Andrew Singleton, PhD

Affiliations: 
Neurogenetics National Institute of Aging, Cabanatuan City, Central Luzon, Philippines 
Area:
http://www.biomedexperts.com/Profile.bme/1999112/Andrew_Singleton
Website:
http://neuroscience.nih.gov/Lab.asp?Org_ID=454
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"Andrew Singleton"
Cross-listing: Neurotree

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Publications

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Marioni RE, McRae AF, Bressler J, et al. (2018) Meta-analysis of epigenome-wide association studies of cognitive abilities. Molecular Psychiatry
Guerreiro R, Ross OA, Kun-Rodrigues C, et al. (2018) Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study. The Lancet. Neurology. 17: 64-74
Roosen DA, Singleton AB. (2017) Leucine rich repeat kinase knockout (LRRK KO) mouse model: Linking pathological hallmarks of inherited and sporadic Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society
Dillman AA, Majounie E, Ding J, et al. (2017) Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological aging. Scientific Reports. 7: 16890
Ridge PG, Karch CM, Hsu S, et al. (2017) Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience. Genome Medicine. 9: 100
Patel T, Brookes KJ, Turton J, et al. (2017) Whole-exome sequencing of the BDR cohort: Evidence to support the role of the PILRA gene in Alzheimer's disease. Neuropathology and Applied Neurobiology
Chaudhury S, Patel T, Barber IS, et al. (2017) Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease. Neurobiology of Aging
Bettencourt C, Salpietro V, Efthymiou S, et al. (2017) Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia. Orphanet Journal of Rare Diseases. 12: 172
Manole A, Jaunmuktane Z, Hargreaves I, et al. (2017) Clinical, pathological and functional characterization of riboflavin-responsive neuropathy. Brain : a Journal of Neurology
Ylönen S, Siitonen A, Nalls MA, et al. (2017) Genetic risk factors in Finnish patients with Parkinson's disease. Parkinsonism & Related Disorders
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