Katariina Hannula‐Jouppi

6.4k citations
37 papers · 1.3k indexed · h-index 17
Topics
Genetic Syndromes and Imprinting (11 papers)Epigenetics and DNA Methylation (11 papers)Skin and Cellular Biology Research (9 papers)
Journals
Proceedings of the National Academy of SciencesSHILAP Revista de lepidopterologíaPLoS ONE
Partner nations
FinlandSwedenNorway

In The Last Decade

Katariina Hannula‐Jouppi

37 papers receiving 1.2k citations

Peers

Katariina Hannula‐Jouppi
Comparison fields: 5 of 99
  • Genetics 653
  • Molecular Biology 550
  • Developmental and Educational Psychology 376
  • Pediatrics, Perinatology and Child Health 226
  • Cell Biology 127
Replace Mark Rabin with:
Mark Rabin United States
Atsuko Nakagawa Japan
Hans Matsson Sweden
Christopher J. Lyons Canada
L. Leigh Field Canada
C. T. R. M. Schrander‐Stumpel Netherlands
Yo Niida Japan
J. P. Fryns Belgium
Jessica Becker Germany
Peter N. Bowers United States
Katariina Hannula‐Jouppi relative to Mark Rabin United States Mark Rabin's profile →
Citations per field
00.5×
Mark Rabin · 1×
Citations per year

Countries citing papers authored by Katariina Hannula‐Jouppi

Since Specialization
Citations

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

Fields of papers citing papers by Katariina Hannula‐Jouppi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katariina Hannula‐Jouppi. 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 Katariina Hannula‐Jouppi. The network helps show where Katariina Hannula‐Jouppi may publish in the future.

Co-authorship network of co-authors of Katariina Hannula‐Jouppi

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

All Works

20 of 20 papers shown
#WorkIndexed citations
1 1
2 2
3 3
4 2
5 63
6 5
7 2
8 12
9 4
10 21
11 10
12 54
13 8
14 23
15 9
16 12
17 52
18 255
19 22
20 94

About Katariina Hannula‐Jouppi

Katariina Hannula‐Jouppi is a scholar working on Genetics, Cell Biology and Pediatrics, Perinatology and Child Health, having authored 37 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (11 papers), Epigenetics and DNA Methylation (11 papers) and Skin and Cellular Biology Research (9 papers). The work is most often cited by research in Developmental and Educational Psychology (376 citations), Genetics (653 citations) and Statistics and Probability (124 citations). Katariina Hannula‐Jouppi has collaborated with scholars based in Finland, Sweden and Norway. Frequent co-authors include Juha Kere, Marita Lipsanen‐Nyman, Mikko Taipale, Nina Kaminen‐Ahola, Jaana Nopola‐Hemmi, Helena Kääriäinen, Heikki Lyytinen, Perttu J. Lindsberg, Tuomas Haltia and Kurt Müller. Their work appears in journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

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

Rankless by CCL
2026