Catarina Lundin

600 total citations
17 papers, 287 citations indexed

About

Catarina Lundin is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Catarina Lundin has authored 17 papers receiving a total of 287 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Cardiology and Cardiovascular Medicine and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Catarina Lundin's work include Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers) and Acute Lymphoblastic Leukemia research (3 papers). Catarina Lundin is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers) and Acute Lymphoblastic Leukemia research (3 papers). Catarina Lundin collaborates with scholars based in Sweden, Denmark and Finland. Catarina Lundin's co-authors include Göran Annerén, Sven Cnattingius, Fredrik Mertens, Bertil Johansson, Mette Klarskov Andersen, Erik Forestier, Ann Nordgren, Claes Wadelius, L. Zech and Kristiina Heinonen and has published in prestigious journals such as Blood, Fertility and Sterility and Investigative Ophthalmology & Visual Science.

In The Last Decade

Catarina Lundin

17 papers receiving 279 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Catarina Lundin Sweden 11 106 98 98 85 63 17 287
A. Romeu Spain 14 95 0.9× 213 2.2× 44 0.4× 69 0.8× 70 1.1× 29 568
Ross Rowsey United States 11 66 0.6× 50 0.5× 131 1.3× 146 1.7× 36 0.6× 30 372
Maribel Forero‐Castro Colombia 8 41 0.4× 90 0.9× 43 0.4× 87 1.0× 36 0.6× 29 269
Ekaterina Kuchinskaya Sweden 10 40 0.4× 76 0.8× 68 0.7× 83 1.0× 108 1.7× 28 287
G. Reza Jalali United Kingdom 13 103 1.0× 210 2.1× 132 1.3× 191 2.2× 184 2.9× 16 456
Csaba Papp United States 13 77 0.7× 87 0.9× 81 0.8× 64 0.8× 79 1.3× 27 495
Varpu Jokimaa Finland 12 127 1.2× 185 1.9× 65 0.7× 115 1.4× 41 0.7× 18 509
Shu‐Chin Chien Taiwan 10 67 0.6× 29 0.3× 73 0.7× 84 1.0× 13 0.2× 32 309
J. P. M. Geraedts Netherlands 11 105 1.0× 117 1.2× 153 1.6× 104 1.2× 95 1.5× 22 422
Shinsuke Hirabayashi Japan 9 22 0.2× 48 0.5× 52 0.5× 65 0.8× 134 2.1× 28 220

Countries citing papers authored by Catarina Lundin

Since Specialization
Citations

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

Fields of papers citing papers by Catarina Lundin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catarina Lundin

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

All Works

17 of 17 papers shown
1.
Svensson, Anneli, Meriam Åström Aneq, Jesper Hastrup Svendsen, et al.. (2020). Evolution of P-wave indices during long-term follow-up as markers of atrial substrate progression in arrhythmogenic right ventricular cardiomyopathy. EP Europace. 23(Supplement_1). i29–i37. 5 indexed citations
2.
Englund, Elisabet, et al.. (2019). Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a de novo novel mosaic mutation in the LAMP2 gene. Investigative Ophthalmology & Visual Science. 60(9). 2949–2949. 1 indexed citations
3.
Platonov, Pyotr G., Aigars Rubulis, Lennart Bergfeldt, et al.. (2019). Idiopathic ventricular fibrillation – Long term prognosis in relation to clinical findings and ECG patterns in a Swedish cohort. Journal of Electrocardiology. 56. 46–51. 8 indexed citations
4.
5.
Paulussen, Aimée, Anja Steyls, Jo Vanoevelen, et al.. (2016). Rare novel variants in the ZIC3 gene cause X-linked heterotaxy. European Journal of Human Genetics. 24(12). 1783–1791. 16 indexed citations
6.
Lundin, Catarina, Erik Forestier, Mette Klarskov Andersen, et al.. (2014). Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries. Journal of Hematology & Oncology. 7(1). 32–32. 10 indexed citations
7.
Guenat, David, Carmelo Rizzari, Catarina Lundin, et al.. (2014). Predisposition to Burkitt Lymphoma in Williams-Beuren Syndrome. Blood. 124(21). 2182–2182. 1 indexed citations
8.
Fernlund, Eva, Catarina Lundin, Eva Hertervig, et al.. (2013). Novel Mutation in the KCNJ2 Gene Is Associated with a Malignant Arrhythmic Phenotype of Andersen‐Tawil Syndrome. Annals of Noninvasive Electrocardiology. 18(5). 471–478. 11 indexed citations
9.
Lundin, Catarina, Lars Hjorth, Mikael Behrendtz, et al.. (2012). Submicroscopic genomic imbalances in burkitt lymphomas/leukemias: Association with age and further evidence that 8q24/MYC translocations are not sufficient for leukemogenesis. Genes Chromosomes and Cancer. 52(4). 370–377. 3 indexed citations
10.
Lundin, Catarina, Lars Hjorth, Mikael Behrendtz, et al.. (2011). High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome. Genes Chromosomes and Cancer. 51(2). 196–206. 20 indexed citations
11.
Stavreus‐Evers, Anneli, Sven Cnattingius, Anders Ekbom, et al.. (2010). Ultrasonographic findings in spontaneous miscarriage: relation to euploidy and aneuploidy. Fertility and Sterility. 95(1). 221–224. 13 indexed citations
12.
Lundin, Catarina, Jesper Heldrup, Tomas Ahlgren, Tor Olofsson, & Bertil Johansson. (2008). B‐cell precursor t(8;14)(q11;q32)‐positive acute lymphoblastic leukemia in children is strongly associated with Down syndrome or with a concomitant Philadelphia chromosome. European Journal Of Haematology. 82(1). 46–53. 11 indexed citations
13.
Cnattingius, Sven, et al.. (2005). Chromosomal anomalies in first‐trimester miscarriages. Acta Obstetricia Et Gynecologica Scandinavica. 84(11). 1103–1107. 84 indexed citations
14.
Forestier, Erik, Sverre Heim, Elisabeth Blennow, et al.. (2003). Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO‐93‐AML trial between 1993 and 2001. British Journal of Haematology. 121(4). 566–577. 42 indexed citations
15.
Lundin, Catarina, et al.. (2002). Trisomy 4q syndrome: presentation of a new case and review of the literature. Annales de Génétique. 45(2). 53–57. 22 indexed citations
16.
Lundin, Catarina & Fredrik Mertens. (1998). Cytogenetics of benign breast lesions. Breast Cancer Research and Treatment. 51(1). 1–15. 23 indexed citations
17.
Lundin, Catarina, Fredrik Mertens, Ingrid Idvall, et al.. (1998). Cytogenetic Changes in Benign Proliferative and Nonproliferative Lesions of the Breast. Cancer Genetics and Cytogenetics. 107(2). 118–120. 11 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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