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  A phenotype-based genetic association study reveals the contribution of neuregulin1 gene variants to age of onset and positive symptom severity in schizophrenia

Papiol, S., Begemann, M., Rosenberger, A., Friedrichs, H., Ribbe, K., Grube, S., et al. (2011). A phenotype-based genetic association study reveals the contribution of neuregulin1 gene variants to age of onset and positive symptom severity in schizophrenia. American Journal of Medical Genetics B: Neuropsychiatric Genetics, 156 B(3), 340-345. doi:10.1002/ajmg.b.31168.

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 Creators:
Papiol, Sergi1, Author              
Begemann, Martin1, Author              
Rosenberger, Albert, Author
Friedrichs, Heidi1, Author              
Ribbe, Katja1, Author              
Grube, Sabrina1, Author              
Schwab, Markus H.2, Author              
Jahn, Henriette, Author
Gunkel, Stefan, Author
Benseler, Fritz3, Author              
Nave, Klaus-Armin2, Author              
Ehrenreich, Hannelore1, Author              
Affiliations:
1Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_2173651              
2Neurogenetics, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_2173664              
3Molecular neurobiology, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_2173659              

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Free keywords: NRG1; PGAS; GWAS; Protective genotypes; PANSS; data base
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Language(s): eng - English
 Dates: 2011-04
 Publication Status: Published in print
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 Rev. Type: Peer
 Identifiers: eDoc: 525573
DOI: 10.1002/ajmg.b.31168
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Title: American Journal of Medical Genetics B: Neuropsychiatric Genetics
  Alternative Title : Am. j. med. gen. B
Source Genre: Journal
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Pages: - Volume / Issue: 156 B (3) Sequence Number: - Start / End Page: 340 - 345 Identifier: -