Katri Pauliina Kantojärvi

Publications

Research output per year 2011 2013 2017 2019 2020 2021 2022 2023 2023

• 22 Article
• 1 Review Article
• 1 Doctoral Thesis

Research output per year

Research output per year

Search results

• 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

  Acosta, H., Kantojärvi, K., Tuulari, J. J., Lewis, J. D., Hashempour, N., Scheinin, N. M., Lehtola, S. J., Nolvi, S., Fonov, V. S., Collins, D. L., Evans, A. C., Parkkola, R., Laehdesmaeki, T., Saunavaara, J., Merisaari, H., Karlsson, L., Paunio, T. & Karlsson, H., Apr 2023, (E-pub ahead of print) In: Development and Psychopathology. 16 p.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

• Maternal executive functioning is associated with infant sustained attention, but not executive functioning, in a sex-specific manner

  Karonen, A., Kataja, E-L., Bridgett, D. J., Paunio, T., Kantojärvi, K., Korja, R., Karlsson, H., Karlsson, L. & Nolvi, S., Mar 2023, (E-pub ahead of print) In: Nordic Psychology. 15 p.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

• Polygenic risk for neuroticism is associated with externalizing symptoms in 2-year-old boys

  Liuhanen, J., Kantojärvi, K., Acosta, H., Pietikäinen, J. T., Nolvi, S., Savukoski, M., Kylliäinen, A., Pölkki, P., Karlsson, H., Karlsson, L., Paavonen, E. J. & Paunio, T., 20 Apr 2023, In: Progress in Neuro-Psychopharmacology and Biological Psychiatry. 123, 8 p., 110720.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File

• Portability of Polygenic Risk Scores for Sleep Duration, Insomnia and Chronotype in 33,493 Individuals

  Perkiö, A., Merikanto, I., Kantojärvi, K., Paunio, T., Sinnott-Armstrong, N., Jones, S. E. & Ollila, H. M., Mar 2023, In: Clocks & sleep. 5, 1, p. 10-20 11 p.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access
• 2022

  Genetic polymorphisms in COMT and BDNF influence synchronization dynamics of human neuronal oscillations

  Simola, J., Siebenhühner, F., Myrov, V., Kantojärvi, K., Paunio, T., Palva, M., Brattico, E. & Palva, S., 16 Sep 2022, In: iScience. 25, 9, 21 p., 104985.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File

• Oxytocin receptor genotype moderates the association between maternal prenatal stress and infant early self-regulation

  Kajanoja, J., Nolvi, S., Kantojärvi, K., Karlsson, L., Paunio, T. & Karlsson, H., Apr 2022, In: Psychoneuroendocrinology. 138, 7 p., 105669.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File
• 2021

  Associations Between IFI44L Gene Variants and Rates of Respiratory Tract Infections During Early Childhood

  Lempainen, J., Korhonen, L. S., Kantojärvi, K., Heinonen, S., Toivonen, L., Räty, P., Ramilo, O., Mejias, A., Vuorinen, T., Waris, M., Karlsson, L., Karlsson, H., Laine, A-P., Paunio, T. & Peltola, V., 1 Jan 2021, In: Journal of Infectious Diseases. 223, 1, p. 157-165 9 p.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File

• A variation in the infant oxytocin receptor gene modulates infant hippocampal volumes in association with sex and prenatal maternal anxiety

  Acosta, H., Tuulari, J. J., Kantojärvi, K., Lewis, J. D., Hashempour, N., Scheinin, N. M., Lehtola, S. J., Fonov, V. S., Collins, D. L., Evans, A., Parkkola, R., Lahdesmaki, T., Saunavaara, J., Merisaari, H., Karlsson, L., Paunio, T. & Karlsson, H., 30 Jan 2021, In: Psychiatry Research. Neuroimaging. 307, 10 p., 111207.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File

• Genetic variants for morningness in relation to habitual sleep-wake behavior and diurnal preference in a population-based sample of 17,243 adults

  Merikanto, I., Kantojärvi, K., Partonen, T., Pesonen, A-K. & Paunio, T., Apr 2021, In: Sleep Medicine. 80, p. 322-332 11 p.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File

• Interactions of genetic variants and prenatal stress in relation to the risk for recurrent respiratory infections in children

