Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study - Wikidata - awgldk - TriplyDB

Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

http://www.wikidata.org/entity/Q36406509

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Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals Different Facets of Copy Number Changes: Permanent, Transient, and Adaptive A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome CHRFAM7A, a human-specific and partially duplicated α7-nicotinic acetylcholine receptor gene with the potential to specify a human-specific inflammatory response to injury The Alzheimer's Disease Neuroimaging Initiative: a review of papers published since its inception Alzheimer's disease--a panorama glimpse Insights on the functional interactions between miRNAs and copy number variations in the aging brain Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers Is there a role for endogenous retroviruses to mediate long-term adaptive phenotypic response upon environmental inputs?2014 Update of the Alzheimer's Disease Neuroimaging Initiative: A review of papers published since its inception.Increased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sample Genome-wide scan for copy number variation association with age at onset of Alzheimer's disease.Identification of candidate single-nucleotide polymorphisms in NRXN1 related to antipsychotic treatment response in patients with schizophrenia.Genome-wide copy-number variation study of psychosis in Alzheimer's disease.Current analysis platforms and methods for detecting copy number variation A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.Integrated copy number and gene expression analysis detects a CREB1 association with Alzheimer's disease Copy Number Variants in Alzheimer's Disease.Genetics of psychosis of Alzheimer disease.17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.Fragile sites in cancer: more than meets the eye.The immunogenetics of neurological disease.Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis.Inference of Causative Genes for Alzheimer's Disease Due to Dosage Imbalance.GSTM1 Null Genotype and GSTP1 Ile105Val Polymorphism Are Associated with Alzheimer's Disease: a Meta-Analysis.

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Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

http://www.wikidata.org/entity/Q36406509

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2012年学术文章

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2012年学术文章

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2012年學術文章

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Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

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Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

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Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

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Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

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Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

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Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

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Current Alzheimer Research

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Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

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P2093

John D West

http://www.w3.org/2001/XMLSchema#string

Kelley M Faber

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Mark Inlow

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NIA-LOAD/NCRAD Family Study Group

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Shanker Swaminathan

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P2860

Organization and evolution of olfactory receptor genes on human chromosome 11

Copy-number variations associated with neuropsychiatric conditions

Role of Genes and Environments for Explaining Alzheimer Disease

Ataxin-1 and Brother of ataxin-1 are components of the Notch signalling pathway

Mature DIABLO/Smac is produced by the IMP protease complex on the mitochondrial inner membrane

The chimeric gene CHRFAM7A, a partial duplication of the CHRNA7 gene, is a dominant negative regulator of α7*nAChR function

Neuromuscular forms of glycogen branching enzyme deficiency

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

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

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801-814

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scholarly article

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10.2174/156720512802455331

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Andrew J. Saykin

Alzheimer's Disease Neuroimaging Initiative

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2012-09-01T00:00:00Z

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Alzheimer's disease

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