Genome-wide and gene-based association implicates FRMD6 in Alzheimer disease (Q35888898)

10 August 2017

Genome-wide and gene-based association implicates FRMD6 in Alzheimer disease (English)

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genome-wide association study

10 August 2017

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5

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10 August 2017

Adina L Feldman

3

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Philippe Amouyel

object named as

Philippe Amouyel

6

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Erik Ingelsson

7

object named as

Erik Ingelsson

1 reference

10 August 2017

8

Nancy L Pedersen

1 reference

10 August 2017

2

Chandra A Reynolds

1 reference

10 August 2017

Mun-Gwan Hong

1

1 reference

10 August 2017

Mikael Kallin

4

1 reference

10 August 2017

Jonathan A Prince

9

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10 August 2017

language of work or name

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23 January 2012

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10 August 2017

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10 August 2017

33

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10 August 2017

3

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10 August 2017

521-529

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

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Non-synonymous and synonymous coding SNPs show similar likelihood and effect size of human disease association

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

A versatile gene-based test for genome-wide association studies

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Common SNPs explain a large proportion of the heritability for human height

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Genome-wide analysis of genetic loci associated with Alzheimer disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Voxelwise genome-wide association study (vGWAS)

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

The Human Gene Mutation Database: providing a comprehensive central mutation database for molecular diagnostics and personalized genomics

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Finding the missing heritability of complex diseases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

A survey of ABCA1 sequence variation confirms association with dementia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Common variants at 30 loci contribute to polygenic dyslipidemia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Personal genomes: The case of the missing heritability

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

High-resolution mapping of expression-QTLs yields insight into human gene regulation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Gene-centric genomewide association study via entropy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

PLINK: a tool set for whole-genome association and population-based linkage analyses

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

A new multipoint method for genome-wide association studies by imputation of genotypes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Role of Genes and Environments for Explaining Alzheimer Disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

The future of association studies: gene-based analysis and replication

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

The Swedish Twin Registry: a unique resource for clinical, epidemiological and genetic studies

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Identification of a variant associated with adult-type hypolactasia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Gene ontology: tool for the unification of biology

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Substantial genetic influence on cognitive abilities in twins 80 or more years old.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

The statistical basis of meta-analysis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

The Swedish Adoption Twin Study of Aging: an update.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3326347

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

27 July 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

Complete ascertainment of dementia in the Swedish Twin Registry: the HARMONY study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

Gender and health: a study of older unlike-sex twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

Strategies and issues in the detection of pathway enrichment in genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

A survey of genetic human cortical gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22009

21 January 2018

Identifiers

DOI

10.1002/HUMU.22009

1 reference

10 August 2017

1 reference

10 August 2017

1 reference