Yvonne Bombard
机构: Associate Professor & Scientist, University of Toronto & Li Ka Shing Knowledge Institute of St
每年引用次数
引用次数
引用: 5,352
H-指数: 34
I10-指数 : 80
出版物: 208
“I just wanted more”: Hereditary cancer syndromes patients’ perspectives on the utility of circulating tumour DNA testing for cancer screening
Yvonne Bombard , Ella Adi-Wauran , Marc Clausen , Salma Shickh
2
2023
Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial.
Yvonne Bombard , Marc Clausen , Salma Shickh , Chloe Mighton
Genetics in Medicine
43
2019
Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial
Salma Shickh , Marc Clausen , Chloe Mighton , Selina Casalino
BMJ open 8 ( 4) e021876 -e021876
23
2022
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery
Salma Shickh , Daena Hirjikaka , Marc Clausen , Rita Kodida
BMJ open 12 ( 4) e060899 -e060899
16
2022
Patient and public preferences for being recontacted with updated genomic results: a mixed methods study
Chloe Mighton , Marc Clausen , Agnes Sebastian , Sarah M Muir
Human Genetics 140 1695 -1708
5
2021
How do members of the public expect to use variants of uncertain significance in their health care? A population-based survey
Chloe Mighton , Marc Clausen , Salma Shickh , Nancy N Baxter
Genetics in Medicine 25 ( 5) 100819 -100819
1
2023
P409: clinical utility of genomic sequencing for hereditary cancer syndromes: an observational chart review
Salma Shickh , Chloe Mighton , Marc Clausen , Rita Kodida
Genetics in Medicine Open 1 ( 1)
1
2023
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings
Jordan Sam , Emma Reble , Rita Kodida , Angela Shaw
Human Genetics 141 ( 12) 1875 -1885
1
2022
Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing.
Marc Clausen , Suvetha Krishnapillai , Daena Hirjikaka , Rita Kodida
Genetics in Medicine Open 101814 -101814
2024
P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT
Yvonne Bombard , Chloe Mighton , Salma Shickh , Marc Clausen
Genetics in Medicine Open 2 101422 -101422
2024
P881: Revealing the hidden costs: Exploring the financial toxicity of hereditary cancer syndromes
Sepideh Rajeziesfahani , Jordan Sam , Carly Butkowsky , Emma Reble
Genetics in Medicine Open 2
2024
P555: Clinical utility returning of all types of medically relevant genomic sequencing findings: An observational study
Chloe Mighton , Rita Kodida , Salma Shickh , Marc Clausen
Genetics in Medicine Open 2 101454 -101454
2024
P553: How do patients with hereditary cancer syndromes navigate the healthcare system? A qualitative comparative study across Canada
Carly Butkowsky , Jordan Sam , Emma Reble , Marc Clausen
Genetics in Medicine Open 2
2024
P892:“Should I let them know I have this?”: Concerns and experiences of genetic discrimination amongst individuals with hereditary cancer syndromes
Ridhi Gopalakrishnan , Emma Reble , Jordan Sam , Carly Butkowsky
Genetics in Medicine Open 2
2024
P867:“I worry I don’t have control”: The psychosocial impacts of living with a hereditary cancer syndrome
Jordan Sam , Brooklyn Sparkes , Marc Clausen , Carly Butkowsky
Genetics in Medicine Open 2
2024
P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results
Salma Shickh , Rita Kodida , Chloe Mighton , Marc Clausen
Genetics in Medicine Open 2
2024
P406: Partnering with patients to explore the psychosocial and socioeconomic impacts of hereditary cancer syndromes
Jordan Sam , Holly Etchegary , Marc Clausen , Derrick Bishop
Genetics in Medicine Open 1 ( 1)
2023
P375: Fragmented systems of care: An overview of Canadian health system care models for hereditary cancer syndromes
Jordan Sam , Carly Butkowsky , Marc Clausen , Chloe Mighton
Genetics in Medicine Open 1 ( 1)
2023
P382: Professionals’ perspectives on the use of digital tools to support patient recontact in clinical genetics
Guylaine D'Amours , Emma Reble , Vernie Aguda , Marc Clausen
Genetics in Medicine Open 1 ( 1)
2023
eP502: How will returning variants of uncertain significance impact healthcare use? A cross-sectional survey
Chloe Mighton , Marc Clausen , Agnes Sebastian , Sarah Muir
Genetics in Medicine 24 ( 3) S319 -S320
2022