Sophie Nadia Gaber, Ing-Britt Rydeman, Elisabet Mattsson, Åsa Kneck (2024). Asking about violence and abuse among patients experiencing homelessness: A focus group study with healthcare professionals

Gustav Bockgård, Elisabet Mattsson, Louise von Essen, Anna Klarare (2024). Collaborative Interpretation of Researcher-Generated Photo-Elicitation Findings: Insights From Women With Lived Experience of Homelessness

Andreas Karlsson Rosenblad, Anna Klarare, Penny Rapaport, Elisabet Mattsson, Sophie Nadia Gaber (2024). Health literacy and its association with mental and spiritual well-being among women experiencing homelessness

Anna Klarare, Johan Vamstad, Elisabet Mattsson, Åsa Kneck, Martin Salzmann-Erikson (2024). Social rights in relation to digitalization, mobile phone, and internet use – experiences of women in homelessness: A qualitative study

Anna Klarare, Veronica Ekström, Tove Godskesen, Jeanette Westman, Elisabet Mattsson, Åsa Kneck (2024). Treatment of trauma-related conditions for people in homelessness: A scoping review

Sophie Gaber, Anna Klarare, Elisabet Mattsson, Andreas Karlsson Rosenblad (2023). A comparison of perceptions of caring behaviours among women in homelessness, Registered Nurses and nursing students

Emma Gerhardsson, Paola Oras, Elisabet Mattsson, Ylva Thernström Blomqvist, Eva-Lotta Funkquist (2023). Health care professionals report positive experience with a breastfeeding training program based on the Baby-Friendly Hospital Initiative for Neonatal Intensive Care

Elisabet Mattsson, Anna Klarare (2023). Kvinnor far illa inom ramen för samhällets institutioner

Maria Gottvall, Calle Brunell, Anna Eldebo, Rogers Kissiti, Elisabet Mattsson, Maria Jirwe, Tommy Carlsson (2023). Nurse education about forced migrants with diverse sexual orientations, gender identities, and gender expressions: An exploratory focus group study

Josefine Agius, Anna Klarare, Elisabet Mattsson, Johan Vamstad, Jenny Eriksson Lundström, Sanna Vahlman (2023). Vilket stöd våldsutsatta får blir ett lotteri: Ge kommuner ett särskilt bostadsförsörjningskrav för våldsutsatta

Elisabet Mattsson, Marléne Lindblad, Åsa Kneck, Martin Salzmann-Eriksson, Anna Klarare (2023). Voices of women in homelessness during the outbreak of the COVID-19 pandemic: A co-created qualitative study

Anna Klarare, Tommy Carlsson, Elisabet Mattsson (2022). Belonging to a community of care: Mothers' experiences of online peer support groups for parents having lost a child with congenital heart defects

Viktoria Wallin, Elisabet Mattsson, Pernilla Omerov, Anna Klarare (2022). Caring for patients with eating deficiencies in palliative care—Registered nurses' experiences: A qualitative study

Josefine Agius, Elisabet Mattsson (2022). Kvinnor på skyddade boenden måste kunna ta tillbaka sina liv

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Viktoria Wallin, Pernilla Omerov, Elisabet Mattsson, Anna Klarare (2022). Patienters erfarenheter av mat och måltider vid kronisk livsbegränsande sjukdom: En litteraturöversikt med mixade metoder

Tommy Carlsson, Elisabet Mattsson (2022). Peer Support Experienced by Mothers of Children With Congenital Heart Defects in Sweden

Åsa Kneck, Anna Klarare, Elisabet Mattsson, Martin Salzmann‐Erikson (2022). Reflections on health among women in homelessness: A qualitative study

Johan Vamstad, Elisabet Mattsson, Anna Klarare (2022). Social rights and street-level services for women in homelessness: A qualitative study

Josefine Agius, Elisabet Mattsson, Elisabet Mattsson (2022). ”Stabil vardag måste ses som en del av traumabehandling”

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Sophie Gaber, Andreas Karlsson Rosenblad, Elisabet Mattsson, Anna Klarare (2022). The relationship between attitudes to homelessness and perceptions of caring behaviours: A cross-sectional study among women experiencing homelessness, nurses and nursing students

Josefine Agius, Anna Klarare, Elisabet Mattsson (2022). Trygg kan ingen vara: Elever som lever med skyddade personuppgifter

Anna Klarare, Mona Söderlund, Anna Wikman, Jenny McGreevy, Elisabet Mattsson, Andreas Rosenblad (2021). Caring Behaviors Inventory-24: Translation, cross-cultural adaptation and psychometric testing for use in a Swedish context

Emma Gerhardsson, Paola Oras, Elisabet Mattsson, Ylva Thernström Blomqvist, Eva-Lotta Funkquist, Andreas Rosenblad (2021). Developing the preterm breastfeeding attitudes instrument: A tool for describing attitudes to breastfeeding among health care professionals in neonatal intensive care

Viktoria Wallin, Pernilla Omerov, Elisabet Mattsson, Anna Klarare (2021). Experiences of food and mealtime from the perspective of patients with chronic life-limiting disease: a mixed-method systematic review

