Jenny Nilsson

2.4k total citations
46 papers, 1.7k citations indexed

About

Jenny Nilsson is a scholar working on Pulmonary and Respiratory Medicine, Rheumatology and Cancer Research. According to data from OpenAlex, Jenny Nilsson has authored 46 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Pulmonary and Respiratory Medicine, 16 papers in Rheumatology and 11 papers in Cancer Research. Recurrent topics in Jenny Nilsson's work include Sarcoma Diagnosis and Treatment (26 papers), Vascular Tumors and Angiosarcomas (8 papers) and Soft tissue tumor case studies (8 papers). Jenny Nilsson is often cited by papers focused on Sarcoma Diagnosis and Treatment (26 papers), Vascular Tumors and Angiosarcomas (8 papers) and Soft tissue tumor case studies (8 papers). Jenny Nilsson collaborates with scholars based in Sweden, United States and United Kingdom. Jenny Nilsson's co-authors include Fredrik Mertens, Linda Magnusson, Karolin H. Nord, Henryk A. Domanski, Fredrik Vult von Steyern, Nils Mandahl, Johnbosco Tayebwa, Jakob Hofvander, Christopher D.�M. Fletcher and Otte Brosjö and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Jenny Nilsson

45 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jenny Nilsson Sweden	26	924	725	395	320	265	46	1.7k
Linda Magnusson Sweden	22	1.1k 1.2×	804 1.1×	558 1.4×	288 0.9×	152 0.6×	47	1.7k
Tetsuo Imamura Japan	21	899 1.0×	651 0.9×	479 1.2×	340 1.1×	249 0.9×	83	1.7k
Nicola Fabbri Italy	26	1.3k 1.4×	944 1.3×	386 1.0×	207 0.6×	592 2.2×	74	1.9k
Riruke Maruyama Japan	24	471 0.5×	358 0.5×	422 1.1×	404 1.3×	895 3.4×	123	2.1k
Matthias Werner Germany	15	1.1k 1.2×	572 0.8×	429 1.1×	477 1.5×	311 1.2×	27	2.3k
Yusuke Shinoda Japan	20	388 0.4×	309 0.4×	470 1.2×	552 1.7×	322 1.2×	75	1.4k
Marc Isler Canada	21	1.2k 1.3×	776 1.1×	397 1.0×	72 0.2×	767 2.9×	43	1.8k
Shuichi Jono Japan	24	545 0.6×	825 1.1×	505 1.3×	1.0k 3.2×	531 2.0×	39	3.9k
Yan Jiang China	25	339 0.4×	459 0.6×	781 2.0×	690 2.2×	426 1.6×	219	2.7k
Steffen Albrecht Canada	23	320 0.3×	204 0.3×	163 0.4×	709 2.2×	322 1.2×	56	1.8k

Countries citing papers authored by Jenny Nilsson

Since Specialization

Citations

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

Fields of papers citing papers by Jenny Nilsson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jenny Nilsson

This figure shows the co-authorship network connecting the top 25 collaborators of Jenny Nilsson. A scholar is included among the top collaborators of Jenny Nilsson 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 Jenny Nilsson. Jenny Nilsson 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

Kováč, Michal, Louise Cornmark, Linda Magnusson, et al.. (2023). Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathway. The Journal of Pathology. 262(2). 147–160. 10 indexed citations

Styring, Emelie, Linda Magnusson, Jenny Nilsson, et al.. (2023). Osteosarcomas With Few Chromosomal Alterations or Adult Onset Are Genetically Heterogeneous. Laboratory Investigation. 104(1). 100283–100283. 4 indexed citations

Nilsson, Jenny, Linda Magnusson, Uta Flucke, et al.. (2023). Insertion of the CXXC domain of KMT2A into YAP1: An unusual mechanism behind the formation of a chimeric oncogenic protein. Genes Chromosomes and Cancer. 62(11). 633–640. 2 indexed citations

Magnusson, Linda, et al.. (2022). Inactivation of RB1, CDKN2A, and TP53 have distinct effects on genomic stability at side‐by‐side comparison in karyotypically normal cells. Genes Chromosomes and Cancer. 62(2). 93–100. 7 indexed citations

Koster, Jan De, Paul Piccinelli, Fredrik Vult von Steyern, et al.. (2022). The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors. Laboratory Investigation. 102(8). 838–845. 3 indexed citations

Puls, Florian, Jodi M. Carter, Nischalan Pillay, et al.. (2021). Overlapping morphological, immunohistochemical and genetic features of superficial CD34-positive fibroblastic tumor and PRDM10-rearranged soft tissue tumor. Modern Pathology. 35(6). 767–776. 19 indexed citations

Hofvander, Jakob, Vickie Y. Jo, Christopher D.�M. Fletcher, et al.. (2020). PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells. Modern Pathology. 33(7). 1331–1340. 27 indexed citations

Andersson, Björn, Linda Lundgren, Gert Lindell, et al.. (2019). A risk score model to predict incidental gallbladder cancer in patients scheduled for cholecystectomy. HPB. 21. S542–S542. 1 indexed citations

Al‐Ibraheemi, Alyaa, Andrew L. Folpe, Antonio R. Pérez‐Atayde, et al.. (2018). Aberrant receptor tyrosine kinase signaling in lipofibromatosis: a clinicopathological and molecular genetic study of 20 cases. Modern Pathology. 32(3). 423–434. 48 indexed citations

10.

Arbajian, Elsa, Florian Puls, Cristina R. Antonescu, et al.. (2017). In-depth Genetic Analysis of Sclerosing Epithelioid Fibrosarcoma Reveals Recurrent Genomic Alterations and Potential Treatment Targets. Clinical Cancer Research. 23(23). 7426–7434. 65 indexed citations

11.

Hofvander, Jakob, Johnbosco Tayebwa, Jenny Nilsson, et al.. (2015). RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts. Laboratory Investigation. 95(6). 603–609. 13 indexed citations

12.

Walther, Charles, Jakob Hofvander, Jenny Nilsson, et al.. (2015). Gene fusion detection in formalin-fixed paraffin-embedded benign fibrous histiocytomas using fluorescence in situ hybridization and RNA sequencing. Laboratory Investigation. 95(9). 1071–1076. 58 indexed citations

13.

Hofvander, Jakob, Johnbosco Tayebwa, Jenny Nilsson, et al.. (2014). Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma. Clinical Cancer Research. 21(4). 864–869. 53 indexed citations

14.

Nord, Karolin H., Henrik Lilljebjörn, Francesco Vezzi, et al.. (2014). GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma. Nature Genetics. 46(5). 474–477. 58 indexed citations

15.

Macchia, Gemma, Karolin H. Nord, Jenny Nilsson, et al.. (2013). Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma. Oncology Reports. 31(2). 807–811. 1 indexed citations

16.

Dencker, Magnus, et al.. (2012). A 4-Year Exercise Program in Children Increases Bone Mass Without Increasing Fracture Risk. PEDIATRICS. 129(6). e1468–e1476. 32 indexed citations

17.

Jin, Yuesheng, Emely Möller, Karolin H. Nord, et al.. (2012). Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genes. Genes Chromosomes and Cancer. 51(5). 510–520. 109 indexed citations

18.

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

19.

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

20.

Nilsson, Jenny, Ina Nordström, Yung‐Wu Chen, et al.. (2006). Novel blocker of NFAT activation inhibits IL-6 production in human myometrial arteries and reduces vascular smooth muscle cell proliferation. American Journal of Physiology-Cell Physiology. 292(3). C1167–C1178. 73 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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