Tammimies, Kristiina

Synaptic, transcriptional and chromatin genes disrupted in autism

Study, T. D., De Rubeis, S., Autism, H. M. C. F., UK10K Consortium, The Autism Sequencing Consortium, He, X., Goldberg, A. P., Poultney, C. S., Samocha, K., Ercument Cicek, A., et al. (2014) · Nature

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 2,746

Whole-genome sequencing of quartet families with autism spectrum disorder

Yuen, R. K. C., Thiruvahindrapuram, B., Merico, D., Walker, S., Tammimies, K., Hoang, N., Chrysler, C., Nalpathamkalam, T., Pellecchia, G., Liu, Y., et al. (2015) · Nature Medicine

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 514

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

Tammimies, K., Marshall, C. R., Walker, S., Kaur, G., Thiruvahindrapuram, B., Lionel, A. C., Yuen, R. K. C., Uddin, M., Roberts, W., Weksberg, R., et al. (2015) · JAMA

Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities

Cited by 419

Genome-wide characteristics of de novo mutations in autism

Yuen, R. K., Merico, D., Cao, H., Pellecchia, G., Alipanahi, B., Thiruvahindrapuram, B., Tong, X., Sun, Y., Cao, D., Zhang, T., et al. (2016) · npj Genomic Medicine

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 216

Fetal and postnatal metal dysregulation in autism

Arora, M., Reichenberg, A., Willfors, C., Austin, C., Gennings, C., Berggren, S., Lichtenstein, P., Anckarsäter, H., Tammimies, K., & Bölte, S. (2017) · Nature Communications

Heavy Metal Exposure and ToxicityAutism Spectrum Disorder Research

Cited by 169

Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder

Uddin, M., Tammimies, K., Pellecchia, G., Alipanahi, B., Hu, P., Wang, Z., Pinto, D., Lau, L., Nalpathamkalam, T., Marshall, C. R., et al. (2014) · Nature Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 163

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

Lionel, A. C., Tammimies, K., Vaags, A. K., Rosenfeld, J. A., Ahn, J. W., Merico, D., Noor, A., Runke, C. K., Pillalamarri, V. K., Carter, M. T., et al. (2014) · Human Molecular Genetics

Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities

Cited by 163

Genetic correlates of phenotypic heterogeneity in autism

Warrier, V., Zhang, X., Reed, P., Havdahl, A., Moore, T. M., Cliquet, F., Leblond, C. S., Rolland, T., Rosengren, A., LEAP, E.-A., et al. (2022) · Nature Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 152

Social Skills Training for Children and Adolescents With Autism Spectrum Disorder: A Randomized Controlled Trial

Choque Olsson, N., Flygare, O., Coco, C., Görling, A., Råde, A., Chen, Q., Lindstedt, K., Berggren, S., Serlachius, E., Jonsson, U., et al. (2017) · Journal of the American Academy of Child & Adolescent Psychiatry

Autism Spectrum Disorder ResearchBehavioral and Psychological Studies

Cited by 120

Dynamical features in fetal and postnatal zinc-copper metabolic cycles predict the emergence of autism spectrum disorder

Curtin, P., Austin, C., Curtin, A., Gennings, C., Arora, M., (for the Emergent Dynamical Systems Group), Tammimies, K., Willfors, C., Berggren, S., Siper, P., et al. (2018) · Science Advances

Trace Elements in HealthAutism Spectrum Disorder Research

Cited by 90

The Roots of Autism and ADHD Twin Study in Sweden (RATSS)

Bölte, S., Willfors, C., Berggren, S., Norberg, J., Poltrago, L., Mevel, K., Coco, C., Fransson, P., Borg, J., Sitnikov, R., et al. (2014) · Twin Research and Human Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 71

Medical history of discordant twins and environmental etiologies of autism

Willfors, C., Carlsson, T., Anderlid, B.-M., Nordgren, A., Kostrzewa, E., Berggren, S., Ronald, A., Kuja-Halkola, R., Tammimies, K., & Bölte, S. (2017) · Translational Psychiatry

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

Cited by 35

EU-AIMS Longitudinal European Autism Project (LEAP): the autism twin cohort

the EU-AIMS LEAP group, Isaksson, J., Tammimies, K., Neufeld, J., Cauvet, É., Lundin, K., Buitelaar, J. K., Loth, E., Murphy, D. G. M., Spooren, W., et al. (2018) · Molecular Autism

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 17

Molecular interactome of HNRNPU reveals regulatory networks in neuronal differentiation and DNA methylation

Oksanen, M., Mastropasqua, F., Mazan-Mamczarz, K., Martindale, J. L., Ye, X., Arora, A., Banskota, N., Gorospe, M., & Tammimies, K. (2026) · Nucleic Acids Research

Genetics and Neurodevelopmental DisordersRNA Research and Splicing

Cited by 7

Quo Vadis clinical genomics of ASD?

Tammimies, K., Falck-Ytter, T., & Bölte, S. (2016) · Autism

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 5