Johanna Rantala

6.5k total citations
6 papers, 100 citations indexed

About

Johanna Rantala is a scholar working on Genetics, Molecular Biology and Sociology and Political Science. According to data from OpenAlex, Johanna Rantala has authored 6 papers receiving a total of 100 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Sociology and Political Science. Recurrent topics in Johanna Rantala's work include BRCA gene mutations in cancer (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Family Support in Illness (2 papers). Johanna Rantala is often cited by papers focused on BRCA gene mutations in cancer (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Family Support in Illness (2 papers). Johanna Rantala collaborates with scholars based in Sweden and Finland. Johanna Rantala's co-authors include Annika Lindblom, Gunilla Lindgren, Brita Arver, Yvonne Brandberg, Bo Nilsson, Simone Picelli, Xiaolei Zhou, Sara Margolin, Bo Song and Barbro Werelius and has published in prestigious journals such as British Journal of Cancer, Familial Cancer and European Journal of Medical Genetics.

In The Last Decade

Johanna Rantala

6 papers receiving 98 citations

Peers

Johanna Rantala
Gord Glendon Canada
T Cole United Kingdom
Lisen Axell United States
Michele Nehrebecky United States
Meera Warby Australia
Hildegunn Høberg‐Vetti Norway
Rosie O’Shea Australia
Christine Kobelka United States
Yoland Antill Australia
Kate Shane-Carson United States
Gord Glendon Canada
Johanna Rantala
Citations per year, relative to Johanna Rantala Johanna Rantala (= 1×) peers Gord Glendon

Countries citing papers authored by Johanna Rantala

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Johanna Rantala

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

All Works

6 of 6 papers shown
1.
Valmari, Antti & Johanna Rantala. (2019). Arithmetic, Logic, Syntax and MathCheck. Jyväskylä University Digital Archive (University of Jyväskylä). 292–299. 1 indexed citations
2.
Rantala, Johanna, Simone Picelli, Tatjana Adamović, et al.. (2015). Whole-genome Linkage Analysis and Sequence Analysis of Candidate Loci in Familial Breast Cancer.. PubMed. 35(6). 3155–65. 3 indexed citations
3.
Rantala, Johanna, et al.. (2012). The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees’ outcome. Familial Cancer. 11(3). 371–379. 35 indexed citations
4.
Rantala, Johanna, Gunilla Lindgren, Bo Nilsson, et al.. (2009). Risk perception after genetic counseling in patients with increased risk of cancer. Hereditary Cancer in Clinical Practice. 7(1). 15–15. 31 indexed citations
5.
Song, Bo, Sara Margolin, Xiaolei Zhou, et al.. (2007). TGFBR1*6A and Int7G24A variants of transforming growth factor-β receptor 1 in Swedish familial and sporadic breast cancer. British Journal of Cancer. 97(8). 1175–1179. 19 indexed citations
6.
Schoumans, Jacqueline, Johan Staaf, Göran Jönsson, et al.. (2005). Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith–Magenis syndrome minimum deletion to ~650 kb. European Journal of Medical Genetics. 48(3). 290–300. 11 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Gord Glendon Breakdown of academic impact, for papers by T Cole Breakdown of academic impact, for papers by Lisen Axell Breakdown of academic impact, for papers by Michele Nehrebecky Breakdown of academic impact, for papers by Meera Warby Breakdown of academic impact, for papers by Hildegunn Høberg‐Vetti Breakdown of academic impact, for papers by Rosie O’Shea Breakdown of academic impact, for papers by Christine Kobelka Breakdown of academic impact, for papers by Yoland Antill Breakdown of academic impact, for papers by Kate Shane-Carson
Rankless by CCL
2026