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Author Details

June C Carroll
University of Toronto
1986
150
29
Vardit Ravitsky (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37217257A model for the return and referral of all clinically significant secondary findings of genomic sequencing.J Med Genet2023
37217337Patient-Guided Tours: A Patient-Centered Methodology to Understand Patient Experiences of Health Care.Ann Fam Med2023
34768014Challenges and practical solutions for managing secondary genomic findings in primary care.Eur J Med Genet2022
35739291A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings.Hum Genet2022
35760333Psychological Distress and Behavioural Changes in Pregnant and Postpartum Individuals During the COVID-19 Pandemic.J Obstet Gynaecol Can2022
35487723Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery.BMJ Open2022
35947109Use of eConsult to enhance genetics service delivery in primary care: A multimethod study.Genet Med2022
33776058Widening the lens of actionability: A qualitative study of primary care providers' views and experiences of managing secondary genomic findings.Eur J Hum Genet2022
33420345Effect of genetics clinical decision support tools on health-care providers' decision making: a mixed-methods systematic review.Genet Med2021
34972506Pregnant during the COVID-19 pandemic: an exploration of patients' lived experiences.BMC Pregnancy Childbirth2021
34587266A Master Class in Family Doctor Leadership: Evaluating an Innovative Program.Fam Med2021
34379295Anticipating the primary care role in genomic medicine: expectations of genetics health professionals.J Community Genet2021
34127476Newborn screening for cystic fibrosis: Role of primary care providers in caring for infants with positive screening results.Can Fam Physician2021
34127469Primary care providers' role in newborn screening result notification for cystic fibrosis.Can Fam Physician2021
34261715Experiences of patients with a disability in receiving primary health care: Using experience-based design for quality improvement.Can Fam Physician2021
32857771Nicotine dependence as a risk factor for upper aerodigestive tract (UADT) cancers: A mediation analysis.PLoS One2020
32008974Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions in Average-Risk Pregnancies: A Cost-Effectiveness Analysis.J Obstet Gynaecol Can2020
33117641Hereditary colorectal cancer screening: A 10-year longitudinal cohort study following an educational intervention.Prev Med Rep2020
29700759Primary care providers' lived experiences of genetics in practice.J Community Genet2019
31661705Family History Taking in Pediatric Practice: A Qualitative Interview Study.Public Health Genomics2019
31824576Informing Integration of Genomic Medicine Into Primary Care: An Assessment of Current Practice, Attitudes, and Desired Resources.Front Genet2019
30059977Mendelian Randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers.Int J Epidemiol2019
31185964Bridging the gap in genetics: a progressive model for primary to specialist care.BMC Med Educ2019
31594892Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.BMJ Open2019
30349099A framework to build capacity for a reflex-testing program for Lynch syndrome.Genet Med2019
30580830Fetal Exome Sequencing on the Horizon.J Obstet Gynaecol Can2019
29368425Genetic assessment wait time indicators in the High Risk Ontario Breast Screening Program.Mol Genet Genomic Med2018
29700101Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.BMJ Open2018
27711070Universal tumor screening for Lynch syndrome: health-care providers' perspectives.Genet Med2017
28279431Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis.J Pediatr2017
28115461Assessing family history of chronic disease in primary care: Prevalence, documentation, and appropriate screening.Can Fam Physician2017
28490923Multigene expression profile testing in breast cancer: is there a role for family physicians?Curr Oncol2017
29025964False-Positive Newborn Screening for Cystic Fibrosis and Health Care Use.Pediatrics2017
28633170Teaching Primary Care Genetics: A Randomized Controlled Trial Comparison.Fam Med2017
27608173A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis.Genet Med2017
27244855Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options.Pediatrics2016
27737998Primary care providers' experiences with and perceptions of personalized genomic medicine.Can Fam Physician2016
27737996Coordination of cancer care between family physicians and cancer specialists: Importance of communication.Can Fam Physician2016
27737991Identification et prise en charge des femmes ayant des antécédents familiaux de cancer du sein: Guide pratique à l⿿intention des médecins.Can Fam Physician2016
27737982Patients' experiences with continuity of cancer care in Canada: Results from the CanIMPACT study.Can Fam Physician2016
27737975Identification and management of women with a family history of breast cancer: Practical guide for clinicians.Can Fam Physician2016
27638987Joint SOGC-CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing.J Obstet Gynaecol Can2016
27583994The Gene Messenger Impact Project: An Innovative Genetics Continuing Education Strategy for Primary Care Providers.J Contin Educ Health Prof2016
27331228Academic family health teams: Part 1: patient perceptions of core primary care domains.Can Fam Physician2016
27331229Academic family health teams: Part 2: patient perceptions of access.Can Fam Physician2016
27329737Supporting genetics in primary care: investigating how theory can inform professional education.Eur J Hum Genet2016
27215612Attitudes to incorporating genomic risk assessments into population screening programs: the importance of purpose, context and deliberation.BMC Med Genomics2016
27485696Parent Experience With False-Positive Newborn Screening Results for Cystic Fibrosis.Pediatrics2016
23369110Expectations and values about expanded newborn screening: a public engagement study.Health Expect2015
26238338Developing clinical decision tools to implement chronic disease prevention and screening in primary care: the BETTER 2 program (building on existing tools to improve chronic disease prevention and screening in primary care).Implement Sci2015
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Collaborators

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Co-authored papers 25
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Co-authored papers 6
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Co-authored papers 6
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Co-authored papers 5
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Co-authored papers 5
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Co-authored papers 3
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Co-authored papers 3
Universite Laval
Co-authored papers 3
The Hospital for Sick Children
Co-authored papers 2
Mayo Clinic
Co-authored papers 2
The Princess Margaret Cancer Centre/University of Toronto
Co-authored papers 2
Lunenfeld-Tanenbaum Research Institute
Co-authored papers 2
Memorial University
Co-authored papers 2
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Co-authored papers 2
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Co-authored papers 2
CHU de Quebec-Universite Laval Research Center
Co-authored papers 2
Co-authored papers 1
Princess Margaret Cancer Centre
Co-authored papers 1
Co-authored papers 1
Arizona State University.
Co-authored papers 1
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Center for Biomedical Ethics, Stanford University School of Medicine
Co-authored papers 1
Health Services Research Unit, University of Aberdeen
Co-authored papers 1
The Hastings Center
Co-authored papers 1
McGill University.
Co-authored papers 1
The First Hospital of Lanzhou University
Co-authored papers 1
and Translational Research Center
Co-authored papers 1
Princess Margaret Cancer Centre, University Health Network, University of Toronto
Co-authored papers 1
University of Liverpool, Molecular & Clinical Cancer Medicine
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