Heidi Johansen

888 total citations
30 papers, 419 citations indexed

About

Heidi Johansen is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Heidi Johansen has authored 30 papers receiving a total of 419 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 10 papers in Pulmonary and Respiratory Medicine and 8 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Heidi Johansen's work include Connective tissue disorders research (13 papers), Aortic Disease and Treatment Approaches (8 papers) and Congenital limb and hand anomalies (5 papers). Heidi Johansen is often cited by papers focused on Connective tissue disorders research (13 papers), Aortic Disease and Treatment Approaches (8 papers) and Congenital limb and hand anomalies (5 papers). Heidi Johansen collaborates with scholars based in Norway, Sweden and Australia. Heidi Johansen's co-authors include Gry Velvin, Ingeborg Beate Lidal, Anne Elise Eggen, Svend Rand‐Hendriksen, Tom Wilsgaard, Laila Arnesdatter Hopstock, Sameline Grimsgaard, Svein O. Fredwall, Trine Bathen and Morten Wang Fagerland and has published in prestigious journals such as PLoS ONE, Nutrients and BMC Public Health.

In The Last Decade

Heidi Johansen

29 papers receiving 405 citations

Peers

Heidi Johansen

GENET

PRM

CCM

SURGE

PHEOH

Nicole Scheuing Germany

Stéphane Travers France

M Wallymahmed United Kingdom

Danilo Marcelo Leite do Prado Brazil

Sarita Dhuper United States

Martino Pavone Italy

Hillarie Slater United States

Gülay Eren Türkiye

Florian F. Hildenbrand Switzerland

Iwona Palczewska Poland

Nicole Scheuing Germany

Heidi Johansen

194 ×1.0

GENET

134 ×1.2

PRM

11 ×0.1

CCM

179 ×2.1

SURGE

28 ×0.6

PHEOH

Citations per year, relative to Heidi Johansen Heidi Johansen (= 1×) peers Nicole Scheuing

Countries citing papers authored by Heidi Johansen

Since Specialization

Citations

This map shows the geographic impact of Heidi Johansen'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 Heidi Johansen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heidi Johansen more than expected).

Fields of papers citing papers by Heidi Johansen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Heidi Johansen. 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 Heidi Johansen. The network helps show where Heidi Johansen may publish in the future.

Co-authorship network of co-authors of Heidi Johansen

This figure shows the co-authorship network connecting the top 25 collaborators of Heidi Johansen. A scholar is included among the top collaborators of Heidi Johansen 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 Heidi Johansen. Heidi Johansen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Velvin, Gry, et al.. (2025). Quality of life in people with syndromic heritable thoracic aortic disease and their relatives: a qualitative interview based study. Orphanet Journal of Rare Diseases. 20(1). 12–12.

Velvin, Gry, et al.. (2023). Fatigue in patients with syndromic heritable thoracic aortic disease: a systematic review of the literature and a qualitative study of patients’ experiences and perceptions. Orphanet Journal of Rare Diseases. 18(1). 119–119. 4 indexed citations

Velvin, Gry, et al.. (2023). Work participation in adults with rare genetic diseases - a scoping review. BMC Public Health. 23(1). 910–910. 4 indexed citations

Johansen, Heidi, Gry Velvin, & Ingeborg Beate Lidal. (2022). Education and employment status among adults with Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome in Norway, a questionnaire based study. PLoS ONE. 17(12). e0279848–e0279848. 2 indexed citations

Hopstock, Laila Arnesdatter, et al.. (2022). The seventh survey of the Tromsø Study (Tromsø7) 2015–2016: study design, data collection, attendance, and prevalence of risk factors and disease in a multipurpose population-based health survey. Scandinavian Journal of Public Health. 50(7). 919–929. 69 indexed citations

Bathen, Trine, Heidi Johansen, Hilde Strømme, & Gry Velvin. (2022). Experienced fatigue in people with rare disorders: a scoping review on characteristics of existing research. Orphanet Journal of Rare Diseases. 17(1). 14–14. 6 indexed citations

Johansen, Heidi, Gry Velvin, Kerstin Fugl-Meyer, & Ingeborg Beate Lidal. (2021). Adults with Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome: A cross-sectional study of life satisfaction. Journal of Rehabilitation Medicine. 53(11 (November)). jrm00236–jrm00236. 6 indexed citations

Velvin, Gry, et al.. (2019). Physical exercise for people with hereditable thoracic aortic disease. A study of patient perspectives. Disability and Rehabilitation. 43(17). 2464–2471. 14 indexed citations

Velvin, Gry, et al.. (2019). Systematic review of quality of life in persons with hereditary thoracic aortic aneurysm and dissection diagnoses. Clinical Genetics. 95(6). 661–676. 18 indexed citations

10.

Hopstock, Laila Arnesdatter, et al.. (2019). Folkehelserapport: Den sjuende Tromsøundersøkelsen 2015-16. Septentrio Academic Publishing (University of Tromsø). 2 indexed citations

11.

Fredwall, Svein O., et al.. (2019). Current knowledge of medical complications in adults with achondroplasia: A scoping review. Clinical Genetics. 97(1). 179–197. 41 indexed citations

12.

Johansen, Heidi, et al.. (2018). Chronic pain and fatigue in adults with congenital unilateral upper limb deficiency in Norway. A cross-sectional study. PLoS ONE. 13(1). e0190567–e0190567. 10 indexed citations

13.

Johansen, Heidi, et al.. (2016). Children with congenital limb deficiency in Norway: issues related to school life and health-related quality of life. A cross-sectional study. Disability and Rehabilitation. 38(18). 1803–1810. 9 indexed citations

14.

Johansen, Heidi, et al.. (2016). Health-related quality of life in adults with congenital unilateral upper limb deficiency in Norway. A cross-sectional study. Disability and Rehabilitation. 38(23). 2305–2314. 12 indexed citations

15.

Johansen, Heidi, et al.. (2015). Adults with congenital limb deficiency in Norway: demographic and clinical features, pain and the use of health care and welfare services. A cross-sectional study. Disability and Rehabilitation. 37(22). 2076–2082. 11 indexed citations

16.

Johansen, Heidi, et al.. (2013). Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two. Health and Quality of Life Outcomes. 11(1). 152–152. 37 indexed citations

17.

Rand‐Hendriksen, Svend, Heidi Johansen, Svein Ove Semb, et al.. (2010). Health-related quality of life in Marfan syndrome: A cross-sectional study of Short Form 36 in 84 adults with a verified diagnosis. Genetics in Medicine. 12(8). 517–524. 47 indexed citations

18.

Smedal, Tori, Heidi Johansen, Kjell‐Morten Myhr, & Liv Inger Strand. (2009). Psychometric properties of a Norwegian version of Multiple Sclerosis Impact Scale (MSIS-29). Acta Neurologica Scandinavica. 122(4). 244–251. 18 indexed citations

19.

Johansen, Heidi, et al.. (2009). Barn med skjelettdysplasi slik deres foreldre ser dem: En kartleggingsstudie. 1 indexed citations

20.

Johansen, Heidi, et al.. (2007). Health status of adults with Short Stature: A comparison with the normal population and one well-known chronic disease (Rheumatoid Arthritis). Orphanet Journal of Rare Diseases. 2(1). 24 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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