Oswaldo Lorenzo‐Betancor

VA Puget Sound Health Care System — United States

Medicine · Health Sciences

27h-index2.8kcitations66works2.52yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Parkinson's Disease Mechanisms and Treatments(38), Neurological diseases and metabolism(18), Neurological disorders and treatments(12), Genetics and Neurodevelopmental Disorders(12), RNA regulation and disease(9)

Publications66 total

Elucidating the Mechanism of p.G192R RAB39B in X-linked Parkinson’s Disease (S4.008)
Neurology·2025
Parkinson's Disease Gene Screening in Familial Cases from Central and South America
Movement Disorders·2024· 5 citedOpen Access
Author Correction: The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson’s disease data
npj Parkinson s Disease·2023Open Access
The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson’s disease data
npj Parkinson s Disease·2023· 7 citedOpen Access
<scp>PNPLA6</scp>‐Related Disorder with Levodopa‐Responsive Parkinsonism
Movement Disorders Clinical Practice·2022· 4 citedOpen Access
Homozygous <scp><i>CADPS2</i></scp> Mutations Cause Neurodegenerative Disease with Lewy Body‐like Pathology in Parrots
Movement Disorders·2022· 10 citedOpen Access
The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson’s disease data
2022Open Access
Homozygous CADPS2 mutations cause neurodegenerative disease with Lewy bodies in amazon parrots (P8-11.006)
Neurology·2022
Homozygous <i>CADPS2</i> mutations cause neurodegenerative disease with Lewy bodies in parrots
2022· 1 citedOpen Access
Novel compound heterozygous FBXO7 mutations in a family with early onset Parkinson's disease
Parkinsonism & Related Disorders·2020· 12 citedOpen Access
<i>RNF213</i> variation, a broader role in neurovascular disease in Caucasian and Japanese populations
2020· 1 citedOpen Access
X-Linked Lymphoproliferative Syndrome Presenting as Adult-Onset Multi-Infarct Dementia
Journal of Neuropathology & Experimental Neurology·2019· 11 citedOpen Access
The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru
Parkinsonism & Related Disorders·2019· 45 citedOpen Access
<i>PCNT</i> point mutations and familial intracranial aneurysms
Neurology·2018· 25 citedOpen Access
Association study between multiple system atrophy and TREM2 p.R47H
Neurology Genetics·2018· 9 citedOpen Access
Data from: PCNT point mutations and familial intracranial aneurysms
Data Archiving and Networked Services (DANS)·2018Open Access
Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease
Autophagy·2018· 136 citedOpen Access
Pooled-DNA target sequencing of Parkinson genes reveals novel phenotypic associations in Spanish population
Neurobiology of Aging·2018· 8 cited
Multiple system atrophy and apolipoprotein E
Movement Disorders·2018· 21 citedOpen Access
Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variants
Neurobiology of Aging·2018· 1 citedOpen Access
page 1 of 4Next →

Frequent Co-authors

Pau Pástor(30), Owen A. Ross(21), Zbigniew K. Wszołek(17), Hortensia Alonso‐Navarro(16), Félix Javier Jiménez‐Jiménez(15), José A. G. Agúndez(15), Elena Garcı́a-Martı́n(15), Dennis W. Dickson(14), Catherine Labbé(13), Ronald L. Walton(13), Alexandra I. Soto‐Ortolaza(12), Ryan J. Uitti(12), Elena Lorenzo(10), Michael G. Heckman(10), Lluı́s Samaranch(9), Sara Ortega‐Cubero(9), Neill R. Graff‐Radford(9), Kotaro Ogaki(9), Ronald C. Petersen(8), Bradley F. Boeve(8)