Australians' views and experience of personal genomic testing: survey findings from the Genioz study
Savard, Jacqueline, Hickerton, Chriselle, Tytherleigh, Rigan, Terrill, Bronwyn, Turbitt, Erin, Newson, Ainsley J, Wilson, Brenda, Gray, Kathleen, Gaff, Clara, Middleton, Anna, Stackpoole, Elaine, Metcalfe, Sylvia A
Published in European journal of human genetics : EJHG (01.05.2019)
Published in European journal of human genetics : EJHG (01.05.2019)
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Journal Article
Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing
Field, Michael, Dudding-Byth, Tracy, Arpone, Marta, Baker, Emma K, Aliaga, Solange M, Rogers, Carolyn, Hickerton, Chriselle, Francis, David, Phelan, Dean G, Palmer, Elizabeth E, Amor, David J, Slater, Howard, Bretherton, Lesley, Ling, Ling, Godler, David E
Published in International journal of molecular sciences (11.08.2019)
Published in International journal of molecular sciences (11.08.2019)
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Journal Article
The expectations and realities of nutrigenomic testing in australia: A qualitative study
Tutty, Erin, Hickerton, Chriselle, Terrill, Bronwyn, McClaren, Belinda, Tytherleigh, Rigan, Stackpoole, Elaine, Savard, Jaqueline, Newson, Ainsley, Middleton, Anna, Nisselle, Amy, Cusack, Marie, Adamski, Melissa, Gaff, Clara, Metcalfe, Sylvia
Published in Health expectations : an international journal of public participation in health care and health policy (01.04.2021)
Published in Health expectations : an international journal of public participation in health care and health policy (01.04.2021)
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Journal Article
"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
Hickerton, Chriselle L., Aitken, MaryAnne, Hodgson, Jan, Delatycki, Martin B.
Published in American journal of medical genetics. Part A (01.02.2012)
Published in American journal of medical genetics. Part A (01.02.2012)
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Journal Article
Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes
Baker, Emma K, Godler, David E, Bui, Minh, Hickerton, Chriselle, Rogers, Carolyn, Field, Mike, Amor, David J, Bretherton, Lesley
Published in Journal of neurodevelopmental disorders (06.08.2018)
Published in Journal of neurodevelopmental disorders (06.08.2018)
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Journal Article
General practitioners' views on genomics, practice and education: A qualitative interview study
Cusack, Marie Brigitte, Hickerton, Chriselle, Nisselle, Amy, McClaren, Belinda, Terrill, Bronwyn, Gaff, Clara, Dunlop, Kate, Metcalfe, Sylvia
Published in Australian journal of general practice (01.10.2021)
Published in Australian journal of general practice (01.10.2021)
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Journal Article
"It's about having the choice": Stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome
Archibald, Alison D., Hickerton, Chriselle L., Jaques, Alice M., Wake, Samantha, Cohen, Jonathan, Metcalfe, Sylvia A.
Published in American journal of medical genetics. Part A (01.01.2013)
Published in American journal of medical genetics. Part A (01.01.2013)
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Journal Article
“It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare
Archibald, Alison D., Hickerton, Chriselle L., Wake, Samantha A., Jaques, Alice M., Cohen, Jonathan, Metcalfe, Sylvia A.
