Genetic heterogeneity in Alzheimer disease and implications for treatment strategies (Q26995802)

3

object named as

Colin L. Masters

1 reference

7

Bernardino Ghetti

1 reference

Neill R Graff-Radford

6

object named as

Neill Graff-Radford

1 reference

John M. Ringman

1

1 reference

Nigel J. Cairns

4

1 reference

Adrian Danek

5

1 reference

John C. Morris

8

1 reference

language of work or name

1 reference

November 2014

1 reference

Current Neurology and Neuroscience Reports

1 November 2014

5 references

25 April 2019

30 June 2019

14 September 2019

15 December 2019

25 January 2021

6 references

25 April 2019

30 June 2019

14 September 2019

15 December 2019

25 January 2021

14

1 reference

page(s)

499

1 reference

issue

11

1 reference

Creative Commons Attribution 4.0 International

copyright license

start time

14 September 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1007/s11910-014-0499-8

0 references

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ApoE-directed therapeutics rapidly clear β-amyloid and reverse deficits in AD mouse models

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Role of Genes and Environments for Explaining Alzheimer Disease

21 March 2017

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

21 March 2017

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The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics

21 March 2017

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Alzheimer's disease and endocytic dysfunction: clues from the Down syndrome-related proteins, DSCR1 and ITSN1

21 March 2017

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

21 March 2017

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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

21 March 2017

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

21 March 2017

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Alzheimer's presenilin 1 mutations impair kinesin-based axonal transport

21 March 2017

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

21 March 2017

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Functional brain abnormalities in young adults at genetic risk for late-onset Alzheimer's dementia

21 March 2017

7 April 2017

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Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein

7 April 2017

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Clinical and biomarker changes in dominantly inherited Alzheimer's disease

7 April 2017

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Decreased clearance of CNS beta-amyloid in Alzheimer's disease

7 April 2017

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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

7 April 2017

1 reference

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The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor

7 April 2017

1 reference

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SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease

7 April 2017

1 reference

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Symptom onset in autosomal dominant Alzheimer disease: a systematic review and meta-analysis

28 September 2017

1 reference

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Clinical predictors of severe cerebral amyloid angiopathy and influence of APOE genotype in persons with pathologically verified Alzheimer disease

28 September 2017

1 reference

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Recent Perspectives on APP, Secretases, Endosomal Pathways and How they Influence Alzheimer's Related Pathological Changes in Down Syndrome

28 September 2017

1 reference

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18F-fluorodeoxyglucose positron emission tomography, aging, and apolipoprotein E genotype in cognitively normal persons

28 September 2017

1 reference

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Regional distribution of synaptic markers and APP correlate with distinct clinicopathological features in sporadic and familial Alzheimer's disease

28 September 2017

1 reference

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APOE ε4 worsens hippocampal CA1 apical neuropil atrophy and episodic memory

28 September 2017

1 reference

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Two phase 3 trials of bapineuzumab in mild-to-moderate Alzheimer's disease

28 September 2017

1 reference

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Brain differences in infants at differential genetic risk for late-onset Alzheimer disease: a cross-sectional imaging study

28 September 2017

1 reference

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Autosomal-dominant Alzheimer's disease mutations at the same codon of amyloid precursor protein differentially alter Aβ production

28 September 2017

1 reference

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Subjects harboring presenilin familial Alzheimer's disease mutations exhibit diverse white matter biochemistry alterations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Preclinical trials in autosomal dominant AD: implementation of the DIAN-TU trial.

28 September 2017

1 reference

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Greater medial temporal hypometabolism and lower cortical amyloid burden in ApoE4-positive AD patients

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Down's syndrome, neuroinflammation, and Alzheimer neuropathogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Increased in vivo amyloid-β42 production, exchange, and loss in presenilin mutation carriers

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

The amyloid precursor protein: a biochemical enigma in brain development, function and disease

28 September 2017

1 reference

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New genes and new insights from old genes: update on Alzheimer disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Association of plasma and cortical amyloid beta is modulated by APOE ε4 status

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Genetic influences on atrophy patterns in familial Alzheimer's disease: a comparison of APP and PSEN1 mutations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Distinct patterns of APP processing in the CNS in autosomal-dominant and sporadic Alzheimer disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Familial Alzheimer's disease mutations differentially alter amyloid β-protein oligomerization

