Samuli Hemmer

1.7k total citations
12 papers, 1.4k citations indexed

About

Samuli Hemmer is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Samuli Hemmer has authored 12 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 6 papers in Pathology and Forensic Medicine and 4 papers in Molecular Biology. Recurrent topics in Samuli Hemmer's work include Genomic variations and chromosomal abnormalities (6 papers), Genetic factors in colorectal cancer (5 papers) and Cancer Genomics and Diagnostics (4 papers). Samuli Hemmer is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetic factors in colorectal cancer (5 papers) and Cancer Genomics and Diagnostics (4 papers). Samuli Hemmer collaborates with scholars based in Finland, Sweden and Argentina. Samuli Hemmer's co-authors include Veli-Matti Wasenius, Sakari Knuutila, Wael El‐Rifai, Kaarle Franssila, Heikki Joensuu, Marcelo L. Larramendy, Ying Zhu, Johanna Tapper, Outi Monni and Maija Wolf and has published in prestigious journals such as American Journal Of Pathology, British Journal of Cancer and The American Journal of Surgical Pathology.

In The Last Decade

Samuli Hemmer

12 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Samuli Hemmer Finland 10 694 473 410 340 312 12 1.4k
Lúcia Roque Portugal 24 506 0.7× 304 0.6× 562 1.4× 199 0.6× 296 0.9× 49 1.5k
Rosangela Donghi Italy 15 909 1.3× 325 0.7× 990 2.4× 313 0.9× 358 1.1× 23 2.0k
Jong-Yeon Shin South Korea 17 967 1.4× 227 0.5× 572 1.4× 529 1.6× 266 0.9× 25 1.8k
Anna Dowe United Kingdom 13 537 0.8× 189 0.4× 245 0.6× 264 0.8× 112 0.4× 15 951
Tuula Kuukasjärvi Finland 20 892 1.3× 602 1.3× 834 2.0× 633 1.9× 245 0.8× 25 1.8k
Yu-Nien Sun United States 10 528 0.8× 145 0.3× 566 1.4× 196 0.6× 152 0.5× 12 1.4k
Agustín Herrero Spain 12 525 0.8× 258 0.5× 464 1.1× 151 0.4× 168 0.5× 14 1.2k
M Brunet France 16 471 0.7× 326 0.7× 763 1.9× 709 2.1× 254 0.8× 26 1.5k
G Sauter United States 7 1.1k 1.6× 251 0.5× 609 1.5× 408 1.2× 158 0.5× 11 1.8k
Patrícia Castro Portugal 20 673 1.0× 313 0.7× 666 1.6× 156 0.5× 343 1.1× 28 1.9k

Countries citing papers authored by Samuli Hemmer

Since Specialization
Citations

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

Fields of papers citing papers by Samuli Hemmer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samuli Hemmer

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

All Works

12 of 12 papers shown
1.
Taskinen, Minna, Matti Nykter, Marja‐Liisa Karjalainen‐Lindsberg, et al.. (2006). Differential gene expression in non‐malignant tumour microenvironment is associated with outcome in follicular lymphoma patients treated with rituximab and CHOP. British Journal of Haematology. 135(1). 33–42. 32 indexed citations
2.
Wasenius, Veli-Matti, Samuli Hemmer, Marja‐Liisa Karjalainen‐Lindsberg, et al.. (2005). MET Receptor Tyrosine Kinase Sequence Alterations in Differentiated Thyroid Carcinoma. The American Journal of Surgical Pathology. 29(4). 544–549. 55 indexed citations
3.
Wasenius, Veli-Matti, Samuli Hemmer, Eeva Kettunen, et al.. (2003). Hepatocyte growth factor receptor, matrix metalloproteinase-11, tissue inhibitor of metalloproteinase-1, and fibronectin are up-regulated in papillary thyroid carcinoma: a cDNA and tissue microarray study.. PubMed. 9(1). 68–75. 142 indexed citations
4.
Hemmer, Samuli, Veli-Matti Wasenius, Caj Haglund, et al.. (2002). Alterations in the suppressor gene PPP2R1B in parathyroid hyperplasias and adenomas. Cancer Genetics and Cytogenetics. 134(1). 13–17. 7 indexed citations
5.
Hemmer, Samuli, Veli-Matti Wasenius, Caj Haglund, et al.. (2001). Deletion of 11q23 and Cyclin D1 Overexpression Are Frequent Aberrations in Parathyroid Adenomas. American Journal Of Pathology. 158(4). 1355–1362. 55 indexed citations
6.
Hemmer, Samuli, Veli-Matti Wasenius, Sakari Knuutila, Kaarle Franssila, & Heikki Joensuu. (1999). DNA Copy Number Changes in Thyroid Carcinoma. American Journal Of Pathology. 154(5). 1539–1547. 93 indexed citations
7.
El‐Rifai, Wael, Samuli Hemmer, Asta Försti, et al.. (1999). DNA Copy Number Losses at 1p32-pter in Monozygotic Twins Concordant for Breast Cancer. Cancer Genetics and Cytogenetics. 112(2). 169–172. 9 indexed citations
8.
Knuutila, Sakari, Yan Aalto, K. Autio, et al.. (1999). DNA Copy Number Losses in Human Neoplasms. American Journal Of Pathology. 155(3). 683–694. 332 indexed citations
9.
Hemmer, Samuli, Veli-Matti Wasenius, Sakari Knuutila, Heikki Joensuu, & Kaarle Franssila. (1998). Comparison of benign and malignant follicular thyroid tumours by comparative genomic hybridization. British Journal of Cancer. 78(8). 1012–1017. 47 indexed citations
10.
Tapper, Johanna, Laura Sarantaus, Pia Vahteristo, et al.. (1998). Genetic changes in inherited and sporadic ovarian carcinomas by comparative genomic hybridization: extensive similarity except for a difference at chromosome 2q24-q32.. PubMed. 58(13). 2715–9. 53 indexed citations
11.
Knuutila, Sakari, K. Autio, Maija Tarkkanen, et al.. (1998). DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies.. PubMed. 152(5). 1107–23. 480 indexed citations
12.
El‐Rifai, Wael, et al.. (1997). Optimization of comparative genomic hybridization using fluorochrome conjugated to dCTP and dUTP nucleotides.. PubMed. 77(6). 699–700. 98 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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