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Genetic variability in the regulation of gene expression in ten regions of the human brain

Nature neuroscience, 2014-10, Vol.17 (10), p.1418-1428

2014

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Widespread sex differences in gene expression and splicing in the adult human brain

Nature communications, 2013-11, Vol.4 (1), p.2771-2771, Article 2771

2013

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Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease

Nature genetics, 2017-09, Vol.49 (9), p.1392-1397

2017

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Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies

Journal of neurochemistry, 2011-10, Vol.119 (2), p.275-282

2011

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Quality control for genome-wide association studies

Methods in molecular biology (Clifton, N.J.), 2010-01, Vol.628, p.341

Weale, Michael E

2010

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Transethnic differences in GWAS signals: A simulation study

Annals of human genetics, 2018-09, Vol.82 (5), p.280-286

2018

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Natural selection on EPAS1 (HIF2α) associated with low hemoglobin concentration in Tibetan highlanders

Proceedings of the National Academy of Sciences - PNAS, 2010-06, Vol.107 (25), p.11459-11464

2010

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A systematic evaluation of the performance and properties of the UK Biobank Polygenic Risk Score (PRS) Release

PloS one, 2024-09, Vol.19 (9), p.e0307270

2024

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MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies

Human molecular genetics, 2012-09, Vol.21 (18), p.4094-4103

2012

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Long-Range LD Can Confound Genome Scans in Admixed Populations

American journal of human genetics, 2008-07, Vol.83 (1), p.132-135

2008

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Analysis of subcellular RNA fractions demonstrates significant genetic regulation of gene expression in human brain post-transcriptionally

Scientific reports, 2023-08, Vol.13 (1), p.13874-13874, Article 13874

2023

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A Bayesian method to incorporate hundreds of functional characteristics with association evidence to improve variant prioritization

PloS one, 2014-05, Vol.9 (5), p.e98122-e98122

2014

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Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain

Neurobiology of disease, 2012-07, Vol.47 (1), p.20-28

2012

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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

Human molecular genetics, 2009-12, Vol.18 (23), p.4650-4661

2009

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Positive Selection on a High-Sensitivity Allele of the Human Bitter-Taste Receptor TAS2R16

Current biology, 2005-07, Vol.15 (14), p.1257-1265

2005

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Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy

Neurobiology of aging, 2014-06, Vol.35 (6), p.1514.e1-1514.e12

2014

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Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis

PloS one, 2011-04, Vol.6 (4), p.e14808-e14808

2011

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Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies

Nucleic acids research, 2013-04, Vol.41 (7), p.e88-e88

2013

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An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks

BMC systems biology, 2017-04, Vol.11 (1), p.47-47, Article 47

2017

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Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy

Brain (London, England : 1878), 2019-06, Vol.142 (6), p.1616-1630

2019

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Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities

Journal of the Royal Statistical Society. Series A, Statistics in society, 2003-06, Vol.166 (2), p.155-188

2003

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Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries

The American journal of cardiology, 2021-06, Vol.148, p.157-164

2021

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Insights into TREM2 biology by network analysis of human brain gene expression data

Neurobiology of aging, 2013-12, Vol.34 (12), p.2699-2714

2013

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Corrigendum to “Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.” [Neurobiol. Aging 35 (2014) 1514.e1–1514.e12]

Neurobiology of aging, 2015-11, Vol.36 (11), p.3118-3118

2015

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Genetic variability in the regulation of gene expression in ten regions of the human brain

Widespread sex differences in gene expression and splicing in the adult human brain

Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease

Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies

Quality control for genome-wide association studies

Transethnic differences in GWAS signals: A simulation study

Natural selection on EPAS1 (HIF2α) associated with low hemoglobin concentration in Tibetan highlanders

A systematic evaluation of the performance and properties of the UK Biobank Polygenic Risk Score (PRS) Release

MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies

Long-Range LD Can Confound Genome Scans in Admixed Populations

Analysis of subcellular RNA fractions demonstrates significant genetic regulation of gene expression in human brain post-transcriptionally

A Bayesian method to incorporate hundreds of functional characteristics with association evidence to improve variant prioritization

Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

Positive Selection on a High-Sensitivity Allele of the Human Bitter-Taste Receptor TAS2R16

Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy

Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis

Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies

An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks

Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy

Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities

Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries

Insights into TREM2 biology by network analysis of human brain gene expression data

Phenome-wide association studies across large population cohorts support drug target validation

Corrigendum to “Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.” [Neurobiol. Aging 35 (2014) 1514.e1–1514.e12]

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