Brendan ONeill
Overview
Explore the profile of Brendan ONeill including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
7
Citations
204
Followers
0
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Recent Articles
1.
Hamilton B, Anderson L, Anglem N, Armstrong S, Baker S, Beable S, et al.
N Z Med J
. 2020 Jun;
133(1517):107-116.
PMID: 32595225
No abstract available.
2.
McLaren K, McCauley E, ONeill B, Tinker S, Jenkins N, Sehulster L
Am J Infect Control
. 2019 Jun;
47(11):1375-1381.
PMID: 31239175
Background: Research on reducing Clostridioides difficile spore contamination of textiles via laundering is needed. We evaluated the sporicidal properties of 5 laundry chemicals and then determined the ability of a...
3.
Varcianna A, Myszczynska M, Castelli L, ONeill B, Kim Y, Talbot J, et al.
EBioMedicine
. 2019 Feb;
40:626-635.
PMID: 30711519
Background: Astrocytes regulate neuronal function, synaptic formation and maintenance partly through secreted extracellular vesicles (EVs). In amyotrophic lateral sclerosis (ALS) astrocytes display a toxic phenotype that contributes to motor neuron...
4.
Subramaniam S, Dand P, Ridout M, Cawley D, Miller S, Valli P, et al.
BMJ Support Palliat Care
. 2018 Mar;
9(3):326-331.
PMID: 29507041
Objectives: In palliative care settings, predicting prognosis is important for patients and clinicians. The Palliative Prognostic Index (PPI), a prognostic tool calculated using clinical indices alone has been validated within...
5.
Colinge J, Lee C, Afzalian A, Akhavan N, Yan R, Ferain I, et al.
Nat Nanotechnol
. 2010 Feb;
5(3):225-9.
PMID: 20173755
All existing transistors are based on the use of semiconductor junctions formed by introducing dopant atoms into the semiconductor material. As the distance between junctions in modern devices drops below...
6.
ONeill B, Simha V, Kotha V, Garg A
Am J Med Genet A
. 2007 May;
143A(13):1421-30.
PMID: 17523150
Neonatal progeroid syndrome (NPS), also known as Wiedemann-Rautenstrauch Syndrome, is a rare autosomal recessive disorder characterized by accelerated aging and lipodystrophy from birth. Affected children have extreme intrauterine growth retardation,...
7.
Bertolino C, Macsweeney M, Tobin J, ONeill B, Sheehan M, Coluccia S, et al.
Biosens Bioelectron
. 2005 Oct;
21(4):565-73.
PMID: 16202869
The aim of this work was to develop an integrated solution to DNA hybridisation monitoring for diagnostics on a monolithic silicon platform. A fabrication process was developed incorporating a gold...