Andrew Singleton, PhD
Affiliations: | Neurogenetics | National Institute of Aging, Cabanatuan City, Central Luzon, Philippines |
Area:
http://www.biomedexperts.com/Profile.bme/1999112/Andrew_SingletonWebsite:
http://neuroscience.nih.gov/Lab.asp?Org_ID=454Google:
"Andrew Singleton"Mean distance: 19.14 (cluster 28)
Cross-listing: Alzheimer's Tree
Children
Sign in to add trainee| Rita Joao Guerreiro | grad student | UCL (Alzheimer's Tree) | |
| Jennifer C. Schymick | grad student | 2005-2009 | National Institute of Health |
BETA: Related publications
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Publications
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| Vitale D, Koretsky M, Kuznetsov N, et al. (2024) GenoTools: An Open-Source Python Package for Efficient Genotype Data Quality Control and Analysis. Biorxiv : the Preprint Server For Biology |
| Ojo OO, Bandres-Ciga S, Makarious MB, et al. (2024) GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians. Movement Disorders : Official Journal of the Movement Disorder Society |
| Chen Z, Gustavsson EK, Macpherson H, et al. (2024) Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4. Movement Disorders : Official Journal of the Movement Disorder Society |
| Li Z, Weller CA, Shah S, et al. (2023) ProtPipe: A Multifunctional Data Analysis Pipeline for Proteomics and Peptidomics. Biorxiv : the Preprint Server For Biology |
| Kim JJ, Vitale D, Otani DV, et al. (2023) Multi-ancestry genome-wide association meta-analysis of Parkinson's disease. Nature Genetics |
| Wu L, Real R, Martinez A, et al. (2023) Investigation of the genetic aetiology of Lewy body diseases with and without dementia. Medrxiv : the Preprint Server For Health Sciences |
| Bandres-Ciga S, Faghri F, Majounie E, et al. (2023) NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations. Medrxiv : the Preprint Server For Health Sciences |
| Reilly L, Lara E, Ramos D, et al. (2023) A fully automated FAIMS-DIA mass spectrometry-based proteomic pipeline. Cell Reports Methods. 100593 |
| Lange LM, Avenali M, Ellis M, et al. (2023) Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2). Npj Parkinson's Disease. 9: 133 |
| Rizig M, Bandres-Ciga S, Makarious MB, et al. (2023) Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study. The Lancet. Neurology |