| The clinical utility of exome and genome sequencing across clinical indications: a systematic review S Shickh, C Mighton, E Uleryk, P Pechlivanoglou, Y Bombard Human genetics 140, 1403-1416, 2021 | 78 | 2021 |
| Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis C Mighton, S Shickh, E Uleryk, P Pechlivanoglou, Y Bombard Genetics in Medicine 23 (1), 22-33, 2021 | 68 | 2021 |
| Variant classification changes over time in BRCA1 and BRCA2 C Mighton, GS Charames, M Wang, KR Zakoor, A Wong, S Shickh, ... Genetics in Medicine 21 (10), 2248-2254, 2019 | 63 | 2019 |
| Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial Y Bombard, M Clausen, S Shickh, C Mighton, S Casalino, THM Kim, ... Genetics in Medicine 22 (4), 727-735, 2020 | 49 | 2020 |
| Patient-facing digital tools for delivering genetic services: a systematic review W Lee, S Shickh, D Assamad, S Luca, M Clausen, C Somerville, A Tafler, ... Journal of medical genetics 60 (1), 1-10, 2023 | 41 | 2023 |
| The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care S Shickh, SA Rafferty, M Clausen, R Kodida, C Mighton, S Panchal, ... Genetics in Medicine 23 (6), 1086-1094, 2021 | 41 | 2021 |
| Quality of life drives patients’ preferences for secondary findings from genomic sequencing C Mighton, L Carlsson, M Clausen, S Casalino, S Shickh, L McCuaig, ... European Journal of Human Genetics 28 (9), 1178-1186, 2020 | 29 | 2020 |
| Development of patient “profiles” to tailor counseling for incidental genomic sequencing results C Mighton, L Carlsson, M Clausen, S Casalino, S Shickh, L McCuaig, ... European Journal of Human Genetics 27 (7), 1008-1017, 2019 | 29 | 2019 |
| Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study S Shickh, MG Salazar, KR Zakoor, C Lázaro, J Gu, J Goltz, D Kleinman, ... Journal of medical genetics 58 (4), 275-283, 2021 | 25 | 2021 |
| Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial S Shickh, M Clausen, C Mighton, S Casalino, E Joshi, E Glogowski, ... BMJ open 8 (4), e021876, 2022 | 23 | 2022 |
| Genetics adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery S Shickh, D Hirjikaka, M Clausen, R Kodida, C Mighton, E Reble, J Sam, ... BMJ open 12 (4), e060899, 2022 | 22 | 2022 |
| Effect of genetics clinical decision support tools on health-care providers’ decision making: a mixed-methods systematic review A Sebastian, JC Carroll, LE Oldfield, C Mighton, S Shickh, E Uleryk, ... Genetics in Medicine 23 (4), 593-602, 2021 | 22 | 2021 |
| Shared decision making in the care of patients with cancer S Shickh, K Leventakos, MA Lewis, Y Bombard, VM Montori American Society of Clinical Oncology Educational Book 43, e389516, 2023 | 21 | 2023 |
| Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings E Reble, M Gutierrez Salazar, KR Zakoor, S Khalouei, M Clausen, ... Human Genetics 140, 493-504, 2021 | 17 | 2021 |
| From the patient to the population: use of genomics for population screening C Mighton, S Shickh, V Aguda, S Krishnapillai, E Adi-Wauran, Y Bombard Frontiers in Genetics 13, 893832, 2022 | 16 | 2022 |
| Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial S Shickh, M Clausen, C Mighton, MG Salazar, KR Zakoor, R Kodida, ... BMJ open 9 (10), e031092, 2019 | 15 | 2019 |
| Widening the lens of actionability: a qualitative study of primary care providers’ views and experiences of managing secondary genomic findings A Sebastian, JC Carroll, M Vanstone, M Clausen, R Kodida, E Reble, ... European Journal of Human Genetics 30 (5), 595-603, 2022 | 14 | 2022 |
| “Game changer”: health professionals’ views on the clinical utility of circulating tumor DNA testing in hereditary cancer syndrome management S Shickh, LE Oldfield, M Clausen, C Mighton, A Sebastian, A Calvo, ... The Oncologist 27 (5), e393-e401, 2022 | 12 | 2022 |
| c. 1289G> A (p. Arg430His) variant in the epsilon isoform of the GFAP gene in a patient with adult onset Alexander disease N Karp, D Lee, S Shickh, ME Jenkins European Journal of Medical Genetics 62 (4), 235-238, 2019 | 11 | 2019 |
| Patient and public preferences for being recontacted with updated genomic results: a mixed methods study C Mighton, M Clausen, A Sebastian, SM Muir, S Shickh, NN Baxter, ... Human Genetics 140, 1695-1708, 2021 | 9 | 2021 |
