Author: Gerard D. Schellenberg

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Preprints

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

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Causal associations between potentially modifiable risk factors and the Alzheimer's phenome: A Mendelian randomization study

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  • In genetics: 963
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  • Site-wide: 21,446

Personalized genetic assessment of age associated Alzheimers disease risk

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  • In genetics: 1,037
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Quality Control and Integration of Genotypes from Two Calling Pipelines for Whole Genome Sequence Data in the Alzheimer's Disease Sequencing Project

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  • In genetics: 1,351
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Inferring the molecular mechanisms of noncoding Alzheimer's disease-associated genetic variants

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INFERNO - INFERring the molecular mechanisms of NOncoding genetic variants

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  • In bioinformatics: 3,695
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Polygenic hazard scores in preclinical Alzheimer's disease

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  • In genetics: 1,927
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Immune-related genetic enrichment in frontotemporal dementia

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  • In genetics: 1,990
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Sex-dependent polygenic effects on the clinical progressions of Alzheimer's disease

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VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing Project

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  • In bioinformatics: 5,564
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CXCR4 involvement in neurodegenerative diseases

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  • In genetics: 3,260
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TSC1 loss-of-function increases risk for tauopathy by inducing tau acetylation and preventing autophagy-mediated tau clearance

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  • In neuroscience: 14,152
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