Tord Jonson

1.8k total citations
28 papers, 1.2k citations indexed

About

Tord Jonson is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Tord Jonson has authored 28 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Oncology and 9 papers in Genetics. Recurrent topics in Tord Jonson's work include Pancreatic and Hepatic Oncology Research (8 papers), Cancer Genomics and Diagnostics (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Tord Jonson is often cited by papers focused on Pancreatic and Hepatic Oncology Research (8 papers), Cancer Genomics and Diagnostics (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Tord Jonson collaborates with scholars based in Sweden, Netherlands and Finland. Tord Jonson's co-authors include Mattias Höglund, David Gisselsson, Fredrik Mertens, Nils Mandahl, Ludmila Gorunova, Felix Mitelman, Markus Heidenblad, Bodil Strömbeck, Paola Dal Cin and Åsa Petersén and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Cancer Research.

In The Last Decade

Tord Jonson

27 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tord Jonson Sweden 16 748 327 300 261 228 28 1.2k
Richard Volckmann Netherlands 11 760 1.0× 514 1.6× 306 1.0× 243 0.9× 91 0.4× 14 1.4k
Jennifer J. Kordich United States 14 889 1.2× 210 0.6× 171 0.6× 168 0.6× 47 0.2× 17 1.3k
Abdullah Mahmood Ali United States 20 1.5k 2.0× 244 0.7× 309 1.0× 178 0.7× 101 0.4× 60 2.0k
Naotoshi Kanda Japan 19 1.0k 1.3× 296 0.9× 306 1.0× 380 1.5× 158 0.7× 40 1.7k
Mascha van Noort Netherlands 10 1.6k 2.1× 317 1.0× 220 0.7× 203 0.8× 51 0.2× 10 2.0k
Zimu Zheng United States 6 1.5k 2.0× 457 1.4× 251 0.8× 324 1.2× 106 0.5× 6 2.0k
Monica Di Padova Italy 18 1.6k 2.1× 196 0.6× 353 1.2× 210 0.8× 132 0.6× 30 1.8k
Monika Goś Poland 19 769 1.0× 134 0.4× 91 0.3× 331 1.3× 77 0.3× 49 1.2k
Nijaguna B. Prasad United States 19 545 0.7× 430 1.3× 202 0.7× 198 0.8× 54 0.2× 25 1.2k

Countries citing papers authored by Tord Jonson

Since Specialization
Citations

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

Fields of papers citing papers by Tord Jonson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tord Jonson

This figure shows the co-authorship network connecting the top 25 collaborators of Tord Jonson. A scholar is included among the top collaborators of Tord Jonson 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 Tord Jonson. Tord Jonson 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.
Stenfeldt, Karin, Alessandro Castiglione, Tord Jonson, et al.. (2025). Diagnostic Yield and Genetic Variation in 85 Swedish Patients with Mild to Profound Hearing Loss Analyzed by Whole Genome Sequencing. Journal of Otolaryngology - Head and Neck Surgery. 54. 2071669311–2071669311.
2.
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
3.
Ehrencrona, Hans, et al.. (2022). Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation. International Journal of Pediatric Otorhinolaryngology. 159. 111218–111218. 9 indexed citations
4.
Brøndum‐Nielsen, Karen, Johan Svensson, Klaus Brusgaard, et al.. (2019). Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism. European Journal of Medical Genetics. 63(1). 103632–103632. 10 indexed citations
5.
Karlsson, Jenny, Anders Valind, Linda Holmquist Mengelbier, et al.. (2018). Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer. Nature Genetics. 50(7). 944–950. 46 indexed citations
6.
Valind, Anders, Niklas Pal, Jenny Karlsson, et al.. (2018). Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers. Pediatric Blood & Cancer. 65(11). e27301–e27301. 4 indexed citations
7.
Régal, Luc, Isabelle Maystadt, Nicol C. Voermans, et al.. (2017). PREPL deficiency: delineation of the phenotype and development of a functional blood assay. Genetics in Medicine. 20(1). 109–118. 24 indexed citations
8.
Gebré‐Medhin, Samuel, Karin Bröberg, Tord Jonson, et al.. (2009). Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone. Cytogenetic and Genome Research. 124(2). 121–127. 12 indexed citations
9.
Heidenblad, Markus, David Lindgren, Tord Jonson, et al.. (2008). Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumors. BMC Medical Genomics. 1(1). 3–3. 58 indexed citations
10.
Jin, Yuesheng, David Lindgren, Attila Frigyesi, et al.. (2007). Distinct Mitotic Segregation Errors Mediate Chromosomal Instability in Aggressive Urothelial Cancers. Clinical Cancer Research. 13(6). 1703–1712. 29 indexed citations
11.
Paulsson, Kajsa, Tord Jonson, Ingrid Øra, et al.. (2007). Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)‐positive acute lymphoblastic leukaemias. British Journal of Haematology. 138(2). 196–201. 17 indexed citations
12.
13.
Heidenblad, Markus, Eric Schoenmakers, Tord Jonson, et al.. (2004). Genome-Wide Array-Based Comparative Genomic Hybridization Reveals Multiple Amplification Targets and Novel Homozygous Deletions in Pancreatic Carcinoma Cell Lines. Cancer Research. 64(9). 3052–3059. 73 indexed citations
14.
Mertens, Fredrik, Ioannis Panagopoulos, Tord Jonson, et al.. (2004). Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation. Cytogenetic and Genome Research. 106(1). 33–38. 6 indexed citations
15.
Jonson, Tord, Markus Heidenblad, Ludmila Gorunova, et al.. (2003). Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1. Genes Chromosomes and Cancer. 36(4). 340–352. 11 indexed citations
16.
Gisselsson, David, Tord Jonson, C. Yu, et al.. (2002). Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres. British Journal of Cancer. 87(2). 202–207. 75 indexed citations
17.
Heidenblad, Markus, Tord Jonson, Eija Mahlamäki, et al.. (2002). Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5‐Mb target region for amplification. Genes Chromosomes and Cancer. 34(2). 211–223. 32 indexed citations
18.
Jonson, Tord, et al.. (1999). Molecular analyses of the 15q and 18qSMAD genes in pancreatic cancer. Genes Chromosomes and Cancer. 24(1). 62–71. 52 indexed citations
19.
Andreasson, Patrik, Mattias Höglund, Tord Jonson, et al.. (1998). Molecular characterization of jumping translocations reveals spatial and temporal breakpoint heterogeneity. Leukemia. 12(9). 1411–1416. 18 indexed citations
20.
Höglund, Mattias, Ludmila Gorunova, Tord Jonson, et al.. (1998). Cytogenetic and FISH analyses of pancreatic carcinoma reveal breaks in 18q11 with consistent loss of 18q12-qter and frequent gain of 18p. British Journal of Cancer. 77(11). 1893–1899. 14 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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