Alison Luk Young (Alison L Young)

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 6

Top Topics

Smoking Cessation

General Practice

Top Venues

Asia-Pacific journal of clinical oncology

European journal of human genetics : EJHG

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

Publications

Alison Luk Young, Emilia Ip, Tahlia Scheinberg, Michelle Harrison, Philip Beale, Annabel Goodwin
An Australian mainstream genetic testing program: Clinicians views about current and future practices. Asia-Pacific journal of clinical oncology (2023)
Alison Luk Young, Aalya Imran, Michael J Spoelma, Rachel Williams, Katherine M Tucker, Jane Halliday, Laura Elenor Forrest, Claire E Wakefield, Phyllis N Butow
Proband-mediated interventions to increase disclosure of genetic risk in families with a BRCA or Lynch syndrome condition: a systematic review. European journal of human genetics : EJHG (2022)
Alison Luk Young, Nicole Marion Rankin, Elena Whippy, Skye Cooke, Chris Milross, Robert R Zielinski, Hayley Brennan, Melissa Grand, Philip Beale
Implementation and evaluation of a smoking cessation checklist implemented within Australian cancer services. Asia-Pacific journal of clinical oncology 18 (5) (2022)
Emilia Ip, Alison Luk Young, Tahlia Scheinberg, Michelle Harrison, Philip Beale, Annabel Goodwin
Evaluation of a mainstream genetic testing program for women with ovarian or breast cancer. Asia-Pacific journal of clinical oncology 18 (5) (2022)
Alison Luk Young, Phyllis N Butow, Katherine M Tucker, Claire E Wakefield, Emma Healey, Rachel Williams
When to break the news and whose responsibility is it? A cross-sectional qualitative study of health professionals' views regarding disclosure of BRCA genetic cancer risk. BMJ open 10 (2) (2020)
Alison Luk Young, Phyllis N Butow, Katherine M Tucker, Claire E Wakefield, Emma Healey, Rachel Williams
Challenges and strategies proposed by genetic health professionals to assist with family communication. European journal of human genetics : EJHG 27 (11) (2019)