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K. Kantojärvi · SciRah

Researcher profile · Semantic Scholar

K. Kantojärvi

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K. Kantojärvi — researcher profile on SciRah

h-index: 14
Works: 67
Citations: 1,146

Most-cited papers

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
C. Leblond, J. Heinrich, R. Delorme, C. Proepper +56 more
2012PLoS Genetics401 citations Open access
Semantic Scholar
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes
He-Ming Wang, J. Lane, S. Jones, H. Dashti +41 more
2019Nature Communications205 citations Open access
Semantic Scholar
Linkage and candidate gene studies of autism spectrum disorders in European populations
R. Holt, G. Barnby, E. Maestrini, E. Bacchelli +9 more
2010European Journal of Human Genetics91 citations Open access
Semantic Scholar
Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample
K. Kantojärvi, P. Onkamo, R. Vanhala, R. Alen +4 more
2010Psychiatric Genetics41 citations
Semantic Scholar
The landscape of copy number variations in Finnish families with autism spectrum disorders
C. Kanduri, K. Kantojärvi, Paula M. Salo, R. Vanhala +4 more
2016Autism Research38 citations
Semantic Scholar
Brain predictive coding processes are associated to COMT gene Val158Met polymorphism
L. Bonetti, S. E. P. Bruzzone, N. A. Sedghi, N. T. Haumann +5 more
2021NeuroImage29 citations Open access
Semantic Scholar
Partial Support for an Interaction Between a Polygenic Risk Score for Major Depressive Disorder and Prenatal Maternal Depressive Symptoms on Infant Right Amygdalar Volumes.
H. Acosta, K. Kantojärvi, N. Hashempour, J. Pelto +14 more
2020Cerebral Cortex29 citations Open access
Semantic Scholar
Fine mapping of Xq11.1‐q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD)
K. Kantojärvi, Ilona Kotala, Karola Rehnström, T. Ylisaukko-oja +4 more
2011Autism Research27 citations
Semantic Scholar
Genetic variants for morningness in relation to habitual sleep-wake behavior and diurnal preference in a population-based sample of 17,243 adults.
I. Merikanto, K. Kantojärvi, T. Partonen, A. Pesonen +1 more
2021Sleep Medicine23 citations Open access
Semantic Scholar
Identification of NCAN as a candidate gene for developmental dyslexia
E. Einarsdottir, M. Peyrard-Janvid, F. Darki, J. Tuulari +15 more
2017Scientific Reports21 citations Open access
Semantic Scholar
Epigenetic dysregulation of genes related to synaptic long-term depression among adolescents with depressive disorder and sleep symptoms.
A. Ämmälä, A. Urrila, A. Lahtinen, Olena Santangeli +6 more
2019Sleep Medicine19 citations Open access
Semantic Scholar
Association and Promoter Analysis of AVPR1A in Finnish Autism Families
K. Kantojärvi, Jaana Oikkonen, Ilona Kotala, Jenni Kallela +3 more
2015Autism Research18 citations
Semantic Scholar
Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants
K. Kantojärvi, J. Liuhanen, O. Saarenpää-Heikkilä, A. Satomaa +9 more
2017PLoS ONE17 citations Open access
Semantic Scholar
Nightmares share genetic risk factors with sleep and psychiatric traits
H. Ollila, N. Sinnott-Armstrong, K. Kantojärvi, M. Broberg +14 more
2024Translational Psychiatry16 citations Open access
Semantic Scholar
Sex‐specific association between infant caudate volumes and a polygenic risk score for major depressive disorder
H. Acosta, K. Kantojärvi, J. Tuulari, J. D. Lewis +13 more
2020Journal of Neuroscience Research13 citations Open access
Semantic Scholar
Oxytocin receptor genotype moderates the association between maternal prenatal stress and infant early self-regulation.
J. Kajanoja, S. Nolvi, K. Kantojärvi, L. Karlsson +2 more
2022Psychoneuroendocrinology11 citations Open access
Semantic Scholar
A variation in the infant oxytocin receptor gene modulates infant hippocampal volumes in association with sex and prenatal maternal anxiety.
H. Acosta, J. Tuulari, K. Kantojärvi, J. D. Lewis +13 more
