Search filters

List of works by Kristiina Tammimies

2D:4D Ratio in Neurodevelopmental Disorders: A Twin Study

Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder

scientific article published on 08 July 2019

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

scientific article

Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs

scientific article published on 22 July 2016

Clinical versus automated assessments of morphological variants in twins with and without neurodevelopmental disorders

scientific article published on 12 March 2020

Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders

scientific article

Copy number variation in Han Chinese individuals with autism spectrum disorder

scientific article

De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature review

scientific article

Derivation of human iPS cell lines from monozygotic twins in defined and xeno free conditions

scientific article published on 9 December 2016

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

scientific article published on 30 December 2013

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

scientific article

Dynamical properties of elemental metabolism distinguish attention deficit hyperactivity disorder from autism spectrum disorder

scientific article published on 25 September 2019

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

scientific article published on 13 April 2018

Enrichment of rare copy number variation in children with developmental language disorder

scientific article published on 25 June 2018

Fetal and postnatal metal dysregulation in autism

scientific article

Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia

scientific article

Genetic mechanisms of regression in autism spectrum disorder

scientific article published on 03 May 2019

Genome-wide characteristics of de novo mutations in autism

scientific article published on August 2016

Human LUHMES and NES cells as models for studying primary cilia in neurons

scientific article published in 2023

Hypogonadotrophic hypogonadism, delayed puberty and risk for neurodevelopmental disorders

scientific article published on 12 November 2019

Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons

scientific article

Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay

scientific article published on July 2016

Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes.

scientific article published on 4 June 2018

Long-term social skills group training for children and adolescents with autism spectrum disorder: a randomized controlled trial

scientific article published on 10 May 2018

Medical history of discordant twins and environmental etiologies of autism

scientific article published on 31 January 2017

Minor physical anomalies in neurodevelopmental disorders: a twin study

scientific article published on 28 November 2017

Modeling SHH-driven medulloblastoma with patient iPS cell-derived neural stem cells

scientific article published on 03 August 2020

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

scientific article published on September 2015

Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins

scientific article

Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders

scientific article published on 05 December 2019

Presynaptic dysfunction in CASK-related neurodevelopmental disorders

scientific article published on 14 September 2020

Quo Vadis clinical genomics of ASD?

scientific article published in April 2016

Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder

scientific article published on 29 April 2015

Recurrence quantification analysis to characterize cyclical components of environmental elemental exposures during fetal and postnatal development

scientific article published on 7 November 2017

SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.

scientific article published on 4 January 2011

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

scientific article

Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium

scientific article published in April 2022

Synaptic, transcriptional and chromatin genes disrupted in autism

scientific article

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

scientific article published on 15 April 2014

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

scientific article

The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder

scientific article published on 12 October 2020

The molecular network of the dyslexia candidate gene DYX1C1 shows connection to neuronal migration genes and cytoskeletal proteins

article

The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation

scientific article

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

scientific article published on 29 November 2014

Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications

scientific article published on 15 November 2019

Whole-genome sequencing of quartet families with autism spectrum disorder

scientific article published on 26 January 2015

X-box promoter motif searches: from C. elegans to humans to novel candidate ciliopathies

scientific article published on 13 July 2015

Paulina is supported by:

About Paulina

Help