Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci. - Wikidata - awgldk - TriplyDB

Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.

Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.

http://www.wikidata.org/entity/Q35987583

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Toward precision medicine in neurological diseases Toward more predictive genetic mouse models of Alzheimer's disease Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals Genetic variants in Alzheimer disease - molecular and brain network approaches ABCA7 frameshift deletion associated with Alzheimer disease in African Americans.African American exome sequencing identifies potential risk variants at Alzheimer disease loci Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.Role of ABCA7 loss-of-function variant in Alzheimer's disease: a replication study in European-Americans Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variants.The Adaptor Protein CD2AP Is a Coordinator of Neurotrophin Signaling-Mediated Axon Arbor Plasticity.Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation.ABCA7 p.G215S as potential protective factor for Alzheimer's disease ABCA7 loss-of-function variants, expression, and neurologic disease risk.MS4A6A genotypes are associated with the atrophy rates of Alzheimer's disease related brain structures.Cellular and molecular modifier pathways in tauopathies: the big picture from screening invertebrate models.Novel susceptibility loci for Alzheimer's disease.Central Nervous System Lipoproteins: ApoE and Regulation of Cholesterol Metabolism.Polygenic risk scores in familial Alzheimer disease.Sex Hormone Decline and Amyloid β Synthesis, Transport and Clearance in the Brain.From Common to Rare Variants: The Genetic Component of Alzheimer Disease.State of Play in Alzheimer's Disease Genetics.Alzheimer's Disease in the Latino Community: Intersection of Genetics and Social Determinants of Health.Untangling Genetic Risk for Alzheimer's Disease.Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease.ABC Transporters Are Key Players in Alzheimer's Disease.ABCA7 and Pathogenic Pathways of Alzheimer's Disease.Genetics of Alzheimer's Disease: the Importance of Polygenic and Epistatic Components.Bin1 and CD2AP polarise the endocytic generation of beta-amyloid.ABCA7 Genotypes Confer Alzheimer's Disease Risk by Modulating Amyloid-β Pathology.An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease.Genetics of dementia in a Finnish cohort.Rare ABCA7 variants in 2 German families with Alzheimer disease.Genetic variations in chromodomain helicase DNA-binding protein 5, gene-environment interactions and risk of sporadic Alzheimer's disease in Chinese population.Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.Linkage analysis of multiplex Caribbean Hispanic families loaded for unexplained early-onset cases identifies novel Alzheimer's disease loci

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P2860

Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.

http://www.wikidata.org/entity/Q35987583

description

2015 nî lūn-bûn

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2015年の論文

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2015年论文

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name

Rare coding mutations identifi ...... wide association studies loci.

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Rare coding mutations identifi ...... wide association studies loci.

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Rare coding mutations identifi ...... wide association studies loci.

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Rare coding mutations identifi ...... wide association studies loci.

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Rare coding mutations identifi ...... wide association studies loci.

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Rare coding mutations identifi ...... wide association studies loci.

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Annals of Neurology

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Rare coding mutations identifi ...... wide association studies loci.

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Amanda Kahn

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Badri N Vardarajan

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Christine Sato

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Dolly Reyes-Dumeyer

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Ivonne Z Jimenez-Velazquez

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Joseph H Lee

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Martin Medrano

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Rafael Lantigua

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Rong Cheng

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Sandra Barral

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P2860

TREM2 Variants in Alzheimer's Disease

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Fast and accurate short read alignment with Burrows-Wheeler transform

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium

ATP-binding cassette transporter A7 regulates processing of amyloid precursor protein in vitro

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487-498

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10.1002/ANA.24466

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3

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78

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Ekaterina Rogaeva

Christiane Reitz

Peter Henry St George-Hyslop

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2015-06-23T00:00:00Z

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26101835

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genome-wide association study

Alzheimer's disease

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4546546

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