2020Psychiatry research. Neuroimaging11 citations
Semantic Scholar
Selected Rapporteur Summaries from the XX World Congress of Psychiatric Genetics, Hamburg, Germany, October 14-18, 2012
H. Anderson-Schmidt, O. Beltcheva, Mariko D Brandon, E. Byrne +22 more
2013American Journal of Medical Genetics Part B: Neuropsychiatric Genetics11 citations Open access
Semantic Scholar
Moderate associations between BDNF Val66Met gene polymorphism, musical expertise, and mismatch negativity
L. Bonetti, S. E. P. Bruzzone, T. Paunio, K. Kantojärvi +4 more
2023Heliyon10 citations Open access
Semantic Scholar
Genetic polymorphisms in COMT and BDNF influence synchronization dynamics of human neuronal oscillations
Jaana Simola, Felix Siebenhühner, V. Myrov, K. Kantojärvi +4 more
2021bioRxiv10 citations Open access
Semantic Scholar
Portability of Polygenic Risk Scores for Sleep Duration, Insomnia and Chronotype in 33,493 Individuals
Anna Perkiö, I. Merikanto, K. Kantojärvi, T. Paunio +3 more
2022Clocks & Sleep9 citations Open access
Semantic Scholar
Association between arterial hypertension and liver outcomes using polygenic risk scores: a population-based study
F. Åberg, K. Kantojärvi, V. Männistö, A. But +8 more
2022Scientific Reports9 citations Open access
Semantic Scholar
The Effects of Genetic Background for Diurnal Preference on Sleep Development in Early Childhood
I. Morales-Muñoz, K. Kantojärvi, Veli-Matti Uhre, O. Saarenpää-Heikkilä +7 more
2021Nature and Science of Sleep9 citations Open access
Semantic Scholar
QSOX2 Deficiency-induced short stature, gastrointestinal dysmotility and immune dysfunction
A. Maharaj, Miho Ishida, A. Rybak, Reem Elfeky +11 more
2024Nature Communications8 citations Open access
Semantic Scholar
Genetic predisposition for morningness-eveningness and economic disadvantage: Evidence from Finland over 25 years.
A. Hazak, K. Kantojärvi, J. Liuhanen, S. Sulkava +5 more
2025Sleep Medicine7 citations Open access
Semantic Scholar
The role of TPH2 variant rs4570625 in shaping infant attention to social signals.
Eeva-Leena Kataja, J. Leppänen, K. Kantojärvi, Juho Pelto +6 more
2020Infant Behavior and Development7 citations
Semantic Scholar
Schizophrenia genetic risk and labour market outcomes in the Finnish general population: Are schizophrenia-related traits penalised or rewarded?
Aaro Hazak, J. Liuhanen, K. Kantojärvi, S. Sulkava +5 more
2025Comprehensive Psychiatry6 citations Open access
Semantic Scholar
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.
H. Acosta, K. Kantojärvi, J. Tuulari, J. D. Lewis +14 more
2023Development and Psychopathology6 citations Open access
Semantic Scholar
Associations between IFI44L gene variants and rates of respiratory tract infections during early childhood.
Johanna Lempainen, Laura S. Korhonen, K. Kantojärvi, S. Heinonen +11 more
2020Journal of Infectious Diseases6 citations Open access
Semantic Scholar
Nightmares share strong genetic risk with sleep and psychiatric disorders
H. Ollila, N. Sinnott-Armstrong, K. Kantojärvi, T. Palviainen +9 more
2019bioRxiv5 citations Open access
Semantic Scholar
Genetic background to attention deficit and hyperactivity disorder and attention deficit and hyperactivity disorder symptoms at the age of 5 years: the role of sleep duration
I. Morales-Muñoz, E. J. Paavonen, K. Kantojärvi, T. Härkänen +4 more
2023Sleep4 citations Open access
Semantic Scholar
Variation near MTNR1A associates with early development and interacts with seasons
S. Sulkava, Antti-Mathias Taka, K. Kantojärvi, P. Pölkki +7 more
2020Journal of Sleep Research4 citations Open access
Semantic Scholar
Genetic disparities in sleep traits and human capital development: A 25-year study in Finnish population-based cohorts
A. Hazak, K. Kantojärvi, S. Sulkava, M. Kukk +5 more
2025Scandinavian Journal of Work, Environment and Health3 citations Open access
Semantic Scholar
Polygenic risk for neuroticism is associated with externalizing symptoms in 2-year-old boys.
