Rebecca R Valentino
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Explore the profile of Rebecca R Valentino including associated specialties, affiliations and a list of published articles.
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15
Citations
109
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Recent Articles
1.
Tamvaka N, Heckman M, Johnson P, Soto-Beasley A, Walton R, Koga S, et al.
Mitochondrion
. 2024 Aug;
78:101948.
PMID: 39179138
Mitochondrial health is an integral factor in aging, with mitochondrial dysfunction known to increase with age and contribute to the development of age-related neurodegenerative disorders. Additionally, the mitochondrial genome (mtDNA)...
2.
Valentino R, Scotton W, Roemer S, Lashley T, Heckman M, Shoai M, et al.
Lancet Neurol
. 2024 Apr;
23(5):487-499.
PMID: 38631765
Background: Pick's disease is a rare and predominantly sporadic form of frontotemporal dementia that is classified as a primary tauopathy. Pick's disease is pathologically defined by the presence in the...
3.
Hou X, Heckman M, Fiesel F, Koga S, Soto-Beasley A, Watzlawik J, et al.
medRxiv
. 2023 Oct;
PMID: 37905059
The PINK1-PRKN pathway mediates a critical quality control to maintain mitochondrial health and function. Together the kinase-ligase pair identifies and decorate damaged mitochondria with phosphorylated ubiquitin (p-S65-Ub). This selective label...
4.
Valentino R, Scotton W, Roemer S, Lashley T, Heckman M, Shoai M, et al.
medRxiv
. 2023 May;
PMID: 37163045
Background: Pick's disease (PiD) is a rare and predominantly sporadic form of frontotemporal dementia that is classified as a primary tauopathy. PiD is pathologically defined by argyrophilic inclusion Pick bodies...
5.
Valentino R, Ramnarine C, Heckman M, Johnson P, Soto-Beasley A, Walton R, et al.
Acta Neuropathol Commun
. 2022 Jul;
10(1):103.
PMID: 35836284
Dementia with Lewy bodies (DLB) is clinically diagnosed when patients develop dementia less than a year after parkinsonism onset. Age is the primary risk factor for DLB and mitochondrial health...
6.
Wernick A, Walton R, Soto-Beasley A, Koga S, Ren Y, Heckman M, et al.
Neurosci Lett
. 2021 Feb;
749:135723.
PMID: 33600908
Multiple system atrophy (MSA) is a rare sporadic, progressive parkinsonism characterised by autonomic dysfunction. A recent genome-wide association study reported an association at the Elongation of Very Long Fatty Acids...
7.
Valentino R, Heckman M, Johnson P, Baker M, Soto-Beasley A, Walton R, et al.
Neurology
. 2021 Feb;
96(13):e1755-e1760.
PMID: 33568542
Objective: To determine whether stable polymorphisms that define mitochondrial haplogroups in mitochondrial DNA (mtDNA) are associated with Pick disease risk, we genotyped 52 pathologically confirmed cases of Pick disease and...
8.
Wernick A, Walton R, Soto-Beasley A, Koga S, Heckman M, Valentino R, et al.
Clin Auton Res
. 2021 Jan;
31(1):117-125.
PMID: 33502644
Purpose: Investigate single nucleotide variants and short tandem repeats in 39 genes related to spinocerebellar ataxia in clinical and pathologically defined cohorts of multiple system atrophy. Methods: Exome sequencing was...
9.
Heckman M, Labbe C, Kolicheski A, Soto-Beasley A, Walton R, Valentino R, et al.
Parkinsonism Relat Disord
. 2021 Jan;
83:22-30.
PMID: 33454605
Introduction: Genome-wide association studies (GWAS) have confirmed the leucine-rich repeat kinase 2 (LRRK2) gene as a susceptibility locus for idiopathic Parkinson's disease (PD) in Caucasians. Though the rs1491942 and rs76904798...
10.
Jabbari E, Koga S, Valentino R, Reynolds R, Ferrari R, Tan M, et al.
Lancet Neurol
. 2020 Dec;
20(2):107-116.
PMID: 33341150
Background: The genetic basis of variation in the progression of primary tauopathies has not been determined. We aimed to identify genetic determinants of survival in progressive supranuclear palsy (PSP). Methods:...