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101 results for Gaff,+Clara

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Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery
Author / Creator:Lynch, Fiona ; Nisselle, Amy ; Stark, Zornitza ; Gaff, Clara L ; McClaren, Belinda
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2022-11, Vol.30 (11), p.1276-1282
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Parents’ experiences of decision making for rapid genomic sequencing in intensive care
Author / Creator:Lynch, Fiona ; Nisselle Amy ; Stark Zornitza ; Gaff, Clara L ; McClaren Belinda
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2021-12, Vol.29 (12), p.1804-1810
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Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness
Author / Creator:Stark, Zornitza ; Schofield, Deborah ; Martyn, Melissa ; Rynehart, Luke ; Shrestha, Rupendra ; Alam, Khurshid ; Lunke, Sebastian ; Tan, Tiong Y. ; Gaff, Clara L. ; White, Susan M.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2019-01, Vol.21 (1), p.173-180
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Meeting the challenges of implementing rapid genomic testing in acute pediatric care
Author / Creator:Stark, Zornitza ; Lunke, Sebastian ; Brett, Gemma R. ; Tan, Natalie B. ; Stapleton, Rachel ; Kumble, Smitha ; Yeung, Alison ; Phelan, Dean G. ; Chong, Belinda ; Fanjul-Fernandez, Miriam ; Marum, Justine E. ; Hunter, Matthew ; Jarmolowicz, Anna ; Prawer, Yael ; Riseley, Jessica R. ; Regan, Matthew ; Elliott, Justine ; Martyn, Melissa ; Best, Stephanie ; Tan, Tiong Y. ; Gaff, Clara L. ; White, Susan M.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2018-12, Vol.20 (12), p.1554-1563
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Clinical impact of genomic testing in patients with suspected monogenic kidney disease
Author / Creator:Jayasinghe, Kushani ; Stark, Zornitza ; Kerr, Peter G. ; Gaff, Clara ; Martyn, Melissa ; Whitlam, John ; Creighton, Belinda ; Donaldson, Elizabeth ; Hunter, Matthew ; Jarmolowicz, Anna ; Johnstone, Lilian ; Krzesinski, Emma ; Lunke, Sebastian ; Lynch, Elly ; Nicholls, Kathleen ; Patel, Chirag ; Prawer, Yael ; Ryan, Jessica ; See, Emily J. ; Talbot, Andrew ; Trainer, Alison ; Tytherleigh, Rigan ; Valente, Giulia ; Wallis, Mathew ; Wardrop, Louise ; West, Kirsty H. ; White, Susan M. ; Wilkins, Ella ; Mallett, Andrew J. ; Quinlan, Catherine
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2021-01, Vol.23 (1), p.183-191
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Known unknowns: building an ethics of uncertainty into genomic medicine
Author / Creator:Newson, Ainsley J. ; Leonard, Samantha J. ; Hall, Alison ; Gaff, Clara L.
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2016-09, Vol.9 (1), p.57, Article 57
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How can a community of practice support healthcare professionals navigating new roles? a case study of genetic counsellors employed to work in medical specialities
Author / Creator:Do, Trang Thu ; McEwen, Alison ; Martyn, Melissa ; Gaff, Clara ; Dawson-McClaren, Belinda
Publisher:England: BioMed Central Ltd
Journal title:BMC health services research, 2025-02, Vol.25 (1), p.314-11, Article 314
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Carrier screening for Beta-thalassaemia: a review of international practice
Author / Creator:Cousens, Nicole E ; Gaff, Clara L ; Metcalfe, Sylvia A ; Delatycki, Martin B
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2010-10, Vol.18 (10), p.1077-1083
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The leadership behaviors needed to implement clinical genomics at scale: a qualitative study
Author / Creator:Best, Stephanie ; Stark, Zornitza ; Brown, Helen ; Long, Janet C. ; Hewage, Kushani ; Gaff, Clara ; Braithwaite, Jeffrey ; Taylor, Natalie
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2020-08, Vol.22 (8), p.1384-1390
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Exome sequencing in infants with congenital hearing impairment: a population-based cohort study
Author / Creator:Downie, Lilian ; Halliday, Jane ; Burt, Rachel ; Lunke Sebastian ; Lynch, Elly ; Martyn, Melissa ; Poulakis Zeffie ; Gaff Clara ; Sung, Valerie ; Wake, Melissa ; Hunter, Matthew F ; Saunders, Kerryn ; Rose, Elizabeth ; Lewis, Sharon ; Jarmolowicz Anna ; Phelan, Dean ; Rehm, Heidi L ; Amor, David J
