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Lack of an association of BDNF Val66Met polymorphism and plasma BDNF with hippocampal volume and memory.
- Published in:
- Cognitive, Affective & Behavioral Neuroscience, 2015, v. 15, n. 3, p. 625, doi. 10.3758/s13415-015-0343-x
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- Publication type:
- Article
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 258, doi. 10.1007/s00439-003-0960-2
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- Publication type:
- Article
Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease.
- Published in:
- Human Genetics, 2001, v. 109, n. 6, p. 646, doi. 10.1007/s00439-001-0614-1
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- Publication type:
- Article
Correction: GWAS on family history of Alzheimer's disease.
- Published in:
- 2019
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- Publication type:
- Correction Notice
GWAS on family history of Alzheimer’s disease.
- Published in:
- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0150-6
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- Publication type:
- Article
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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- Publication type:
- Article
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.
- Published in:
- 2009
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- Publication type:
- journal article
Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy.
- Published in:
- Scientific Reports, 2014, p. 1, doi. 10.1038/srep04497
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- Publication type:
- Article
Cell Type-Specific In Vitro Gene Expression Profiling of Stem Cell-Derived Neural Models.
- Published in:
- Cells (2073-4409), 2020, v. 9, n. 6, p. 1406, doi. 10.3390/cells9061406
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- Publication type:
- Article
Single-nucleus RNA-sequencing of autosomal dominant Alzheimer disease and risk variant carriers.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37437-5
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- Publication type:
- Article
Discovery and validation of dominantly inherited Alzheimer's disease mutations in populations from Latin America.
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- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-01052-1
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- Publication type:
- Article
Progranulin promotes neurite outgrowth and neuronal differentiation by regulating GSK-3β.
- Published in:
- Protein & Cell, 2010, v. 1, n. 6, p. 552, doi. 10.1007/s13238-010-0067-1
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- Publication type:
- Article
Evaluation of Gene-Based Family-Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease.
- Published in:
- Frontiers in Neuroscience, 2018, p. 1, doi. 10.3389/fnins.2018.00209
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- Publication type:
- Article
APOE4 Allele Disrupts Resting State fMRI Connectivity in the Absence of Amyloid Plaques or Decreased CSF Aβ42.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 50, p. 17035, doi. 10.1523/JNEUROSCI.3987-10.2010
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- Publication type:
- Article
Twenty years of Alzheimer's disease-causing mutations.
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- Journal of Neurochemistry, 2012, v. 120, p. 3, doi. 10.1111/j.1471-4159.2011.07575.x
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- Publication type:
- Article
Pathogenic cysteine mutations affect progranulin function and production of mature granulins.
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- Journal of Neurochemistry, 2010, v. 112, n. 5, p. 1305, doi. 10.1111/j.1471-4159.2009.06546.x
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- Publication type:
- Article
Conserved residues in juxtamembrane region of the extracellular domain of nicastrin are essential for γ-secretase complex formation.
- Published in:
- Journal of Neurochemistry, 2006, v. 98, n. 1, p. 300, doi. 10.1111/j.1471-4159.2006.03881.x
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- Publication type:
- Article
C-terminal PAL motif of presenilin and presenilin homologues required for normal active site conformation.
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- Journal of Neurochemistry, 2006, v. 96, n. 1, p. 218, doi. 10.1111/j.1471-4159.2005.03548.x
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- Publication type:
- Article
Presenilin 2 familial Alzheimer's disease mutations result in partial loss of function and dramatic changes in Aβ 42/40 ratios.
- Published in:
- Journal of Neurochemistry, 2005, v. 92, n. 2, p. 294, doi. 10.1111/j.1471-4159.2004.02858.x
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- Publication type:
- Article
Chitinase-3-like 1 protein (CHI3L1) locus influences cerebrospinal fluid levels of YKL-40.
- Published in:
- BMC Neurology, 2016, v. 16, p. 1, doi. 10.1186/s12883-016-0742-9
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- Publication type:
- Article
A globally diverse reference alignment and panel for imputation of mitochondrial DNA variants.
- Published in:
- BMC Bioinformatics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12859-021-04337-8
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- Publication type:
- Article
Alzheimer’s disease risk variants show association with cerebrospinal fluid amyloid beta.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 13, doi. 10.1007/s10048-008-0150-4
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- Publication type:
- Article
Copy Number Variation Accuracy in Genome-Wide Association Studies.
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- Human Heredity, 2011, v. 71, n. 3, p. 141, doi. 10.1159/000324683
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- Publication type:
- Article
Beyond cigarettes per day. A genome-wide association study of the biomarker carbon monoxide.
