Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants - sprookjes - yvandenbroek - TriplyDB

Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants

Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants

http://www.wikidata.org/entity/Q56769911

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SORL1 variants and risk of late-onset Alzheimer's disease Evidence for an association between KIBRA and late-onset Alzheimer's disease Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Assessment of Alzheimer's disease case-control associations using family-based methods Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease Genetics of late-onset Alzheimer's disease: update from the alzgene database and analysis of shared pathways Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease Association studies of 22 candidate SNPs with late-onset Alzheimer's disease Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study Genome-wide association studies in Alzheimer's disease Endophenotypes in normal brain morphology and Alzheimer's disease: a review Sumoylation in Synaptic Function and Dysfunction The sodium leak channel, NALCN, in health and disease The genetics and neuropathology of Alzheimer's disease Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease Intermediate phenotypes identify divergent pathways to Alzheimer's disease Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities Genome-wide association study of Alzheimer's disease Genomic variants, genes, and pathways of Alzheimer's disease: An overview.Association of CLU and PICALM variants with Alzheimer's disease.Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 families.Genome scan of age-at-onset in the NIMH Alzheimer disease sample uncovers multiple loci, along with evidence of both genetic and sample heterogeneity.Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs.The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2.Assessing batch effects of genotype calling algorithm BRLMM for the Affymetrix GeneChip Human Mapping 500 K array set using 270 HapMap samples.Use of genetic variation as biomarkers for Alzheimer's disease.Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer disease Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.Late onset Alzheimer's disease genetics implicates microglial pathways in disease risk.GAB2 as an Alzheimer disease susceptibility gene: follow-up of genomewide association results Clinical genetics of Alzheimer's disease Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data A putative Alzheimer's disease risk allele in PCK1 influences brain atrophy in multiple sclerosis.Genome-wide association studies: progress and potential for drug discovery and development.Alzheimer's disease: insights from Drosophila melanogaster models.Recent insights into the molecular genetics of dementia Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE Genetics of Alzheimer disease in the pre- and post-GWAS era Genetic variation at a single locus and age of onset for Alzheimer's disease.

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Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants

http://www.wikidata.org/entity/Q56769911

description

article

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im Februar 2007 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в лютому 2007

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name

Evidence for novel susceptibil ...... f putative functional variants

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Evidence for novel susceptibil ...... f putative functional variants

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type

label

Evidence for novel susceptibil ...... f putative functional variants

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Evidence for novel susceptibil ...... f putative functional variants

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prefLabel

Evidence for novel susceptibil ...... f putative functional variants

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Evidence for novel susceptibil ...... f putative functional variants

@nl

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Human Molecular Genetics

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Evidence for novel susceptibil ...... f putative functional variants

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Andrew Grupe

http://www.w3.org/2001/XMLSchema#string

Angharad Morgan

http://www.w3.org/2001/XMLSchema#string

Brian Lawlor

http://www.w3.org/2001/XMLSchema#string

Charles Rowland

http://www.w3.org/2001/XMLSchema#string

David Rubinsztein

http://www.w3.org/2001/XMLSchema#string

David Stone

http://www.w3.org/2001/XMLSchema#string

Eric Schadt

http://www.w3.org/2001/XMLSchema#string

John C. Morris

http://www.w3.org/2001/XMLSchema#string

John Sninsky

http://www.w3.org/2001/XMLSchema#string

Joseph Catanese

http://www.w3.org/2001/XMLSchema#string

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Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

Characterization of the tyrosine kinase Tnk1 and its binding with phospholipase C-gamma1

Promoter polymorphism in PCK1 (phosphoenolpyruvate carboxykinase gene) associated with type 2 diabetes mellitus

Lysosomal processing of amyloid precursor protein to A beta peptides: a distinct role for cathepsin S

High-resolution whole-genome association study of Parkinson disease.

Identification of four gene variants associated with myocardial infarction.

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

Complement factor H polymorphism in age-related macular degeneration

Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family

Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease

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865-873

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scholarly article

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10.1093/HMG/DDM031

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8

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16

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Michael C O'Donovan

Simon Lovestone

Ricardo Segurado

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2007-02-22T00:00:00Z

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17317784

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genome-wide association study