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Multi‐ancestry genome‐wide gene × age interaction study identifies novel loci associated with late‐onset Alzheimer's Disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.093279
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- Article
Indian‐enriched genetic variants are associated with cognitive function.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.093199
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- Article
The Alzheimer's Disease Sequencing Project – Discovery, Discovery Extension and Follow Up Study (ADSP‐FUS): APOE genotype status and demographic characteristics across datasets.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.092629
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- Article
Genetic factors modify the effect of chronic viral infections on Alzheimer disease risk.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.091644
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- Article
Genome‐wide Interaction and Stratified Study with Smoking Identifies Association of APAF1 and MIXL1/LIN9 with Alzheimer's Disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.091434
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- Article
Short tandem repeat expansions are a novel genetic risk factor for Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.089952
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- Article
Variant‐to‐function mapping of late‐onset Alzheimer's disease GWAS loci in human microglial models implicates RTFDC1 as an effector gene at the CASS4 locus.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.089683
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- Article
Genomic Frontiers in Alzheimer's Research: A Primer on the Alzheimer's Disease Sequencing Project (ADSP) and its AI/ML Opportunities.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.087888
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- Article
Variant‐gene pair in silico analyses and functional validation of LOAD GWAS loci in human brain‐relevant cell types identify EGFR as a target gene for potential drug repurposing.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.087633
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- Article
A genomic sequence analysis of the mouse and human microtubule-associated protein tau.
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- Mammalian Genome, 2001, v. 12, n. 9, p. 700, doi. 10.1007/s00335-001-2044-8
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- Article
A comparative study of structural variant calling in WGS from Alzheimer's disease families.
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- Life Science Alliance, 2024, v. 7, n. 5, p. 1, doi. 10.26508/lsa.202302181
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- Article
Progress in Molecular Genetics of Alzheimer's Disease.
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- Neuroscientist, 1996, v. 2, n. 1, p. 3, doi. 10.1177/107385849600200106
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- Article
Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability.
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- Science Translational Medicine, 2010, v. 2, n. 49, p. 1, doi. 10.1126/scitranslmed.3001267
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- Article
Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease.
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- Genetic Epidemiology, 2010, v. 34, n. 1, p. 92, doi. 10.1002/gepi.20439
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- Article
The Seattle Alzheimer's disease data set.
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- Genetic Epidemiology, 1993, v. 10, n. 6, p. 365, doi. 10.1002/gepi.1370100606
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- Article
Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis.
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- Acta Neuropathologica, 2010, v. 119, n. 4, p. 409, doi. 10.1007/s00401-010-0659-0
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- Article
Aging-associated neuropathology in Werner syndrome.
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- Acta Neuropathologica, 1998, v. 96, n. 4, p. 421, doi. 10.1007/s004010050914
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- Publication type:
- Article
Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type.
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- Journal of Neurogenetics, 1987, v. 4, n. 2, p. 97, doi. 10.3109/01677068709167221
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- Article
Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type.
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- Journal of Neurogenetics, 1987, v. 4, n. 1, p. 97, doi. 10.3109/01677068709102337
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- Article
High copy wildtype human 1N4R tau expression promotes early pathological tauopathy accompanied by cognitive deficits without progressive neurofibrillary degeneration.
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- Acta Neuropathologica Communications, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40478-015-0210-6
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- Article
Genomic variants, genes, and pathways of Alzheimer's disease: An overview.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 1, p. 5, doi. 10.1002/ajmg.b.32499
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- Article
Genome Scan in Familial Late-Onset Alzheimer's Disease: A Locus on Chromosome 6 Contributes to Age-at-Onset.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 2, p. 201, doi. 10.1002/ajmg.b.32133
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- Article
Report of the APOE4 National Institute on Aging/Alzheimer Disease Sequencing Project Consortium Working Group: Reducing APOE4 in Carriers is a Therapeutic Goal for Alzheimer's Disease.
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- Annals of Neurology, 2024, v. 95, n. 4, p. 625, doi. 10.1002/ana.26864
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- Article
Causal Associations Between Modifiable Risk Factors and the Alzheimer's Phenome.
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- Annals of Neurology, 2021, v. 89, n. 1, p. 54, doi. 10.1002/ana.25918
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- Article
Polygenic hazard scores in preclinical Alzheimer disease.
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- 2017
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- journal article
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation.
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- 2014
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- journal article
PLXNA 4 is associated with Alzheimer disease and modulates tau phosphorylation.
- Published in:
- Annals of Neurology, 2014, v. 76, n. 3, p. 379, doi. 10.1002/ana.24219
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- Article
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.
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- 2011
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- Publication type:
- journal article
Familial prion disease with alzheimer disease?like tau pathology and clinical phenotype.
