MaryAnne Aitken
Overview
Explore the profile of MaryAnne Aitken including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
30
Citations
370
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Hodgson J, Metcalfe S, Gaff C, Donath S, Delatycki M, Winship I, et al.
Eur J Hum Genet
. 2015 Jul;
24(3):356-60.
PMID: 26130486
When an inherited genetic condition is diagnosed in an individual it has implications for other family members. Privacy legislation and ethical considerations can restrict health professionals from communicating directly with...
2.
Hodgson J, Metcalfe S, Aitken M, Donath S, Gaff C, Winship I, et al.
BMC Med Genet
. 2014 Mar;
15:33.
PMID: 24628824
Background: Genetic information given to an individual newly diagnosed with a genetic condition is likely to have important health implications for other family members. The task of communicating with these...
3.
McClaren B, Aitken M, Massie J, Amor D, Ukoumunne O, Metcalfe S
Genet Med
. 2013 Jan;
15(7):533-40.
PMID: 23348769
Purpose: Newborn screening for cystic fibrosis is increasingly available, but cascade testing following the diagnosis in a child has received little attention. We previously reported low levels of cascade testing...
4.
Wolthuizen M, Nisselle A, Halliday J, Metcalfe S, Aitken M, Allen K, et al.
Genet Test Mol Biomarkers
. 2012 Oct;
17(1):21-4.
PMID: 23098241
Aim: Hemochromatosis is a common disorder of iron overload most commonly due to homozogosity for the HFE C282Y substitution. A workplace-screening program was conducted in which over 11,000 individuals were...
5.
Schapper C, Dwyer T, Tregear G, Aitken M, Clay M
Aust Health Rev
. 2012 May;
36(2):218-23.
PMID: 22624645
Background: Evaluation of the social and economic outcomes of health research funding is an area of intense interest and debate. Typically, approaches have sought to assess the impact of research...
6.
Flouris A, Hawthorne G, Aitken M, Gaff C, Metcalfe S
J Community Genet
. 2012 Mar;
1(4):175-83.
PMID: 22460300
To support developments in genetics education, we constructed the GPGeneQ questionnaire to assess skills required for the practice of genetics by general practitioners (GPs). We describe the process of developing...
7.
Forrest L, Delatycki M, Curnow L, Gen Couns M, Skene L, Aitken M
Genet Med
. 2012 Jan;
14(1):122-8.
PMID: 22237441
Purpose: The aim of this study was to investigate the uptake of genetic testing by at-risk family members for four genetic conditions: chromosomal translocations, fragile X syndrome, Huntington disease, and...
8.
Delatycki M, Wolthuizen M, Collins V, Varley E, Craven J, Allen K, et al.
Eur J Hum Genet
. 2012 Jan;
20(5):505-9.
PMID: 22234159
As the results of the Human Genome Project are realised, screening for genetic mutations that predispose to preventable disease is becoming increasingly possible. How and where such screening should best...
9.
Hickerton C, Aitken M, Hodgson J, Delatycki M
Am J Med Genet A
. 2011 Dec;
158A(2):373-83.
PMID: 22140089
The availability of tests to detect genetic conditions prenatally has expanded considerably in recent decades. These advances allow women and couples choices; the choice of whether or not to undergo...
10.
McClaren B, Metcalfe S, Amor D, Aitken M, Massie J
Med J Aust
. 2011 Mar;
194(4):208-9.
PMID: 21401469
No abstract available.