Margareth Isaksson

2.0k total citations
32 papers, 1.3k citations indexed

About

Margareth Isaksson is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Rheumatology. According to data from OpenAlex, Margareth Isaksson has authored 32 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Pulmonary and Respiratory Medicine and 9 papers in Rheumatology. Recurrent topics in Margareth Isaksson's work include Sarcoma Diagnosis and Treatment (13 papers), Acute Myeloid Leukemia Research (8 papers) and Musculoskeletal synovial abnormalities and treatments (4 papers). Margareth Isaksson is often cited by papers focused on Sarcoma Diagnosis and Treatment (13 papers), Acute Myeloid Leukemia Research (8 papers) and Musculoskeletal synovial abnormalities and treatments (4 papers). Margareth Isaksson collaborates with scholars based in Sweden, Italy and Belgium. Margareth Isaksson's co-authors include Ioannis Panagopoulos, Nils Mandahl, Fredrik Mertens, Henryk A. Domanski, Bertil Johansson, Felix Mitelman, Bodil Strömbeck, Otte Brosjö, Clelia Tiziana Storlazzi and Raf Sciot and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Oncogene and Biochemical and Biophysical Research Communications.

In The Last Decade

Margareth Isaksson

31 papers receiving 1.3k citations

Peers

Margareth Isaksson
Aurelia Meloni‐Ehrig United States
Paola Dal Cin Belgium
Kristina Arheden Sweden
Sheng Xiao United States
Jerian F. Lim Canada
Nils Mandahl Sweden
Chandrika Sreekantaiah United States
Marcia L. Lux United States
Maria Fernanda Amary United Kingdom
Diane L. Pickering United States
Aurelia Meloni‐Ehrig United States
Margareth Isaksson
Citations per year, relative to Margareth Isaksson Margareth Isaksson (= 1×) peers Aurelia Meloni‐Ehrig

Countries citing papers authored by Margareth Isaksson

Since Specialization
Citations

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

Fields of papers citing papers by Margareth Isaksson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Margareth Isaksson

This figure shows the co-authorship network connecting the top 25 collaborators of Margareth Isaksson. A scholar is included among the top collaborators of Margareth Isaksson 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 Margareth Isaksson. Margareth Isaksson 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.
Bartuma, Hammurabi, Karolin H. Nord, Gemma Macchia, et al.. (2011). Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion. Genes Chromosomes and Cancer. 50(8). 619–632. 41 indexed citations
2.
Nord, Karolin H., Linda Magnusson, Margareth Isaksson, et al.. (2010). Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma. Proceedings of the National Academy of Sciences. 107(49). 21122–21127. 45 indexed citations
3.
Mengelbier, Linda Holmquist, Jenny Karlsson, David Lindgren, et al.. (2010). Deletions of 16q in Wilms Tumors Localize to Blastemal-Anaplastic Cells and Are Associated with Reduced Expression of the IRXB Renal Tubulogenesis Gene Cluster. American Journal Of Pathology. 177(5). 2609–2621. 12 indexed citations
4.
Soller, Maria, et al.. (2009). The expression of pluripotency marker Oct 3/4 in prostate cancer and benign prostate hyperplasia. The Prostate. 69(9). 909–916. 25 indexed citations
5.
6.
Panagopoulos, Ioannis, Emely Möller, Margareth Isaksson, & Fredrik Mertens. (2008). A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1. Genes Chromosomes and Cancer. 47(6). 521–529. 10 indexed citations
7.
Möller, Emely, Margareth Isaksson, Nils Mandahl, Fredrik Mertens, & Ioannis Panagopoulos. (2007). Comparison of the proximal promoter regions of the PAX3 and PAX7 genes. Cancer Genetics and Cytogenetics. 178(2). 114–119. 10 indexed citations
8.
Panagopoulos, Ioannis, Bodil Strömbeck, Margareth Isaksson, et al.. (2006). Fusion of ETV6 with an intronic sequence of the BAZ2A gene in a paediatric pre‐B acute lymphoblastic leukaemia with a cryptic chromosome 12 rearrangement. British Journal of Haematology. 133(3). 270–275. 18 indexed citations
9.
Panagopoulos, Ioannis, Emely Möller, Anna Dahlén, et al.. (2006). Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera. Genes Chromosomes and Cancer. 46(2). 181–191. 37 indexed citations
10.
Panagopoulos, Ioannis, Thérèse Nilsson, Henryk A. Domanski, et al.. (2005). Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor. International Journal of Cancer. 118(5). 1181–1186. 88 indexed citations
11.
Panagopoulos, Ioannis, et al.. (2004). MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23). Genes Chromosomes and Cancer. 41(4). 400–404. 12 indexed citations
12.
Storlazzi, Clelia Tiziana, Fredrik Mertens, Nils Mandahl, et al.. (2003). A novel fusion gene, SS18L1/SSX1, in synovial sarcoma. Genes Chromosomes and Cancer. 37(2). 195–200. 74 indexed citations
13.
Panagopoulos, Ioannis, Thoas Fioretos, Margareth Isaksson, et al.. (2002). Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment‐related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15). Genes Chromosomes and Cancer. 34(2). 249–254. 10 indexed citations
14.
Panagopoulos, Ioannis, Margareth Isaksson, Rolf Billström, et al.. (2002). Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13). Genes Chromosomes and Cancer. 36(1). 107–112. 55 indexed citations
15.
Panagopoulos, Ioannis, Fredrik Mertens, Margareth Isaksson, et al.. (2002). Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma. Genes Chromosomes and Cancer. 35(4). 340–352. 78 indexed citations
16.
Panagopoulos, Ioannis, Fredrik Mertens, Maria Dêbiec‐Rychter, et al.. (2002). Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses. International Journal of Cancer. 99(4). 560–567. 109 indexed citations
17.
Panagopoulos, Ioannis, Fredrik Mertens, Henryk A. Domanski, et al.. (2001). NoEWS/FLI1 fusion transcripts in giant-cell tumors of bone. International Journal of Cancer. 93(6). 769–772. 29 indexed citations
18.
Panagopoulos, Ioannis, Fredrik Mertens, Margareth Isaksson, & Nils Mandahl. (2000). A Novel FUS/CHOP Chimera in Myxoid Liposarcoma. Biochemical and Biophysical Research Communications. 279(3). 838–845. 38 indexed citations
19.
Panagopoulos, Ioannis, Margareth Isaksson, Charlotta Lindvall, et al.. (2000). RT-PCR analysis of theMOZ-CBP andCBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13). Genes Chromosomes and Cancer. 28(4). 415–424. 27 indexed citations
20.
Panagopoulos, Ioannis, Carin Lassen, Margareth Isaksson, et al.. (1997). Characteristic sequence motifs at the breakpoints of the hybrid genes FUS/CHOP, EWS/CHOP and FUS/ERG in myxoid liposarcoma and acute myeloid leukemia. Oncogene. 15(11). 1357–1362. 55 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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