| Using grounded theory method to capture and analyze health care experiences G Foley, V Timonen Health services research 50 (4), 1195-1210, 2015 | 600 | 2015 |
| Using grounded theory method to capture and analyze health care experiences G Foley, V Timonen Health services research 50 (4), 1195-1210, 2015 | 600 | 2015 |
| Challenges when using grounded theory: A pragmatic introduction to doing GT research V Timonen, G Foley, C Conlon International journal of qualitative methods 17 (1), 1609406918758086, 2018 | 584 | 2018 |
| Confused about theoretical sampling? Engaging theoretical sampling in diverse grounded theory studies C Conlon, V Timonen, C Elliott-O’Dare, S O’Keeffe, G Foley Qualitative health research 30 (6), 947-959, 2020 | 222 | 2020 |
| Amyotrophic lateral sclerosis: improving care with a multidisciplinary approach A Hogden, G Foley, RD Henderson, N James, SM Aoun Journal of multidisciplinary healthcare, 205-215, 2017 | 162 | 2017 |
| Interviewing as a vehicle for theoretical sampling in grounded theory G Foley, V Timonen, C Conlon, CE O’Dare International Journal of Qualitative Methods 20, 1609406920980957, 2021 | 115 | 2021 |
| Exerting control and adapting to loss in amyotrophic lateral sclerosis G Foley, V Timonen, O Hardiman Social Science & Medicine 101, 113-119, 2014 | 101 | 2014 |
| Perceptions of quality of life in people with ALS: effects of coping and health care G Foley, P O'Mahony, O Hardiman Amyotrophic lateral sclerosis 8 (3), 164-169, 2007 | 90 | 2007 |
| Patients’ perceptions of services and preferences for care in amyotrophic lateral sclerosis: a review G Foley, V Timonen, O Hardiman Amyotrophic Lateral Sclerosis 13 (1), 11-24, 2012 | 77 | 2012 |
| Acceptance and decision making in amyotrophic lateral sclerosis from a life-course perspective G Foley, V Timonen, O Hardiman Qualitative health research 24 (1), 67-77, 2014 | 70 | 2014 |
| “I hate being a burden”: the patient perspective on carer burden in amyotrophic lateral sclerosis G Foley, V Timonen, O Hardiman Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 17 (5-6), 351-357, 2016 | 50 | 2016 |
| Understanding psycho-social processes underpinning engagement with services in motor neurone disease: a qualitative study G Foley, V Timonen, O Hardiman Palliative Medicine 28 (4), 318-325, 2014 | 49 | 2014 |
| Video-based online interviews for palliative care research: A new normal in COVID-19? G Foley Palliative Medicine 35 (3), 625-626, 2021 | 46 | 2021 |
| Experience of services as a key outcome in amyotrophic lateral sclerosis (ALS) care: the case for a better understanding of patient experiences G Foley, V Timonen, O Hardiman American Journal of Hospice and Palliative Medicine® 29 (5), 362-367, 2012 | 38 | 2012 |
| Experience of services as a key outcome in amyotrophic lateral sclerosis (ALS) care: the case for a better understanding of patient experiences G Foley, V Timonen, O Hardiman American Journal of Hospice and Palliative Medicine® 29 (5), 362-367, 2012 | 38 | 2012 |
| Mutual support between patients and family caregivers in palliative care: a systematic review and narrative synthesis R McCauley, R McQuillan, K Ryan, G Foley Palliative Medicine 35 (5), 875-885, 2021 | 34 | 2021 |
| Decision-making among patients and their family in ALS care: a review G Foley, G Hynes Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19 (3-4), 173-193, 2018 | 30 | 2018 |
| Decision-making in palliative care: patient and family caregiver concordance and discordance—systematic review and narrative synthesis SM Symmons, K Ryan, SM Aoun, LE Selman, AN Davies, N Cornally, ... BMJ supportive & palliative care 13 (4), 374-385, 2023 | 25 | 2023 |
| The complexity of care in amyotrophic lateral sclerosis G Foley Amyotrophic Lateral Sclerosis 12 (3), 160, 2011 | 15 | 2011 |
| The supportive relationship between palliative patients and family caregivers G Foley BMJ Supportive & Palliative Care 8 (2), 184-186, 2018 | 13 | 2018 |
