SORL1 variants across Alzheimer's disease European American cohorts.

about

Analysis of neurodegenerative Mendelian genes in clinically diagnosed Alzheimer Disease.Association between SORL1 polymorphisms and the risk of Alzheimer's disease.Genetic variants associated with Alzheimer's disease confer different cerebral cortex cell-type population structure.

P2860

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P2860

SORL1 variants across Alzheimer's disease European American cohorts.

Item

http://www.wikidata.org/entity/Q45658615

description

2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

name

SORL1 variants across Alzheimer's disease European American cohorts.

@en

SORL1 variants across Alzheimer's disease European American cohorts.

@nl

type

Item

label

SORL1 variants across Alzheimer's disease European American cohorts.

@en

SORL1 variants across Alzheimer's disease European American cohorts.

@nl

prefLabel

SORL1 variants across Alzheimer's disease European American cohorts.

@en

SORL1 variants across Alzheimer's disease European American cohorts.

@nl

P1476

SORL1 variants across Alzheimer's disease European American cohorts.

@en

P2093

Ben Saef

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

Bill Howells

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

Carlos Cruchaga

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

Catherine Bi

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

David Carrell

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

Joanne Norton

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

Jorge L Del-Aguila

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

Kathleen Black

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

Maria Victoria Fernández

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

NIA-LOAD family study group, NCRAD

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

P2860

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The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.

GEE-based SNP set association test for continuous and discrete traits in family-based association studies

Rare-variant association testing for sequencing data with the sequence kernel association test.

Coding variants in TREM2 increase risk for Alzheimer's disease

P2888

ejhg.2016.122

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1828-1830

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scholarly article

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10.1038/EJHG.2016.122

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2016-09-21T00:00:00Z

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1033601703

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27650968

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P921

Alzheimer's disease

P932

5117924

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SORL1 variants across Alzheimer's disease European American cohorts.

about

P2860

P2860

SORL1 variants across Alzheimer's disease European American cohorts.

description

name

type

label

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P1433

P1476

P2093

P2860

P2888

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P921

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P2888

P304

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P478

P50

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P932