Stefanie Witt

928 total citations
45 papers, 511 citations indexed

About

Stefanie Witt is a scholar working on Surgery, Pediatrics, Perinatology and Child Health and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Stefanie Witt has authored 45 papers receiving a total of 511 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Surgery, 18 papers in Pediatrics, Perinatology and Child Health and 9 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Stefanie Witt's work include Childhood Cancer Survivors' Quality of Life (13 papers), Esophageal and GI Pathology (11 papers) and Congenital Diaphragmatic Hernia Studies (8 papers). Stefanie Witt is often cited by papers focused on Childhood Cancer Survivors' Quality of Life (13 papers), Esophageal and GI Pathology (11 papers) and Congenital Diaphragmatic Hernia Studies (8 papers). Stefanie Witt collaborates with scholars based in Germany, Sweden and Portugal. Stefanie Witt's co-authors include Julia Quitmann, Monika Bullinger, Jens Dingemann, Michaela Dellenmark‐Blom, Carmen Dingemann, Rachel Sommer, Benno Ure, Vladimir Gatzinsky, Linus Jönsson and John Eric Chaplin and has published in prestigious journals such as International Journal of Environmental Research and Public Health, Quality of Life Research and Health and Quality of Life Outcomes.

In The Last Decade

Stefanie Witt

42 papers receiving 497 citations

Peers

Stefanie Witt
Julia Quitmann Germany
Kristine Wolter‐Warmerdam United States
Sarah M. Lambert United States
Nicola Williamson United Kingdom
Heléne E.K. Sundelin Sweden
Laurie Stevens United States
Alı Annagür Türkiye
Andrew Yaworsky United States
Sophie Guilmin‐Crépon France
Pamela Mudd United States
Julia Quitmann Germany
Stefanie Witt
Citations per year, relative to Stefanie Witt Stefanie Witt (= 1×) peers Julia Quitmann

Countries citing papers authored by Stefanie Witt

Since Specialization
Citations

This map shows the geographic impact of Stefanie Witt's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Stefanie Witt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefanie Witt more than expected).

Fields of papers citing papers by Stefanie Witt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stefanie Witt. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Stefanie Witt. The network helps show where Stefanie Witt may publish in the future.

Co-authorship network of co-authors of Stefanie Witt

This figure shows the co-authorship network connecting the top 25 collaborators of Stefanie Witt. A scholar is included among the top collaborators of Stefanie Witt based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stefanie Witt. Stefanie Witt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Adedeji, Adekunle, Tosin Yinka Akintunde, Franka Metzner, et al.. (2025). Perceived microaggressions and quality of life: the mediating role of personal resources and social support among people with African migration background in Germany. Cogent Social Sciences. 11(1). 1 indexed citations
2.
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Witt, Stefanie, Jessika Johannsen, Deike Weiss, et al.. (2024). DySMA – an Instrument to Monitor Swallowing Function in Children with Spinal Muscular Atrophy ages 0 to 24 Months: Development, Consensus, and Pilot Testing. Journal of Neuromuscular Diseases. 11(2). 473–483. 2 indexed citations
4.
Adedeji, Adekunle, et al.. (2024). A comprehensive systematic review of health-related quality of life measures in short stature paediatric patients. Endocrine. 86(2). 478–504. 1 indexed citations
5.
Witt, Stefanie, Julia Quitmann, Anna T. Höglund, et al.. (2023). Effects of a Pretend Play Intervention on Health-Related Quality of Life in Children With Cancer: A Swedish–German Study. PubMed. 40(3). 158–169. 3 indexed citations
6.
Quitmann, Julia, et al.. (2023). Health-Related Quality of Life, Stress, Caregiving Burden and Special Needs of Parents Caring for a Short-Statured Child—Review and Recommendations for Future Research. International Journal of Environmental Research and Public Health. 20(16). 6558–6558. 7 indexed citations
7.
Witt, Stefanie, Katharina Schuett, Silke Wiegand‐Grefe, Johannes Boettcher, & Julia Quitmann. (2023). Living with a rare disease - experiences and needs in pediatric patients and their parents. Orphanet Journal of Rare Diseases. 18(1). 242–242. 35 indexed citations
8.
Quitmann, Julia, et al.. (2023). Caregiving burden and special needs of parents in the care of their short-statured children – a qualitative approach. Frontiers in Endocrinology. 14. 1093983–1093983. 3 indexed citations
9.
Höglund, Anna T., et al.. (2022). Parent Perceptions of a Pretend Play Intervention for Their Children With Cancer. Journal of Nursing Research. 31(1). e253–e253. 3 indexed citations
10.
Dellenmark‐Blom, Michaela, Kate Abrahamsson, Jens Dingemann, et al.. (2022). Factors of family impact in a Swedish–German cohort of children born with esophageal atresia. Orphanet Journal of Rare Diseases. 17(1). 207–207. 7 indexed citations
11.
Witt, Stefanie, Jens Dingemann, Michaela Dellenmark‐Blom, & Julia Quitmann. (2021). Parent-Child Assessment of Strengths and Difficulties of German Children and Adolescents Born With Esophageal Atresia. Frontiers in Pediatrics. 9. 723410–723410. 6 indexed citations
12.
Witt, Stefanie, Kaja Kristensen, Silke Wiegand‐Grefe, et al.. (2021). Rare pediatric diseases and pathways to psychosocial care: a qualitative interview study with professional experts working with affected families in Germany. Orphanet Journal of Rare Diseases. 16(1). 497–497. 12 indexed citations
13.
Kristensen, Kaja, Julia Quitmann, & Stefanie Witt. (2021). Health-Related Quality of Life of Children and Adolescents With Congenital Hyperinsulinism – A Scoping Review. Frontiers in Endocrinology. 12. 784932–784932. 1 indexed citations
14.
Quitmann, Julia, Neuza Silva, Monika Bullinger, et al.. (2019). Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment. Frontiers in Pediatrics. 7. 164–164. 17 indexed citations
15.
Silva, Neuza, et al.. (2019). Psychometric properties of the quality of life in short statured youth (QoLISSY) questionnaire within the course of growth hormone treatment. Health and Quality of Life Outcomes. 17(1). 49–49. 9 indexed citations
16.
17.
Witt, Stefanie, et al.. (2019). Quality of life of children with achondroplasia and their parents - a German cross-sectional study. Orphanet Journal of Rare Diseases. 14(1). 194–194. 39 indexed citations
18.
Sommer, Rachel, Stefanie Witt, Monika Bullinger, et al.. (2019). Cross-cultural selection and validation of instruments to assess patient-reported outcomes in children and adolescents with achondroplasia. Quality of Life Research. 28(9). 2553–2563. 15 indexed citations
19.
Dellenmark‐Blom, Michaela, Kate Abrahamsson, Julia Quitmann, et al.. (2017). Development and pilot-testing of a condition-specific instrument to assess the quality-of-life in children and adolescents born with esophageal atresia. Diseases of the Esophagus. 30(7). 1–9. 31 indexed citations
20.
Wirth, Stephan, A. Wieser, Stefanie Witt, W. Mutschler, & Mario Reiser. (2003). Nachweis einer radiographisch okkulten Osteochondrosis dissecans tali mit der MRT. Der Unfallchirurg. 106(3). 238–240. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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2026