Predicting white matter integrity from multiple common genetic variants. - Wikidata - awgldk - TriplyDB

Predicting white matter integrity from multiple common genetic variants.

Predicting white matter integrity from multiple common genetic variants.

http://www.wikidata.org/entity/Q36100330

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Genetics of the connectome The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data Neuroimaging and genetic risk for Alzheimer's disease and addiction-related degenerative brain disorders.A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations Recent advances in imaging Alzheimer's disease.Improved DTI registration allows voxel-based analysis that outperforms tract-based spatial statistics.Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure Genetic underpinnings of white matter 'connectivity': heritability, risk, and heterogeneity in schizophrenia.Obesity gene NEGR1 associated with white matter integrity in healthy young adults A neurogenetics approach to defining differential susceptibility to institutional care Differential contributions of dorso-ventral and rostro-caudal prefrontal white matter tracts to cognitive control in healthy older adults.Heritability and genetic association analysis of neuroimaging measures in the Diabetes Heart Study Reprint of: Mapping connectivity in the developing brain.Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2.How a common variant in the growth factor receptor gene, NTRK1, affects white matter.Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA-DTI working group.Relation between variants in the neurotrophin receptor gene, NTRK3, and white matter integrity in healthy young adults.Mechanisms of sporadic cerebral small vessel disease: insights from neuroimaging.Agenesis of the corpus callosum: classifying functional manifestations with the ICF-CY.Applying imaging genetics to ADHD: the promises and the challenges.Reduced Cerebral White Matter Integrity Assessed by DTI in Cognitively Normal H63D-HFE Polymorphism Carriers.The BDNF Val66Met Polymorphism Affects the Vulnerability of the Brain Structural Network Revolution of Resting-State Functional Neuroimaging Genetics in Alzheimer's Disease.Reduced white matter MRI transverse relaxation rate in cognitively normal H63D-HFE human carriers and H67D-HFE mice.Sex-specific effects of COMT Val158Met polymorphism on corpus callosum structure: A whole-brain diffusion-weighted imaging study.The effect of feature image on sensitivity of the statistical analysis in the pipeline of a tractography atlas-based analysis.The development of brain white matter microstructure.Abnormal white matter integrity during pain-free periovulation is associated with pain intensity in primary dysmenorrhea.Magnified effects of the COMT gene on white-matter microstructure in very old age.Impacts of PICALM and CLU variants associated with Alzheimer's disease on the functional connectivity of the hippocampus in healthy young adults.Neuroimaging genetic risk for Alzheimer's disease in preclinical individuals: From candidate genes to polygenic approaches

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Predicting white matter integrity from multiple common genetic variants.

http://www.wikidata.org/entity/Q36100330

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2012 nî lūn-bûn

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2012年论文

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2012年论文

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name

Predicting white matter integrity from multiple common genetic variants.

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Predicting white matter integrity from multiple common genetic variants.

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Predicting white matter integrity from multiple common genetic variants.

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Predicting white matter integrity from multiple common genetic variants.

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Predicting white matter integrity from multiple common genetic variants.

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Predicting white matter integrity from multiple common genetic variants.

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P2860

Genetics of austim: complex aetiology for a heterogeneous disorder

Multilocus genetic analysis of brain images

Altered neuregulin 1-erbB4 signaling contributes to NMDA receptor hypofunction in schizophrenia

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

Brain-derived neurotrophic factor

Common variants in the trichohyalin gene are associated with straight hair in Europeans

Intermediate phenotypes and genetic mechanisms of psychiatric disorders

The involvement of ErbB4 with schizophrenia: association and expression studies

Clusterin promotes amyloid plaque formation and is critical for neuritic toxicity in a mouse model of Alzheimer's disease

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

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