Johanna Rantala
Impact in
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- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
- Childhood Cancer Survivors' Quality of Life
Papers in
- Genetics 3
- BRCA gene mutations in cancer 2
- Genomic variations and chromosomal abnormalities 1
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- Advanced biosensing and bioanalysis techniques 1
- TGF-β signaling in diseases 1
- Co-authors
- Annika Lindblom (4 shared papers)Yvonne Brandberg (2 shared papers)Brita Arver (2 shared papers)Gunilla Lindgren (2 shared papers)Bo Nilsson (1 shared paper)Simone Picelli (2 shared papers)Barbro Werelius (1 shared paper)Xiaolei Zhou (1 shared paper)
In The Last Decade
Johanna Rantala
6 papers receiving 99 citations
Peers
Comparison fields: 5 of 27
- Genetics 67
- Pediatrics, Perinatology and Child Health 19
- Issues, ethics and legal aspects 1
- Pathology and Forensic Medicine 11
- Oncology 14
Countries citing papers authored by Johanna Rantala
This map shows the geographic impact of Johanna Rantala'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 Johanna Rantala with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Johanna Rantala more than expected).
Fields of papers citing papers by Johanna Rantala
This network shows the impact of papers produced by Johanna Rantala. 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 Johanna Rantala. The network helps show where Johanna Rantala may publish in the future.
Co-authors
The 20 scholars most cited alongside Johanna Rantala, 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 | 2012 | 35 | |
| 2 | 2009 | 32 | |
| 3 | 2007 | 19 | |
| 4 | 2005 | 11 | |
| 5 | Whole-genome Linkage Analysis and Sequence Analysis of Candidate Loci in Familial Breast Cancer. | 2015 | 3 |
| 6 | 2019 | 1 |
About Johanna Rantala
Johanna Rantala is a scholar working on Genetics, Molecular Biology, Genetics, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 6 papers that have together received 101 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (2 papers), History and Theory of Mathematics (1 paper), Childhood Cancer Survivors' Quality of Life (1 paper), Genetic factors in colorectal cancer (1 paper), Advanced biosensing and bioanalysis techniques (1 paper), Family Support in Illness (1 paper), TGF-β signaling in diseases (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Genetics (67 citations), Pediatrics, Perinatology and Child Health (19 citations), Issues, ethics and legal aspects (1 citation), Pathology and Forensic Medicine (11 citations) and Oncology (14 citations). Johanna Rantala has collaborated with scholars based in Sweden and Finland. Frequent co-authors include Annika Lindblom, Yvonne Brandberg, Brita Arver, Gunilla Lindgren, Bo Nilsson, Simone Picelli, Barbro Werelius, Xiaolei Zhou, Sara Margolin and Bo Song. Their work appears in journals such as Familial Cancer, European Journal of Medical Genetics, British Journal of Cancer, Hereditary Cancer in Clinical Practice and PubMed.
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.