about
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataRare coding variants in the phospholipase D3 gene confer risk for Alzheimer's diseaseMultiple origins of Ashkenazi Levites: Y chromosome evidence for both Near Eastern and European ancestries.Genes predict village of origin in rural EuropeFounding mothers of Jewish communities: geographically separated Jewish groups were independently founded by very few female ancestorsLittle genetic differentiation as assessed by uniparental markers in the presence of substantial language variation in peoples of the Cross River region of NigeriaNatural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlandersA genome-wide study of common SNPs and CNVs in cognitive performance in the CANTABGenetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutationRecursive splicing in long vertebrate genes.Novel genetic loci underlying human intracranial volume identified through genome-wide associationHigh-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of JewsArmenian Y chromosome haplotypes reveal strong regional structure within a single ethno-national groupNew genetic evidence supports isolation and drift in the Ladin communities of the South Tyrolean Alps but not an ancient origin in the Middle EastUsing functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysisA genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies.Insights into TREM2 biology by network analysis of human brain gene expression data.Sex-Specific Genetic Data Support One of Two Alternative Versions of the Foundation of the Ruling Dynasty of the Nso' in Cameroon.Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS.A genome-wide investigation of SNPs and CNVs in schizophrenia.An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks.A Bayesian method to incorporate hundreds of functional characteristics with association evidence to improve variant prioritization.Gene expression changes with age in skin, adipose tissue, blood and brain.Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.The T allele of a single-nucleotide polymorphism 13.9 kb upstream of the lactase gene (LCT) (C-13.9kbT) does not predict or cause the lactase-persistence phenotype in AfricansGenetic signatures reveal high-altitude adaptation in a set of ethiopian populationsGenetic variability in the regulation of gene expression in ten regions of the human brain.Common genetic variants influence human subcortical brain structuresEvolution of a length polymorphism in the human PER3 gene, a component of the circadian system.Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosisFine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus.Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genesIdentifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene.Assessing models for genetic prediction of complex traits: a comparison of visualization and quantitative methodsChromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.Alternative ion channel splicing in mesial temporal lobe epilepsy and Alzheimer's diseaseIntegration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain.MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies.
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P50
description
hulumtues
@sq
researcher
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wetenschapper
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հետազոտող
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name
Michael E. Weale
@ast
Michael E. Weale
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Michael E. Weale
@es
Michael E. Weale
@nl
Michael E. Weale
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type
label
Michael E. Weale
@ast
Michael E. Weale
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Michael E. Weale
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Michael E. Weale
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Michael E. Weale
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altLabel
Michael Weale
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prefLabel
Michael E. Weale
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Michael E. Weale
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Michael E. Weale
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Michael E. Weale
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Michael E. Weale
@sl
P1053
F-2587-2010
P106
P1153
36744609500
P21
P31
P3829
P496
0000-0003-4593-1186