9. Centre of Urban Epidemiology, Institute of Medical Informatics, Biometry and Epidemiology; Essen Germany

10. Department of Psychiatry and Psychotherapy; University of Bonn; Bonn Germany

11. Department of Psychiatry; University of Tübingen

12. Department of Psychiatry; University of Halle; Halle Germany

13. German Center for Neurodegenerative Diseases (DZNE); Bonn Germany

14. Department of Biostatistics; Harvard School of Public Health; Boston Massachusetts

Funder

BMBF

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

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1. A typical variant in TCF4 exon 18 is not associated with P itt– H opkins syndrome but with a familial case of mild and nonspecific neurodevelopmental disorder;American Journal of Medical Genetics Part A;2022-12-27

2. Functional consequences of TCF4 missense substitutions associated with Pitt-Hopkins syndrome, mild intellectual disability, and schizophrenia;Journal of Biological Chemistry;2021-12

3. Transcription factor 4 and its association with psychiatric disorders;Translational Psychiatry;2021-01-05

4. Region and Cell Type Distribution of TCF4 in the Postnatal Mouse Brain;Frontiers in Neuroanatomy;2020-07-17

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