H. Matsson

发表

Identification of NCAN as a candidate gene for developmental dyslexia

T. Paunio, J. Kere, T. Klingberg, 2017, Scientific Reports.

Cognitive DCDC 2 Polymorphism Is Associated with Left Temporoparietal Gray and White Matter Structures during Development

J. Kere, T. Klingberg, F. Darki, 2014 .

DCDC2 Polymorphism Is Associated with Left Temporoparietal Gray and White Matter Structures during Development

Torkel Klingberg, Fahimeh Darki, Juha Kere, 2014, The Journal of Neuroscience.

Diamond-Blackfan anemia blocks erythroid development and mimics defects seen in Deficiency of ribosomal protein S19 in CD34+ cells generated by siRNA

S. Karlsson, M. Wiznerowicz, D. Trono, 2013 .

Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia

D. Bowers, N. Dahl, E. D. de Bont, 1999, Human Genetics.

Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glands

R. Jonsson, A. Bolstad, Y. Hayashi, 2005, Nature Genetics.

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

J. Kere, E. Castrén, U. Landegren, 2009, Human molecular genetics.

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

J. Kere, A. Ameur, T. Klingberg, 2015, Human Genetics.

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

J. Kere, K. Humphreys, T. Klingberg, 2012, Developmental psychology.

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

J. Kere, T. Klingberg, F. Vezzi, 2014, Journal of Medical Genetics.

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

J. Kere, F. Pasquier, J. Lambert, 2011, Journal of Alzheimer's disease : JAD.

Alpha-cardiac actin mutations produce atrial septal defects.

M. Vikkula, A. Jonzon, K. Trybus, 2008, Human molecular genetics.

Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia

D. Bowers, N. Dahl, E. D. de Bont, 1999, Human Genetics.

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

Peter Gustavsson, Hans Matsson, I. Dianzani, 1999, Nature Genetics.

Erythropoiesis in the Rps19 disrupted mouse: Analysis of erythropoietin response and biochemical markers for Diamond-Blackfan anemia.

S. Karlsson, G. Ronquist, K. Miyake, 2006, Blood cells, molecules & diseases.

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

Jessica M. Lindvall, J. Kere, A. Ameur, 2015, Human Genetics.

Polymorphisms in DCDC2 and S100B associate with developmental dyslexia

M. Nöthen, J. Kere, P. Leppänen, 2015, Journal of Human Genetics.

This is an electronic reprint of the original article. This reprint may differ from the original in pagination and typographic detail.

J. Kere, H. Lyytinen, A. Warnke, 2011 .

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

J. Kere, J. Eisfeldt, A. Lindstrand, 2020, BMC Medical Genetics.

Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia

J. Kere, J. Eisfeldt, A. Lindstrand, 2020, bioRxiv.

Molecular Networks of DYX1C1 Gene Show Connection to Neuronal Migration Genes and Cytoskeletal Proteins

Carsten O. Daub, Staffan Strömblad, Tiina Öhman, 2013, Biological Psychiatry.

Three Dyslexia Susceptibility Genes, DYX1C1, DCDC2, and KIAA0319, Affect Temporo-Parietal White Matter Structure

Torkel Klingberg, Fahimeh Darki, Juha Kere, 2012, Biological Psychiatry.

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

D. Hougaard, B. Feenstra, H. Boyd, 2018, Human molecular genetics.

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

M. Perola, A. Chakravarti, D. Hougaard, 2018, European Journal of Human Genetics.

Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons

Juha Kere, Hans Matsson, J. Kere, 2011, PloS one.

Deficiency of ribosomal protein S19 in CD34+ cells generated by siRNA blocks erythroid development and mimics defects seen in Diamond-Blackfan anemia.

Koichi Miyake, Johan Richter, Hans Matsson, 2005, Blood.

Targeted Disruption of the Ribosomal Protein S19 Gene Is Lethal Prior to Implantation

S. Karlsson, N. Dahl, I. Hamaguchi, 2004, Molecular and Cellular Biology.

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

Y. Bossé, D. Postma, J. Kere, 2016, BMC Pulmonary Medicine.

Variant Profiling of Candidate Genes in Pancreatic Ductal Adenocarcinoma.

J. Kere, A. Iafrate, Zongli Zheng, 2015, Clinical Chemistry.

Variant Proﬁling of Candidate Genes in Pancreatic Ductal Adenocarcinoma

J. Kere, A. Iafrate, Zongli Zheng, 2015 .

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

J. Kere, M. Jansson, S. Lehmann, 2015, Haematologica.

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

D. Nilsson, G. Barker, A. Nordenskjöld, 2018, Human Genome Variation.

Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene

N. Dahl, J. Henter, E. Forestier, 2002, British journal of haematology.

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

Heikki Lyytinen, Bertram Müller-Myhsok, Andreas Warnke, 2007, Human molecular genetics.

Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine 1356 Studies of the Ribosomal Protein S19 in Erythropoiesis

H. Matsson, 2004 .

Influence of the COMT Genotype on Working Memory and Brain Activity Changes During Development

Iroise Dumontheil, Chantal Roggeman, Torkel Klingberg, 2011, Biological Psychiatry.

SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations

Heikki Lyytinen, Andreas Warnke, Markus M. Nöthen, 2011, Behavior genetics.

Working memory brain activity and capacity link MAOA polymorphism to aggressive behavior during development

T Klingberg, J. Kere, T. Klingberg, 2012, Translational Psychiatry.

Polymorphisms in the Dopamine Receptor 2 Gene Region Influence Improvements during Working Memory Training in Children and Adolescents

Torkel Klingberg, Juha Kere, Stina Söderqvist, 2014, Journal of Cognitive Neuroscience.

The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure

Dianne F. Newbury, Torkel Klingberg, Fahimeh Darki, 2012, PloS one.

The SNAP25 Gene Is Linked to Working Memory Capacity and Maturation of the Posterior Cingulate Cortex During Childhood

J. Kere, K. Humphreys, T. Klingberg, 2010, Biological Psychiatry.

Human ROBO1 regulates white matter structure in corpus callosum

Torkel Klingberg, Fahimeh Darki, Elina Salmela, 2016, Brain Structure and Function.

Multiple epiphyseal dysplasia

N. Dahl, K. Gustavson, T. Lönnerholm, 2009, Acta orthopaedica.

A clinical and genetic study of 12 cases in a Swedish 6-generation family

N. Dahl, K. Gustavson, T. Lönnerholm, 2009 .

Influence of the COMT Genotype on Working Memory and Brain Activity Changes During Development

J. Kere, T. Klingberg, C. Roggeman, 2011, Biological Psychiatry.

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

T. Klingberg, Sissela Bergman Nutley, Stina Söderqvist, 2012, Developmental psychology.

Dopamine, Working Memory, and Training Induced Plasticity: Implications for Developmental Research Dopamine and Working Memory Evidence from Primates

J. Kere, K. Humphreys, T. Klingberg, 2022 .