List of works - Alison H Trainer

A cost-effectiveness model of genetic testing and periodical clinical screening for the evaluation of families with dilated cardiomyopathy

scientific article published on 20 June 2019

An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome

scientific article published on 17 June 2019

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

scientific article published on 16 December 2019

Changing landscape of hereditary breast and ovarian cancer germline genetic testing in Australia

article

Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs

scientific article published on 9 January 2018

Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk

scientific article

Germline whole exome sequencing of a family with appendiceal mucinous tumours presenting with pseudomyxoma peritonei

scientific article published on 01 May 2020

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

scientific article published on 01 September 2019

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015: Szczecin, Poland. 24-25 September, 2015.

scientific article published on 10 October 2017

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

scientific article published on 15 February 2018

Mutations in RECQL are not associated with breast cancer risk in an Australian population

scientific article published on 01 October 2018

Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls

scientific article

Rare variants in XRCC2 as breast cancer susceptibility alleles

scientific article published on October 2012

Reevaluation of RINT1 as a breast cancer predisposition gene

scientific article

Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context

scientific article

The iPrevent Online Breast Cancer Risk Assessment and Risk Management Tool: Usability and Acceptability Testing

scientific article published on 07 November 2018

List of works by Alison H Trainer

A cost-effectiveness model of genetic testing and periodical clinical screening for the evaluation of families with dilated cardiomyopathy

An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

Changing landscape of hereditary breast and ovarian cancer germline genetic testing in Australia

Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs

Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk

Germline whole exome sequencing of a family with appendiceal mucinous tumours presenting with pseudomyxoma peritonei

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015: Szczecin, Poland. 24-25 September, 2015.

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

Mutations in RECQL are not associated with breast cancer risk in an Australian population

Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls

Rare variants in XRCC2 as breast cancer susceptibility alleles

Reevaluation of RINT1 as a breast cancer predisposition gene

Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context

The iPrevent Online Breast Cancer Risk Assessment and Risk Management Tool: Usability and Acceptability Testing