Lucinda Freeman

Sydney, NSW, Australia

Last Updated: 09/26/2026

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Found 25 publications

Developing general practitioner and consumer supports for genomics in Australian primary care: a mixed-methods protocol.

Developing general practitioner and consumer supports for genomics in Australian primary care: a mixed-methods protocol.

Journal: BMJ open

Published: June 16, 2026

Prenatal Screening for Common Aneuploidy in Southeast Asian Countries: A Systematic Review of Challenges and Opportunities.

Prenatal Screening for Common Aneuploidy in Southeast Asian Countries: A Systematic Review of Challenges and Opportunities.

Journal: Prenatal diagnosis

Published: January 01, 2026

Perspectives of women who receive an increased chance result on non-invasive prenatal testing or combined first trimester screening: a qualitative study.

Perspectives of women who receive an increased chance result on non-invasive prenatal testing or combined first trimester screening: a qualitative study.

Journal: Midwifery

Published: August 07, 2025

Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation.

Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation.

Journal: European journal of human genetics : EJHG

Published: July 22, 2025

Nationwide, Couple-Based Genetic Carrier Screening.

Nationwide, Couple-Based Genetic Carrier Screening.

Journal: The New England journal of medicine

Published: November 20, 2024

Empowering midwives with genetic knowledge: A systematic review of educational needs in genomics.

Empowering midwives with genetic knowledge: A systematic review of educational needs in genomics.

Journal: Nurse education in practice

Published: October 08, 2024

Perceptions of severity and their influence on reproductive decision-making following reproductive genetic carrier screening.

Perceptions of severity and their influence on reproductive decision-making following reproductive genetic carrier screening.

Journal: European journal of human genetics : EJHG

Published: May 09, 2024

Considering severity in the design of reproductive genetic carrier screening programs: screening for severe conditions.

Considering severity in the design of reproductive genetic carrier screening programs: screening for severe conditions.

Journal: European journal of human genetics : EJHG

Published: March 31, 2024

Beyond severity: utility as a criterion for setting the scope of RGCS.

Beyond severity: utility as a criterion for setting the scope of RGCS.

Journal: European journal of human genetics : EJHG

Published: January 30, 2024

Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness.

Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness.

Journal: Journal of genetic counseling

Published: April 08, 2023

Scaling-up and future sustainability of a national reproductive genetic carrier screening program.

Scaling-up and future sustainability of a national reproductive genetic carrier screening program.

Journal: NPJ genomic medicine

Published: November 19, 2022

Genetic Counsellors play a key role in supporting ethically responsible expanded universal carrier screening.

Genetic Counsellors play a key role in supporting ethically responsible expanded universal carrier screening.

Journal: European journal of human genetics : EJHG

Published: October 06, 2022

Showing 1-12 of 25

Last Updated: 09/26/2026