Genetic variation at CR1 increases risk of cerebral amyloid angiopathy. - Wikidata - awgldk - TriplyDB

Genetic variation at CR1 increases risk of cerebral amyloid angiopathy.

Genetic variation at CR1 increases risk of cerebral amyloid angiopathy.

http://www.wikidata.org/entity/Q30422717

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Genes associated with Alzheimer's disease: an overview and current status From development to dysfunction: microglia and the complement cascade in CNS homeostasis Current and future implications of basic and translational research on amyloid-β peptide production and removal pathways Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhage Personalized management of atrial fibrillation: Proceedings from the fourth Atrial Fibrillation competence NETwork/European Heart Rhythm Association consensus conference.Cerebral amyloid angiopathy: emerging concepts TOMM40 in Cerebral Amyloid Angiopathy Related Intracerebral Hemorrhage: Comparative Genetic Analysis with Alzheimer's Disease.Clinical predictors of severe cerebral amyloid angiopathy and influence of APOE genotype in persons with pathologically verified Alzheimer disease.Vascular disruption and blood-brain barrier dysfunction in intracerebral hemorrhage.Epigenomics of Alzheimer's disease.Advances in our Understanding of the Pathophysiology, Detection and Management of Cerebral Amyloid Angiopathy.A kernel machine method for detecting effects of interaction between multidimensional variable sets: an imaging genetics application.New insights into the genetics of glioblastoma multiforme by familial exome sequencing.International epidemiology of intracerebral hemorrhage.Overview and findings from the religious orders study Overview and findings from the rush Memory and Aging Project Microglial malfunction: the third rail in the development of Alzheimer's disease.Apolipoprotein E, amyloid-ß clearance and therapeutic opportunities in Alzheimer's disease A shift in microglial β-amyloid binding in Alzheimer's disease is associated with cerebral amyloid angiopathy.Pathways to neurodegeneration: mechanistic insights from GWAS in Alzheimer's disease, Parkinson's disease, and related disorders Clinical neurogenetics: stroke.Cerebral microbleeds: a review of clinical, genetic, and neuroimaging associations.The pathophysiology and clinical presentation of cerebral amyloid angiopathy.Alternative Approaches in Gene Discovery and Characterization in Alzheimer's Disease.Alzheimer's silent partner: cerebral amyloid angiopathy.CR1 in Alzheimer's disease.UNC5C variants are associated with cerebral amyloid angiopathy.Genetic risk factors for spontaneous intracerebral haemorrhage.Pharmacogenomics of angiotensin receptor/neprilysin inhibitor and its long-term side effects.Predicting cerebral amyloid angiopathy-related intracerebral hemorrhages and other cerebrovascular disorders in Alzheimer's disease.HYDRA: Revealing heterogeneity of imaging and genetic patterns through a multiple max-margin discriminative analysis framework.Genome-wide significant, replicated and functional risk variants for Alzheimer's disease.Risk Factors Associated With Early vs Delayed Dementia After Intracerebral Hemorrhage.The role of amyloid beta clearance in cerebral amyloid angiopathy: more potential therapeutic targets.De-regulation of gene expression and alternative splicing affects distinct cellular pathways in the aging hippocampus.Effect of CR1 Genetic Variants on Cerebrospinal Fluid and Neuroimaging Biomarkers in Healthy, Mild Cognitive Impairment and Alzheimer's Disease Cohorts.Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+).

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P2860

Genetic variation at CR1 increases risk of cerebral amyloid angiopathy.

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Genetic variation at CR1 increases risk of cerebral amyloid angiopathy.

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Genetic variation at CR1 increases risk of cerebral amyloid angiopathy.

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Genetic variation at CR1 increases risk of cerebral amyloid angiopathy.

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

PLINK: a tool set for whole-genome association and population-based linkage analyses

Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

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

Variants at APOE influence risk of deep and lobar intracerebral hemorrhage.

Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies

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

Aspirin and recurrent intracerebral hemorrhage in cerebral amyloid angiopathy.

Genetic variation and neuroimaging measures in Alzheimer disease.

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