Kristiina Tammimies
Kristiina Tammimies
Centre of Neurodevelopmental Disorders at Karolinska Institutet
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Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
Whole-genome sequencing of quartet families with autism spectrum disorder
RKC Yuen, B Thiruvahindrapuram, D Merico, S Walker, K Tammimies, ...
Nature medicine 21 (2), 185-191, 2015
Molecular diagnostic yield of chromosomal microarray analysis and whole-exome sequencing in children with autism spectrum disorder
K Tammimies, CR Marshall, S Walker, G Kaur, B Thiruvahindrapuram, ...
Jama 314 (9), 895-903, 2015
Genome-wide characteristics of de novo mutations in autism
RKC Yuen, D Merico, H Cao, G Pellecchia, B Alipanahi, ...
NPJ genomic medicine 1 (1), 1-10, 2016
Social skills training for children and adolescents with autism spectrum disorder: a randomized controlled trial
NC Olsson, O Flygare, C Coco, A Görling, A Råde, Q Chen, K Lindstedt, ...
Journal of the American Academy of Child & Adolescent Psychiatry 56 (7), 585-592, 2017
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
AC Lionel, K Tammimies, AK Vaags, JA Rosenfeld, JW Ahn, D Merico, ...
Human molecular genetics 23 (10), 2752-2768, 2014
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder
M Uddin, K Tammimies, G Pellecchia, B Alipanahi, P Hu, Z Wang, D Pinto, ...
Nature genetics 46 (7), 742-747, 2014
Fetal and postnatal metal dysregulation in autism
M Arora, A Reichenberg, C Willfors, C Austin, C Gennings, S Berggren, ...
Nature communications 8 (1), 15493, 2017
Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons
S Massinen, ME Hokkanen, H Matsson, K Tammimies, I Tapia-Páez, ...
PloS one 6 (6), e20580, 2011
A novel way to measure and predict development: A heuristic approach to facilitate the early detection of neurodevelopmental disorders
PB Marschik, FB Pokorny, R Peharz, D Zhang, J O’Muircheartaigh, ...
Current neurology and neuroscience reports 17, 1-15, 2017
The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia
I Tapia-Páez, K Tammimies, S Massinen, AL Roy, J Kere
The FASEB Journal 22 (8), 3001, 2008
The roots of autism and ADHD twin study in Sweden (RATSS)
S Bölte, C Willfors, S Berggren, J Norberg, L Poltrago, K Mevel, C Coco, ...
Twin Research and Human Genetics 17 (3), 164-176, 2014
Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia
S Massinen, K Tammimies, I Tapia-Páez, H Matsson, ME Hokkanen, ...
Human molecular genetics 18 (15), 2802-2812, 2009
Dynamical features in fetal and postnatal zinc-copper metabolic cycles predict the emergence of autism spectrum disorder
P Curtin, C Austin, A Curtin, C Gennings, M Arora, ...
Science advances 4 (5), eaat1293, 2018
Copy number variation in Han Chinese individuals with autism spectrum disorder
MJ Gazzellone, X Zhou, AC Lionel, M Uddin, B Thiruvahindrapuram, ...
Journal of neurodevelopmental disorders 6, 1-7, 2014
Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins
K Tammimies, M Vitezic, H Matsson, S Le Guyader, TR Bürglin, T Öhman, ...
Biological psychiatry 73 (6), 583-590, 2013
Genetic mechanisms of regression in autism spectrum disorder
K Tammimies
Neuroscience & Biobehavioral Reviews 102, 208-220, 2019
The association between somatic health, autism spectrum disorder, and autistic traits
PY Pan, K Tammimies, S Bölte
Behavior Genetics 50 (4), 233-246, 2020
Derivation of human iPS cell lines from monozygotic twins in defined and xeno free conditions
E Uhlin, H Rönnholm, K Day, M Kele, K Tammimies, S Bölte, A Falk
Stem cell research 18, 22-25, 2017
SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations
H Matsson, K Tammimies, M Zucchelli, H Anthoni, P Onkamo, ...
Behavior genetics 41, 134-140, 2011
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