Sara Rollinson
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Explore the profile of Sara Rollinson including associated specialties, affiliations and a list of published articles.
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68
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6128
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Recent Articles
1.
Manzoni C, Kia D, Ferrari R, Leonenko G, Costa B, Saba V, et al.
Am J Hum Genet
. 2024 Jun;
111(7):1316-1329.
PMID: 38889728
Frontotemporal dementia (FTD) is the second most common cause of early-onset dementia after Alzheimer disease (AD). Efforts in the field mainly focus on familial forms of disease (fFTDs), while studies...
2.
Chia R, Ray A, Shah Z, Ding J, Ruffo P, Fujita M, et al.
Neuron
. 2024 May;
112(13):2142-2156.e5.
PMID: 38701790
Multiple system atrophy (MSA) is an adult-onset, sporadic synucleinopathy characterized by parkinsonism, cerebellar ataxia, and dysautonomia. The genetic architecture of MSA is poorly understood, and treatments are limited to supportive...
3.
Wegscheider A, Gorniak J, Rollinson S, Gough L, Dhaliwal N, Guardiola A, et al.
Diagnostics (Basel)
. 2024 Feb;
14(3).
PMID: 38337757
Background: An accurate status determination of breast cancer biomarkers (ER, PR, HER2, Ki67) is crucial for guiding patient management. The "gold standard" for assessing these biomarkers in FFPE tissue is...
4.
Ryan S, Rollinson S, Hobbs E, Pickering-Brown S
Sci Rep
. 2022 Mar;
12(1):4799.
PMID: 35314728
A repeat expansion in C9orf72 is the major cause of both frontotemporal dementia and amyotrophic lateral sclerosis, accounting for approximately 1 in 12 cases of either disease. The expansion is...
5.
Johnson J, Miller D, Li R, Kumaran R, Alahmady N, Cookson M, et al.
JAMA Neurol
. 2021 Aug;
78(10):1236-1248.
PMID: 34459874
Importance: Juvenile amyotrophic lateral sclerosis (ALS) is a rare form of ALS characterized by age of symptom onset less than 25 years and a variable presentation. Objective: To identify the...
6.
Saxon J, Thompson J, Harris J, Richardson A, Langheinrich T, Rollinson S, et al.
J Neurol Neurosurg Psychiatry
. 2020 Oct;
91(12):1304-1311.
PMID: 33055142
Objective: The precise relationship between frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) is incompletely understood. The association has been described as a continuum, yet data suggest that this may...
7.
Costa B, Manzoni C, Bernal-Quiros M, Kia D, Aguilar M, Alvarez I, et al.
Neurology
. 2020 Sep;
95(24):e3288-e3302.
PMID: 32943482
Objective: We sought to characterize expansions in relation to genetic ancestry and age at onset (AAO) and to use these measures to discriminate the behavioral from the language variant syndrome...
8.
Ryan S, Hobbs E, Rollinson S, Pickering-Brown S
Neurobiol Aging
. 2019 Nov;
84:235.e1-235.e8.
PMID: 31676125
A C9orf72 repeat expansion is the most common cause of both frontotemporal dementia and motor neuron disease. The expansion is translated to produce dipeptide repeat proteins (DPRs), which are toxic...
9.
Pottier C, Ren Y, Perkerson 3rd R, Baker M, Jenkins G, van Blitterswijk M, et al.
Acta Neuropathol
. 2019 Feb;
137(6):879-899.
PMID: 30739198
Frontotemporal lobar degeneration with neuronal inclusions of the TAR DNA-binding protein 43 (FTLD-TDP) represents the most common pathological subtype of FTLD. We established the international FTLD-TDP whole-genome sequencing consortium to...
10.
Zhang M, Ferrari R, Tartaglia M, Keith J, Surace E, Wolf U, et al.
Brain
. 2018 Sep;
141(10):2895-2907.
PMID: 30252044
The G4C2-repeat expansion in C9orf72 is the most common known cause of amyotrophic lateral sclerosis and frontotemporal dementia. The high phenotypic heterogeneity of C9orf72 patients includes a wide range in...