Katri Kantojärvi

1.3k total citations
33 papers, 340 citations indexed

About

Katri Kantojärvi is a scholar working on Cognitive Neuroscience, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Katri Kantojärvi has authored 33 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Cognitive Neuroscience, 11 papers in Genetics and 10 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Katri Kantojärvi's work include Maternal Mental Health During Pregnancy and Postpartum (7 papers), Child and Adolescent Psychosocial and Emotional Development (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Katri Kantojärvi is often cited by papers focused on Maternal Mental Health During Pregnancy and Postpartum (7 papers), Child and Adolescent Psychosocial and Emotional Development (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Katri Kantojärvi collaborates with scholars based in Finland, United Kingdom and United States. Katri Kantojärvi's co-authors include Irma Järvelä, Tiina Paunio, Raija Vanhala, Päivi Onkamo, Linnéa Karlsson, Hasse Karlsson, Chakravarthi Kanduri, Christine Blancher, Anthony P. Monaco and Harri Lähdesmäki and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Katri Kantojärvi

31 papers receiving 321 citations

Peers

Katri Kantojärvi

GENET

ECP

PPCH

Weiqiu Cheng Norway

Juthamas Wirojanan Thailand

Althea Robinson Shelton United States

Kathryn M. Harper United States

Sophia Docherty United Kingdom

Justin D. Tubbs Hong Kong

Maria Tropeano United Kingdom

Daniël Roelfs Norway

Mihoko Shimada Japan

Weiqiu Cheng Norway

Katri Kantojärvi

87 ×0.7

192 ×1.6

GENET

126 ×1.2

50 ×0.9

ECP

20 ×0.4

PPCH

Citations per year, relative to Katri Kantojärvi Katri Kantojärvi (= 1×) peers Weiqiu Cheng

Countries citing papers authored by Katri Kantojärvi

Since Specialization

Citations

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

Fields of papers citing papers by Katri Kantojärvi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katri Kantojärvi

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

All Works

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20 of 20 papers shown

Kantojärvi, Katri, Sonja Sulkava, Tuija Jääskeläinen, et al.. (2025). Genetic predisposition for morningness-eveningness and economic disadvantage: Evidence from Finland over 25 years. Sleep Medicine. 136. 106811–106811.

Kantojärvi, Katri, Sonja Sulkava, Tuija Jääskeläinen, et al.. (2025). Schizophrenia genetic risk and labour market outcomes in the Finnish general population: Are schizophrenia-related traits penalised or rewarded?. Comprehensive Psychiatry. 140. 152600–152600. 1 indexed citations

Ollila, Hanna M., Nasa Sinnott-Armstrong, Katri Kantojärvi, et al.. (2024). Nightmares share genetic risk factors with sleep and psychiatric traits. Translational Psychiatry. 14(1). 123–123. 8 indexed citations

Kantojärvi, Katri, Jetro J. Tuulari, John D. Lewis, et al.. (2023). Association of cumulative prenatal adversity with infant subcortical structure volumes and child problem behavior and its moderation by a coexpression polygenic risk score of the serotonin system. Development and Psychopathology. 36(3). 1027–1042. 3 indexed citations

Bonetti, Leonardo, Tiina Paunio, Katri Kantojärvi, et al.. (2023). Moderate associations between BDNF Val66Met gene polymorphism, musical expertise, and mismatch negativity. Heliyon. 9(5). e15600–e15600. 3 indexed citations

Kantojärvi, Katri, Saara Nolvi, Minna Savukoski, et al.. (2023). Polygenic risk for neuroticism is associated with externalizing symptoms in 2-year-old boys. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 123. 110720–110720. 2 indexed citations

Åberg, Fredrik, Katri Kantojärvi, Ville Männistö, et al.. (2022). Association between arterial hypertension and liver outcomes using polygenic risk scores: a population-based study. Scientific Reports. 12(1). 15581–15581. 2 indexed citations

Simola, Jaana, Felix Siebenhühner, Vladislav Myrov, et al.. (2022). Genetic polymorphisms in COMT and BDNF influence synchronization dynamics of human neuronal oscillations. iScience. 25(9). 104985–104985. 4 indexed citations

Merikanto, Ilona, Katri Kantojärvi, Tiina Paunio, et al.. (2022). Portability of Polygenic Risk Scores for Sleep Duration, Insomnia and Chronotype in 33,493 Individuals. SHILAP Revista de lepidopterología. 5(1). 10–20. 7 indexed citations

10.

Bonetti, Leonardo, Niels Trusbak Haumann, Tiina Paunio, et al.. (2021). Brain predictive coding processes are associated to COMT gene Val158Met polymorphism. NeuroImage. 233. 117954–117954. 16 indexed citations

11.

Morales‐Muñoz, Isabel, Katri Kantojärvi, Outi Saarenpää‐Heikkilä, et al.. (2021). The Effects of Genetic Background for Diurnal Preference on Sleep Development in Early Childhood. Nature and Science of Sleep. Volume 13. 219–228. 9 indexed citations

12.

Kantojärvi, Katri, Juho Pelto, Noora M. Scheinin, et al.. (2020). Partial Support for an Interaction Between a Polygenic Risk Score for Major Depressive Disorder and Prenatal Maternal Depressive Symptoms on Infant Right Amygdalar Volumes. Cerebral Cortex. 30(12). 6121–6134. 21 indexed citations

13.

Kataja, Eeva‐Leena, Jukka Leppänen, Katri Kantojärvi, et al.. (2020). The role of TPH2 variant rs4570625 in shaping infant attention to social signals. Infant Behavior and Development. 60. 101471–101471. 5 indexed citations

14.

Tuulari, Jetro J., Katri Kantojärvi, John D. Lewis, et al.. (2020). A variation in the infant oxytocin receptor gene modulates infant hippocampal volumes in association with sex and prenatal maternal anxiety. Psychiatry Research Neuroimaging. 307. 111207–111207. 8 indexed citations

15.

Kantojärvi, Katri, Jetro J. Tuulari, John D. Lewis, et al.. (2020). Sex‐specific association between infant caudate volumes and a polygenic risk score for major depressive disorder. Journal of Neuroscience Research. 98(12). 2529–2540. 11 indexed citations

16.

Einarsdóttir, Elísabet, Myriam Peyrard‐Janvid, Fahimeh Darki, et al.. (2017). Identification of NCAN as a candidate gene for developmental dyslexia. Scientific Reports. 7(1). 9294–9294. 15 indexed citations

17.

Kantojärvi, Katri, Outi Saarenpää‐Heikkilä, Anneli Kylliäinen, et al.. (2017). Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants. PLoS ONE. 12(8). e0180652–e0180652. 13 indexed citations

18.

Kantojärvi, Katri, Karola Rehnström, Tero Ylisaukko‐oja, et al.. (2011). Fine mapping of Xq11.1‐q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD). Autism Research. 4(3). 228–233. 13 indexed citations

19.

Holt, Richard, Gabrielle Barnby, Elena Maestrini, et al.. (2010). Linkage and candidate gene studies of autism spectrum disorders in European populations. European Journal of Human Genetics. 18(9). 1013–1019. 64 indexed citations

20.

Kantojärvi, Katri, Päivi Onkamo, Raija Vanhala, et al.. (2010). Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample. Psychiatric Genetics. 20(3). 102–108. 27 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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