Author: Denis Baird

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Preprints

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

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Multi-omics study revealing tissue-dependent putative mechanisms of SARS-CoV-2 drug targets on viral infections and complex diseases

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Using Y chromosomal haplogroups in genetic association studies and suggested implications

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Brain expression quantitative trait locus and network analysis reveals downstream effects and putative drivers for brain-related diseases

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Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

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Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual through variant-to-gene mapping

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Mendelian Randomization analysis reveals a causal influence of circulating sclerostin levels on bone mineral density and fractures

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Genome-wide study of DNA methylation in Amyotrophic Lateral Sclerosis identifies differentially methylated loci and implicates metabolic, inflammatory and cholesterol pathways

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