Aideen M McInerney-Leo (A M McInerney-Leo, Aideen McInerney-Leo)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 43

Top Venues

European journal of human genetics : EJHG

American journal of medical genetics. Part A

The Medical journal of Australia

Journal of medical genetics

University of Queensland

University of Queensland (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Queensland

Australia

NHMRC research fellow :: Dermatology Research Centre, University of Queensland Diamantina Institute

Queensland University of Technology

Australia

Genetic Counsellor, Post-doctoral researcher :: Institute of Health and Biomedical Innovation

Education History

University of Queensland

Australia

PHD

University of Manchester

United Kingdom

MSC

University College London

United Kingdom

BSC

Publications

Ellie J Maas, Emily DeBortoli, Vaishnavi Nathan, Ned P Freeman, Adam Mothershaw, Darren J Smit, Brigid Betz-Stablein, Lauren G Aoude, Mitchell S Stark, Richard A Sturm, Hans Peter Soyer, Aideen M McInerney-Leo
POT1 and multiple primary melanomas: the dermatological phenotype. Journal of medical genetics (2024)
Cassandra Muller, Lyndon Gallacher, Louise Keogh, Aideen M McInerney-Leo, Tiffany F Boughtwood, Penny Gleeson, Kristine Barlow-Stewart, Martin B Delatycki, Ingrid Winship, Kristen J Nowak, Margaret Otlowski, Paul A Lacaze, Jane M Tiller
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance. European journal of human genetics : EJHG 32 (7) (2024)
Danya F Vears, Alison McLean, Chloe La Spina, Aideen M McInerney-Leo, null null
Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children. Twin research and human genetics : the official journal of the International Society for Twin Studies (2024)
Danya F Vears, Alison McLean, Chloe La Spina, Aideen M McInerney-Leo, null null
Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children. Twin research and human genetics : the official journal of the International Society for Twin Studies 27 (2) (2024)
Rebecca Kriukelis, Michael T Gabbett, Rachael Beswick, Aideen M McInerney-Leo, Carlie Driscoll, Karen Liddle
The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates. European journal of human genetics : EJHG (2024)
Rebecca Kriukelis, Michael T Gabbett, Rachael Beswick, Aideen M McInerney-Leo, Carlie Driscoll, Karen Liddle
The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates. European journal of human genetics : EJHG (2024)
Cassandra Muller, Lyndon Gallacher, Louise Keogh, Aideen M McInerney-Leo, Tiffany F Boughtwood, Penny Gleeson, Kristine Barlow-Stewart, Martin B Delatycki, Ingrid Winship, Kristen J Nowak, Margaret Otlowski, Paul A Lacaze, Jane M Tiller
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance. European journal of human genetics : EJHG 32 (7) (2024)
Cassandra Muller, Lyndon Gallacher, Louise Keogh, Aideen M McInerney-Leo, Tiffany F Boughtwood, Penny Gleeson, Kristine Barlow-Stewart, Martin B Delatycki, Ingrid Winship, Kristen J Nowak, Margaret Otlowski, Paul A Lacaze, Jane M Tiller
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance. European journal of human genetics : EJHG 32 (7) (2024)
Cassandra Muller, Lyndon Gallacher, Louise Keogh, Aideen M McInerney-Leo, Tiffany F Boughtwood, Penny Gleeson, Kristine Barlow-Stewart, Martin B Delatycki, Ingrid Winship, Kristen J Nowak, Margaret Otlowski, Paul A Lacaze, Jane M Tiller
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance. European journal of human genetics : EJHG (2024)
Ellie J Maas, Emily DeBortoli, Vaishnavi Nathan, Ned P Freeman, Adam Mothershaw, Darren J Smit, Brigid Betz-Stablein, Lauren G Aoude, Mitchell S Stark, Richard A Sturm, Hans Peter Soyer, Aideen M McInerney-Leo
