"This graft-vs.-host disease determines my life. That's it."-A qualitative analysis of the experiences and needs of allogenic hematopoietic stem cells transplantation survivors in Germany

- Parisek, Mira, Loss, Julika, Holler, Ernst, Barata, Anna, Weber, Daniela, Edinger, Matthias, Wolff, Daniel, Schoemans, Helene, Herrmann, Anne

A discrete choice experiment to assess cancer patients' preferences for when and how to make treatment decisions

- Herrmann, Anne, Sanson-Fisher, Rob, Hall, Alix, Wall, Laura, Zdenkowski, Nicholas, Waller, Amy

A qualitative study on patients' and their support persons' preferences for receiving one longer consultation or two shorter consultations when being informed about allogeneic hematopoietic stem cell transplantation

- Herrmann, Anne, Holler, Ernst, Edinger, Matthias, Eickmann, Sascha, Wolff, Daniel

Assessing patients' experiences of cancer care across the treatment pathway: a mapping review of recent psychosocial cancer care publications

- Sanson-Fisher, Rob, Fakes, Kristy, Waller, Amy, Mackenzie, Lisa, Bryant, Jamie, Herrmann, Anne

Australian GPs' perceptions of barriers and enablers to best practice palliative care: a qualitative study

- Herrmann, Anne, Carey, Mariko L., Zucca, Alison C., Boyd, Lucy A. P., Roberts, Bernadette J.

Do haematological cancer patients get the information they need about their cancer and its treatment? Results of a cross-sectional survey

- Watson, Rochelle, Bryant, Jamie, Sanson-Fisher, Robert, Turon, Heidi, Hyde, Lisa, Herrmann, Anne

Exploring health literacy and preferences for risk communication among medical oncology patients

- Carey, Mariko, Herrmann, Anne, Hall, Alix, Mansfield, Elise, Fakes, Kristy

Exploring women's experiences with a decision aid for neoadjuvant systemic therapy for operable breast cancer

- Herrmann, Anne, Boyle, Frances, Butow, Phyllis, Hall, Alix E., Zdenkowski, Nicholas

General practitioners' perceptions of best practice care at the end of life: a qualitative study.

- Herrmann, Anne, Carey, Mariko, Zucca, Alison, Boyd, Lucy, Roberts, Bernadette

Not asking cancer patients about their preferences does make a difference. A cross-sectional study examining cancer patients' preferred and perceived role in decision-making regarding their last important cancer treatment

- Herrmann, Anne, Hall, Alix, Sanson-Fisher, Rob, Zdenkowski, Nicholas, Watson, Rochelle, Turon, Heidi

Not having adequate time to make a treatment decision can impact on cancer patients' care experience: results of a cross-sectional study

- Herrmann, Anne, Sanson-Fisher, Rob, Hall, Alix

Perceived problems with involvement in decision making about breast cancer treatment and care: a cross-sectional study

- Mackenzie, Lisa, Mansfield, Elise, Herrmann, Anne, Grady, Alice, Evans, Tiffany-Jane, Sanson-Fisher, Robert

Support persons' preferences for the type of consultation and the format of information provided when making a cancer treatment decision

- Herrmann, Anne, Sanson-Fisher, Rob, Hall, Alix, Wall, Laura, Zdenkowski, Nicholas, Waller, Amy

Systematic review of barriers and enablers to the delivery of palliative care by primary care practitioners

- Carey, Mariko L., Zucca, Alison C., Freund, Megan A. G., Bryant, Jamie, Herrmann, Anne, Roberts, Bernadette J.

Use of the supportive care framework to explore haematological cancer survivors' unmet needs: a qualitative study

- Herrmann, Anne, Mansfield, Elise, Tzelepis, Flora, Lynagh, Marita, Hall, Alix

Wilfully out of sight? A literature review on the effectiveness of cancer-related decision aids and implementation strategies

- Herrmann, Anne, Mansfield, Elise, Hall, Alix E., Sanson-Fisher, Rob, Zdenkowski, Nicholas

Women's experiences with deciding on neoadjuvant systemic therapy for operable breast cancer: a qualitative study

- Herrmann, Anne, Hall, Alix, Zdenkowski, Nicholas

Working towards patient-centred decision making in cancer care

- Herrmann, Anne