Genetic insights in Alzheimer's disease (Q38067204)

28 August 2017

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title

Genetic insights in Alzheimer's disease (English)

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Christine Van Broeckhoven

28 August 2017

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series ordinal

3

object named as

Christine Van Broeckhoven

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Kristel Sleegers

series ordinal

2

object named as

Kristel Sleegers

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28 August 2017

Karolien Bettens

1

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28 August 2017

1 January 2013

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28 August 2017

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28 August 2017

12

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28 August 2017

92-104

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28 August 2017

1

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Neuropathological stageing of Alzheimer-related changes

28 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Candidate gene for the chromosome 1 familial Alzheimer's disease locus

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https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Role of Genes and Environments for Explaining Alzheimer Disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genome-wide analysis of genetic loci associated with Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

A new amyloid beta variant favoring oligomerization in Alzheimer's-type dementia.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Role of common and rare APP DNA sequence variants in Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Deficiency of presenilin-1 inhibits the normal cleavage of amyloid precursor protein

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Presenilin clinical mutations can affect gamma-secretase activity by different mechanisms

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Abeta42 and decreased Abeta40.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

APOE and Alzheimer disease: a major gene with semi-dominant inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Exome sequencing reveals VCP mutations as a cause of familial ALS

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western Europe

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Repeat expansion in C9ORF72 in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Meta-analysis of the association between variants in SORL1 and Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

A mutation that creates a pseudoexon in SOD1 causes familial ALS.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Promoter mutations that increase amyloid precursor-protein expression are associated with Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Clinical and biomarker changes in dominantly inherited Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Replication of CLU, CR1, and PICALM associations with alzheimer disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Association of CLU and PICALM variants with Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Identification of novel loci for Alzheimer disease and replication of CLU, PICALM, and BIN1 in Caribbean Hispanic individuals

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Complement receptor 1 polymorphisms and risk of late-onset Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Identification and confirmation of an exonic splicing enhancer variation in exon 5 of the Alzheimer disease associated PICALM gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Clusterin in cerebrospinal fluid: analysis of carbohydrates and quantification of native and glycosylated forms.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Alzheimer's risk variants in the clusterin gene are associated with alternative splicing

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genetic variability in CLU and its association with Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Association of plasma clusterin concentration with severity, pathology, and progression in Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Plasma clusterin and the risk of Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Serum clusterin levels are not increased in presymptomatic Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Association of the Alzheimer's disease clusterin risk allele with plasma clusterin concentration.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Personal genomes: The case of the missing heritability

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Finding the missing heritability of complex diseases

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Deep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Structural organization of the human MS4A gene cluster on Chromosome 11q12.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Role of ATP-binding cassette transporters in brain lipid transport and neurological disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

SP-40,40, a protein involved in the control of the complement pathway, possesses a unique array of disulphide bridges

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Complement Receptor 1: disease associations and therapeutic implications.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

ATP-binding cassette transporter A7 enhances phagocytosis of apoptotic cells and associated ERK signaling in macrophages

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genetic evidence for the involvement of lipid metabolism in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Putative dual role of ephrin-Eph receptor interactions in inflammation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Clathrin assembly lymphoid myeloid leukemia (CALM) protein: localization in endocytic-coated pits, interactions with clathrin, and the impact of overexpression on clathrin-mediated traffic

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Amphiphysin heterodimers: potential role in clathrin-mediated endocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Distinct endocytic mechanisms of CD22 (Siglec-2) and Siglec-F reflect roles in cell signaling and innate immunity

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

A Cortactin-CD2-associated protein (CD2AP) complex provides a novel link between epidermal growth factor receptor endocytosis and the actin cytoskeleton

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Clusterin: a forgotten player in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genetic association of CR1 with Alzheimer's disease: a tentative disease mechanism.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Evidence for CALM in directing VAMP2 trafficking

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Implication of the Immune System in Alzheimer's Disease: Evidence from Genome-Wide Pathway Analysis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Proteome-based identification of plasma proteins associated with hippocampal metabolism in early Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

CLU, CR1 and PICALM genes associate with Alzheimer's-related senile plaques

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Functional links between Aβ toxicity, endocytic trafficking, and Alzheimer's disease risk factors in yeast

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Functional screening of Alzheimer pathology genome-wide association signals in Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genetic variation and neuroimaging measures in Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Neural hyperactivation in carriers of the Alzheimer's risk variant on the clusterin gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

CR1 genotype is associated with entorhinal cortex volume in young healthy adults.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Identification of common variants associated with human hippocampal and intracranial volumes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Biological, clinical and population relevance of 95 loci for blood lipids

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

No evidence that extended tracts of homozygosity are associated with Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Genome-wide scan of copy number variation in late-onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Olfactory copy number association with age at onset of Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

The mystery of missing heritability: Genetic interactions create phantom heritability

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Modeling familial Alzheimer's disease with induced pluripotent stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

Probing sporadic and familial Alzheimer's disease using induced pluripotent stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970259-4

7 January 2021

10.1016/S1474-4422(12)70259-4

Identifiers

DOI

1 reference

28 August 2017

1 reference

PubMed ID

23237904