Overview
Background
I am a clinician-academic whose interactions with patients have shaped my research questions and fuelled my enthusiasm for the importance of clinical research. I trained as a genetic counsellor and my research now focuses on the integration of genomics into clinical care. My research program has had three primary themes: evaluating the psychosocial impact of genetic conditions and/or genetic testing; evaluating genetics education preferences for patients and healthcare providers; and using next-generation sequencing to increase diagnostic yield for rare disorders.
Current research projects include:
- Exploring whether genetic fatalism affects sun-related health behaviours in high-risk individuals following genetic testing.
- Exploring the referral journey to genetic services for individuals with rare diseases
- Assessing Human Research Ethics Committee (HREC) members’ confidence in reviewing genomic research applications.
- Mainstreaming Genetic Testing for Melanoma into Dermatology Practice.
- Using Exome sequencing to identify new genes in families with inherited melanoma, negative for mutations in known genes.
Availability
- Associate Professor Aideen McInerney-Leo is:
- Available for supervision
Qualifications
- Masters (Coursework) of Science, The University of Manchester
- Doctor of Philosophy, The University of Queensland
Research interests
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Integrating genetic testing for melanoma into dermatology practice
Our study explores whether upskilling dermatologists to offer genetic testing for melanoma is acceptable to dermatologists and whether patient outcomes, as compared to when genetic testing is offered by a genetic counsellor.
Works
Search Professor Aideen McInerney-Leo’s works on UQ eSpace
2004
Journal Article
BRCA1/2 testing in hereditary breast and ovarian cancer families: effectiveness of problem-solving training as a counseling intervention
McInerney-Leo, Aideen, Biesecker, Barbara Bowles, Hadley, Donald W., Kase, Ronald G., Giambarresi, Therese R., Johnson, Elizabeth, Lerman, Caryn and Struewing, Jeffery P. (2004). BRCA1/2 testing in hereditary breast and ovarian cancer families: effectiveness of problem-solving training as a counseling intervention. American Journal of Medical Genetics Part A, 130A (3), 221-227. doi: 10.1002/ajmg.a.30265
2004
Journal Article
SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies
Johnson, J., Hague, S. M., Hanson, M., Gibson, A., Wilson, K. E., Evans, E. W., Singleton, A. A., McInerney-Leo, A., Nussbaum, R. L., Hernandez, D. G., Gallardo, M., McKeith, I. G., Burn, D. J., Ryu, M., Hellstrom, O., Ravina, B., Eerola, J., Perry, R. H., Jaros, E., Tienari, P., Weiser, R., Gwinn-Hardy, K., Morris, C. M., Hardy, J. and Singleton, A. B. (2004). SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies. Neurology, 63 (3), 554-556. doi: 10.1212/01.WNL.0000133401.09043.44
2004
Journal Article
Prevalence of Parkinson's disease in populations of African ancestry: a review
McInerney-Leo, Aideen, Gwinn-Hardy, Katrina and Nussbaum, Robert L. (2004). Prevalence of Parkinson's disease in populations of African ancestry: a review. Journal of the National Medical Association, 96 (7), 974-979.
2001
Journal Article
Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome
Kelberman, D., Tyson, J., Chandler, D. C., McInerney, A. M., Slee, J., Albert, D., Aymat, A., Botma, M., Calvert, M., Goldblatt, J., Haan, E. A., Laing, N. G., Lim, J., Malcolm, S., Singer, S. L., Winter, R. M. and Bitner-Glindzicz, M. (2001). Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome. Human Genetics, 109 (6), 638-645. doi: 10.1007/s00439-001-0626-x
2001
Journal Article
An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility
Green, Michael J., Biesecker, Barbara B., McInerney, Aideen M., Mauger, David and Fost, Norman (2001). An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility. American Journal of Medical Genetics, 103 (1), 16-23. doi: 10.1002/ajmg.1500
2001
Journal Article
Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor
Green, Michael J., McInerney, Aideen M., Biesecker, Barbara B. and Fost, Norman (2001). Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor. American Journal of Medical Genetics, 103 (1), 24-31. doi: 10.1002/ajmg.1501
2000
Journal Article
Minocycline-induced generalized postinflammatory elastolysis
Ho, Nicola C, McInerney, Aideen, Levy, Howard, Francomano, Clair A and Elkayam, Ori (2000). Minocycline-induced generalized postinflammatory elastolysis. The American Journal of Medicine, 109 (4), 340-340. doi: 10.1016/s0002-9343(00)00499-x
Funding
Current funding
Past funding
Supervision
Availability
- Associate Professor Aideen McInerney-Leo is:
- Available for supervision
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Supervision history
Current supervision
-
Doctor Philosophy
Developing and implementing interventions to facilitate the utilisation of polygenic risk scores in risk stratifying older populations for degenerative eye disease
Principal Advisor
Other advisors: Dr Tatiane Yanes
-
Doctor Philosophy
Unusual suspects in hereditary melanoma: phenotype-genotype characterisation of POT1, POLE, BAP1 and CDKN2A carriers
Principal Advisor
Other advisors: Professor Peter Soyer
-
Doctor Philosophy
Integrating genomics and deep phenotyping to optimise care for paediatric hearing loss
Principal Advisor
-
Doctor Philosophy
Multiple Primary Melanoma: Defining phenotypic, behavioural, and genetic risk profile for invasive versus in situ lesions
Principal Advisor
Other advisors: Professor Peter Soyer
-
Doctor Philosophy
Artificial Intelligence Tools for Automated Melanoma Risk Assessment: Potential Utility and Validation
Associate Advisor
Other advisors: Professor Peter Soyer
-
Doctor Philosophy
Translating polygenic and personalised risk scores: Acceptability and impact of providing polygenic and personalised risk information for melanoma
Associate Advisor
Other advisors: Professor Peter Soyer, Dr Tatiane Yanes
-
Doctor Philosophy
Development and evaluation of model of care for implementation of genomic testing for paediatric healthcare
Associate Advisor
Other advisors: Dr Tatiane Yanes
-
Doctor Philosophy
Mainstreaming polygenic risk testing for common cancers into clinical practice
Associate Advisor
Other advisors: Dr Tatiane Yanes
Completed supervision
-
2024
Doctor Philosophy
Unusual suspects in hereditary melanoma: phenotype-genotype characterisation of POT1, POLE and BAP1
Principal Advisor
Other advisors: Professor Peter Soyer
-
2023
Doctor Philosophy
Mainstreaming Genetic Testing for Familial Melanoma: evaluating whether psycho-behavioural outcomes differ depending on provider type
Principal Advisor
Other advisors: Professor Peter Soyer
-
2024
Doctor Philosophy
Translating polygenic and personalised risk scores: Acceptability and impact of providing polygenic and personalised risk information for melanoma
Associate Advisor
Other advisors: Professor Peter Soyer, Dr Tatiane Yanes
Media
Enquiries
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