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"Cross-listing: Neurotree
Children
Sign in to add trainee| Rita Joao Guerreiro | grad student | UCL | |
| Jennifer C. Schymick | grad student | 2005-2009 | National Institute of Health (Neurotree) |
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Publications
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| Lange LM, Levine K, Fox SH, et al. (2025) The LRRK2 p.L1795F variant causes Parkinson's disease in the European population. Npj Parkinson's Disease. 11: 58 |
| Dilliott AA, Costanzo MC, Bandres-Ciga S, et al. (2025) The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources. Neurology. Genetics. 11: e200246 |
| Akçimen F, Paquette K, Crea PW, et al. (2025) Large-scale genetic characterization of Parkinson's disease in the African and African admixed populations. Medrxiv : the Preprint Server For Health Sciences |
| Jerez PÁ, Wild Crea PA, Ramos DM, et al. (2024) African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1. Medrxiv : the Preprint Server For Health Sciences |
| Álvarez Jerez P, Wild Crea P, Ramos DM, et al. (2024) African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1. Nature Structural & Molecular Biology. 31: 1955-1963 |
| Chen Z, Alvarez Jerez P, Anderson C, et al. (2024) The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder. Movement Disorders : Official Journal of the Movement Disorder Society |
| Khani M, Akçimen F, Grant SM, et al. (2024) Biobank-scale characterization of Alzheimer's disease and related dementias identifies potential disease-causing variants, risk factors, and genetic modifiers across diverse ancestries. Medrxiv : the Preprint Server For Health Sciences |
| Kuznetsov N, Daida K, Makarious MB, et al. (2024) CNV-Finder: Streamlining Copy Number Variation Discovery. Biorxiv : the Preprint Server For Biology |
| Li Z, Weller CA, Shah S, et al. (2024) ProtPipe: A Multifunctional Data Analysis Pipeline for Proteomics and Peptidomics. Genomics, Proteomics & Bioinformatics |
| Acosta-Uribe J, Piña Escudero SD, Cochran JN, et al. (2024) Genetic Contributions to Alzheimer's Disease and Frontotemporal Dementia in Admixed Latin American Populations. Medrxiv : the Preprint Server For Health Sciences |