Hanna Karlsson, Anna Klarare, Elisabet Mattsson, Johan Vamstad (2021). Låt berörda vara del i forskning

Elsa Karlsson, Anna Klarare, Elisabet Mattsson (2021). Låt våra hemlösa få bo på de tomma hotellen

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Åsa Kneck, Elisabet Mattsson, Martin Salzmann-Erikson, Anna Klarare (2021). “Stripped of dignity” - Women in homelessness and their perspectives of healthcare services: A qualitative study

Lisa Ljungman, Matilda Köhler, Emma Hovén, Karin Stålberg, Elisabet Mattsson, Anna Wikman (2021). "There should be some kind of checklist for the soul": A qualitative interview study of support needs after end of treatment for gynecologic cancer in young women

Anna Klarare, Anna Wikman, Mona Söderlund, Jenny McGreevy, Elisabet Mattsson, Andreas Rosenblad (2021). Translation, Cross-Cultural Adaptation, and Psychometric Analysis of the Attitudes Towards Homelessness Inventory for Use in Sweden

Elisabet Mattsson, Josefine Agius (2021). Öka kunskapen i vården kring skyddad identitet

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Tommy Carlsson, Ulla Melander Marttala, Elisabet Mattsson (2020). Being involved in research as a collaborator with experience of a prenatal diagnosis of congenital heart defect in the fetus: A qualitative study

Elisabet Mattsson (2020). Hur kan hemlösa kvinnor få samma vård som andra i samhället?

Emma Gerhardsson, Andreas Rosenblad, Elisabet Mattsson, Eva-Lotta Funquist (2020). Mothers' Adaptation to a Late Preterm Infant When Breastfeeding

Tommy Carlsson, Anna Klarare, Elisabet Mattsson (2020). Peer support among parents of children with congenital heart defects: A qualitative analysis of written responses submitted via an online survey

Elisabet Mattsson, Lisa Ljungman, Kim Einhorn, Inger Sundström Poromaa, Karin Stålberg, Anna Wikman (2020). Perceptions of care after end-of-treatment among younger women with different gynecologic cancer diagnoses: a qualitative analysis of written responses submitted via a survey

Pernilla Omerov, Åsa Gransjön Craftman, Elisabet Mattsson, Anna Klarare (2019). Homeless persons' experiences of health- and social care: A systematic integrative review

Tommy Carlsson, Banaz Balbas, Elisabet Mattsson (2019). Written narratives from immigrants following a prenatal diagnosis: qualitative exploratory study.

Tommy Carlsson, Elisabet Mattsson (2018). Emotional and cognitive experiences during the time of diagnosis and decision-making following a prenatal diagnosis: A qualitative study of males presented with congenital heart defect in the fetus carried by their pregnant partner.

Anna Wikman, Elisabet Mattsson, Louise von Essen, Emma Hovén (2018). Prevalence and predictors of symptoms of anxiety and depression, and comorbid symptoms of distress in parents of childhood cancer survivors and bereaved parents five years after end of treatment or a child's death.

Emma Gerhardsson, Ingegerd Hildingsson, Elisabet Mattsson, Eva-Lotta Funkquist (2018). Prospective questionnaire study showed that higher self-efficacy predicted longer exclusive breastfeeding by the mothers of late preterm infants.

Elisabet Mattsson, Kim Einhorn, Lisa Ljungman, Inger Sundström-Poromaa, Karin Stålberg, Anna Wikman (2018). Women treated for gynaecological cancer during young adulthood: A mixed-methods study of perceived psychological distress and experiences of support from health care following end-of-treatment.

Kerstin Hedberg Nyqvist, Andreas Rosenblad, Helena Volgsten, Eva-Lotta Funkquist, Elisabet Mattsson (2017). Early skin-to-skin contact between healthy late preterm infants and their parents: an observational cohort study

Ulla Melander Marttala, Elisabet Mattsson (2017). Fackord i samtal och texter om barns hjärtfel

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Tommy Carlsson, Ulla Melander Marttala, Barbro Wadensten, Gunnar Bergman, Ove Axelsson, Elisabet Mattsson (2017). Quality of Patient Information Websites About Congenital Heart Defects: Mixed-Methods Study of Perspectives Among Individuals With Experience of a Prenatal Diagnosis.

Tommy Carlsson, Veronica Starke, Elisabet Mattsson (2017). The emotional process from diagnosis to birth following a prenatal diagnosis of fetal anomaly: A qualitative study of messages in online discussion boards

Tommy Carlsson, Mats Landqvist, Elisabet Mattsson (2016). Communication of support and critique in Swedish virtual community threads about prenatal diagnoses of fetal anomalies.

Malin Ander, Helena Grönqvist, Martin Cernvall, Gunn Engvall, Mariann Hedström, Gustaf Ljungman, Johan Lyhagen, Elisabet Mattsson, Louise von Essen (2016). Development of health-related quality of life and symptoms of anxiety and depression among persons diagnosed with cancer during adolescence: a 10-year follow-up study

Tommy Carlsson, Ulla Melander Marttala, Elisabet Mattsson, Anders Ringnér (2016). Experiences and preferences of care among Swedish immigrants following a prenatal diagnosis of congenital heart defect in the fetus: A qualitative interview study.

