日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Young people's experience of predictive genetic testing for inherited cardiac conditions: a qualitative study

年轻人对遗传性心脏病预测基因检测的体验：一项定性研究

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-025-01988-6
Mulhern, Sarah; Morrish, Ansley M; Connell, Vanessa; Hickerton, Chriselle; Macciocca, Ivan
心脏病
心血管
发表日期：2026
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The expectations and realities of nutrigenomic testing in australia: A qualitative study

澳大利亚营养基因组学检测的期望与现实：一项定性研究

期刊:Health Expectations
影响因子:3.2
doi:10.1111/hex.13216
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
发表日期：2021
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Australians' views and experience of personal genomic testing: survey findings from the Genioz study

澳大利亚人对个人基因组检测的看法和体验：Genioz 研究的调查结果

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-018-0325-x
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
发表日期：2019
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Australians' views on personal genomic testing: focus group findings from the Genioz study

澳大利亚人对个人基因组检测的看法：Genioz 研究的焦点小组调查结果

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-018-0151-1
Metcalfe, Sylvia A; Hickerton, Chriselle; Savard, Jacqueline; Terrill, Bronwyn; Turbitt, Erin; Gaff, Clara; Gray, Kathleen; Middleton, Anna; Wilson, Brenda; Newson, Ainsley J
发表日期：2018
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Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes

探索澳大利亚一组患有普拉德-威利综合征和安格曼综合征的患者的自闭症症状

期刊:Journal of Neurodevelopmental Disorders
影响因子:4
doi:10.1186/s11689-018-9242-0
Baker, Emma K; Godler, David E; Bui, Minh; Hickerton, Chriselle; Rogers, Carolyn; Field, Mike; Amor, David J; Bretherton, Lesley
自闭症
神经科学
发表日期：2018
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Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X

脆性X染色体综合征男性儿童队列中颊上皮细胞内基因DNA甲基化与智力功能的关系

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-018-21990-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
上皮细胞
细胞生物学
表观遗传
DNA甲基化
发表日期：2018
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A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy

采用混合方法探索家庭对儿童脊髓性肌萎缩症诊断的经历

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/ejhg.2014.147
Lawton, Sally; Hickerton, Chriselle; Archibald, Alison D; McClaren, Belinda J; Metcalfe, Sylvia A
神经科学
肌萎缩症
发表日期：2015
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ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible

ironXS：高中阶段开展遗传性血色素沉着症筛查是可接受且可行的。

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/ejhg.2011.247
Delatycki, Martin B; Wolthuizen, Michelle; Collins, Veronica; Varley, Elizabeth; Craven, Joanna; Allen, Katrina J; Gurrin, Lyle C; Aitken, Maryanne; Trembath, M Kaye; Bond, Lyndal; Wilson, Gabrielle R; Stephenson, Sarah E M; Macciocca, Ivan; Hickerton, Chriselle; Lockhart, Paul J; Metcalfe, Sylvia A
发表日期：2012
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