Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.
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Toward precision medicine in neurological diseasesToward more predictive genetic mouse models of Alzheimer's diseaseAssociation of Long Runs of Homozygosity With Alzheimer Disease Among African American IndividualsGenetic variants in Alzheimer disease - molecular and brain network approachesABCA7 frameshift deletion associated with Alzheimer disease in African Americans.African American exome sequencing identifies potential risk variants at Alzheimer disease lociRare 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-AmericansOverlap 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 diseaseABCA7 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
P2860
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P2860
Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Rare coding mutations identifi ...... wide association studies loci.
@ast
Rare coding mutations identifi ...... wide association studies loci.
@en
type
label
Rare coding mutations identifi ...... wide association studies loci.
@ast
Rare coding mutations identifi ...... wide association studies loci.
@en
prefLabel
Rare coding mutations identifi ...... wide association studies loci.
@ast
Rare coding mutations identifi ...... wide association studies loci.
@en
P2093
P2860
P50
P356
P1433
P1476
Rare coding mutations identifi ...... wide association studies loci.
@en
P2093
Amanda Kahn
Badri N Vardarajan
Christine Sato
Dolly Reyes-Dumeyer
Ivonne Z Jimenez-Velazquez
Joseph H Lee
Martin Medrano
Rafael Lantigua
Rong Cheng
Sandra Barral
P2860
P304
P356
10.1002/ANA.24466
P577
2015-06-23T00:00:00Z