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“It's good to know”: Experiences of gene identification and result disclosure in familial epilepsies

Epilepsy research, 2015-05, Vol.112, p.64-71

2015

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Genetics, Insurance and Professional Practice: Survey of the Australasian Clinical Genetics Workforce

Frontiers in public health, 2018-11, Vol.6, p.333-333

2018

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“It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare

Journal of community genetics, 2016-04, Vol.7 (2), p.159-171

2016

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Alerting genetic relatives to a risk of serious inherited disease without a patient's consent

Medical journal of Australia, 2011-04, Vol.194 (8), p.385-386

2011

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

Genetics in medicine, 2008-07, Vol.10 (7), p.525-535

2008

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Doctors breaching patient privacy: Orwell redux

Medical journal of Australia, 2011-06, Vol.194 (12), p.670-671

2011

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Family communication following a diagnosis of myotonic dystrophy: To tell or not to tell?

Journal of genetic counseling, 2019-10, Vol.28 (5), p.1029-1041

2019

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Genetic Counsellors and Private Practice: Professional Turbulence and Common Values

Journal of genetic counseling, 2018-08, Vol.27 (4), p.782-791

2018

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Educating Genetic Counselors in Australia—Developing a Masters Program

Journal of genetic counseling, 2013-12, Vol.22 (6), p.897-901

2013

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Communicating microarray results of uncertain clinical significance in consultation summary letters and implications for practice

European journal of human genetics : EJHG, 2016-01, Vol.25 (1), p.22-30

2016

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Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS)

European journal of human genetics : EJHG, 2015-02, Vol.23 (2), p.152-158

2015

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

American journal of medical genetics. Part A, 2013-01, Vol.161A (1), p.48-58

2013

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

American journal of medical genetics. Part A, 2009-12, Vol.149A (12), p.2731-2738

2009

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Use and disclosure of genetic information without consent: a decision-making tool for health practitioners - who, when, why and how?

Internal medicine journal, 2011-08, Vol.41 (8), p.634-638

Anon

2011

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Cystic fibrosis carrier screening in two New South Wales country towns

Medical journal of Australia, 1996-04, Vol.164 (8), p.471-474

1996

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Effects of exercise training and dietary manipulation on insulin-regulatable glucose-transporter mRNA in rat muscle

Diabetes (New York, N.Y.), 1991-02, Vol.40 (2), p.275-279

1991

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Dizygous twinning and premature menopause in fragile X syndrome

The Lancet (British edition), 1994-11, Vol.344 (8935), p.1500-1500

1994

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Case finding for the fragile X syndrome and its consequences

BMJ, 1997-11, Vol.315 (7117), p.1223-1226

International edition, 1997

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An analysis of the rate of metallothionein mRNA POLY(A)-shortening using RNA blot hybridization

Nucleic acids research, 1985-11, Vol.13 (22), p.7929-7943

1985

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Developmental variation in copper, zinc and metallothionein mRNA in brindled mutant and nutritionally copper deficient mice

Biochimica et biophysica acta. Molecular basis of disease, 1991-10, Vol.1097 (3), p.205-211

1991

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NcoI and HinfI RFLPs detected with a dihydropteridine reductase cDNA probe

Nucleic acids research, 1988-04, Vol.16 (7), p.3124-3124

1988

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Analysis of DNA probes for the prenatal diagnosis of cystic fibrosis

Medical journal of Australia, 1989-08, Vol.151 (3), p.131, 133-136

1989

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The primary structure of the imported mitochondrial protein, ornithine transcarbamylase from rat liver: mRNA levels during ontogeny

DNA (New York, N.Y.), 1985-04, Vol.4 (2), p.147-156

1985

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SDSS-IV MaNGA: faint quenched galaxies – I. Sample selection and evidence for environmental quenching

Monthly notices of the Royal Astronomical Society, 2016-11, Vol.462 (4), p.3955-3978

2016

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Pharmacogenomics of medications given via nonconventional administration routes: a scoping review

Pharmacogenomics, 2022-11, Vol.23 (16), p.933-948

2022

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“It's good to know”: Experiences of gene identification and result disclosure in familial epilepsies

Genetics, Insurance and Professional Practice: Survey of the Australasian Clinical Genetics Workforce

“It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare

Alerting genetic relatives to a risk of serious inherited disease without a patient's consent

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

Doctors breaching patient privacy: Orwell redux

Family communication following a diagnosis of myotonic dystrophy: To tell or not to tell?

Genetic Counsellors and Private Practice: Professional Turbulence and Common Values

Educating Genetic Counselors in Australia—Developing a Masters Program

Communicating microarray results of uncertain clinical significance in consultation summary letters and implications for practice

Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS)

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

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

Use and disclosure of genetic information without consent: a decision-making tool for health practitioners - who, when, why and how?

Cystic fibrosis carrier screening in two New South Wales country towns

Effects of exercise training and dietary manipulation on insulin-regulatable glucose-transporter mRNA in rat muscle

Dizygous twinning and premature menopause in fragile X syndrome

Case finding for the fragile X syndrome and its consequences

An analysis of the rate of metallothionein mRNA POLY(A)-shortening using RNA blot hybridization

Developmental variation in copper, zinc and metallothionein mRNA in brindled mutant and nutritionally copper deficient mice

NcoI and HinfI RFLPs detected with a dihydropteridine reductase cDNA probe

Analysis of DNA probes for the prenatal diagnosis of cystic fibrosis

The primary structure of the imported mitochondrial protein, ornithine transcarbamylase from rat liver: mRNA levels during ontogeny

SDSS-IV MaNGA: faint quenched galaxies – I. Sample selection and evidence for environmental quenching

Pharmacogenomics of medications given via nonconventional administration routes: a scoping review

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