Singleton, Andrew B.

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DLB and PDD boundary issues: Diagnosis, treatment, molecular pathology, and biomarkers

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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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A genome-wide association study identifies protein quantitative trait loci (pQTLs)

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Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

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Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

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Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

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Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

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Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

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Genome-Wide Association Study of Plasma Polyunsaturated Fatty Acids in the InCHIANTI Study

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Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis

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Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis

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Frontotemporal dementia and its subtypes: a genome-wide association study

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Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement

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Genome-wide pleiotropy between Parkinson disease and autoimmune diseases

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Virus exposure and neurodegenerative disease risk across national biobanks

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Novel genetic loci associated with hippocampal volume

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A novel Alzheimer disease locus located near the gene encoding tau protein

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Meta-analysis of genome-wide association data identifies two loci influencing age at menarche

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Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

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A CRISPRi/a platform in human iPSC-derived microglia uncovers regulators of disease states

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

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Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals

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