Tommy Carlsson, Gunnar Bergman, Barbro Wadensten, Elisabet Mattsson (2016). Experiences of Informational Needs and Received Information Following a Prenatal Diagnosis of Congenital Heart Defect

Tommy Carlsson, Gunnar Bergman, Anna-Malin Karlsson, Barbro Wadensten, Elisabet Mattsson (2016). Experiences of termination of pregnancy for a fetal anomaly: A qualitative study of virtual community messages.

Tommy Carlsson, Ulla Melander Marttala, Barbro Wadensten, Gunnar Bergman, Elisabet Mattsson (2016). Involvement of persons with lived experience of a prenatal diagnosis of congenital heart defect: An explorative study to gain insights into perspectives on future research

Tommy Carlsson, Gunnar Bergman, Anna-Malin Karlsson, Elisabet Mattsson (2015). Content and quality of information websites about congenital heart defects following a prenatal diagnosis

Elisabet Mattsson, Eva-Lotta Funkquist, Maria Wickström, Kerstin Hedberg Nyqvist, Helena Volgsten (2015). Healthy late preterm infants and supplementary artificial milk feeds: Effects on breast feeding and associated clinical parameters

Tommy Carlsson, Gunnar Bergman, Ulla Melander Marttala, Barbro Wadensten, Elisabet Mattsson (2015). Information following a Diagnosis of Congenital Heart Defect: Experiences among Parents to Prenatally Diagnosed Children

Vicky Lehmann, Helena Grönqvist, Gunn Engvall, Malin Ander, Marrit A Tuinman, Mariët Hagedoorn, Robbert Sanderman, Elisabet Mattsson, Louise von Essen (2014). Negative and positive consequences of adolescent cancer 10 years after diagnosis: An interview-based longitudinal study in Sweden

Emma Gerhardsson, Kerstin Hedberg Nyqvist, Elisabet Mattsson, Helena Volgsten, Ingegerd Hildingsson, Eva-Lotta Funkquist (2014). The Swedish Version of the Breastfeeding Self-Efficacy Scale-Short Form: Reliability and Validity Assessment

Anna-Malin Karlsson, Ulla Melander Marttala, Elisabet Mattsson (2014). "Vi kan inte visa ett normalt hjärta": Kommunikativa praktiker i samband med hjärtfel hos foster

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Gunn Engvall, Inger Skolin, Elisabet Mattsson, Mariann Hedström, Louise von Essen (2011). Are nurses and physicians able to assess which strategies adolescents recently diagnosed with cancer use to cope with disease- and treatment-related distress?

Gunn Engvall, Martin Cernvall, Gunnel Larsson, Louise von Essen, Elisabet Mattsson (2011). Cancer during adolescence: negative and positive consequences reported three and four years after diagnosis

Gunn Engvall, Elisabet Mattsson, Louise von Essen, Mariann Hedström (2011). Findings on how adolescents cope with cancer: a matter of methodology?

Lena Wettergren, Elisabet Mattsson, Louise von Essen (2011). Mode of administration only has a small effect on data quality and self-reported health status and emotional distress among Swedish adolescents and young adults

Gunnel Larsson, Elisabet Mattsson, Louise von Essen (2010). Aspects of quality of life, anxiety, and depression among persons diagnosed with cancer during adolescence: a long-term follow-up study

Elisabet Mattsson, Bassam El-Khouri, Gustaf Ljungman, Louise von Essen (2009). Empirically derived psychosocial states among adolescents diagnosed with cancer during the acute and extended phase of survival

Elisabet Mattsson, Björn Lindgren, Louise von Essen (2008). Are there any positive consequences of childhood cancer?: A review of the literature

Anna Jörngården, Elisabet Mattsson, Louise von Essen (2007). Health-related quality of life, anxiety and depression among adolescents and young adults with cancer: A prospective longitudinal study

Elisabet Mattsson, Anders Ringnér, Gustaf Ljungman, Louise von Essén (2007). Positive and negative consequences with regard to cancer during adolescence: Experiences two years after diagnosis

Louise von Essen, Per Olow Sjödén, Elisabet Mattsson (2004). Swedish Mothers and Fathers of a Child Diagnosed with Cancer: A Look at Their Quality of Life

G Sandblom, Lars Holmberg, J-E Damber, J Hugosson, J-E Johansson, R Lundgren, Elisabet Mattsson, J Nilsson, E Varenhorst (2002). Prostate-specific antigen as surrogate for characterizing prostate cancer subgroups

G. Sandblom, L. Holmberg, J-E. Damber, J. Hugosson, J-E. Johansson, R. Lundgren, Elisabet Mattsson, J. Nilsson, E. Varenhorst (2002). Prostate-specific antigen for prostate cancer staging in a population-based register.

Gabriel Sandblom, Elisabet Mattsson, Jonas Nilsson, Jan-Erik Damber, Jan-Erik Johansson, Rolf Lundgren, Eberhard Varenhorst (1999). Prostate cancer registration in four Swedish regions 1996: differences in incidence, age structure and management