  Korhonen, L. S., Lukkarinen, M., Kantojärvi, K., Räty, P., Karlsson, H., Paunio, T., Peltola, V. & Karlsson, L., 7 Apr 2021, In: Scientific Reports. 11, 1, 9 p., 7589.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File
• 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

  Acosta, H., Kantojärvi, K., Hashempour, N., Pelto, J., Scheinin, N. M., Lehtola, S. J., Lewis, J. D., Fonov, V. S., Collins, D. L., Evans, A., Parkkola, R., Lahdesmaki, T., Saunavaara, J., Karlsson, L., Merisaari, H., Paunio, T., Karlsson, H. & Tuulari, J. J., Dec 2020, In: Cerebral Cortex. 30, 12, p. 6121-6134 14 p.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File

• Sex-specific association between infant caudate volumes and a polygenic risk score for major depressive disorder

  Acosta, H., Kantojarvi, K., Tuulari, J. J., Lewis, J. D., Hashempour, N., Scheinin, N. M., Lehtola, S. J., Fonov, V. S., Collins, D. L., Evans, A., Parkkola, R., Lähdesmäki, T., Saunavaara, J., Merisaari, H., Karlsson, L., Paunio, T. & Karlsson, H., Dec 2020, In: Journal of Neuroscience Research. 98, 12, p. 2529-2540 12 p.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File

• The role of TPH2 variant rs4570625 in shaping infant attention to social signals

  Kataja, E-L., Leppänen, J. M., Kantojärvi, K., Pelto, J., Häikiö, T., Korja, R., Nolvi, S., Karlsson, H., Paunio, T. & Karlsson, L., Aug 2020, In: Infant Behavior and Development. 60, 12 p., 101471.

  Research output: Contribution to journal › Article › Scientific › peer-review

• Variation near MTNR1A associates with early development and interacts with seasons

  Sulkava, S. M., Taka, A-M., Kantojärvi, K., Pölkki, P., Morales-Munoz, I., Milani, L., Porkka-Heiskanen, T., Saarenpää-Heikkilä, O., Kylliäinen, A., Paavonen, E. J. & Paunio, T., Dec 2020, In: Journal of Sleep Research. 29, 6, 9 p., 12925.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File
• 2019

  Epigenetic dysregulation of genes related to synaptic long-term depression among adolescents with depressive disorder and sleep symptoms

  Ämmälä, A. J., Urrila, A. S., Lahtinen, A., Santangeli, O., Hakkarainen, A., Kantojärvi, K., Castaneda, A. E., Lundbom, N., Marttunen, M. & Paunio, T., Sep 2019, In: Sleep Medicine. 61, p. 95-103 9 p.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File

• Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes

  Wang, H., Lane, J. M., Jones, S. E., Dashti, H. S., Ollila, H. M., Wood, A. R., van Hees, V. T., Brumpton, B., Winsvold, B. S., Kantojärvi, K., Palviainen, T., Cade, B. E., Sofer, T., Song, Y., Patel, K., Anderson, S. G., Bechtold, D. A., Bowden, J., Emsley, R., Kyle, S. D., & 25 othersLittle, M. A., Loudon, A. S., Scheer, F. A. J. L., Purcell, S. M., Richmond, R. C., Spiegelhalder, K., Tyrrell, J., Zhu, X., Hublin, C., Kaprio, J. A., Kristiansson, K., Sulkava, S., Paunio, T., Hveem, K., Nielsen, J. B., Willer, C. J., Zwart, J. A., Strand, L. B., Frayling, T. M., Ray, D., Lawlor, D. A., Rutter, M. K., Weedon, M. N., Redline, S. & Saxena, R., 13 Aug 2019, In: Nature Communications. 10, 1, 12 p., 3503.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File
• 2017

  Identification of NCAN as a candidate gene for developmental dyslexia

  Einarsdottir, E., Peyrard-Janvid, M., Darki, F., Tuulari, J. J., Merisaari, H., Karlsson, L., Scheinin, N. M., Saunavaara, J., Parkkola, R., Kantojarvi, K., Ammala, A-J., Yu, N. Y-L., Matsson, H., Nopola-Hemmi, J., Karlsson, H., Paunio, T., Klingberg, T., Leinonen, E. & Kere, J., 24 Aug 2017, In: Scientific Reports. 7, 11 p., 9294.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File

• Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants

  Kantojärvi, K., Liuhanen, J., Saarenpää-Heikkilä, O., Satomaa, A-L., Kylliäinen, A., Pölkki, P., Jaatela, J., Toivola, A., Milani, L., Himanen, S-L., Porkka-Heiskanen, T., Paavonen, J. & Paunio, T., 9 Aug 2017, In: PLoS One. 12, 8, 12 p., 0180652.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File
• 2016

  The landscape of copy number variations in Finnish families with autism spectrum disorders

  Kanduri, C., Kantojärvi, K., Salo, P. M., Vanhala, R., Buck, G., Blancher, C., Lahdesmaki, H. & Jarvela, I., Jan 2016, In: Autism Research. 9, 1, p. 9-16 8 p.

  Research output: Contribution to journal › Article › Scientific › peer-review
• 2015

  Association and Promoter Analysis of AVPR1A in Finnish Autism Families

  Kantojärvi, K., Oikkonen, J., Kotala, I., Kallela, J., Vanhala, R., Onkamo, P. & Jarvela, I., Oct 2015, In: Autism Research. 8, 5, p. 634-639 6 p.

  Research output: Contribution to journal › Article › Scientific › peer-review
• 2013

  Exploring genetic susceptibility to autism spectrum disorders

  Kantojärvi, K., 2013, Helsinki: [K. Kantojärvi]. 116 p.

  Research output: Thesis › Doctoral Thesis › Collection of Articles

• Selected rapporteur summaries from the XX world congress of psychiatric genetics, Hamburg, Germany, october 1418, 2012

  Anderson-Schmidt, H., Beltcheva, O., Brandon, M. D., Byrne, E. M., Diehl, E. J., Duncan, L., Gonzalez, S. D., Hannon, E., Kantojärvi, K., Karagiannidis, I., Kos, M. Z., Kotyuk, E., Laufer, B. I., Mantha, K., McGregor, N. W., Meier, S., Nieratschker, V., Spiers, H., Squassina, A., Thakur, G. A., & 6 othersTiwari, Y., Viswanath, B., Way, M. J., Wong, C. C. P., O'Shea, A. & DeLisi, L. E., Mar 2013, In: American journal of medical genetics. Part B, Neuropsychiatric genetics. 162B, 2, p. 96-121 26 p.

  Research output: Contribution to journal › Review Article › peer-review
• 2012

  Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

  Leblond, C. S., Heinrich, J., Delorme, R., Proepper, C., Betancur, C., Huguet, G., Konyukh, M., Chaste, P., Ey, E., Rastam, M., Anckarsater, H., Nygren, G., Gillberg, I. C., Melke, J., Toro, R., Regnault, B., Fauchereau, F., Mercati, O., Lemiere, N., Skuse, D., & 40 othersPoot, M., Holt, R., Monaco, A. P., Jarvela, I., Kantojärvi, K., Vanhala, R., Curran, S., Collier, D. A., Bolton, P., Chiocchetti, A., Klauck, S. M., Poustka, F., Freitag, C. M., Waltes, R., Kopp, M., Duketis, E., Bacchelli, E., Minopoli, F., Ruta, L., Battaglia, A., Mazzone, L., Maestrini, E., Sequeira, A. F., Oliveira, B., Vicente, A., Oliveira, G., Pinto, D., Scherer, S. W., Zelenika, D., Delepine, M., Lathrop, M., Bonneau, D., Guinchat, V., Devillard, F., Assouline, B., Mouren, M-C., Leboyer, M., Gillberg, C., Boeckers, T. M. & Bourgeron, T., 2012, In: PLoS Genetics. 8, 2, p. e1002521 17 p.

  Research output: Contribution to journal › Article › Scientific › peer-review

  Open Access

  File
• 2011

  Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD)

  Kantojärvi, K., Kotala, I., Rehnström, K., Ylisaukko-oja, T., Vanhala, R., Nieminen von Wendt, T., von Wendt, L. & Järvelä, I., 2011, In: Autism Research. 4, 3, p. 228-33 5 p.

  Research output: Contribution to journal › Article › Scientific › peer-review