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Validating Predicted Biological Effects of Alzheimer's Disease Associated SNPs Using CSF Biomarker Levels.
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- Journal of Alzheimer's Disease, 2010, v. 21, n. 3, p. 833, doi. 10.3233/JAD-2010-091711
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- Article
Population stratification and patterns of linkage disequilibrium.
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- Genetic Epidemiology, 2009, v. 33, n. S1, p. S88, doi. 10.1002/gepi.20478
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- Article
Genotyping errors, pedigree errors, and missing data.
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- Genetic Epidemiology, 2005, v. 29, n. S1, p. S120, doi. 10.1002/gepi.20120
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- Article
Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs.
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- Human Molecular Genetics, 2007, v. 16, n. 1, p. 36, doi. 10.1093/hmg/ddl438
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- Article
Novel genes identified in a high-density genome wide association study for nicotine dependence.
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- Human Molecular Genetics, 2007, v. 16, n. 1, p. 24, doi. 10.1093/hmg/ddl441
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- Article
Evidence of common and specific genetic effects: association of the muscarinic acetylcholine receptor M2 (CHRM2) gene with alcohol dependence and major depressive syndrome.
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- Human Molecular Genetics, 2004, v. 13, n. 17, p. 1903, doi. 10.1093/hmg/ddh194
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- Article
Interplay of genetic risk factors and parent monitoring in risk for nicotine dependence.
- Published in:
- Addiction, 2009, v. 104, n. 10, p. 1731, doi. 10.1111/j.1360-0443.2009.02697.x
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- Article
Further evidence for an association between the gamma-aminobutyric acid receptor A, subunit 4 genes on chromosome 4 and Fagerström Test for Nicotine Dependence.
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- Addiction, 2009, v. 104, n. 3, p. 471, doi. 10.1111/j.1360-0443.2008.02445.x
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- Article
Gamma-aminobutyric acid receptor genes and nicotine dependence: evidence for association from a case–control study.
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- Addiction, 2008, v. 103, n. 6, p. 1027, doi. 10.1111/j.1360-0443.2008.02236.x
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- Article
TMEM106B gene polymorphism is associated with age at onset in granulin mutation carriers and plasma granulin protein levels in healthy individuals
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- 2010
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- Abstract
Validating predicted biological effects of Alzheimer's disease associated SNPs using cerebrospinal fluid biomarker levels
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- 2010
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- Abstract
P2-016: Cortical binding of Pittsburgh compound B, an endophenotype for genetic studies of Alzheimer's disease
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- 2008
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- Abstract
IC-01-01: Cortical binding of Pittsburgh compound B, an endophenotype for genetic studies of Alzheimer's disease
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- 2008
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- Abstract
P1-341: Are common variants in APP risk factors for late-onset Alzheimer’s disease?
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- 2006
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- Abstract
P1-341: Are common variants in APP risk factors for late-onset Alzheimer’s disease?
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- 2006
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- Abstract
Escitalopram reduces attentional performance in anxious older adults with high-expression genetic variants at serotonin 2A and IB receptors.
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- International Journal of Neuropsychopharmacology, 2013, v. 16, n. 2, p. 279, doi. 10.1017/S1461145712000351
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- Article
Identifying cryptic population structure in multigenerational pedigrees in a Mexican American sample.
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- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S4
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- Article
Linkage analysis merging replicate phenotypes: an application to three quantitative phenotypes in two African samples.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S81
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- Article
Stratify or adjust? Dealing with multiple populations when evaluating rare variants.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S101
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- Article
Power and false-positive rates for the restricted partition method (RPM) in a large candidate gene data set.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S74
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- Article
A search for non-chromosome 6 susceptibility loci contributing to rheumatoid arthritis.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S15
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- Article
Detecting population stratification using related individuals.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S106
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- Article
Incorporating linkage information into a common disease/rare variant framework.
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- Genetic Epidemiology, 2011, v. 35, p. S74, doi. 10.1002/gepi.20654
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- Article
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin.
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- Annals of Neurology, 2006, v. 60, n. 3, p. 314
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- Article
Ubiquilin 1 polymorphisms are not associated with late‐onset Alzheimer's disease.
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- Annals of Neurology, 2006, v. 59, n. 1, p. 21, doi. 10.1002/ana.20673
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- Article
Association of GABRA2 with Drug Dependence in the Collaborative Study of the Genetics of Alcoholism Sample.
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- Behavior Genetics, 2006, v. 36, n. 5, p. 640, doi. 10.1007/s10519-006-9069-4
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- Article
In search of causal variants: refining disease association signals using cross-population contrasts.
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- BMC Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2156-9-58
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- Article
Microsatellites versus single-nucleotide polymorphisms in linkage analysis for quantitative and qualitative measures.
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- BMC Genetics, 2005, v. 6, p. S122, doi. 10.1186/1471-2156-6-S1-S122
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- Article