(Q44031576)

29 November 2017

title

Examination of the current top candidate genes for AD in a genome-wide association study (English)

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genome-wide association study

29 November 2017

main subject

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author

Simon M. Laws

2

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29 November 2017

Matthias Riemenschneider

13

object named as

M Riemenschneider

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29 November 2017

11

H Förstl

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29 November 2017

T M Feulner

1

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29 November 2017

P Friedrich

3

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29 November 2017

S Wagenpfeil

4

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29 November 2017

S H R Wurst

5

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29 November 2017

C Riehle

6

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29 November 2017

K A Kuhn

7

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29 November 2017

M Krawczak

8

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29 November 2017

S Schreiber

9

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29 November 2017

S Nikolaus

10

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29 November 2017

A Kurz

12

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29 November 2017

language of work or name

English

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publication date

6 January 2009

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29 November 2017

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29 November 2017

volume

15

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29 November 2017

issue

7

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29 November 2017

page(s)

756-766

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describes a project that uses

29 November 2017

genome-wide association study

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Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

inferred from title

cites work

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Apolipoprotein E genotypes and age of onset in early-onset familial Alzheimer's disease.

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Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

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Gene identification in Alzheimer's disease

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APOE epsilon 4 lowers age at onset and is a high risk factor for Alzheimer's disease; a case control study from central Norway

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Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

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Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

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Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer disease

21 January 2018

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The number of trait loci in late-onset Alzheimer disease

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2008.141

Susceptibility locus for Alzheimer's disease on chromosome 10.

21 January 2018

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Full genome screen for Alzheimer disease: Stage II analysis

21 January 2018

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Age at onset in two common neurodegenerative diseases is genetically controlled

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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

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Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database

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SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease

21 January 2018

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Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association

21 January 2018

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Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease

21 January 2018

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GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

21 January 2018

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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

21 January 2018

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Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

21 January 2018

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CAMDEX. A standardised instrument for the diagnosis of mental disorder in the elderly with special reference to the early detection of dementia.

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The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part V. A normative study of the neuropsychological battery.

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A genome-wide scalable SNP genotyping assay using microarray technology

21 January 2018

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Whole-genome genotyping with the single-base extension assay

21 January 2018

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A haplotype map of the human genome

21 January 2018

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A worldwide survey of haplotype variation and linkage disequilibrium in the human genome

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2008.141

Common deletions and SNPs are in linkage disequilibrium in the human genome

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2008.141

Common deletion polymorphisms in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

The structure of haplotype blocks in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

Candidate gene association studies of the alpha 4 (CHRNA4) and beta 2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2008.141

Cholesterol 25-hydroxylase on chromosome 10q is a susceptibility gene for sporadic Alzheimer's disease

21 January 2018

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Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease.

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2008.141

A polymorphism in the cystatin C promoter region is not associated with an increased risk of AD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2008.141

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2008.141

The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

A novel mutation in AlphaA-crystallin (CRYAA) caused autosomal dominant congenital cataract in a large Chinese family

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2008.141

Influence of SORL1 gene variants: association with CSF amyloid-beta products in probable Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

Association between genetic variants in SORL1 and autopsy-confirmed Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

Association analysis of genes involved in cholesterol metabolism located within the linkage region on chromosome 10 and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

Efficacy assessment of SNP sets for genome-wide disease association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

Evidence for genetic linkage of Alzheimer's disease to chromosome 10q

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

7 January 2021

Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees

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https://api.crossref.org/works/10.1038%2FMP.2008.141

7 January 2021

A high-resolution survey of deletion polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

7 January 2021

Cystatin C as a risk factor for Alzheimer disease

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

7 January 2021

Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

7 January 2021

Fine mapping of the MAPT locus using quantitative trait analysis identifies possible causal variants in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

7 January 2021

SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population

1 reference

https://api.crossref.org/works/10.1038%2FMP.2008.141

7 January 2021

Identifiers

DOI

10.1038/MP.2008.141

1 reference

Dimensions Publication ID

29 November 2017

1013602583

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