Published in Journal of community genetics (01.04.2016)
Published in Journal of community genetics (01.04.2016)
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Journal Article
Experiences of prenatal diagnosis and decision-making about termination of pregnancy: A qualitative study
Hodgson, Jan, Pitt, Penelope, Metcalfe, Sylvia, Halliday, Jane, Menezes, Melody, Fisher, Jane, Hickerton, Chriselle, Petersen, Kerry, McClaren, Belinda
Published in Australian & New Zealand journal of obstetrics & gynaecology (01.12.2016)
Published in Australian & New Zealand journal of obstetrics & gynaecology (01.12.2016)
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Journal Article
Australians' views on personal genomic testing: focus group findings from the Genioz study
Metcalfe, Sylvia A, Hickerton, Chriselle, Savard, Jacqueline, Terrill, Bronwyn, Turbitt, Erin, Gaff, Clara, Gray, Kathleen, Middleton, Anna, Wilson, Brenda, Newson, Ainsley J
Published in European journal of human genetics : EJHG (01.08.2018)
Published in European journal of human genetics : EJHG (01.08.2018)
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Journal Article
A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy
Lawton, Sally, Hickerton, Chriselle, Archibald, Alison D, McClaren, Belinda J, Metcalfe, Sylvia A
Published in European journal of human genetics : EJHG (01.05.2015)
Published in European journal of human genetics : EJHG (01.05.2015)
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Journal Article
Australians’ perspectives on support around use of personal genomic testing: Findings from the Genioz study
Metcalfe, Sylvia A., Hickerton, Chriselle, Savard, Jacqueline, Stackpoole, Elaine, Tytherleigh, Rigan, Tutty, Erin, Terrill, Bronwyn, Turbitt, Erin, Gray, Kathleen, Middleton, Anna, Wilson, Brenda, Newson, Ainsley J., Gaff, Clara
Published in European journal of medical genetics (01.05.2019)
Published in European journal of medical genetics (01.05.2019)
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Journal Article
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X
Arpone, Marta, Baker, Emma K., Bretherton, Lesley, Bui, Minh, Li, Xin, Whitaker, Simon, Dissanayake, Cheryl, Cohen, Jonathan, Hickerton, Chriselle, Rogers, Carolyn, Field, Mike, Elliott, Justine, Aliaga, Solange M., Ling, Ling, Francis, David, Hearps, Stephen J. C., Hunter, Matthew F., Amor, David J., Godler, David E.
Published in Scientific reports (26.02.2018)
Published in Scientific reports (26.02.2018)
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Journal Article
Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening
Metcalfe, Sylvia A, Martyn, Melissa, Ames, Alice, Anderson, Vicki, Archibald, Alison D, Couns, Grad Dip Gen, Carter, Rob, Cohen, Jonathan, Cotter, Megan, GenCouns, M, Dang, William, Delatycki, Martin B, Donath, Susan, Edwards, Samantha, Educ, PGrad Dip, Couns, Grad Dip Gen, Forbes, Robin, Couns, Grad Dip Gen, Gavrila, Mioara, MedSci, M, Halliday, Jane, Hickerton, Chriselle, Hill, Melissa, Couns, Grad Dip Gen, Jacobs, Lorilli, Ultrasound, PGrad Dip, Petrou, Vicki, Couns, Grad Dip Gen, Plunkett, Loren, GenCouns, M, Sheffield, Leslie, RACP, F, Thornton, Alison, Younie, Sandra, Econ, PGrad Dip Hlth, Emery, Jon D
Published in Genetics in medicine (01.12.2017)
Published in Genetics in medicine (01.12.2017)
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Journal Article
12 ‘Recreational’ consumer genomics: no such thing as a non-medical test
Wilson, Brenda, Savard, Jacqueline, Hickerton, Chriselle, Terrill, Bronwyn, Newson, Ainsley, Gaff, Clara, Gray, Kathleen, Middleton, Anna, Metcalfe, Sylvia
Published in BMJ evidence-based medicine (01.12.2019)
Published in BMJ evidence-based medicine (01.12.2019)
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Journal Article
Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing
Gray, Kathleen, Stephen, Remya, Terrill, Bronwyn, Wilson, Brenda, Middleton, Anna, Tytherleigh, Rigan, Turbitt, Erin, Gaff, Clara, Savard, Jacqueline, Hickerton, Chriselle, Newson, Ainsley, Metcalfe, Sylvia
Published in Studies in health technology and informatics (2017)
Published in Studies in health technology and informatics (2017)
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ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible
DELATYCKI, Martin B, WOLTHUIZEN, Michelle, WILSON, Gabrielle R, STEPHENSON, Sarah Em, MACCIOCCA, Ivan, HICKERTON, Chriselle, LOCKHART, Paul J, METCALFE, Sylvia A, COLLINS, Veronica, VARLEY, Elizabeth, CRAVEN, Joanna, ALLEN, Katrina J, GURRIN, Lyle C, AITKEN, Maryanne, KAYE TREMBATH, M, BOND, Lyndal
Published in European journal of human genetics : EJHG (01.05.2012)
Published in European journal of human genetics : EJHG (01.05.2012)
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Journal Article
General practitioners' views on genomics, practice and education: A qualitative interview study
Cusack, Marie Brigitte, Hickerton, Chriselle, Nisselle, Amy, McClaren, Belinda, Terrill, Bronwyn, Gaff, Clara, Dunlop, Kate, Metcalfe, Sylvia
Published in Australian family physician (01.10.2021)
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Published in Australian family physician (01.10.2021)
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