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

Papiol, Sergi; Begemann, Martin; Rosenberger, Albert; Friedrichs, Heidi; Ribbe, Katja; Grube, Sabrina; Schwab, Markus H.; Jahn, Henriette; Gunkel, Stefan; Benseler, Fritz; Nave, Klaus-Armin; Ehrenreich, Hannelore

doi:10.1002/ajmg.b.31168

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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

MPS-Authors

/persons/resource/persons182342

Papiol, Sergi
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182563

Begemann, Martin
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182154

Friedrichs, Heidi
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182315

Ribbe, Katja
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182168

Grube, Sabrina
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182402

Schwab, Markus H.
Neurogenetics, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182084

Benseler, Fritz
Molecular neurobiology, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182320

Nave, Klaus-Armin
Neurogenetics, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182138

Ehrenreich, Hannelore
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

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引用

Papiol, S., Begemann, M., Rosenberger, A., Friedrichs, H., Ribbe, K., Grube, S., Schwab, M. H., Jahn, H., Gunkel, S., Benseler, F., Nave, K.-A., & Ehrenreich, H. (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 Part B: Neuropsychiatric Genetics, 156(3), 340-345. doi:10.1002/ajmg.b.31168.

引用: https://hdl.handle.net/11858/00-001M-0000-002A-3D15-8

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