POT1 and multiple primary melanomas: the dermatological phenotype. Journal of medical genetics 61 (9) (2024)
Tatiane Yanes, Marisa Blencoe, Antonia Howard, Jane Tiller, Courtney Wallingford, Margaret Otlowski, Louise Keogh, Paul Lacaze, Aideen M McInerney-Leo
Australian researcher's perspectives on the Australian industry-led moratorium on genetic tests in life insurance. American journal of medical genetics. Part A (2024)
Tatiane Yanes, Marisa Blencoe, Antonia Howard, Jane Tiller, Courtney Wallingford, Margaret Otlowski, Louise Keogh, Paul Lacaze, Aideen M McInerney-Leo
Australian researcher's perspectives on the Australian industry-led moratorium on genetic tests in life insurance. American journal of medical genetics. Part A 194 (6) (2024)
Tatiane Yanes, Marisa Blencoe, Antonia Howard, Jane Tiller, Courtney Wallingford, Margaret Otlowski, Louise Keogh, Paul Lacaze, Aideen M McInerney-Leo
Australian researcher's perspectives on the Australian industry-led moratorium on genetic tests in life insurance. American journal of medical genetics. Part A 194 (6) (2024)
Ellie J Maas, Emily DeBortoli, Vaishnavi Nathan, Ned P Freeman, Adam Mothershaw, Darren J Smit, Brigid Betz-Stablein, Lauren G Aoude, Mitchell S Stark, Richard A Sturm, Hans Peter Soyer, Aideen M McInerney-Leo
POT1 and multiple primary melanomas: the dermatological phenotype. Journal of medical genetics 61 (9) (2024)
Rebecca Kriukelis, Michael T Gabbett, Rachael Beswick, Aideen M McInerney-Leo, Carlie Driscoll, Karen Liddle
The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates. European journal of human genetics : EJHG (2024)
Neelam Hassan, Celia L Gregson, Haotian Tang, Marc van der Kamp, Paul Leo, Aideen M McInerney-Leo, Jie Zheng, Maria Luisa Brandi, Jonathan Cy Tang, William Fraser, Michael D Stone, Elin Grundberg, null null, Matthew A Brown, Emma L Duncan, Jonathan H Tobias
Rare and common variants in GALNT3 may affect bone mass independently of phosphate metabolism. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (2023)
Neelam Hassan, Celia L Gregson, Haotian Tang, Marc W Van der Kamp, Paul Leo, Aideen M McInerney-Leo, Yufang Bi, Maria Luisa Brandi, Jonathan C Y Tang, William D Fraser, Michael D Stone, Elin Grundberg, null null, Matthew A Brown, Emma L Duncan, Jonathan H Tobias
Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (2023)
Prachi Bhave, Jessica Wong, Aideen M McInerney-Leo, Amelia K Smit, Craig Lawn, Monika Janda, Victoria J Mar
Management of cutaneous melanoma in Australia: a narrative review. The Medical journal of Australia 218 (9) (2023)
Ellie J Maas, Courtney K Wallingford, Emily DeBortoli, Darren J Smit, Brigid Betz-Stablein, Lauren G Aoude, Mitchell S Stark, Richard A Sturm, Hans Peter Soyer, Aideen M McInerney-Leo
GOLM1 : expanding our understanding of melanoma susceptibility. Journal of medical genetics (2023)
Jane M Tiller, Andrew Bakshi, Grace Dowling, Louise Keogh, Aideen M McInerney-Leo, Kristine Barlow-Stewart, Tiffany F Boughtwood, Penny Gleeson, Martin B Delatycki, Ingrid Winship, Margaret Otlowski, Paul A Lacaze
Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing. European journal of human genetics : EJHG (2023)
Danya F Vears, Jackie Boyle, Chris Jacobs, Aideen M McInerney-Leo, Ainsley Janelle Newson, null null
Human Genetics Society of Australasia Position Statement: Genetic Carrier Testing for Recessive Conditions. Twin research and human genetics : the official journal of the International Society for Twin Studies (2023)
Prachi Bhave, Jessica Wong, Aideen M McInerney-Leo, Amelia K Smit, Craig Lawn, Monika Janda, Victoria J Mar
Management of cutaneous melanoma in Australia: a narrative review. The Medical journal of Australia 218 (9) (2023)
