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Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning

Frontiers in genetics, 2020-03, Vol.11, p.151-151

2020

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Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education

Frontiers in genetics, 2020-03, Vol.11, p.59-59

2020

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A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy

European journal of human genetics : EJHG, 2015-10, Vol.23 (10), p.1294-1300

2015

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Editorial: Educating Health Professionals in Genomic Medicine: Evidence-Based Strategies and Approaches

Frontiers in genetics, 2020-08, Vol.11, p.696-696

2020

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Genetic counselling, patient education, and informed decision-making in the genomic era

Seminars in fetal & neonatal medicine, 2018-04, Vol.23 (2), p.142-149

Metcalfe, Sylvia A.

2018

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Responsible implementation of expanded carrier screening

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.e1-e12

2016

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Carrier screening for Beta-thalassaemia: a review of international practice

European journal of human genetics : EJHG, 2010-10, Vol.18 (10), p.1077-1083

2010

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Human Genetics Society of Australasia Position Statement: Online DNA Testing

Twin research and human genetics, 2020-08, Vol.23 (4), p.256-258

2020

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“Testing Times, Challenging Choices”: An Australian Study of Prenatal Genetic Counseling

Journal of genetic counseling, 2010-02, Vol.19 (1), p.22-37

2010

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Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research

Genetics in medicine, 2014-03, Vol.16 (3), p.207-216

2014

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Australians' views on personal genomic testing: focus group findings from the Genioz study

European journal of human genetics : EJHG, 2018-08, Vol.26 (8), p.1101-1112

2018

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Carrier screening in preconception consultation in primary care

Journal of community genetics, 2012-07, Vol.3 (3), p.193-203

Metcalfe, Sylvia A.

2012

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A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy

European journal of human genetics : EJHG, 2015-05, Vol.23 (5), p.575-580

2015

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Personal genomic testing for nutrition and wellness in Australia: A content analysis of online information

Nutrition & dietetics, 2019-07, Vol.76 (3), p.263-270

2019

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Australians' views and experience of personal genomic testing: survey findings from the Genioz study

European journal of human genetics : EJHG, 2019-05, Vol.27 (5), p.711-720

2019

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Fragile X population carrier screening

Genetics in medicine, 2018-09, Vol.20 (9), p.1091-1092

2018

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Australians’ perspectives on support around use of personal genomic testing: Findings from the Genioz study

European journal of medical genetics, 2019-05, Vol.62 (5), p.290-299

2019

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FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts

Genetics in medicine, 2018-12, Vol.20 (12), p.1627-1634

2018

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An exploration of genetic health professionals' experience with direct-to-consumer genetic testing in their clinical practice

European journal of human genetics : EJHG, 2012-08, Vol.20 (8), p.825-830

2012

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Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2014-01, Vol.165B (1), p.41-51

2014

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A systematic review of population screening for fragile X syndrome

Genetics in medicine, 2010-07, Vol.12 (7), p.396-410

2010

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From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing

AJOB empirical bioethics, 2020-01, Vol.11 (1), p.63-76

2020

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Responsible implementation of expanded carrier screening

European journal of human genetics : EJHG, 2017-11, Vol.25 (11), p.1291-1291

2017

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Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women

Neurology, 2015-04, Vol.84 (16), p.1631

2015

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Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning

Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education

A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy

Editorial: Educating Health Professionals in Genomic Medicine: Evidence-Based Strategies and Approaches

Genetic counselling, patient education, and informed decision-making in the genomic era

Responsible implementation of expanded carrier screening

Carrier screening for Beta-thalassaemia: a review of international practice

Human Genetics Society of Australasia Position Statement: Online DNA Testing

“Testing Times, Challenging Choices”: An Australian Study of Prenatal Genetic Counseling

Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research

Australians' views on personal genomic testing: focus group findings from the Genioz study

Carrier screening in preconception consultation in primary care

A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy

Personal genomic testing for nutrition and wellness in Australia: A content analysis of online information

Australians' views and experience of personal genomic testing: survey findings from the Genioz study

Fragile X population carrier screening

Australians’ perspectives on support around use of personal genomic testing: Findings from the Genioz study

FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts

An exploration of genetic health professionals' experience with direct-to-consumer genetic testing in their clinical practice

Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers

A systematic review of population screening for fragile X syndrome

From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing

Responsible implementation of expanded carrier screening

Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women

Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening

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