(Q34731149)

4 August 2017

title

Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease (English)

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4 August 2017

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13

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D Harold

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Simon Lovestone

object named as

S Lovestone

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author name string

A R Morgan

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G Hamilton

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D Turic

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L Jehu

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R Abraham

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P Hollingworth

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V Moskvina

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C Brayne

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D C Rubinsztein

10

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A Lynch

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B Lawlor

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J Powell

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J Williams

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M J Owen

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publication date

1 September 2008

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

4 August 2017

published in

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4 August 2017

volume

147B

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4 August 2017

issue

6

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4 August 2017

page(s)

727-731

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Prevalence of dementia and probable senile dementia of the Alzheimer type in the Framingham Study

4 August 2017

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Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

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Insulin degrading enzyme and alpha-3 catenin polymorphisms in Italian patients with Alzheimer disease.

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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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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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Identification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community.

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

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TET1, a member of a novel protein family, is fused to MLL in acute myeloid leukemia containing the t(10;11)(q22;q23).

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Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease

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Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease

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Streamlined analysis of pooled genotype data in SNP-based association studies

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High-throughput SNP genotyping by allele-specific PCR with universal energy-transfer-labeled primers

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Susceptibility locus for Alzheimer's disease on chromosome 10.

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Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

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DNA Pooling: a tool for large-scale association studies

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Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.

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Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease

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Full genome screen for Alzheimer disease: Stage II analysis

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Identifiers

DOI

10.1002/AJMG.B.30670

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4 August 2017

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