Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study
about
A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer diseaseAnalysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individualsCHRFAM7A, a human-specific and partially duplicated α7-nicotinic acetylcholine receptor gene with the potential to specify a human-specific inflammatory response to injuryThe Alzheimer's Disease Neuroimaging Initiative: a review of papers published since its inceptionAltered CSMD1 Expression Alters Cocaine-Conditioned Place Preference: Mutual Support for a Complex Locus from Human and Mouse ModelsGenetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkersGenome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics2014 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 sampleGenome-wide scan for copy number variation association with age at onset of Alzheimer's disease.Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family StudyA genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.Association of fish oil supplement use with preservation of brain volume and cognitive functionCHRNA7 Polymorphisms and Dementia Risk: Interactions with Apolipoprotein ε4 and Cigarette Smoking.Association between copy number variations of HLA-DQA1 and ankylosing spondylitis in the Chinese Han population.Copy Number Variants in Alzheimer's Disease.Association between TLR7 copy number variations and hepatitis B virus infection outcome in Chinese.Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.Transposable elements and psychiatric disorders.Adult neurogenesis and neurodegenerative diseases: A systems biology perspective.Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson diseaseAssociation between HLA-DQA1 gene copy number polymorphisms and susceptibility to rheumatoid arthritis in Chinese Han population.Neural effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253.Analysis of Association of Genetic Markers in the LUZP2 and FBXO40 Genes with the Normal Variability in Cognitive Performance in the Elderly.
P2860
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P2860
Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Genomic Copy Number Analysis i ...... tive Impairment: An ADNI Study
@ast
Genomic Copy Number Analysis i ...... tive Impairment: An ADNI Study
@en
type
label
Genomic Copy Number Analysis i ...... tive Impairment: An ADNI Study
@ast
Genomic Copy Number Analysis i ...... tive Impairment: An ADNI Study
@en
prefLabel
Genomic Copy Number Analysis i ...... tive Impairment: An ADNI Study
@ast
Genomic Copy Number Analysis i ...... tive Impairment: An ADNI Study
@en
P2093
P2860
P50
P356
P1476
Genomic Copy Number Analysis i ...... tive Impairment: An ADNI Study
@en
P2093
David W Craig
Matthew J Huentelman
Shanker Swaminathan
The Alzheimer's Disease Neuroimaging Initiative Adni
P2860
P304
P356
10.4061/2011/729478
P50
P577
2011-06-02T00:00:00Z