Anne Kallioniemi
Impact in
- Cancer Research top 0.2%
- Cancer Genomics and Diagnostics
- Genetics top 0.1%
- Genomic variations and chromosomal abnormalities
Papers in
-
- Genomics and Chromatin Dynamics 16
- TGF-β signaling in diseases 15
- Gene expression and cancer classification 11
- Genetics 63
- Genomic variations and chromosomal abnormalities 53
- BRCA gene mutations in cancer 13
- Co-authors
- Olli Kallioniemi (46 shared papers)Joe W. Gray (12 shared papers)Fred Waldman (6 shared papers)Dan Pinkel (4 shared papers)Damir Sudar (4 shared papers)Denis Rutovitz (3 shared papers)Ritva Karhu (29 shared papers)Jorma Isola (12 shared papers)
- Journals
- Genes Chromosomes and Cancer (18 papers)Breast Cancer Research and Treatment (6 papers)International Journal of Cancer (6 papers)Proceedings of the National Academy of Sciences (5 papers)BMC Cancer (5 papers)
- Partner nations
- FinlandUnited StatesSwitzerland
In The Last Decade
Anne Kallioniemi
137 papers receiving 13.8k citations
Anne Kallioniemi's Hit Papers
Peers
Comparison fields: 5 of 138
- Cancer Research 3.6k
- Genetics 5.2k
- Oncology 3.3k
- Pathology and Forensic Medicine 1.9k
- Molecular Biology 7.2k
Countries citing papers authored by Anne Kallioniemi
This map shows the geographic impact of Anne Kallioniemi'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 Anne Kallioniemi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anne Kallioniemi more than expected).
Fields of papers citing papers by Anne Kallioniemi
This network shows the impact of papers produced by Anne Kallioniemi. 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 Anne Kallioniemi. The network helps show where Anne Kallioniemi may publish in the future.
Co-authors
The 25 scholars most cited alongside Anne Kallioniemi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 138 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors Hit paper breakdown → | 1992 | 2508 |
| 2 | Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors Hit paper breakdown → | 1994 | 893 |
| 3 | Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization. Hit paper breakdown → | 1994 | 637 |
| 4 | 1992 | 445 | |
| 5 | Genetic changes in primary and recurrent prostate cancer by comparative genomic hybridization. | 1995 | 411 |
| 6 | Impact of DNA amplification on gene expression patterns in breast cancer. | 2002 | 370 |
| 7 | 2002 | 350 | |
| 8 | Genetic heterogeneity and clonal evolution underlying development of asynchronous metastasis in human breast cancer. | 1997 | 333 |
| 9 | 1998 | 314 | |
| 10 | 2000 | 234 | |
| 11 | Comparative genomic hybridization analysis of 38 breast cancer cell lines: a basis for interpreting complementary DNA microarray data. | 2000 | 228 |
| 12 | 1995 | 224 | |
| 13 | 1997 | 219 | |
| 14 | 2001 | 194 | |
| 15 | 1995 | 183 | |
| 16 | New amplified and highly expressed genes discovered in the ERBB2 amplicon in breast cancer by cDNA microarrays. | 2001 | 177 |
| 17 | Comparative genomic hybridization: a rapid new method for detecting and mapping DNA amplification in tumors. | 1993 | 175 |
| 18 | 1999 | 171 | |
| 19 | Independent amplification and frequent co-amplification of three nonsyntenic regions on the long arm of chromosome 20 in human breast cancer. | 1996 | 162 |
| 20 | 2008 | 161 |
About Anne Kallioniemi
Anne Kallioniemi is a scholar working on Molecular Biology, Genetics, Cancer Research, Oncology and Pathology and Forensic Medicine, having authored 138 papers that have together received 14.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (53 papers), Cancer Genomics and Diagnostics (31 papers), Cancer-related Molecular Pathways (17 papers), Genomics and Chromatin Dynamics (16 papers), TGF-β signaling in diseases (15 papers), BRCA gene mutations in cancer (13 papers), Gene expression and cancer classification (11 papers) and Chromosomal and Genetic Variations (11 papers). The work is most often cited by research in Cancer Research (3.6k citations), Genetics (5.2k citations), Oncology (3.3k citations), Pathology and Forensic Medicine (1.9k citations) and Molecular Biology (7.2k citations). Anne Kallioniemi has collaborated with scholars based in Finland, United States and Switzerland. Frequent co-authors include Olli Kallioniemi, Joe W. Gray, Fred Waldman, Dan Pinkel, Damir Sudar, Denis Rutovitz, Ritva Karhu, Jorma Isola, Päivikki Kauraniemi and Outi Monni. Their work appears in journals such as Genes Chromosomes and Cancer, Breast Cancer Research and Treatment, International Journal of Cancer, Proceedings of the National Academy of Sciences and BMC Cancer.
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.