Ulla‐Maria Flodérus

913 total citations
14 papers, 746 citations indexed

About

Ulla‐Maria Flodérus is a scholar working on Obstetrics and Gynecology, Pulmonary and Respiratory Medicine and Reproductive Medicine. According to data from OpenAlex, Ulla‐Maria Flodérus has authored 14 papers receiving a total of 746 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Obstetrics and Gynecology, 5 papers in Pulmonary and Respiratory Medicine and 5 papers in Reproductive Medicine. Recurrent topics in Ulla‐Maria Flodérus's work include Uterine Myomas and Treatments (10 papers), Sarcoma Diagnosis and Treatment (5 papers) and Ovarian cancer diagnosis and treatment (5 papers). Ulla‐Maria Flodérus is often cited by papers focused on Uterine Myomas and Treatments (10 papers), Sarcoma Diagnosis and Treatment (5 papers) and Ovarian cancer diagnosis and treatment (5 papers). Ulla‐Maria Flodérus collaborates with scholars based in Sweden, Switzerland and Italy. Ulla‐Maria Flodérus's co-authors include Felix Mitelman, Nils Mandahl, Sverre Heim, Helena Willén, Mef Nilbert, Tanja Pejović, Stefan Furgyik, G. Helm, Bengt Elmfors and Nikos Pandis and has published in prestigious journals such as International Journal of Cancer, Genes Chromosomes and Cancer and Cytogenetic and Genome Research.

In The Last Decade

Ulla‐Maria Flodérus

14 papers receiving 737 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ulla‐Maria Flodérus Sweden 13 283 275 227 185 166 14 746
Jaime Prat Spain 10 274 1.0× 242 0.9× 94 0.4× 169 0.9× 120 0.7× 13 648
M F Kohler United States 7 132 0.5× 280 1.0× 58 0.3× 195 1.1× 168 1.0× 9 622
Yvonne Hennig Germany 9 166 0.6× 115 0.4× 109 0.5× 183 1.0× 108 0.7× 11 466
Pilar Fernández Machín Spain 9 262 0.9× 198 0.7× 66 0.3× 280 1.5× 210 1.3× 19 710
Greg A. Miller United States 13 116 0.4× 157 0.6× 114 0.5× 162 0.9× 105 0.6× 39 684
Mervi Aavikko Finland 15 585 2.1× 501 1.8× 209 0.9× 352 1.9× 186 1.1× 27 1.3k
R. Tucker Burks United States 6 412 1.5× 348 1.3× 90 0.4× 159 0.9× 132 0.8× 9 706
Lisbeth Haugom Norway 13 104 0.4× 103 0.4× 206 0.9× 192 1.0× 104 0.6× 19 486
Gianluigi Taddei Italy 15 268 0.9× 243 0.9× 66 0.3× 191 1.0× 77 0.5× 40 659

Countries citing papers authored by Ulla‐Maria Flodérus

Since Specialization
Citations

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

Fields of papers citing papers by Ulla‐Maria Flodérus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ulla‐Maria Flodérus. 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 Ulla‐Maria Flodérus. The network helps show where Ulla‐Maria Flodérus may publish in the future.

Co-authorship network of co-authors of Ulla‐Maria Flodérus

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

All Works

14 of 14 papers shown
1.
Pejović, Tanja, Sverre Heim, Felix Mitelman, et al.. (1992). Chromosome aberrations in 35 primary ovarian carcinomas. Genes Chromosomes and Cancer. 4(1). 58–68. 120 indexed citations
2.
Pandis, Nikos, Sverre Heim, Georgia Bardi, et al.. (1991). Chromosome analysis of 96 uterine leiomyomas. Cancer Genetics and Cytogenetics. 55(1). 11–18. 110 indexed citations
3.
Pejović, Tanja, Sverre Heim, Nils Mandahl, et al.. (1991). Bilateral ovarian carcinoma: Cytogenetic evidence of unicentric origin. International Journal of Cancer. 47(3). 358–361. 46 indexed citations
4.
Nilbert, Mef, Sverre Heim, Nils Mandahl, et al.. (1990). Trisomy 12 in uterine leiomyomas. Cancer Genetics and Cytogenetics. 45(1). 63–66. 48 indexed citations
5.
Nilbert, Mef, Yuesheng Jin, Sverre Heim, et al.. (1990). Chromosome rearrangements in two uterine sarcomas. Cancer Genetics and Cytogenetics. 44(1). 27–35. 26 indexed citations
6.
Pandis, Nikos, Sverre Heim, Georgia Bardi, et al.. (1990). Parallel karyotypic evolution and tumor progression in uterine leiomyoma. Genes Chromosomes and Cancer. 2(4). 311–317. 27 indexed citations
7.
Pejović, Tanja, Sverre Heim, Nils Mandahl, et al.. (1990). Trisomy 12 is a consistent chromosomal aberration in benign ovarian tumors. Genes Chromosomes and Cancer. 2(1). 48–52. 46 indexed citations
8.
Pejović, Tanja, Sverre Heim, Nils Mandahl, et al.. (1990). Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovary. Cancer Genetics and Cytogenetics. 46(1). 65–69. 11 indexed citations
9.
Nilbert, Mef, Sverre Heim, Nils Mandahl, et al.. (1989). Complex karyotypic anomalies in a bizarre leiomyoma of the uterus. Genes Chromosomes and Cancer. 1(2). 131–134. 17 indexed citations
10.
Pejović, Tanja, Sverre Heim, Nils Mandahl, et al.. (1989). Consistent occurrence of a 19p+ marker chromosome and loss of 11p material in ovarian seropapillary cystadenocarcinomas. Genes Chromosomes and Cancer. 1(2). 167–171. 50 indexed citations
11.
Nilbert, Mef, Sverre Heim, Nils Mandahl, et al.. (1989). Different karyotypic abnormalities, t(1;6) and del(7), in two uterine leiomyomas from the same patient. Cancer Genetics and Cytogenetics. 42(1). 51–53. 27 indexed citations
12.
Nilbert, Mef, Sverre Heim, Nils Mandahl, et al.. (1988). Karyotypic rearrangements in 20 uterine leiomyomas. Cytogenetic and Genome Research. 49(4). 300–304. 53 indexed citations
13.
Heim, Sverre, Mef Nilbert, Roberta Vanni, et al.. (1988). A specific translocation, t(12;14)(q14–15; q23–24), characterizes a subgroup of uterine leiomyomas. Cancer Genetics and Cytogenetics. 32(1). 13–17. 124 indexed citations
14.
Nilbert, Mef, Sverre Heim, Nils Mandahl, et al.. (1988). Ring formation and structural rearrangements of chromosome 1 as secondary changes in uterine leiomyomas with t(12;14)(q14–15;q23–24). Cancer Genetics and Cytogenetics. 36(2). 183–190. 41 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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