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Down's syndrome and Alzheimer's disease: towards secondary prevention

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Plasma signaling proteins in persons at genetic risk for Alzheimer disease: influence of APOE genotype

28 September 2017

1 reference

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Comparison of clinical characteristics between familial and non-familial early onset Alzheimer's disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Hippocampal sclerosis in advanced age: clinical and pathological features.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Distinct cerebrospinal fluid amyloid beta peptide signatures in sporadic and PSEN1 A431E-associated familial Alzheimer's disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

The role of apolipoprotein E in Alzheimer's disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Epilepsy and cognitive impairments in Alzheimer disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Early onset familial Alzheimer Disease with spastic paraparesis, dysarthria, and seizures and N135S mutation in PSEN1.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Mosaicism for trisomy 21 in a patient with young-onset dementia: a case report and brief literature review

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Cerebral amyloid angiopathy: pathogenetic mechanisms and link to dense amyloid plaques.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Amyloid deposition begins in the striatum of presenilin-1 mutation carriers from two unrelated pedigrees

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Regulated intramembrane proteolysis of amyloid precursor protein and regulation of expression of putative target genes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Oxidative stress: a bridge between Down's syndrome and Alzheimer's disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

What the study of persons at risk for familial Alzheimer's disease can tell us about the earliest stages of the disorder: a review

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Amyloid mediates the association of apolipoprotein E e4 allele to cognitive function in older people

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Presenilin regulates capacitative calcium entry dependently and independently of gamma-secretase activity.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Notch and Presenilin: regulated intramembrane proteolysis links development and degeneration.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Apolipoprotein E epsilon4 allele, AD pathology, and the clinical expression of Alzheimer's disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Synthesis, aggregation, neurotoxicity, and secondary structure of various A beta 1-42 mutants of familial Alzheimer's disease at positions 21-23.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Relationship between severe amyloid angiopathy, apolipoprotein E genotype, and vascular lesions in Alzheimer's disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

What the evolution of the amyloid protein precursor supergene family tells us about its function

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Familial Alzheimer's disease-linked presenilin 1 variants elevate Abeta1-42/1-40 ratio in vitro and in vivo

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

A familial Alzheimer's disease locus on chromosome 1.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Neuronal origin of a cerebral amyloid: neurofibrillary tangles of Alzheimer's disease contain the same protein as the amyloid of plaque cores and blood vessels

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Neuritic plaques and cerebrovascular amyloid in Alzheimer disease are antigenically related

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Mutation of the beta-amyloid precursor protein in familial Alzheimer's disease increases beta-protein production

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Molecular mapping of Alzheimer-type dementia in Down's syndrome.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Amyloid A4 protein and its precursor in Down's syndrome and Alzheimer's disease.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

The pattern of acquisition of plaques and tangles in the brains of patients under 50 years of age with Down's syndrome

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

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

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

An English translation of Alzheimer's 1907 paper, "Uber eine eigenartige Erkankung der Hirnrinde".

31 May 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: association with age, hippocampal sclerosis and clinical phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

The apolipoprotein E epsilon 4 allele is associated with increased neuritic plaques and cerebral amyloid angiopathy in Alzheimer's disease and Lewy body variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

High striatal amyloid beta-peptide deposition across different autosomal Alzheimer disease mutation types

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Low PiB PET retention in presence of pathologic CSF biomarkers in Arctic APP mutation carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

The exception makes the rule: not all Aβ plaques are created equal.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

The E280A presenilin 1 Alzheimer mutation produces increased A beta 42 deposition and severe cerebellar pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

A novel mutation in the PSEN1 gene (L286P) associated with familial early-onset dementia of Alzheimer type and lobar haematomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Amyloid imaging results from the Australian Imaging, Biomarkers and Lifestyle (AIBL) study of aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Differential effect of APOE genotype on amyloid load and glucose metabolism in AD dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Insensitivity to Abeta42-lowering nonsteroidal anti-inflammatory drugs and gamma-secretase inhibitors is common among aggressive presenilin-1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

The effect of APOE genotype on clinical phenotype in Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-014-0499-8

Endocytic disturbances distinguish among subtypes of Alzheimer's disease and related disorders.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162987

28 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/25217249