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- Annals of Neurology, 2011, v. 69, n. 4, p. 712, doi. 10.1002/ana.22264
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- Article
Integrated Model of <i>De Novo</i> and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes.
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- PLoS Genetics, 2013, v. 9, n. 8, p. 1, doi. 10.1371/journal.pgen.1003671
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- Article
Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene.
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- Human Mutation, 1998, v. 11, n. 3, p. 216, doi. 10.1002/(SICI)1098-1004(1998)11:3<216::AID-HUMU6>3.0.CO;2-F
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- Article
DRAW+SneakPeek: Analysis workflow and quality metric management for DNA-seq experiments.
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- Bioinformatics, 2013, v. 29, n. 19, p. 2498, doi. 10.1093/bioinformatics/btt422
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- Article
The Effect of Apolipoprotein E ε4 in the Relationships of Smoking and Drinking to Cognitive Function.
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- Neuroepidemiology, 1999, v. 18, n. 3, p. 125, doi. 10.1159/000026204
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- Article
Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci.
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- Annals of Human Genetics, 2013, v. 77, n. 2, p. 85, doi. 10.1111/ahg.12000
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- Article
Presenilin-1 mutation alters NGF-induced neurite outgrowth, calcium homeostasis, and transcription factor (AP-1) activation in PC12 cells.
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- Journal of Neuroscience Research, 1998, v. 52, n. 5, p. 618, doi. 10.1002/(SICI)1097-4547(19980601)52:5<618::AID-JNR14>3.0.CO;2-Y
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- Article
A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death.
- Published in:
- Nature Medicine, 2014, v. 20, n. 12, p. 1452, doi. 10.1038/nm.3736
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- Article
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutation.
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- Journal of Neurochemistry, 2003, v. 87, n. 2, p. 427, doi. 10.1046/j.1471-4159.2003.02020.x
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- Article
CXCR4 involvement in neurodegenerative diseases.
- Published in:
- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-017-0049-7
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- Article
INFERNO: inferring the molecular mechanisms of noncoding genetic variants.
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- Nucleic Acids Research, 2018, v. 46, n. 17, p. 8740, doi. 10.1093/nar/gky686
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- Article
Neuropsychiatric Symptoms and Caregiver Burden in Individuals With Alzheimer's Disease: The TEAM-AD VA Cooperative Study.
- Published in:
- 2018
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- Publication type:
- journal article
Apolipoprotein E ε4 and Change in Cognitive Functioning in Community-Dwelling Older Adults.
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- Journal of Geriatric Psychiatry & Neurology, 2005, v. 18, n. 4, p. 196, doi. 10.1177/0891988705281864
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- Publication type:
- Article
Enhancing the Power of Genetic Association Studies through the Use of Silver Standard Cases Derived from Electronic Medical Records.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0063481
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- Publication type:
- Article
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 59, doi. 10.1007/s00439-010-0899-z
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- Publication type:
- Article
C9orf72 Hexanucleotide Repeat Expansion and Guam Amyotrophic Lateral Sclerosis--Parkinsonism-Dementia Complex.
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- JAMA Neurology, 2013, v. 70, n. 6, p. 742, doi. 10.1001/jamaneurol.2013.1817
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- Article
Effects of insulin and octreotide on memory and growth hormone in Alzheimer's disease.
- Published in:
- 2009
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- Publication type:
- journal article
Apolipoprotein E Highly Correlates with AβPP- and Tau-Related Markers in Human Cerebrospinal Fluid.
- Published in:
- Journal of Alzheimer's Disease, 2008, v. 15, n. 3, p. 409, doi. 10.3233/JAD-2008-15307
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- Publication type:
- Article
Intranasal insulin administration dose-dependently modulates verbal memory and plasma amyloid-beta in memory-impaired older adults.
- Published in:
- 2008
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- Publication type:
- journal article
Multiple SNPs Within and Surrounding the Apolipoprotein E Gene Influence Cerebrospinal Fluid Apolipoprotein E Protein Levels.
- Published in:
- Journal of Alzheimer's Disease, 2008, v. 13, n. 3, p. 255, doi. 10.3233/JAD-2008-13303
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- Publication type:
- Article
Intranasal Insulin Administration Dose-Dependently Modulates Verbal Memory and Plasma Amyloid-β in Memory-Impaired Older Adults.
- Published in:
- Journal of Alzheimer's Disease, 2008, v. 13, n. 3, p. 323, doi. 10.3233/JAD-2008-13309
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- Publication type:
- Article
Effect of statins on Alzheimer's disease biomarkers in cerebrospinal fluid.
- Published in:
- Journal of Alzheimer's Disease, 2006, v. 10, n. 4, p. 399, doi. 10.3233/JAD-2006-10408
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- Article