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Agricola

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Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes

• Authors : Baker, Emma K.; Godler, David E.; Bui, Minh

• Source: Journal of Neurodevelopmental Disorders. August 6, 2018, Vol. 10 Issue 1

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The expectations and realities of nutrigenomic testing in australia: A qualitative study.

• Authors : Tutty, Erin; Hickerton, Chriselle; Terrill, Bronwyn

Subjects: NUTRITIONAL assessment; ATTITUDE (Psychology); RESEARCH methodologyAUSTRALIA

• Source: Health Expectations. Apr2021, Vol. 24 Issue 2, p670-686. 17p. 3 Diagrams, 4 Charts.

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General practitioners' views on genomics, practice and education: A qualitative interview study.

• Authors : Cusack, Marie Brigitte; Hickerton, Chriselle; Nisselle, Amy

Subjects: GENERAL practitioners; GENOMICS; EARLY detection of cancer

• Source: Australian Journal of General Practice; Oct2021, Vol. 50 Issue 10, p747-752, 6p

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

• Authors : Savard, Jacqueline; Hickerton, Chriselle; Metcalfe, Sylvia A.

Subjects: CONSUMER preferences; AUTONOMY (Psychology); CONSUMER behaviorAUSTRALIA

• Source: AJOB Empirical Bioethics; Jan-Mar2020, Vol. 11 Issue 1, p63-76, 14p

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

• Authors : Savard, Jacqueline; Hickerton, Chriselle; Tytherleigh, Rigan

• Source: European Journal of Human Genetics: EJHG; May 2019, Vol. 27 Issue: 5 p711-720, 10p

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Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing.

• Authors : Gray, Kathleen; Stephen, Remya; Terrill, Bronwyn

Subjects: MEDICAL informatics; MEDICAL telematics; CONSUMERS

• Source: Medinfo; 2017, p89-93, 5p

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

• Authors : Metcalfe, Sylvia; Hickerton, Chriselle; Savard, Jacqueline

• Source: European Journal of Human Genetics: EJHG; August 2018, Vol. 26 Issue: 8 p1101-1112, 12p

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

• Authors : Lawton, Sally; Hickerton, Chriselle; Archibald, Alison D

Subjects: SPINAL muscular atrophy; MUSCULAR atrophy in children; NEUROMUSCULAR diseases in children

• Source: European Journal of Human Genetics. May2015, Vol. 23 Issue 5, p575-580. 6p.

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Experiences of prenatal diagnosis and decision-making about termination of pregnancy: A qualitative study.

• Authors : Hodgson, Jan; Pitt, Penelope; Metcalfe, Sylvia

Subjects: ABORTION; DECISION making; DNAAUSTRALIA

• Source: Australian & New Zealand Journal of Obstetrics & Gynaecology; Dec2016, Vol. 56 Issue 6, p605-613, 9p, 5 Charts

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

• Authors : Metcalfe, Sylvia A; Martyn, Melissa; Ames, Alice

• Source: Genetics in Medicine; December 2017, Vol. 19 Issue: 12 p1346-1355, 10p

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

• Authors : Archibald, Alison; Hickerton, Chriselle; Wake, Samantha

• Source: Journal of Community Genetics; Apr2016, Vol. 7 Issue 2, p159-171, 13p

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

• Authors : Delatycki, Martin B; Wolthuizen, Michelle; Collins, Veronica

Subjects: HEMOCHROMATOSIS; HUMAN genome; GENETIC mutation

• Source: European Journal of Human Genetics. May2012, Vol. 20 Issue 5, p505-509. 5p. 1 Diagram, 3 Charts.

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

• Authors : Archibald, Alison D.; Hickerton, Chriselle L.; Jaques, Alice M.

• Source: American Journal of Medical Genetics. Part A; Jan2013, Vol. 161A Issue 1, p48-58, 11p

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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.

• Authors : Hickerton, Chriselle L.; Aitken, MaryAnne; Hodgson, Jan

• Source: American Journal of Medical Genetics. Part A; Feb2012, Vol. 158A Issue 2, p373-383, 11p

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Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing.

• Authors : Field, Michael; Dudding-Byth, Tracy; Arpone, Marta

Subjects: MOSAICISM; FRAGILE X syndrome; AUTISM

• Source: International Journal of Molecular Sciences; Aug2019, Vol. 20 Issue 16, p3907-3907, 1p, 4 Graphs

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

• Authors : Metcalfe, Sylvia A.^1,2 (AUTHOR) ; Hickerton, Chriselle² (AUTHOR); Savard, Jacqueline^1,3,4 (AUTHOR)

Subjects: *INTERNET forums; *CONFORMANCE testing; *DOWNLOADINGAUSTRALIA

• Source: European Journal of Medical Genetics. May2019, Vol. 62 Issue 5, p290-299. 10p.

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Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X.

• Authors : Arpone M; Faculty of Medicine, Dentistry and Health Sciences, Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia. .; Cyto-Molecular Diagnostics Research, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia. .

Subjects: DNA Methylation/DNA Methylation/DNA Methylation/*genetics ; Epithelial Cells/Epithelial Cells/Epithelial Cells/*metabolism; Adolescent

• Source: Scientific reports [Sci Rep] 2018 Feb 26; Vol. 8 (1), pp. 3644. Date of Electronic Publication: 2018 Feb 26.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing.

• Authors : Gray K; The University of Melbourne, VIC Australia.; Stephen R

Subjects: Consumer Health Informatics* ; Consumer Health Information* ; Direct-To-Consumer Screening and Testing*

• Source: Studies in health technology and informatics [Stud Health Technol Inform] 2017; Vol. 245, pp. 89-93.Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9214582 Publication Model: Print Cited Medium: Internet ISSN: 1879-8365

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