Author

Oswaldo Lorenzo‐Betancor

University of WashingtonORCID 0000-0002-5607-8363Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:benchmarking· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:human· 1 Organism:non-human primate· 1 Research Focus:software / tool· 1

Frequent Co-Authors

Alastair John NoyceiD· 1 shared Alejandro Martínez-CarrascoiD· 1 shared Alexandra I. Soto‐BeasleyiD· 1 shared Alina Jama· 1 shared Amica Corda Müller-NedebockiD· 1 shared Ana Luisa Gil-MartíneziD· 1 shared Anastasia IllarionovaiD· 1 shared Andrew SingletoniD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperGenetics

Alastair John NoyceORCID

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3 papers

Recent·Most cited

Geneticsnpj Parkinson s DiseasePeer-reviewedMar 4, 2023

The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data

Hampton L. Leonard, Ruqaya Murtadha, Alejandro Martínez-Carrasco…·Alastair John Noyce

The paper describes a virtual hackathon event that brought together early career scientists to develop tools for Parkinson's disease research using open science principles.

7 citations

experimental assaysoftware / tool

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NeurosciencebioRxivPreprintMar 30, 2022

Homozygous CADPS2 mutations cause neurodegenerative disease with Lewy bodies in parrots

Oswaldo Lorenzo‐Betancor, Livio Galosi, Laura Bonfili…·Cyrus P. Zabetian

This study identifies a homozygous CADPS2 mutation in parrots causing neurodegenerative disease with Lewy bodies and reduced proteasome activity.

1 citation

non-human primatestatistical model

𝕏 PostBluesky

NeurosciencebioRxivPreprintMar 31, 2020

RNF213 variation, a broader role in neurovascular disease in Caucasian and Japanese populations

Oswaldo Lorenzo‐Betancor, Patrick R. Blackburn, Luca P. Farrugia…·Owen A. Ross

The paper investigates RNF213 variation's role in neurovascular diseases across Caucasian and Japanese populations, finding linkage disequilibrium between SLC26A11 and RNF213 variants associated with ischemic stroke and aneurysms.

1 citation

humanGWAS summary statistics

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