(Q84485275)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

title

Genome-wide association studies: the key to unlocking neurodegeneration? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

genome-wide association study

6 February 2020

main subject

1 reference

1 reference

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

author name string

Sonia Gandhi

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

publication date

1 July 2010

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

page(s)

789-794

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/nn.2584

6 February 2020

exact match

0 references

cites work

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12 December 2020

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

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12 December 2020

Identification of the Alzheimer beta/A4 amyloid precursor protein in clathrin-coated vesicles purified from PC12 cells.

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Lack of apolipoprotein E dramatically reduces amyloid beta-peptide deposition.

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12 December 2020

A second generation human haplotype map of over 3.1 million SNPs

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Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

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12 December 2020

Human genetic variation and its contribution to complex traits

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12 December 2020

Genome-wide association study reveals genetic risk underlying Parkinson's disease

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12 December 2020

A common LRRK2 mutation in idiopathic Parkinson's disease

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12 December 2020

Genome-wide association studies in neurological disorders

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12 December 2020

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

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Linking Abeta and tau in late-onset Alzheimer's disease: a dual pathway hypothesis

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Inhibition of dynamin-dependent endocytosis increases shedding of the amyloid precursor protein ectodomain and reduces generation of amyloid beta protein

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12 December 2020

Clusterin promotes amyloid plaque formation and is critical for neuritic toxicity in a mouse model of Alzheimer's disease

1 reference

12 December 2020

Drinking from the fire hose--statistical issues in genomewide association studies

1 reference

12 December 2020

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

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12 December 2020

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

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12 December 2020

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

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12 December 2020

alpha-Synuclein locus triplication causes Parkinson's disease

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12 December 2020

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

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12 December 2020

Genome-wide association studies: theoretical and practical concerns

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12 December 2020

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

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12 December 2020

Common vs. rare allele hypotheses for complex diseases

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12 December 2020

Distribution of clusterin in Alzheimer brain tissue

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12 December 2020

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

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

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12 December 2020

Untangling the tau gene association with neurodegenerative disorders.

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12 December 2020

Transport pathways for clearance of human Alzheimer's amyloid beta-peptide and apolipoproteins E and J in the mouse central nervous system

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12 December 2020

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

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12 December 2020

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

12 December 2020

Long-term effects of Abeta42 immunisation in Alzheimer's disease: follow-up of a randomised, placebo-controlled phase I trial

1 reference

12 December 2020

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

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12 December 2020

Evidence for CALM in directing VAMP2 trafficking

1 reference

12 December 2020

Multiplicity of Ca2+ messengers and Ca2+ stores: a perspective from cyclic ADP-ribose and NAADP.

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12 December 2020

Rare variants create synthetic genome-wide associations

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12 December 2020

A hundred years of Alzheimer's disease research

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12 December 2020

Genetic variation in an individual human exome

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12 December 2020

Molecular genetics of Alzheimer's disease: an update

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12 December 2020

Peripheral clearance of amyloid beta peptide by complement C3-dependent adherence to erythrocytes.

1 reference

12 December 2020

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

1 reference

12 December 2020

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease

1 reference

12 December 2020

Clusterin: a forgotten player in Alzheimer's disease

1 reference

12 December 2020

Calcium, cellular aging, and selective neuronal vulnerability in Parkinson's disease

1 reference

12 December 2020

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

1 reference

12 December 2020

Complement C3 and C4 expression in C1q sufficient and deficient mouse models of Alzheimer's disease

1 reference

12 December 2020

Apolipoprotein E: risk factor for Alzheimer disease

1 reference

12 December 2020

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

1 reference

12 December 2020

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

1 reference

12 December 2020

Identifiers

DOI

10.1038/NN.2584

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20581814%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

1 reference