Found: 19
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Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 19, n. 1, p. 69, doi. 10.3233/JAD-2010-1212
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- Article
Exome sequence analysis of Finnish patients with clozapine-induced agranulocytosis.
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- Molecular Psychiatry, 2014, v. 19, n. 4, p. 403, doi. 10.1038/mp.2013.74
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- Article
Genome-wide tagging for everyone.
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- Nature Genetics, 2006, v. 38, n. 11, p. 1227, doi. 10.1038/ng1106-1227
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- Article
Priorities and standards in pharmacogenetic research.
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- Nature Genetics, 2005, v. 37, n. 7, p. 671, doi. 10.1038/ng1593
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- Article
Handling and environmental enrichment do not rescue learning and memory impairments in αCamKII<sup>T286A</sup> mutant mice.
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- Genes, Brain & Behavior, 2003, v. 2, n. 3, p. 132, doi. 10.1034/j.1601-183X.2003.00020.x
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- Article
Corrigendum to: Common genetic variation and performance on standardized cognitive tests.
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- 2010
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- Correction Notice
Common genetic variation and performance on standardized cognitive tests.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 7, p. 815, doi. 10.1038/ejhg.2010.2
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- Article
Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis.
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- European Journal of Human Genetics, 2009, v. 17, n. 7, p. 946, doi. 10.1038/ejhg.2008.264
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- Article
Obesity is Associated with Genetic Variants That Alter Dopamine Availability.
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- Annals of Human Genetics, 2006, v. 70, n. 3, p. 293, doi. 10.1111/j.1529-8817.2005.00228.x
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- Article
Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.
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- Human Molecular Genetics, 2018, v. 27, n. 14, p. 2454, doi. 10.1093/hmg/ddy146
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- Article
COMT Val108/158 Met Genotype Affects Neural but not Cognitive Processing in Healthy Individuals.
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- Cerebral Cortex, 2010, v. 20, n. 3, p. 672, doi. 10.1093/cercor/bhp132
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- Article
Copy Number Variation of KIR Genes Influences HIV-1 Control.
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- PLoS Biology, 2011, v. 9, n. 11, p. 1, doi. 10.1371/journal.pbio.1001208
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- Article
One gene, many neuropsychiatric disorders: lessons from Mendelian diseases.
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- Nature Neuroscience, 2014, v. 17, n. 6, p. 773, doi. 10.1038/nn.3713
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- Article
Learning and memory impairments in K[sub v] β1.1-null mutants are rescued by environmental enrichment or ageing.
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- European Journal of Neuroscience, 2003, v. 18, n. 6, p. 1640, doi. 10.1046/j.1460-9568.2003.02889.x
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- Article
A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci.
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- PLoS Genetics, 2009, v. 5, n. 3, p. 1, doi. 10.1371/journal.pgen.1000421
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- Article
A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia.
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- PLoS Genetics, 2009, v. 5, n. 2, p. 1, doi. 10.1371/journal.pgen.1000373
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- Article
Brain-derived neurotrophic factor val66met polymorphism and hippocampal activation during episodic encoding and retrieval tasks.
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- Hippocampus, 2011, v. 21, n. 9, p. 980, doi. 10.1002/hipo.20809
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- Article
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4650, doi. 10.1093/hmg/ddp413
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- Article
SVA: software for annotating and visualizing sequenced human genomes.
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- Bioinformatics, 2011, v. 27, n. 14, p. 1998, doi. 10.1093/bioinformatics/btr317
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- Article