Neelam Hassan, Celia L Gregson, Haotian Tang, Marc W Van der Kamp, Paul Leo, Aideen M McInerney-Leo, Yufang Bi, Maria Luisa Brandi, Jonathan C Y Tang, William D Fraser, Michael D Stone, Elin Grundberg, null null, Matthew A Brown, Emma L Duncan, Jonathan H Tobias
Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (2023)
Prachi Bhave, Jessica Wong, Aideen M McInerney-Leo, Amelia K Smit, Craig Lawn, Monika Janda, Victoria J Mar
Management of cutaneous melanoma in Australia: a narrative review. The Medical journal of Australia 218 (9) (2023)
Jane M Tiller, Andrew Bakshi, Grace Dowling, Louise Keogh, Aideen M McInerney-Leo, Kristine Barlow-Stewart, Tiffany F Boughtwood, Penny Gleeson, Martin B Delatycki, Ingrid Winship, Margaret Otlowski, Paul A Lacaze
Correction: Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing. European journal of human genetics : EJHG (2023)
Courtney K Wallingford, Anastassia Demeshko, Asha Krishnankutty Krishnakripa, Darren J Smit, David L Duffy, Brigid Betz-Stablein, Annette Pflugfelder, Kasturee Jagirdar, Elizabeth Holland, Graham J Mann, Clare A Primiero, Tatiane Yanes, Josep Malvehy, Cèlia Badenas, Cristina Carrera, Paula Aguilera, Catherine M Olsen, Sarah V Ward, Nikolas K Haass, Richard A Sturm, Susanna Puig, David C Whiteman, Matthew H Law, Amelia K Smit, Miriam Potrony, Hans Peter Soyer, Aideen M McInerney-Leo
MC1R 'r' allele does not increase melanoma risk in MITF E318K carriers. The British journal of dermatology (2023)
Prachi Bhave, Jessica Wong, Aideen M McInerney-Leo, Amelia K Smit, Craig Lawn, Monika Janda, Victoria J Mar
Management of cutaneous melanoma in Australia: a narrative review. The Medical journal of Australia 218 (9) (2023)
Prachi Bhave, Jessica Wong, Aideen M McInerney-Leo, Amelia K Smit, Craig Lawn, Monika Janda, Victoria J Mar
Management of cutaneous melanoma in Australia: a narrative review. The Medical journal of Australia (2023)
Jane M Tiller, Andrew Bakshi, Grace Dowling, Louise Keogh, Aideen M McInerney-Leo, Kristine Barlow-Stewart, Tiffany F Boughtwood, Penny Gleeson, Martin B Delatycki, Ingrid Winship, Margaret Otlowski, Paul A Lacaze
Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing. European journal of human genetics : EJHG (2023)
Grace Dowling, Jane M Tiller, Aideen M McInerney-Leo, Andrea Belcher, Casey Haining, Kristine Barlow-Stewart, Tiffany F Boughtwood, Penny Gleeson, Martin B Delatycki, Ingrid Winship, Margaret Otlowski, Chris Jacobs, Louise Keogh, Paul A Lacaze
Health professionals' views and experiences of the Australian moratorium on genetic testing and life insurance: A qualitative study. European journal of human genetics : EJHG 30 (11) (2022)
Aideen M McInerney-Leo, Hui Yi Chew, Po-Ling Inglis, Paul J Leo, Shannon R Joseph, Caroline L Cooper, Satomi Okano, Tim Hassall, Lisa K Anderson, Rayleen V Bowman, Michael Gattas, Jessica E Harris, Mhairi S Marshall, Janet G Shaw, Lawrie Wheeler, Ian A Yang, Matthew A Brown, Kwun M Fong, Fiona Simpson, Emma L Duncan
Germline ERBB3 mutation in familial non-small-cell lung carcinoma: expanding ErbB's role in oncogenesis. Human molecular genetics 30 (24) (2022)
Ellie J Maas, Courtney K Wallingford, Jessica J McGuire, Chantal Rutjes, Darren J Smit, Brigid Betz-Stablein, Richard A Sturm, Hans Peter Soyer, Aideen M McInerney-Leo
Amelanotic/hypopigmented melanoma in a sibship with oculocutaneous albinism. The Journal of dermatology 49 (11) (2022)
Andrew Bakshi, Mabel Yan, Moeen Riaz, Galina Polekhina, Suzanne G Orchard, Jane M Tiller, Rory Wolfe, Amit Joshi, Yin Cao, Aideen M McInerney-Leo, Tatiane Yanes, Monika Janda, H Peter Soyer, Amelia K Smit, Matthew H Law, Peter Gibbs, Catriona McLean, Andrew T Chan, John J McNeil, Victoria J Mar, Paul A Lacaze
