Markus Heidenblad

2.2k total citations
19 papers, 1.7k citations indexed

About

Markus Heidenblad is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Markus Heidenblad has authored 19 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 8 papers in Cancer Research. Recurrent topics in Markus Heidenblad's work include Genomic variations and chromosomal abnormalities (10 papers), Cancer Genomics and Diagnostics (7 papers) and Pancreatic and Hepatic Oncology Research (5 papers). Markus Heidenblad is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Cancer Genomics and Diagnostics (7 papers) and Pancreatic and Hepatic Oncology Research (5 papers). Markus Heidenblad collaborates with scholars based in Sweden, Netherlands and United States. Markus Heidenblad's co-authors include Mattias Höglund, Ludmila Gorunova, Nils Mandahl, Fredrik Mertens, Johan Staaf, Tord Jonson, Göran Jönsson, Camila O. dos Santos, Susanna Obad and Oliver Broom and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Markus Heidenblad

19 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Markus Heidenblad Sweden 14 1.1k 655 332 316 261 19 1.7k
Tove Kirkegaard Denmark 17 828 0.8× 547 0.8× 583 1.8× 250 0.8× 164 0.6× 30 1.5k
Binaifer Balsara United States 20 924 0.9× 331 0.5× 398 1.2× 290 0.9× 370 1.4× 38 1.6k
Hena R. Ashar United States 12 1.2k 1.1× 380 0.6× 522 1.6× 177 0.6× 150 0.6× 13 1.6k
Lakjaya Buluwela United Kingdom 20 935 0.9× 227 0.3× 436 1.3× 276 0.9× 120 0.5× 28 1.6k
Yasmin Akbarali United States 17 1.1k 1.1× 264 0.4× 420 1.3× 169 0.5× 200 0.8× 17 1.8k
Naoki Kitabayashi United States 17 844 0.8× 472 0.7× 207 0.6× 208 0.7× 525 2.0× 19 1.5k
Stine H. Kresse Norway 21 877 0.8× 604 0.9× 350 1.1× 127 0.4× 443 1.7× 30 1.5k
Igor Matushansky United States 21 1.1k 1.1× 313 0.5× 593 1.8× 122 0.4× 576 2.2× 48 1.8k
Jin Sung Jang United States 24 1.0k 1.0× 420 0.6× 516 1.6× 122 0.4× 324 1.2× 49 1.7k
Tuula Kuukasjärvi Finland 20 892 0.8× 633 1.0× 834 2.5× 602 1.9× 232 0.9× 25 1.8k

Countries citing papers authored by Markus Heidenblad

Since Specialization
Citations

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

Fields of papers citing papers by Markus Heidenblad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Markus Heidenblad

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

All Works

19 of 19 papers shown
1.
Liedberg, Fredrik, Carina Bernardo, Anders Edsjö, et al.. (2022). UROSCAN and UROSCANSEQ: a large-scale multicenter effort towards translation of molecular bladder cancer subtypes into clinical practice – from biobank to RNA-sequencing in real time. Scandinavian Journal of Urology. 57(1-6). 2–9. 4 indexed citations
2.
Pfisterer, Ulrich, et al.. (2021). Single‐cell sequencing in translational cancer research and challenges to meet clinical diagnostic needs. Genes Chromosomes and Cancer. 60(7). 504–524. 11 indexed citations
3.
Obad, Susanna, Camila O. dos Santos, Andreas Petri, et al.. (2011). Silencing of microRNA families by seed-targeting tiny LNAs. Nature Genetics. 43(4). 371–378. 498 indexed citations
4.
Nord, Karolin H., Raf Sciot, Johan Staaf, et al.. (2009). Two genetic pathways, t(1;10) and amplification of 3p11–12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions. The Journal of Pathology. 217(5). 716–727. 108 indexed citations
5.
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
6.
Jönsson, Göran, Johan Staaf, Eleonor Olsson, et al.. (2007). High‐resolution genomic profiles of breast cancer cell lines assessed by tiling BAC array comparative genomic hybridization. Genes Chromosomes and Cancer. 46(6). 543–558. 156 indexed citations
7.
8.
Nord, Karolin H., Johan Staaf, Göran Jönsson, et al.. (2007). Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation. British Journal of Cancer. 98(2). 434–442. 81 indexed citations
9.
Paulsson, Kajsa, Markus Heidenblad, Bodil Strömbeck, et al.. (2006). High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration. Leukemia. 20(5). 840–846. 58 indexed citations
10.
Heidenblad, Markus, Karolin H. Nord, Johan Staaf, et al.. (2006). Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays. Oncogene. 25(53). 7106–7116. 38 indexed citations
11.
Nord, Karolin H., Markus Heidenblad, Otte Brosjö, Nils Mandahl, & Fredrik Mertens. (2006). Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone. Cancer Genetics and Cytogenetics. 172(1). 80–83. 4 indexed citations
12.
Paulsson, Kajsa, Markus Heidenblad, Helena Mörse, et al.. (2006). Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia. Leukemia. 20(11). 2002–2007. 27 indexed citations
13.
14.
Paulsson, Kajsa, Markus Heidenblad, Bodil Strömbeck, et al.. (2005). High Resolution Genome-Wide Array-Based Comparative Genome Hybridization Reveals Cryptic Chromosome Changes in AML and MDS Cases with Trisomy 8 as the Sole Cytogenetic Aberration.. Blood. 106(11). 2847–2847. 11 indexed citations
15.
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
16.
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
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, Jan Axelson, Markus Heidenblad, et al.. (2001). Altered expression of TGFB receptors and mitogenic effects of TGFB in pancreatic carcinomas. International Journal of Oncology. 19(1). 71–81. 50 indexed citations
19.
Gisselsson, David, Louise Pettersson, Mattias Höglund, et al.. (2000). Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. Proceedings of the National Academy of Sciences. 97(10). 5357–5362. 323 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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