(Q59399481)

April 2022 Public Data File from Crossref

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https://scigraph.springernature.com/pub.10.1007/s13311-014-0295-9

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cites work

Are rare variants responsible for susceptibility to complex diseases?

1 reference

12 December 2020

Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations

1 reference

12 December 2020

The possible role of complement activation in Alzheimer disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Amyloid deposition as the central event in the aetiology of Alzheimer's disease

1 reference

12 December 2020

Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease

1 reference

12 December 2020

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

Aspartate residue 7 in amyloid beta-protein is critical for classical complement pathway activation: implications for Alzheimer's disease pathogenesis

1 reference

12 December 2020

Genetic Linkage Analysis

1 reference

12 December 2020

Neuronal sorting protein-related receptor sorLA/LR11 regulates processing of the amyloid precursor protein

1 reference

12 December 2020

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

1 reference

12 December 2020

Blockade of TREM-2 exacerbates experimental autoimmune encephalomyelitis.

1 reference

12 December 2020

TREM2-transduced myeloid precursors mediate nervous tissue debris clearance and facilitate recovery in an animal model of multiple sclerosis

1 reference

12 December 2020

TREM2 is upregulated in amyloid plaque-associated microglia in aged APP23 transgenic mice

1 reference

12 December 2020

A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesis.

1 reference

12 December 2020

Genomewide association studies and human disease

1 reference

12 December 2020

Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease

1 reference

12 December 2020

Finding the missing heritability of complex diseases

1 reference

12 December 2020

Whole genome analysis in a consanguineous family with early onset Alzheimer's disease.

1 reference

12 December 2020

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

1 reference

12 December 2020

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

1 reference

12 December 2020

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

1 reference

12 December 2020

Autosomal recessive causes likely in early-onset Alzheimer disease

1 reference

12 December 2020

Extended kindred with recessive late-onset Alzheimer disease maps to locus 8p22-p21.2: a genome-wide linkage analysis.

1 reference

12 December 2020

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

1 reference

12 December 2020

Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis

1 reference

12 December 2020

Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease

1 reference

12 December 2020

High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease.

1 reference

12 December 2020

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

1 reference

12 December 2020

TREM2 Variants in Alzheimer's Disease

1 reference

12 December 2020

Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement

1 reference

12 December 2020

Functional impairment of microglia coincides with Beta-amyloid deposition in mice with Alzheimer-like pathology

1 reference

12 December 2020

Alzheimer's disease risk gene CD33 inhibits microglial uptake of amyloid beta

1 reference

12 December 2020

Amish revisited: next-generation sequencing studies of psychiatric disorders among the Plain people

1 reference

12 December 2020

Sorting receptor SORLA--a trafficking path to avoid Alzheimer disease

1 reference

12 December 2020

SnapShot: genetics of Alzheimer's disease

1 reference

12 December 2020

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

1 reference

12 December 2020

Evidence of recessive Alzheimer disease loci in a Caribbean Hispanic data set: genome-wide survey of runs of homozygosity

1 reference

12 December 2020

Antiamyloid therapy for Alzheimer's disease--are we on the right road?

1 reference

12 December 2020

A critique of the drug discovery and phase 3 clinical programs targeting the amyloid hypothesis for Alzheimer disease

1 reference

12 December 2020

Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype

1 reference

12 December 2020