Lone Sunde

8.1k total citations
117 papers, 2.6k citations indexed

About

Lone Sunde is a scholar working on Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Genetics. According to data from OpenAlex, Lone Sunde has authored 117 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Pediatrics, Perinatology and Child Health, 44 papers in Public Health, Environmental and Occupational Health and 35 papers in Genetics. Recurrent topics in Lone Sunde's work include Prenatal Screening and Diagnostics (44 papers), Gestational Trophoblastic Disease Studies (36 papers) and Genetic factors in colorectal cancer (23 papers). Lone Sunde is often cited by papers focused on Prenatal Screening and Diagnostics (44 papers), Gestational Trophoblastic Disease Studies (36 papers) and Genetic factors in colorectal cancer (23 papers). Lone Sunde collaborates with scholars based in Denmark, United States and Sweden. Lone Sunde's co-authors include Isa Niemann, Inge Bernstein, Lars Bolund, T Myrhøj, Heikki Järvinen, Henry T. Lynch, Markku Aarnio, Juul Wijnen, Hans F. A. Vasen and Patrice Watson and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Lone Sunde

112 papers receiving 2.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Lone Sunde Denmark 30 795 771 725 627 619 117 2.6k
Daniel L. Van Dyke United States 41 1.9k 2.4× 853 1.1× 669 0.9× 248 0.4× 1.8k 2.9× 183 4.7k
Ulf Kristoffersson Sweden 33 1.9k 2.4× 935 1.2× 390 0.5× 503 0.8× 1.3k 2.1× 156 4.2k
Diane C. Arthur United States 33 395 0.5× 895 1.2× 283 0.4× 945 1.5× 1.0k 1.7× 78 4.1k
Roland P. Kuiper Netherlands 35 758 1.0× 1.1k 1.4× 756 1.0× 1.2k 1.9× 2.6k 4.2× 123 5.4k
Brian E. Ward United States 25 1.6k 2.0× 406 0.5× 446 0.6× 213 0.3× 870 1.4× 41 2.6k
Helga Rehder Germany 26 1.2k 1.5× 183 0.2× 777 1.1× 241 0.4× 906 1.5× 119 2.3k
Franck Bourdeaut France 33 341 0.4× 1.0k 1.3× 260 0.4× 317 0.5× 2.2k 3.6× 130 3.9k
Miguel Urioste Spain 28 779 1.0× 663 0.9× 209 0.3× 102 0.2× 990 1.6× 110 2.4k
Daynna J. Wolff United States 24 1.2k 1.5× 392 0.5× 222 0.3× 120 0.2× 1.0k 1.6× 80 2.8k
Marjan M. Weiss Netherlands 29 992 1.2× 715 0.9× 362 0.5× 73 0.1× 1.0k 1.6× 87 2.9k

Countries citing papers authored by Lone Sunde

Since Specialization
Citations

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

Fields of papers citing papers by Lone Sunde

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lone Sunde

This figure shows the co-authorship network connecting the top 25 collaborators of Lone Sunde. A scholar is included among the top collaborators of Lone Sunde 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 Lone Sunde. Lone Sunde 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.
Møller, Pål, Aysel Ahadova, Matthias Kloor, et al.. (2025). Colorectal carcinogenesis in the Lynch syndromes and familial adenomatous polyposis: trigger events and downstream consequences. Hereditary Cancer in Clinical Practice. 23(1). 3–3. 1 indexed citations
3.
Maher, Geoffrey J., et al.. (2023). When to Consult a Geneticist Specialising in Gestational Trophoblastic Disease. Gynecologic and Obstetric Investigation. 89(3). 198–213. 4 indexed citations
4.
Lildballe, Dorte L., Anja Lisbeth Frederiksen, Bitten Schönewolf‐Greulich, et al.. (2023). National clinical Genetic Networks - GENets - Establishment of expert collaborations in Denmark. European Journal of Medical Genetics. 66(12). 104872–104872.
5.
Jelsig, Anne Marie, Thomas van Overeem Hansen, Niels Qvist, et al.. (2023). Survival, surveillance, and genetics in patients with Peutz–Jeghers syndrome: A nationwide study. Clinical Genetics. 104(1). 81–89. 7 indexed citations
6.
Lildballe, Dorte L., et al.. (2021). Clinical genetic diagnostics in Danish autosomal dominant polycystic kidney disease patients reveal possible founder variants. European Journal of Medical Genetics. 64(4). 104183–104183. 4 indexed citations
7.
Lildballe, Dorte L., Maria Rasmussen, Lone Sunde, et al.. (2021). Functional megalin is expressed in renal cysts in a mouse model of adult polycystic kidney disease. Clinical Kidney Journal. 14(11). 2420–2427. 3 indexed citations
9.
Niemann, Isa, et al.. (2020). A rare case of urothelial carcinoma with syncytiotrophoblastic cell differentiation. Scandinavian Journal of Urology. 54(4). 358–359. 1 indexed citations
10.
Sunde, Lone, Ripudaman Singh, Estrid Stæhr Hansen, et al.. (2020). Hydatidiform mole diagnostics using circulating gestational trophoblasts isolated from maternal blood. Molecular Genetics & Genomic Medicine. 9(1). e1565–e1565. 3 indexed citations
11.
Sunde, Lone, et al.. (2019). The pivotal roles of the NOD-like receptors with a PYD domain, NLRPs, in oocytes and early embryo development†. Biology of Reproduction. 101(2). 284–296. 18 indexed citations
12.
Rasmussen, Maria, Lone Sunde, Mette Ramsing, et al.. (2017). Targeted gene sequencing and whole‐exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies. Clinical Genetics. 93(4). 860–869. 40 indexed citations
13.
Lautrup, Charlotte Kvist, Ellen M. Mikkelsen, Timothy L. Lash, Niels Katballe, & Lone Sunde. (2015). Familial colorectal cancer risk may be lower than previously thought: A Danish cohort study. Cancer Epidemiology. 39(5). 714–719. 6 indexed citations
14.
Sunde, Lone, Neil J. Sebire, Anni Grove, et al.. (2015). Paternal Hemizygosity in 11p15 in Mole-like Conceptuses. Medicine. 94(44). e1776–e1776. 6 indexed citations
15.
16.
Rasmussen, Maria, Steen Pedersen, Lone Sunde, et al.. (2014). A novel FBN1 variant in a large Marfan family with high penetrance of aortic dissection or rupture.. PubMed. 61(11). A4949–A4949. 1 indexed citations
17.
Binderup, Marie Louise Mølgaard, Marie Luise Bisgaard, Hans Ulrik Møller, et al.. (2013). Von Hippel-Lindau disease (vHL): National clinical guideline for diagnosis and surveillance in Denmark. University of Southern Denmark Research Portal (University of Southern Denmark). 60(12). 11 indexed citations
18.
Aretz, Stefan, Dietlinde Stienen, Siegfried Uhlhaas, et al.. (2007). High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome. Journal of Medical Genetics. 44(11). 702–709. 151 indexed citations
19.
Petersen, C. M., Poul Henning Jensen, Anne Bukh, et al.. (1990). Pregnancy zone protein: a re-evaluation of serum levels in healthy women and in women suffering from breast cancer or trophoblastic disease. Scandinavian Journal of Clinical and Laboratory Investigation. 50(5). 479–485. 13 indexed citations
20.
Sunde, Lone, et al.. (1983). Metodebetingede forskelle i vitalkapacitet. Ugeskrift for Læger. 145(36). 2 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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