| Pulsed radiofrequency in interventional pain management: cellular and molecular mechanisms of action–an update and review S Jordan, M Catapano, S Sahni, F Ma, A Abd-Elsayed, O Visnjevac Pain Physician 24 (8), 525, 2021 | 45 | 2021 |
| 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 | 16 | 2022 |
| “Doctors shouldn’t have to cheat the system”: Clinicians’ real-world experiences of the utility of genomic sequencing S Shickh, C Mighton, M Clausen, E Adi-Wauran, D Hirjikaka, R Kodida, ... Genetics in Medicine 24 (9), 1888-1898, 2022 | 6 | 2022 |
| Clinical Radiofrequency Ablation Outcomes of Combined Sensory Nerve Branch and Dorsal Entry Root Zone Complex Lesions for Sacroiliac Joint Complex Pain J Sam, M Pastrak, L Duda, N Vladicic, B Vrooman, F Ma, F Khandwalla, ... Advances in Therapy 39 (8), 3539-3546, 2022 | 5 | 2022 |
| Review of opioid sparing interventional pain management options and techniques for radiofrequency ablations for sacroiliac joint pain M Pastrak, N Vladicic, J Sam, B Vrooman, F Ma, A Mahmoud, JS Khan, ... Current Pain and Headache Reports 26 (11), 855-862, 2022 | 3 | 2022 |
| A model for the return and referral of all clinically significant secondary findings of genomic sequencing R Kodida, E Reble, M Clausen, S Shickh, C Mighton, J Sam, N Forster, ... Journal of Medical Genetics 60 (8), 733-739, 2023 | 2 | 2023 |
| “I just wanted more”: Hereditary cancer syndromes patients’ perspectives on the utility of circulating tumour DNA testing for cancer screening Y Bombard, E Adi-Wauran, M Clausen, S Shickh, A Gagliardi, A Denburg, ... | 2 | 2023 |
| P409: clinical utility of genomic sequencing for hereditary cancer syndromes: an observational chart review S Shickh, C Mighton, M Clausen, R Kodida, J Sam, D Hirjikaka, E Reble, ... Genetics in Medicine Open 1 (1), 2023 | 1 | 2023 |
| A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings J Sam, E Reble, R Kodida, A Shaw, M Clausen, MG Salazar, S Shickh, ... Human Genetics 141 (12), 1875-1885, 2022 | 1 | 2022 |
| “I just wanted more”: Hereditary cancer syndromes patients’ perspectives on the utility of circulating tumour DNA testing for cancer screening E Adi-Wauran, M Clausen, S Shickh, AR Gagliardi, A Denburg, ... European Journal of Human Genetics 32 (2), 176-181, 2024 | | 2024 |
| Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing. M Clausen, S Krishnapillai, D Hirjikaka, R Kodida, S Shickh, E Reble, ... Genetics in Medicine Open, 101814, 2024 | | 2024 |
| P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT Y Bombard, C Mighton, S Shickh, M Clausen, R Kodida, E Reble, J Sam, ... Genetics in Medicine Open 2, 101422, 2024 | | 2024 |
| P881: Revealing the hidden costs: Exploring the financial toxicity of hereditary cancer syndromes S Rajeziesfahani, J Sam, C Butkowsky, E Reble, M Clausen, B Sparkes, ... Genetics in Medicine Open 2, 2024 | | 2024 |
| P555: Clinical utility returning of all types of medically relevant genomic sequencing findings: An observational study C Mighton, R Kodida, S Shickh, M Clausen, E Reble, J Sam, S Grewal, ... Genetics in Medicine Open 2, 101454, 2024 | | 2024 |
| P553: How do patients with hereditary cancer syndromes navigate the healthcare system? A qualitative comparative study across Canada C Butkowsky, J Sam, E Reble, M Clausen, S Rajeziesfahani, B Sparkes, ... Genetics in Medicine Open 2, 2024 | | 2024 |
| P892:“Should I let them know I have this?”: Concerns and experiences of genetic discrimination amongst individuals with hereditary cancer syndromes R Gopalakrishnan, E Reble, J Sam, C Butkowsky, M Clausen, ... Genetics in Medicine Open 2, 2024 | | 2024 |
| P867:“I worry I don’t have control”: The psychosocial impacts of living with a hereditary cancer syndrome J Sam, B Sparkes, M Clausen, C Butkowsky, E Reble, S Rajeziesfahani, ... Genetics in Medicine Open 2, 2024 | | 2024 |
| P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results S Shickh, R Kodida, C Mighton, M Clausen, E Reble, J Sam, S Grewal, ... Genetics in Medicine Open 2, 2024 | | 2024 |
| “I don’t need any more unknowns hanging over my head”: Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing S Shickh, C Mighton, M Clausen, R Kodida, E Adi-Wauran, D Hirjikaka, ... Genetics in Medicine 25 (12), 100960, 2023 | | 2023 |
| Sunlight on First Snow S Shickh, C Mighton, M Clausen, R Kodida, E Adi-Wauran, D Hirjikaka, ... | | 2023 |