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2020-05, Vol.28 (5), p.587-596
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Return of individual research results from genomic research: A systematic review of stakeholder perspectives
Author / Creator:Vears, Danya F. ; Minion, Joel T. ; Roberts, Stephanie J. ; Cummings, James ; Machirori, Mavis ; Blell, Mwenza ; Budin-Ljøsne, Isabelle ; Cowley, Lorraine ; Dyke, Stephanie O. M. ; Gaff, Clara ; Green, Robert ; Hall, Alison ; Johns, Amber L. ; Knoppers, Bartha M. ; Mulrine, Stephanie ; Patch, Christine ; Winkler, Eva ; Murtagh, Madeleine J.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2021-11, Vol.16 (11), p.e0258646
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A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis
Author / Creator:Tiong Yang Tan ; Lunke, Sebastian ; Chong, Belinda ; Phelan, Dean ; Fanjul-Fernandez, Miriam ; Marum, Justine E ; Vanessa Siva Kumar ; Stark, Zornitza ; Yeung, Alison ; Brown, Natasha J ; Stutterd, Chloe ; Delatycki, Martin B ; Sadedin, Simon ; Martyn, Melissa ; Goranitis, Ilias ; Thorne, Natalie ; Gaff, Clara L ; White, Susan M
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2019-12, Vol.27 (12), p.1791-1799
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Measuring physician practice, preparedness and preferences for genomic medicine: a national survey
Author / Creator:Nisselle, Amy ; King, Emily A ; McClaren, Belinda ; Janinski, Monika ; Metcalfe, Sylvia ; Gaff, Clara ; Dunlop, Kate ; Graves, Debra ; Terrill, Bronwyn
Publisher:London: British Medical Journal Publishing Group
Journal title:BMJ open, 2021-07, Vol.11 (7), p.e044408
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Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care
Author / Creator:Stark Zornitza ; Nisselle Amy ; McClaren Belinda ; Lynch, Fiona ; Best, Stephanie ; Long, Janet C ; Martyn, Melissa ; Patel, Chirag ; Schlapbach, Luregn J ; Barnett, Christopher ; Theda Christiane ; Pinner, Jason ; Dinger, Marcel E ; Lunke Sebastian ; Gaff, Clara L
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2019-10, Vol.27 (10), p.1493-1501
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Evaluating the resource implications of different service delivery models for offering additional genomic findings
Author / Creator:Vu, Martin ; Degeling, Koen ; Martyn, Melissa ; Lynch, Elly ; Chong, Belinda ; Gaff, Clara ; IJzerman, Maarten J.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2021-04, Vol.23 (4), p.606-613
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Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics)
Author / Creator:Nisselle, Amy ; Janinski, Monika ; Martyn, Melissa ; McClaren, Belinda ; Kaunein, Nadia ; Maguire, Jane ; Riggs, Erin Rooney ; Barlow-Stewart, Kristine ; Belcher, Andrea ; Bernat, John A. ; Best, Stephanie ; Bishop, Michelle ; Carroll, June C. ; Cornel, Martina ; Dissanayake, Vajira H.W. ; Dodds, Agnes ; Dunlop, Kate ; Garg, Gunjan ; Gear, Russell ; Graves, Debra ; Knight, Ken ; Korf, Bruce ; Kumar, Dhavendra ; Laurino, Mercy ; Ma, Alan ; Mallett, Andrew ; McCarthy, Maria ; McEwen, Alison ; Mulder, Nicola ; Patel, Chirag ; Quinlan, Catherine ; Reed, Kate ; Sinnerbrink, Ingrid ; Slavotinek, Anne ; Suppiah, Vijayaprakash ; Terrill, Bronwyn ; Tobias, Edward S. ; Tonkin, Emma ; Trumble, Steve ; Wessels, Tina-Marie ; Metcalfe, Sylvia ; Jordan, Helen ; Gaff, Clara
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2021-07, Vol.23 (7), p.1356-1365
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Aligning intuition and theory: a novel approach to identifying the determinants of behaviours necessary to support implementation of evidence into practice
Author / Creator:Taylor, Natalie ; McKay, Skye ; Long, Janet C. ; Gaff, Clara ; North, Kathryn ; Braithwaite, Jeffrey ; Francis, Jill J. ; Best, Stephanie
Publisher:England: BioMed Central Ltd
Journal title:Implementation science : IS, 2023-07, Vol.18 (1), p.29-17, Article 29
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Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol
Author / Creator:Bouffler, Sophie E ; Lee, Ling ; Lynch, Fiona ; Martyn, Melissa ; Lynch, Elly ; Macciocca, Ivan ; Curnow, Lisette ; McCorkell, Giulia ; Lunke, Sebastian ; Chong, Belinda ; Marum, Justine E ; Delatycki, Martin ; Downie, Lilian ; Goranitis, Ilias ; Vears, Danya F ; Best, Stephanie ; Clausen, Marc ; Bombard, Yvonne ; Stark, Zornitza ; Gaff, Clara L
