Publications by authors named "Hans Matsson"

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Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder.
Stephanie Efthymiou, Cailyn P Leo, Chenghong Deng, Sheng-Jia Lin, Reza Maroofian, Hans Matsson

Am J Hum Genet· May 2025

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Case report: a novel deep intronic splice-altering variant in as a cause of Becker muscular dystrophy.
Shala Ghaderi Berntsson, Hans Matsson, Anna Kristoffersson, Valter Niemelä, Hermine A van Duyvenvoorde

Front Genet· September 2023

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Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report.
Andrea Bieder, Elisabet Einarsdottir, Hans Matsson, Harriet E Nilsson, Jesper Eisfeldt

BMC Med Genet· May 2020

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Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis.
João Fadista, Line Skotte, Frank Geller, Jonas Bybjerg-Grauholm, Sanne Gørtz, Hans Matsson

Hum Mol Genet· January 2019

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Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.
João Fadista, Marie Lund, Line Skotte, Frank Geller, Priyanka Nandakumar, Hans Matsson

Eur J Hum Genet· April 2018

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Evaluation of the gene in the pathogenesis of bladder exstrophy in a Swedish cohort.
Samara Arkani, Jia Cao, Johanna Lundin, Daniel Nilsson, Thomas Källman, Hans Matsson

Hum Genome Var· March 2018

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Identification of NCAN as a candidate gene for developmental dyslexia.
Elisabet Einarsdottir, Myriam Peyrard-Janvid, Fahimeh Darki, Jetro J Tuulari, Harri Merisaari, Hans Matsson

Sci Rep· August 2017

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Human ROBO1 regulates white matter structure in corpus callosum.
Fahimeh Darki, Satu Massinen, Elina Salmela, Hans Matsson, Myriam Peyrard-Janvid

Brain Struct Funct· March 2017

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Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease.
Hans Matsson, Cilla Söderhäll, Elisabet Einarsdottir, Maxime Lamontagne, Sanna Gudmundsson

BMC Pulm Med· November 2016

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Variant Profiling of Candidate Genes in Pancreatic Ductal Adenocarcinoma.
Jiaqi Huang, Johannes-Matthias Löhr, Magnus Nilsson, Ralf Segersvärd, Hans Matsson

Clin Chem· November 2015

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Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family.
Elisabet Einarsdottir, Idor Svensson, Fahimeh Darki, Myriam Peyrard-Janvid, Jessica M Lindvall, Hans Matsson

Hum Genet· November 2015

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Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Hans Matsson, Mikael Huss, Helena Persson, Elisabet Einarsdottir, Ettore Tiraboschi

J Hum Genet· July 2015

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High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia.
Mohsen Karimi, Christer Nilsson, Marios Dimitriou, Monika Jansson, Hans Matsson

Haematologica· June 2015

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CTNND2-a candidate gene for reading problems and mild intellectual disability.
Wolfgang Hofmeister, Daniel Nilsson, Alexandra Topa, Britt-Marie Anderlid, Fahimeh Darki, Hans Matsson

J Med Genet· February 2015

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DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development.
Fahimeh Darki, Myriam Peyrard-Janvid, Hans Matsson, Juha Kere, Torkel Klingberg

J Neurosci· October 2014

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Polymorphisms in the dopamine receptor 2 gene region influence improvements during working memory training in children and adolescents.
Stina Söderqvist, Hans Matsson, Myriam Peyrard-Janvid, Juha Kere, Torkel Klingberg

J Cogn Neurosci· January 2014

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The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
Thomas S Scerri, Fahimeh Darki, Dianne F Newbury, Andrew J O Whitehouse, Myriam Peyrard-Janvid, Hans Matsson

PLoS One· June 2013

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Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins.
Kristiina Tammimies, Morana Vitezic, Hans Matsson, Sylvie Le Guyader, Thomas R Bürglin

Biol Psychiatry· March 2013

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Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.
Fahimeh Darki, Myriam Peyrard-Janvid, Hans Matsson, Juha Kere, Torkel Klingberg

Biol Psychiatry· October 2012

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Dopamine, working memory, and training induced plasticity: implications for developmental research.
Stina Söderqvist, Sissela Bergman Nutley, Myriam Peyrard-Janvid, Hans Matsson, Keith Humphreys

Dev Psychol· May 2012

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Study of estrogen receptor-α and receptor-β gene polymorphisms on Alzheimer's disease.
Louisa Goumidi, Karin Dahlman-Wright, Isabel Tapia-Paez, Hans Matsson, Florence Pasquier

J Alzheimers Dis· January 2012

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Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons.
Satu Massinen, Marie-Estelle Hokkanen, Hans Matsson, Kristiina Tammimies, Isabel Tapia-Páez

PLoS One· November 2011

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Influence of the COMT genotype on working memory and brain activity changes during development.
Iroise Dumontheil, Chantal Roggeman, Tim Ziermans, Myriam Peyrard-Janvid, Hans Matsson

Biol Psychiatry· August 2011

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SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.
Hans Matsson, Kristiina Tammimies, Marco Zucchelli, Heidi Anthoni, Päivi Onkamo

Behav Genet· January 2011

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The SNAP25 gene is linked to working memory capacity and maturation of the posterior cingulate cortex during childhood.
Stina Söderqvist, Fiona McNab, Myriam Peyrard-Janvid, Hans Matsson, Keith Humphreys

Biol Psychiatry· December 2010

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