(Q37066475)

English

An inflection point in gene discovery efforts for neurodegenerative diseases: from syndromic diagnoses toward endophenotypes and the epigenome

scientific article published on June 2013

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

An inflection point in gene discovery efforts for neurodegenerative diseases: from syndromic diagnoses toward endophenotypes and the epigenome (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

neurodegeneration

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

David A Bennett

2

object named as

David A Bennett

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Philip L. De Jager

1

object named as

Philip L De Jager

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Europe PubMed Central

PMC publication ID

18 August 2017

language of work or name

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publication date

1 June 2013

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Europe PubMed Central

PMC publication ID

18 August 2017

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

70

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

719-726

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

TREM2 Variants in Alzheimer's Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

1 reference

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29 September 2017

Developing an international network for Alzheimer research: The Dominantly Inherited Alzheimer Network

1 reference

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29 September 2017

An integrated map of genetic variation from 1,092 human genomes

1 reference

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29 September 2017

Relation of neuropathology to cognition in persons without cognitive impairment

1 reference

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29 September 2017

Coordinating GWAS results with gene expression in a systems immunologic paradigm in autoimmunity

1 reference

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29 September 2017

Systematic localization of common disease-associated variation in regulatory DNA

1 reference

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29 September 2017

An integrated encyclopedia of DNA elements in the human genome

1 reference

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29 September 2017

Relationship between genetic risk factors and markers for Alzheimer's disease pathology

1 reference

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29 September 2017

Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants

1 reference

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29 September 2017

Common variants at 12q14 and 12q24 are associated with hippocampal volume

1 reference

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29 September 2017

Identification of common variants associated with human hippocampal and intracranial volumes

1 reference

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29 September 2017

Nigral pathology and parkinsonian signs in elders without Parkinson disease

1 reference

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29 September 2017

A coding variant in CR1 interacts with APOE-ε4 to influence cognitive decline

1 reference

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29 September 2017

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

1 reference

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29 September 2017

A genome-wide scan for common variants affecting the rate of age-related cognitive decline

1 reference

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29 September 2017

Alzheimer's Prevention Initiative: a plan to accelerate the evaluation of presymptomatic treatments

1 reference

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29 September 2017

Pervasive sharing of genetic effects in autoimmune disease

1 reference

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29 September 2017

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

1 reference

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29 September 2017

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

VPS35 mutations in Parkinson disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Mapping and analysis of chromatin state dynamics in nine human cell types

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

CR1 is associated with amyloid plaque burden and age-related cognitive decline

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Parkinson's Disease: Genetics and Pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

The genetics of Alzheimer disease: back to the future

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

The NIH Roadmap Epigenomics Mapping Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Disclosure of APOE genotype for risk of Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Neuropathologic intermediate phenotypes enhance association to Alzheimer susceptibility alleles

1 reference

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29 September 2017

Genetic control of human brain transcript expression in Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Fibrillar amyloid-beta burden in cognitively normal people at 3 levels of genetic risk for Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Parkinson's disease: from monogenic forms to genetic susceptibility factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines

1 reference

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29 September 2017

Variation in MAPT is associated with cerebrospinal fluid tau levels in the presence of amyloid-beta deposition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

29 September 2017

Effect of early versus delayed interferon beta-1b treatment on disability after a first clinical event suggestive of multiple sclerosis: a 3-year follow-up analysis of the BENEFIT study

1 reference

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29 September 2017

Phenotypic plasticity and the epigenetics of human disease

1 reference

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29 September 2017

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

1 reference

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29 September 2017

Molecular biology of amyotrophic lateral sclerosis: insights from genetics

1 reference

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29 September 2017

The International HapMap Project

1 reference

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29 September 2017

The future of genetic studies of complex human diseases

1 reference

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29 September 2017

Identification of cis-regulatory variation influencing protein abundance levels in human plasma.

1 reference

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4 September 2018

A 17q12 allele is associated with altered NK cell subsets and function.

1 reference

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4 September 2018

Rare variants in the CYP27B1 gene are associated with multiple sclerosis.

1 reference

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4 September 2018

The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels.

1 reference

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4 September 2018

Effect of glatiramer acetate on conversion to clinically definite multiple sclerosis in patients with clinically isolated syndrome (PreCISe study): a randomised, double-blind, placebo-controlled trial

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

4 September 2018

Cumulative Effects of High Cholesterol Levels, High Blood Pressure, and Cigarette Smoking on Carotid Stenosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732174

4 December 2018

Identifiers

10.1001/JAMANEUROL.2013.275

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

release_mal6vvq5tvdu3b6lsyndnbfugi

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https://api.fatcat.wiki/v0/release/mal6vvq5tvdu3b6lsyndnbfugi

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

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