Samuli Hemmer
Impact in
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
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- Genetic factors in colorectal cancer
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 6
- BRCA gene mutations in cancer 3
- Genetic Syndromes and Imprinting 2
- Digestive system and related health 1
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- Genetic factors in colorectal cancer 5
- Co-authors
- Veli-Matti Wasenius (7 shared papers)Sakari Knuutila (5 shared papers)Heikki Joensuu (6 shared papers)Kaarle Franssila (6 shared papers)Wael El‐Rifai (4 shared papers)Marcelo L. Larramendy (3 shared papers)Ying Zhu (4 shared papers)Johanna Tapper (3 shared papers)
In The Last Decade
Samuli Hemmer
12 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 64
- Cancer Research 305
- Pathology and Forensic Medicine 274
- Genetics 442
- Oncology 364
- Endocrinology, Diabetes and Metabolism 179
Countries citing papers authored by Samuli Hemmer
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
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-authors
The 25 scholars most cited alongside Samuli Hemmer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies. | 1998 | 487 |
| 2 | 1999 | 340 | |
| 3 | 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. | 2003 | 144 |
| 4 | Optimization of comparative genomic hybridization using fluorochrome conjugated to dCTP and dUTP nucleotides. | 1997 | 98 |
| 5 | 1999 | 95 | |
| 6 | 2001 | 66 | |
| 7 | 2005 | 58 | |
| 8 | Genetic changes in inherited and sporadic ovarian carcinomas by comparative genomic hybridization: extensive similarity except for a difference at chromosome 2q24-q32. | 1998 | 54 |
| 9 | 1998 | 51 | |
| 10 | 2006 | 33 | |
| 11 | 1999 | 9 | |
| 12 | 2002 | 8 |
About Samuli Hemmer
Samuli Hemmer is a scholar working on Genetics, Pathology and Forensic Medicine, Cancer Research, Molecular Biology and Oncology, having authored 12 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genetic factors in colorectal cancer (5 papers), Cancer Genomics and Diagnostics (4 papers), BRCA gene mutations in cancer (3 papers), Pancreatic and Hepatic Oncology Research (2 papers), Genetic Syndromes and Imprinting (2 papers), Parathyroid Disorders and Treatments (2 papers) and Digestive system and related health (1 paper). The work is most often cited by research in Cancer Research (305 citations), Pathology and Forensic Medicine (274 citations), Genetics (442 citations), Oncology (364 citations) and Endocrinology, Diabetes and Metabolism (179 citations). Samuli Hemmer has collaborated with scholars based in Finland, Hungary and Egypt. Frequent co-authors include Veli-Matti Wasenius, Sakari Knuutila, Heikki Joensuu, Kaarle Franssila, Wael El‐Rifai, Marcelo L. Larramendy, Ying Zhu, Johanna Tapper, Outi Monni and Sakari Knuutila. Their work appears in journals such as American Journal Of Pathology, British Journal of Cancer, British Journal of Haematology, The American Journal of Surgical Pathology and Cancer Genetics and Cytogenetics.
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.