Samuli Ripatti

2.2k total citations
4 papers, 66 citations indexed

About

Samuli Ripatti is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Samuli Ripatti has authored 4 papers receiving a total of 66 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Cardiology and Cardiovascular Medicine. Recurrent topics in Samuli Ripatti's work include BRCA gene mutations in cancer (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Genomics and Rare Diseases (1 paper). Samuli Ripatti is often cited by papers focused on BRCA gene mutations in cancer (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Genomics and Rare Diseases (1 paper). Samuli Ripatti collaborates with scholars based in Finland, United Kingdom and United States. Samuli Ripatti's co-authors include Priit Palta, Stacey Gabriel, Eric S. Lander, Andres Metspalu, Mario Mitt, Mart Kals, Kalle Pärn, Andrew P. Morris, Aarno Palotie and Tōnu Esko and has published in prestigious journals such as Nature, European Heart Journal and Human Molecular Genetics.

In The Last Decade

Samuli Ripatti

4 papers receiving 63 citations

Peers

Samuli Ripatti
Jee Yeon Heo South Korea
Reeta Metta United States
Alex Felmeister United States
Lindsay Guare United States
Carol Smee United Kingdom
Anu Reigo Estonia
Amelia L.M. Tan United States
Colleen Morse Kripke United States
Jee Yeon Heo South Korea
Samuli Ripatti
Citations per year, relative to Samuli Ripatti Samuli Ripatti (= 1×) peers Jee Yeon Heo

Countries citing papers authored by Samuli Ripatti

Since Specialization
Citations

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

Fields of papers citing papers by Samuli Ripatti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samuli Ripatti

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

All Works

4 of 4 papers shown
1.
Schunkert, Heribert, Emanuele Di Angelantonio, Michael Inouye, et al.. (2024). Clinical utility and implementation of polygenic risk scores for predicting cardiovascular disease. European Heart Journal. 46(15). 1372–1383. 25 indexed citations
2.
Mitt, Mario, Mart Kals, Kalle Pärn, et al.. (2017). Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel. Nature. 20 indexed citations
3.
Pietiläinen, Olli, Karola Rehnström, Eveliina Jakkula, et al.. (2011). Phenotype mining in CNV carriers from a population cohort †. Human Molecular Genetics. 20(13). 2686–2695. 12 indexed citations
4.
Korpela, Mikko, et al.. (2007). Local, Regional and National Interoperability in Hospital-level Systems Architecture. Methods of Information in Medicine. 46(4). 470–475. 9 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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