Publisher:England: British Medical Journal Publishing Group
Journal title:BMJ open, 2023-06, Vol.13 (6), p.e072999
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Process and outcome in communication of genetic information within families: a systematic review
Author / Creator:Gaff, Clara L ; Clarke, Angus J ; Atkinson, Paul ; Sivell, Stephanie ; Elwyn, Glyn ; Iredale, Rachel ; Thornton, Hazel ; Dundon, Joanna ; Shaw, Chris ; Edwards, Adrian
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2007-10, Vol.15 (10), p.999-1011
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A cost-effectiveness analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients
Author / Creator:Yeung, Alison ; Tan, Natalie B. ; Tan, Tiong Y. ; Stark, Zornitza ; Brown, Natasha ; Hunter, Matthew F. ; Delatycki, Martin ; Stutterd, Chloe ; Savarirayan, Ravi ; Mcgillivray, George ; Stapleton, Rachel ; Kumble, Smitha ; Downie, Lilian ; Regan, Matthew ; Lunke, Sebastian ; Chong, Belinda ; Phelan, Dean ; Brett, Gemma R. ; Jarmolowicz, Anna ; Prawer, Yael ; Valente, Giulia ; Smagarinsky, Yana ; Martyn, Melissa ; McEwan, Callum ; Goranitis, Ilias ; Gaff, Clara ; White, Susan M.
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2020-12, Vol.22 (12), p.1986-1993
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Showing 1 to 20 of 101 results

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Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery

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Parents’ experiences of decision making for rapid genomic sequencing in intensive care

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Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness

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Meeting the challenges of implementing rapid genomic testing in acute pediatric care

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Clinical impact of genomic testing in patients with suspected monogenic kidney disease

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Known unknowns: building an ethics of uncertainty into genomic medicine

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How can a community of practice support healthcare professionals navigating new roles? a case study of genetic counsellors employed to work in medical specialities

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Carrier screening for Beta-thalassaemia: a review of international practice

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The leadership behaviors needed to implement clinical genomics at scale: a qualitative study

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Exome sequencing in infants with congenital hearing impairment: a population-based cohort study

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Return of individual research results from genomic research: A systematic review of stakeholder perspectives

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A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis

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Measuring physician practice, preparedness and preferences for genomic medicine: a national survey

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Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care

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Evaluating the resource implications of different service delivery models for offering additional genomic findings

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Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics)

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Aligning intuition and theory: a novel approach to identifying the determinants of behaviours necessary to support implementation of evidence into practice

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Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol

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Process and outcome in communication of genetic information within families: a systematic review

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A cost-effectiveness analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients

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