Found: 13
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Risk variant of oligodendrocyte lineage transcription factor 2 is associated with reduced white matter integrity.
- Published in:
- Human Brain Mapping, 2013, v. 34, n. 9, p. 2025, doi. 10.1002/hbm.22045
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- Publication type:
- Article
P3-265: Testing for association between Alzheimer's disease with psychosis and variants identified as influencing risk of schizophrenia
- Published in:
- 2008
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- Publication type:
- Abstract
P3-196: A genome-wide association study for late-onset Alzheimer's disease using DNA pooling
- Published in:
- 2008
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- Publication type:
- Abstract
Identification of loci associated with schizophrenia by genome-wide association and follow-up.
- Published in:
- Nature Genetics, 2008, v. 40, n. 9, p. 1053, doi. 10.1038/ng.201
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- Article
Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping.
- Published in:
- BMC Psychiatry, 2008, v. 8, p. 1, doi. 10.1186/1471-244X-8-11
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- Article
First Report of DHA-1 Producing Enterobacter cloacae Complex Isolate in Bulgaria.
- Published in:
- Folia Medica, 2019, v. 61, n. 3, p. 458, doi. 10.3897/folmed.61.e39349
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- Article
De novo CNVs in bipolar affective disorder and schizophrenia.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6677, doi. 10.1093/hmg/ddu379
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- Publication type:
- Article
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 6, p. 1669
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- Publication type:
- Article
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 10, p. 2055, doi. 10.1093/hmg/ddt056
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- Article
De novo mutations in schizophrenia implicate synaptic networks.
- Published in:
- Nature, 2014, v. 506, n. 7487, p. 179, doi. 10.1038/nature12929
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- Article
A network of dopaminergic gene variations implicated as risk factors for schizophrenia.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 5, p. 747, doi. 10.1093/hmg/ddm347
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- Article
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.
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- Human Molecular Genetics, 2008, v. 17, n. 3, p. 458
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- Publication type:
- Article
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
- Published in:
- PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1005993
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- Publication type:
- Article