Rosie OShea
Overview
Explore the profile of Rosie OShea including associated specialties, affiliations and a list of published articles.
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20
Citations
74
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Recent Articles
1.
Keels J, Thomas J, Calzone K, Badzek L, Dewell S, Murthy V, et al.
Front Genet
. 2024 Dec;
15:1481948.
PMID: 39678377
Introduction: Genomics is a lifespan competency that is important for improving health outcomes for individuals, families, and communities. Nurses play a key role in genomic healthcare and realizing the potential...
2.
Jayasinghe K, Biros E, Harris T, Wood A, OShea R, Hill L, et al.
Kidney Int Rep
. 2024 Aug;
9(8):2372-2385.
PMID: 39156154
Introduction: Diagnostic genomic sequencing is the emerging standard of care in nephrology. There is a growing need to scale up the implementation of genomic diagnostics nationally to improve patient outcomes....
3.
Mallawaarachchi A, Fowles L, Wardrop L, Wood A, OShea R, Biros E, et al.
Clin J Am Soc Nephrol
. 2024 Jun;
19(7):887-897.
PMID: 38861662
No abstract available.
4.
Genomic multidisciplinary teams: A model for navigating genetic mainstreaming and precision medicine
Ma A, Newing T, OShea R, Gokoolparsadh A, Murdoch E, Hayward J, et al.
J Paediatr Child Health
. 2024 Apr;
60(4-5):118-124.
PMID: 38605555
Aim: Recent rapid advances in genomics are revolutionising patient diagnosis and management of genetic conditions. However, this has led to many challenges in service provision, education and upskilling requirements for...
5.
Ma A, OShea R, Wedd L, Wong C, Jamieson R, Rankin N
Eur J Hum Genet
. 2024 Feb;
32(4):381-391.
PMID: 38378794
Due to the increasing complexity of genomic data interpretation, and need for close collaboration with clinical, laboratory, and research expertise, genomics often requires a multidisciplinary team (MDT) approach. This systematic...
6.
Luermans J, Fleming J, OShea R, Barlow-Stewart K, Palmer E, Leffler M
Am J Med Genet A
. 2023 Nov;
194(4):e63470.
PMID: 37974553
A diagnosis of the X-linked condition Fragile X syndrome (FXS) in a child commonly reveals the mother's carrier status. Previous research focused on the genetic counseling process for the child...
7.
OShea R, Crook A, Jacobs C, Kentwell M, Gleeson M, Tucker K, et al.
Front Oncol
. 2023 Jun;
13:1140135.
PMID: 37305562
Introduction: "Mainstreaming" is a proposed strategy to integrate genomic testing into oncology. The aim of this paper is to develop a mainstreaming oncogenomics model by identifying health system interventions and...
8.
Wedd L, Gleeson M, Meiser B, OShea R, Barlow-Stewart K, Spurdle A, et al.
J Community Genet
. 2023 Apr;
14(3):307-317.
PMID: 37012465
The complexity of genetic variant interpretation means that a proportion of individuals who undergo genetic testing for a hereditary cancer syndrome will have their test result reclassified over time. Such...
9.
OShea R, Ma A, Jamieson R, Rankin N
Med J Aust
. 2023 Mar;
218(7):331.
PMID: 36924106
No abstract available.
10.
OShea R, Ma A, Jamieson R, Rankin N
Med J Aust
. 2022 Nov;
217(11):559-563.
PMID: 36436133
No abstract available.