Publications by authors named "Simone McInerny"

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Assessment of candidate high-grade serous ovarian carcinoma predisposition genes through integrated germline and tumour sequencing.
Deepak N Subramanian, Maia Zethoven, Kathleen I Pishas, Evanny R Marinović, Simone McInerny

NPJ Genom Med· January 2025

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Using polygenic risk modification to improve breast cancer prevention: study protocol for the PRiMo multicentre randomised controlled trial.
Simone McInerny, Lyon Mascarenhas, Tatiane Yanes, Lara Petelin, Georgia Chenevix-Trench

BMJ Open· August 2024

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Development and evaluation of a novel educational program for providers on the use of polygenic risk scores.
Tatiane Yanes, Courtney K Wallingford, Mary-Anne Young, Aideen M McInerney-Leo, Amanda M Willis, Simone McInerny

Genet Med· August 2023

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ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.
Lenka Stolarova, Petra Kleiblova, Petra Zemankova, Barbora Stastna, Marketa Janatova, Simone McInerny

Clin Cancer Res· August 2023

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Contribution of large genomic rearrangements in to familial breast cancer: implications for genetic testing.
Na Li, Magnus Zethoven, Simone McInerny, Eliza Healey, Dilanka DeSilva

J Med Genet· February 2023

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Somatic inactivation of breast cancer predisposition genes in tumors associated with pathogenic germline variants.
Belle W X Lim, Na Li, Sakshi Mahale, Simone McInerny, Magnus Zethoven

J Natl Cancer Inst· February 2023

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Gene-Expression Profiling of Mucinous Ovarian Tumors and Comparison with Upper and Lower Gastrointestinal Tumors Identifies Markers Associated with Adverse Outcomes.
Nicola S Meagher, Kylie L Gorringe, Matthew Wakefield, Adelyn Bolithon, Chi Nam Ignatius Pang, Simone McInerny

Clin Cancer Res· December 2022

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Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk.
Gillian Gregory, Kuheli Das Gupta, Bettina Meiser, Kristine Barlow-Stewart, Peter Geelan-Small, Simone McInerny

J Genet Couns· February 2022

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Integration of tumour sequencing and case-control data to assess pathogenicity of RAD51C missense variants in familial breast cancer.
Belle W X Lim, Na Li, Simone M Rowley, Ella R Thompson, Simone McInerny

NPJ Breast Cancer· January 2022

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Breast cancer polygenic risk scores: a 12-month prospective study of patient reported outcomes and risk management behavior.
Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, Mary-Anne Young, Philip B Mitchell, Simone McInerny

Genet Med· December 2021

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Communicating polygenic risk scores in the familial breast cancer clinic.
Kuheli Das Gupta, Gillian Gregory, Bettina Meiser, Rajneesh Kaur, Maatje Scheepers-Joynt, Simone McInerny

Patient Educ Couns· October 2021

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Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study.
Na Li, Belle W X Lim, Ella R Thompson, Simone McInerny, Magnus Zethoven

NPJ Breast Cancer· June 2021

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Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects.
Na Li, Magnus Zethoven, Simone McInerny, Lisa Devereux, Yu-Kuan Huang

NPJ Breast Cancer· May 2021

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Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes.
Deepak N Subramanian, Magnus Zethoven, Simone McInerny, James A Morgan, Simone M Rowley

Nat Commun· April 2020

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Uptake of polygenic risk information among women at increased risk of breast cancer.
Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, Maatje Scheepers-Joynt, Simone McInerny

Clin Genet· March 2020

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Combined Tumor Sequencing and Case-Control Analyses of RAD51C in Breast Cancer.
Na Li, Simone McInerny, Magnus Zethoven, Dane Cheasley, Belle W X Lim

J Natl Cancer Inst· December 2019

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Mutations in RECQL are not associated with breast cancer risk in an Australian population.
Na Li, Simone M Rowley, David L Goode, Kaushalya C Amarasinghe, Simone McInerny

Nat Genet· October 2018

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Molecular analysis of PALB2-associated breast cancers.
Jue Er Amanda Lee, Na Li, Simone M Rowley, Dane Cheasley, Magnus Zethoven, Simone McInerny

J Pathol· May 2018

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Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.
Na Li, Simone M Rowley, Ella R Thompson, Simone McInerny, Lisa Devereux

Breast Cancer Res· January 2018

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Reevaluation of RINT1 as a breast cancer predisposition gene.
Na Li, Ella R Thompson, Simone M Rowley, Simone McInerny, Lisa Devereux

Breast Cancer Res Treat· September 2016

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Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.
Ella R Thompson, Simone M Rowley, Na Li, Simone McInerny, Lisa Devereux

J Clin Oncol· May 2016

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rAAV-compatible MiniPromoters for restricted expression in the brain and eye.
Charles N de Leeuw, Andrea J Korecki, Garrett E Berry, Jack W Hickmott, Siu Ling Lam, Simone C McInerny

Mol Brain· May 2016

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Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context.
Ella R Thompson, Kylie L Gorringe, Simone M Rowley, Na Li, Simone McInerny

Sci Rep· October 2015

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Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls.
Ella R Thompson, Kylie L Gorringe, Simone M Rowley, Michelle W Wong-Brown, Simone McInerny

Breast Cancer Res· August 2015

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Targeted CNS Delivery Using Human MiniPromoters and Demonstrated Compatibility with Adeno-Associated Viral Vectors.
Charles N de Leeuw, Frank M Dyka, Sanford L Boye, Stéphanie Laprise, Michelle Zhou, Simone C McInerny

Mol Ther Methods Clin Dev· January 2014

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