- Published in:
- 2014
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- Publication type:
- journal article
Polygenic Scores for Major Depressive Disorder and Risk of Alcohol Dependence.
- Published in:
- 2017
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- Publication type:
- journal article
Heterogeneous effects of genetic risk for Alzheimer's disease on the phenome.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01518-0
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- Publication type:
- Article
Coding variants in TREM2 increase risk for Alzheimer's disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 21, p. 5838, doi. 10.1093/hmg/ddu277
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- Publication type:
- Article
Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 810, doi. 10.1093/hmg/ddt463
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- Publication type:
- Article
Variants in two adjacent genes, EGLN2 and CYP2A6, influence smoking behavior related to disease risk via different mechanisms.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 2, p. 555, doi. 10.1093/hmg/ddt432
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- Publication type:
- Article
Cerebrospinal fluid APOE levels: an endophenotype for genetic studies for Alzheimer's disease.
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- Human Molecular Genetics, 2012, v. 21, n. 20, p. 4558, doi. 10.1093/hmg/dds296
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- Publication type:
- Article
Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6.
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- Human Molecular Genetics, 2012, v. 21, n. 13, p. 3050, doi. 10.1093/hmg/dds114
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- Publication type:
- Article
Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 647, doi. 10.1093/hmg/ddr498
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- Publication type:
- Article
A regulatory variation in OPRK1, the gene encoding the κ-opioid receptor, is associated with alcohol dependence.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 12, p. 1783, doi. 10.1093/hmg/ddn068
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- Publication type:
- Article
Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 5, p. 759, doi. 10.1093/hmg/ddm348
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- Publication type:
- Article
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease.
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- Human Molecular Genetics, 2007, v. 16, n. 22, p. 2703, doi. 10.1093/hmg/ddm224
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- Publication type:
- 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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- Publication type:
- Article
Novel genes identified in a high-density genome wide association study for nicotine dependence.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 1, p. 24, doi. 10.1093/hmg/ddl441
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- Publication type:
- Article
Association of alcohol dehydrogenase genes with alcohol dependence: a comprehensive analysis.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 9, p. 1539, doi. 10.1093/hmg/ddl073
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- Publication type:
- Article
Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohort.
- Published in:
- Alzheimer's Research & Therapy, 2012, v. 4, n. 4, p. 34, doi. 10.1186/alzrt137
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- Publication type:
- Article
Multiple distinct CHRNB3- CHRNA6 variants are genetic risk factors for nicotine dependence in African Americans and European Americans.
- Published in:
- Addiction, 2014, v. 109, n. 5, p. 814, doi. 10.1111/add.12478
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- Publication type:
- Article
Pharmacotherapy effects on smoking cessation vary with nicotine metabolism gene ( CYP2A6)
- Published in:
- 2014
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- Publication type:
- Journal Article
Pharmacotherapy effects on smoking cessation vary with nicotine metabolism gene ( CYP2A6).
- Published in:
- Addiction, 2014, v. 109, n. 1, p. 128, doi. 10.1111/add.12353
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- Publication type:
- Article
CHRNB3 is more strongly associated with Fagerström Test for Cigarette Dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results.
- Published in:
- 2012
- By:
- Publication type:
- Journal Article
CHRNB3 is more strongly associated with Fagerström Test for Cigarette Dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results.
- Published in:
- Addiction, 2012, v. 107, n. 11, p. 2019, doi. 10.1111/j.1360-0443.2012.03922.x
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- Publication type:
- 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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- Publication type:
- 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.
- Published in:
- Addiction, 2009, v. 104, n. 3, p. 471, doi. 10.1111/j.1360-0443.2008.02445.x
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- Publication type:
- Article
Gamma-aminobutyric acid receptor genes and nicotine dependence: evidence for association from a case–control study.
- Published in:
- Addiction, 2008, v. 103, n. 6, p. 1027, doi. 10.1111/j.1360-0443.2008.02236.x
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- Publication type:
- Article
Alcohol dependence with comorbid drug dependence: genetic and phenotypic associations suggest a more severe form of the disorder with stronger genetic contribution to risk.
- Published in:
- Addiction, 2007, v. 102, n. 7, p. 1131, doi. 10.1111/j.1360-0443.2007.01871.x
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- Publication type:
- Article
Dissection of the Phenotypic and Genotypic Associations With Nicotinic Dependence.
- Published in:
- Nicotine & Tobacco Research, 2012, v. 14, n. 4, p. 425
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- Publication type:
- Article
Genetic Heterogeneity in Alzheimer Disease and Implications for Treatment Strategies.
- Published in:
- Current Neurology & Neuroscience Reports, 2014, v. 14, n. 11, p. 1, doi. 10.1007/s11910-014-0499-8
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- Publication type:
- Article