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List of works by Hans Matsson

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

scientific article

CTNND2-a candidate gene for reading problems and mild intellectual disability

scientific article published on 3 December 2014

DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development.

scientific article published in October 2014

Dopamine, working memory, and training induced plasticity: implications for developmental research

scientific article

Evaluation of the ISL1 gene in the pathogenesis of bladder exstrophy in a Swedish cohort

scientific article published on 29 March 2018

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

scientific article

Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus

scientific article

Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis

scientific article published on 01 January 2019

High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia

scientific article published on 13 March 2015

Human ROBO1 regulates white matter structure in corpus callosum

scientific article published on 30 May 2016

Identification of NCAN as a candidate gene for developmental dyslexia

scientific article published on 24 August 2017

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

scientific article

Influence of the COMT genotype on working memory and brain activity changes during development

scientific article published on 22 April 2011

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

scientific article

Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family

scientific article

Polymorphisms in DCDC2 and S100B associate with developmental dyslexia

scientific article published on 16 April 2015

Polymorphisms in the dopamine receptor 2 gene region influence improvements during working memory training in children and adolescents

scientific article published on 3 September 2013

Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report

scientific article published on 01 May 2020

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

Study of estrogen receptor-α and receptor-β gene polymorphisms on Alzheimer's disease

scientific article published in January 2011

Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease

scientific article

The SNAP25 gene is linked to working memory capacity and maturation of the posterior cingulate cortex during childhood

scientific article published on 15 October 2010

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure

scientific article

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

article

Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.

scientific article published on 9 June 2012

Variant Profiling of Candidate Genes in Pancreatic Ductal Adenocarcinoma

scientific article published on 16 September 2015

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