Staff profile
Overview
https://apps.dur.ac.uk/biography/image/4149
Johanna Thren
PDRA
BA, MSc, PhD, FHEA
| Affiliation |
|---|
| PDRA in the Department of Anthropology |
| Post Doctoral Research Associate in the Department of Anthropology |
Research interests
- - Patient and public involvement and engagement
- - The relationship between physical activity, identity and wellbeing
- - Kinship, ritual, grief and loss
- - Developmental evaluation and contribution analysis
- - Research governance and culture
Esteem Indicators
- 2023: Sutasoma Award: The Sutasoma Award was awarded by the Trustees of the Radcliffe-Brown Fund in recognition of research of potentially outstanding merit.
Publications
Journal Article
- Organ donation for research purposes: a qualitative focus group study on the views of donor families, transplant recipients and heart failure patients in the UK.Louca, J. O., Asemota, N., Thren, J., Manara, A., Bhagra, S., Wang, L., Bargehr, J., Burton, N., Burton, S., Rockell, K., Nuñes, J. P., White, P., Berman, M., Pettit, S., Rubino, A., Reyahi, A., Large, S., Sinha, S., Wilson, C., … Wilson, C. (2025). Organ donation for research purposes: a qualitative focus group study on the views of donor families, transplant recipients and heart failure patients in the UK. BMJ Open, 15(12), Article e107992. https://doi.org/10.1136/bmjopen-2025-107992
- NGS-Panel Diagnosis Developed for the Differential Diagnosis of Idiopathic Toe Walking and Its Application for the Investigation of Possible Genetic Causes for the Gait AnomalyPomarino, D., Emelina, A., Heidrich, J., Rostásy, K., Schirmer, S., Schönfeldt, J. O., Thren, A., Wagner, F., Thren, J. R., & Berger, N. (2023). NGS-Panel Diagnosis Developed for the Differential Diagnosis of Idiopathic Toe Walking and Its Application for the Investigation of Possible Genetic Causes for the Gait Anomaly. Global Medical Genetics, 10(02), 063-071. https://doi.org/10.1055/s-0043-57230
- Toe Walking as the Initial Symptom of a Spinocerebellar Ataxia 13 in a Patient Presenting with a Mutation in the KCNC3 GenePomarino, D., Thren, J. R., Thren, A., Rostasy, K., & Schoenfeldt, J. (2022). Toe Walking as the Initial Symptom of a Spinocerebellar Ataxia 13 in a Patient Presenting with a Mutation in the KCNC3 Gene. Global Medical Genetics, 9(1), 51-53. https://doi.org/10.1055/s-0041-1736483