Genomic Risk Score for Melanoma in a Prospective Study of Older Individuals. Journal of the National Cancer Institute 113 (10) (2022)
Aideen M McInerney-Leo, Jennifer West, Bettina Meiser, Malcolm West, Maree R Toombs, Matthew A Brown, Emma L Duncan
The impact of Marfan syndrome on an Aboriginal Australian family: 'I don't like it as much as I don't like cancer'. Journal of genetic counseling (2021)
Anu Närhi, Andrea Fernandes, Sanna Toiviainen-Salo, Jessica Harris, Aideen M McInerney-Leo, Syndia Lazarus, Kristiina Avela, Emma L Duncan
A family with partially penetrant multicentric carpotarsal osteolysis due to gonadal mosaicism: First reported case. American journal of medical genetics. Part A 185 (8) (2021)
Ryan Pysar, Courtney K Wallingford, Jackie Boyle, Scott B Campbell, Lisa Eckstein, Rebekah McWhirter, Bronwyn Terrill, Chris Jacobs, Aideen M McInerney-Leo
Australian human research ethics committee members' confidence in reviewing genomic research applications. European journal of human genetics : EJHG 29 (12) (2021)
Aideen M McInerney-Leo, Jennifer West, Lawrie Wheeler, Paul J Leo, Kim M Summers, Lisa Anderson, Matthew A Brown, Malcolm West, Emma L Duncan
Compound heterozygous mutations in FBN1 in a large family with Marfan syndrome. Molecular genetics & genomic medicine 8 (3) (2020)
Chelsea M Withers, Jane Fleming, Courtney K Wallingford, Michael T Gabbett, Madelyn Peterson, Linda Humphreys, Aideen M McInerney-Leo
Waiting for a diagnosis in Rubinstein-Taybi: The journey from "ignorance is bliss" to the value of "a label". American journal of medical genetics. Part A 185 (1) (2020)
Aideen M McInerney-Leo, Jennifer A West, Jim J McGill, Matthew A Brown, Emma L Duncan, Malcolm J West
Use of the arm-span to height ratio as a criterion for Marfan syndrome in Aboriginal Australians: Diagnostically challenging. American journal of medical genetics. Part A 182 (4) (2020)
Erin K McMeniman, David L Duffy, Kasturee Jagirdar, Katie J Lee, E Peach, Aideen M McInerney-Leo, Brian De'Ambrosis, Jenna E Rayner, Bernard Mark Smithers, Hans Peter Soyer, Richard A Sturm
The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls. The British journal of dermatology 183 (2) (2020)
Anastassia Demeshko, David J Pennisi, Sushil Narayan, Stacy W Gray, Matthew A Brown, Aideen M McInerney-Leo
Factors influencing cancer genetic somatic mutation test ordering by cancer physician. Journal of translational medicine 18 (1) (2020)
Avinaash V Maharaj, Federica Buonocore, Eirini Meimaridou, Gerard Ruiz-Babot, Leonardo Guasti, Hwei-Ming Peng, Cameron P Capper, Neikelyn Burgos-Tirado, Rathi Prasad, Claire R Hughes, Ashwini Maudhoo, Elizabeth C Crowne, Timothy D Cheetham, Caroline E Brain, Jenifer P Suntharalingham, Niccolò Striglioni, Bilgin Yuksel, Fatih Gurbuz, Sangay Gupta, Robert S Lindsay, Robert Couch, Helen A Spoudeas, Tülay Güran, Stephanie R Johnson, Dallas J Fowler, Louise S Conwell, Aideen M McInerney-Leo, Delphine Drui, Bertrand Cariou, Juan Pedro López-Siguero, Mark Harris, Emma L Duncan, Peter C Hindmarsh, Richard J Auchus, Malcolm D Donaldson, John C Achermann, Louise A Metherell
Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing. Journal of the Endocrine Society 3 (1) (2018)
Aideen M McInerney-Leo, Lawrie Wheeler, Mhairi S Marshall, Lisa K Anderson, Andreas Zankl, Matthew A Brown, Paul J Leo, Carol Wicking, Emma L Duncan
Homozygous variant in C21orf2 in a case of Jeune syndrome with severe thoracic involvement: Extending the phenotypic spectrum. American journal of medical genetics. Part A 173 (6) (2017)

Aideen M McInerney-Leo (A M McInerney-Leo, Aideen McInerney-Leo)

Publication Activity (10 Years)

Top Topics

Top Venues