עקוב אחר
Kristiina Tammimies
Kristiina Tammimies
Centre of Neurodevelopmental Disorders at Karolinska Institutet
כתובת אימייל מאומתת בדומיין ki.se
כותרת
צוטט על ידי
צוטט על ידי
שנה
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
27032014
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
5862015
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
4162015
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
2322016
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
184*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
1772014
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
1702014
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
1672017
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
1522011
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
942008
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
932017
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
812014
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
802009
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
772018
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
632014
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
572013
Genetic mechanisms of regression in autism spectrum disorder
K Tammimies
Neuroscience & Biobehavioral Reviews 102, 208-220, 2019
512019
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
472017
The association between somatic health, autism spectrum disorder, and autistic traits
PY Pan, K Tammimies, S Bölte
Behavior Genetics 50 (4), 233-246, 2020
462020
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
432011
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מאמרים 1–20