“I'm Healthy, It's Not Going To Be Me”: Exploring experiences of carriers identified through a population reproductive genetic carrier screening panel in Australia

Expanded Carrier Screening in Reproductive Medicine—Points to Consider

(2015) Janice G. Edwards et al.   OBSTETRICS AND GYNECOLOGY

Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention

(2014) Jan M Hodgson et al.   BMC Medical Genetics

Population-based genetic carrier screening for cystic fibrosis in Victoria

(2014) Alison D Archibald et al.   MEDICAL JOURNAL OF AUSTRALIA

Current Practice and Attitudes of Australian Obstetricians Toward Population-Based Carrier Screening for Inherited Conditions

(2013) Zornitza Stark et al.   Twin Research and Human Genetics

“It's about having the choice”: Stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome

(2012) Alison D. Archibald et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Enhancing Family Communication About Genetics: Ethical and Professional Dilemmas

(2012) Jan Hodgson et al.   Journal of Genetic Counseling

Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing

(2011) C. J. Bell et al.   Science Translational Medicine

Newborn and carrier screening for spinal muscular atrophy

(2010) Thomas W. Prior et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Evaluation of a multi-disease carrier screening programme in Ashkenazi Jewish high schools

(2010) L Ioannou et al.   CLINICAL GENETICS

Uptake of carrier testing in families after cystic fibrosis diagnosis through newborn screening

(2010) Belinda J McClaren et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Population-Based Genetic Screening for Cystic Fibrosis: Attitudes and Outcomes

(2010) L. Ioannou et al.   Public Health Genomics

“It's something I need to consider”: Decisions about carrier screening for fragile X syndrome in a population of non-pregnant women

(2009) Alison D. Archibald et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study

(2009) Sylvia Metcalfe et al.   GENETICS IN MEDICINE