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Research performance evaluation: the experience of an independent medical research institute

Australian health review, 2012-01, Vol.36 (2), p.218

2012

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Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication

European journal of human genetics : EJHG, 2016-03, Vol.24 (3), p.356-360

2016

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Communicating genetic information in families - a review of guidelines and position papers

European journal of human genetics : EJHG, 2007-06, Vol.15 (6), p.612-618

2007

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"Did you find that out in time?": New life trajectories of parents who choose to continue a pregnancy where a genetic disorder is diagnosed or likely

American journal of medical genetics. Part A, 2012-02, Vol.158A (2), p.373-383

2012

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Bullying among doctors in training: cross sectional questionnaire survey

BMJ (Online), 2004-09, Vol.329 (7467), p.658-659

International edition, 2004

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Cascade carrier testing after a child is diagnosed with cystic fibrosis through newborn screening: investigating why most relatives do not have testing

Genetics in medicine, 2013-07, Vol.15 (7), p.533-540

2013

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Genetic health professionals and the communication of genetic information in families: Practice during and after a genetic consultation

American journal of medical genetics. Part A, 2010-06, Vol.152A (6), p.1458-1466

2010

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'It is not in my world': an exploration of attitudes and influences associated with cystic fibrosis carrier screening

European journal of human genetics : EJHG, 2008-04, Vol.16 (4), p.435-444

2008

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Health first, genetics second: exploring families' experiences of communicating genetic information

European journal of human genetics : EJHG, 2008-11, Vol.16 (11), p.1329-1335

2008

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

BMC medical genetics, 2014-03, Vol.15 (1), p.33-33, Article 33

2014

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

European journal of human genetics : EJHG, 2010-10, Vol.18 (10), p.1084-1089

2010

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A case for cystic fibrosis carrier testing in the general population

Medical journal of Australia, 2011-02, Vol.194 (4), p.208-209

2011

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An audit of clinical service examining the uptake of genetic testing by at-risk family members

Genetics in medicine, 2012-01, Vol.14 (1), p.122-128

2012

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A model for the development of genetics education programs for health professionals

Genetics in medicine, 2007-07, Vol.9 (7), p.451-457

2007

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Trainees' attitudes to shift work depend on grade and specialty

BMJ, 2003-01, Vol.326 (7379), p.48-48

International edition, 2003

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ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible

European journal of human genetics : EJHG, 2012-05, Vol.20 (5), p.505-509

2012

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Development of a questionnaire for evaluating genetics education in general practice

Journal of community genetics, 2010-12, Vol.1 (4), p.175-183

2010

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Consumer contribution to the delivery of genetic health services

American journal of medical genetics. Part A, 2008-09, Vol.146A (17), p.2266-2274

2008

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The Importance of Program Evaluation: How Can it be Applied to Diverse Genetics Education Settings?

Journal of genetic counseling, 2008-04, Vol.17 (2), p.170-179

2008

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“It’s Challenging on a Personal Level”—Exploring the ‘Lived Experience’ of Australian and Canadian Prenatal Genetic Counselors

Journal of genetic counseling, 2010-12, Vol.19 (6), p.640-652

2010

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Educating general practitioners about prenatal testing: approaches and challenges

Prenatal diagnosis, 2005-07, Vol.25 (7), p.592-601

2005

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Tay Sachs disease carrier screening in schools: Educational alternatives and cheekbrush sampling

Genetics in medicine, 2005-11, Vol.7 (9), p.626-632

2005

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Harry Potter and the recessive allele

Nature, 2005-08, Vol.436 (7052), p.776-776

2005

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Why do people choose not to have screening for hemochromatosis?

Genetic testing and molecular biomarkers, 2013-01, Vol.17 (1), p.21-24

2013

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Trainee satisfaction before and after the Calman reforms of specialist training: questionnaire survey

BMJ (Online), 2000-03, Vol.320 (7238), p.832-836

International edition, 2000

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Research performance evaluation: the experience of an independent medical research institute

Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication

Communicating genetic information in families - a review of guidelines and position papers

"Did you find that out in time?": New life trajectories of parents who choose to continue a pregnancy where a genetic disorder is diagnosed or likely

Bullying among doctors in training: cross sectional questionnaire survey

Cascade carrier testing after a child is diagnosed with cystic fibrosis through newborn screening: investigating why most relatives do not have testing

Genetic health professionals and the communication of genetic information in families: Practice during and after a genetic consultation

'It is not in my world': an exploration of attitudes and influences associated with cystic fibrosis carrier screening

Health first, genetics second: exploring families' experiences of communicating genetic information

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

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

A case for cystic fibrosis carrier testing in the general population

An audit of clinical service examining the uptake of genetic testing by at-risk family members

A model for the development of genetics education programs for health professionals

Trainees' attitudes to shift work depend on grade and specialty

ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible

Development of a questionnaire for evaluating genetics education in general practice

Consumer contribution to the delivery of genetic health services

The Importance of Program Evaluation: How Can it be Applied to Diverse Genetics Education Settings?

“It’s Challenging on a Personal Level”—Exploring the ‘Lived Experience’ of Australian and Canadian Prenatal Genetic Counselors

Educating general practitioners about prenatal testing: approaches and challenges

Tay Sachs disease carrier screening in schools: Educational alternatives and cheekbrush sampling

Harry Potter and the recessive allele

Why do people choose not to have screening for hemochromatosis?

Trainee satisfaction before and after the Calman reforms of specialist training: questionnaire survey

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