J. Liuhanen, K. Kantojärvi, H. Acosta, J. Pietikäinen +8 more
2023Progress in Neuro-psychopharmacology and Biological Psychiatry3 citations Open access
Semantic Scholar
Maternal executive functioning is associated with infant sustained attention, but not executive functioning, in a sex-specific manner
Anniina Karonen, Eeva-Leena Kataja, David J. Bridgett, T. Paunio +5 more
2023Nordic Psychology3 citations Open access
Semantic Scholar
Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups
He-Ming Wang, J. Lane, S. Jones, H. Dashti +38 more
2018bioRxiv3 citations Open access
Semantic Scholar
Polygenic Risks for Mood Disorders and Economic Well‐being: Study of Finnish Cohorts
A. Hazak, J. Liuhanen, K. Kantojärvi, M. Kukk +6 more
2026Depression and Anxiety2 citations Open access
Semantic Scholar
Neuroticism Genetic Risk, Gender, and Economic Disadvantage
A. Hazak, J. Liuhanen, K. Kantojärvi, S. Sulkava +5 more
2026European Journal of Personality2 citations Open access
Semantic Scholar
Sleep and schizophrenia polygenic scores in non-affective and affective psychotic disorders
Erik Cederlöf, M. Holm, A. Kämpe, Ari V. Ahola-Olli +17 more
2025Psychological Medicine2 citations Open access
Semantic Scholar
Early life gut microbial and metabolic shifts reflected in stool consistency- a gut transit time proxy
A. Aatsinki, Matilda Kråkström, Katja Salonen, H. Isokääntä +13 more
2025bioRxiv2 citations Open access
Semantic Scholar
Interactions of genetic variants and prenatal stress in relation to the risk for recurrent respiratory infections in children
Laura S. Korhonen, M. Lukkarinen, K. Kantojärvi, Panu Räty +4 more
2021Scientific Reports2 citations Open access
Semantic Scholar
Temporal Associations Between Human Milk Metabolites and the Infant Gut Microbiome and metabolome
H. Isokääntä, L. Perasto, S. Lamichhane, Minka Ovaska +12 more
2025bioRxiv1 citations Open access
Semantic Scholar
Direct and indirect genetic pathways between parental neuroticism and offspring emotional problems across development: evidence from 7 cohorts across 5 European nations
H. Sallis, I. Costantini, T. M. Chuong, K. Kantojärvi +20 more
2024medRxiv1 citations Open access
Semantic Scholar
BDNF Val66Met polymorphism as putative genetic substrate of music-induced plasticity in auditory prediction
S. E. P. Bruzzone, L. Bonetti, T. Paunio, K. Kantojärvi +3 more
2021bioRxiv1 citations Open access
Semantic Scholar
Exploring Genetic Susceptibility to Autism Spectrum Disorders
K. Kantojärvi
20131 citations
Semantic Scholar
Polygenic risk for schizophrenia is associated with psychomotor vigilance performance impairment during sleep deprivation in women
J. Liuhanen, L. Skeiky, K. Kantojärvi, Paavo Laitinen +4 more
2026Translational Psychiatry0 citations Open access
Semantic Scholar
Nature's Curriculum: Genes Linked to Educational Attainment and Adult Socioeconomic Status Across Birth Cohorts in a Nordic Welfare State.
Henrik Dobewall, M. Vaalavuo, P. Böckerman, Jutta Viinikainen +5 more
2026Demography0 citations Open access
Semantic Scholar
Evening chronotype and disability pensions: 12-year register-based follow-up of middle-aged adults from the Northern Finland birth cohort 1966.
Tapio Räihä, I. Merikanto, Iiro Nerg, Marko Korhonen +3 more
2026Occupational and Environmental Medicine0 citations
Semantic Scholar
Associations of ADHD genetic risk with objective and subjective economic wellbeing: evidence from Finnish population-based cohorts
A. Hazak, J. Liuhanen, K. Kantojärvi, S. Sulkava +4 more
2026Social Psychiatry and Psychiatric Epidemiology0 citations Open access
Semantic Scholar
Cumulative vulnerabilities increase perceived unmet needs and delays in access to social services in migrant origin and Finnish-born populations
K. Kantojärvi, Regina García Velázquez, J. Maki-Opas, H. Kuusio +1 more
2026International Journal for Equity in Health0 citations Open access
Semantic Scholar

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