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Hardy, John

Reta Lila Weston Institute, Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, United Kingdom

TitleYearPMID
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets. 2021 33523105
Common genetic variants influence human subcortical brain structures. 2015 25607358
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. 2015 25158072
Genetic variability in the regulation of gene expression in ten regions of the human brain. 2014 25174004
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. 2014 24399358
Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain. 2012 22433082
Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies. 2011 21848658
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. 2010 20154673
Genetic control of human brain transcript expression in Alzheimer disease. 2009 19361613
Genomewide association studies and human disease. 2009 19369657
Genotypic analysis of gene expression in the dissection of the aetiology of complex neurological and psychiatric diseases. 2009 19734301
Whole genome expression as a quantitative trait. 2009 19909261
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals. 2007 17116639
Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. 2005 15714520
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