Hans Matsson

837 total citations
15 papers, 610 citations indexed

About

Hans Matsson is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Hans Matsson has authored 15 papers receiving a total of 610 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Hans Matsson's work include Genetics and Neurodevelopmental Disorders (5 papers), RNA modifications and cancer (3 papers) and Congenital heart defects research (3 papers). Hans Matsson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), RNA modifications and cancer (3 papers) and Congenital heart defects research (3 papers). Hans Matsson collaborates with scholars based in Sweden, Finland and United States. Hans Matsson's co-authors include Niklas Dahl, Juha Kere, Isabel Tapia‐Páez, Edward J. Davey, Stefan Karlsson, Satu Massinen, Kristiina Tammimies, Erik Forsberg, Isao Hamaguchi and Per Levéen and has published in prestigious journals such as PLoS ONE, Molecular and Cellular Biology and Biological Psychiatry.

In The Last Decade

Hans Matsson

14 papers receiving 602 citations

Peers

Hans Matsson

GENET

DEP

EPIDE

CCM

Isabel Tapia‐Páez Sweden

Rebeca Diaz United Kingdom

L. Leigh Field Canada

Hamao Hirota Japan

Theresa A. Grebe United States

Benno Röthlisberger Switzerland

Alexandra Matthews United Kingdom

Estelle Colin France

Elisa Giorgio Italy

Maaike Vreeburg Netherlands

Isabel Tapia‐Páez Sweden

Hans Matsson

393 ×1.0

454 ×1.8

GENET

191 ×1.3

DEP

27 ×0.5

EPIDE

12 ×0.3

CCM

Citations per year, relative to Hans Matsson Hans Matsson (= 1×) peers Isabel Tapia‐Páez

Countries citing papers authored by Hans Matsson

Since Specialization

Citations

This map shows the geographic impact of Hans Matsson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hans Matsson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hans Matsson more than expected).

Fields of papers citing papers by Hans Matsson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hans Matsson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hans Matsson. The network helps show where Hans Matsson may publish in the future.

Co-authorship network of co-authors of Hans Matsson

This figure shows the co-authorship network connecting the top 25 collaborators of Hans Matsson. A scholar is included among the top collaborators of Hans Matsson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hans Matsson. Hans Matsson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Berntsson, Shala Ghaderi, Hans Matsson, Hermine A. van Duyvenvoorde, et al.. (2023). Case report: a novel deep intronic splice-altering variant in DMD as a cause of Becker muscular dystrophy. Frontiers in Genetics. 14. 1226766–1226766.

Einarsdóttir, Elísabet, Hans Matsson, Harriet E. Nilsson, et al.. (2020). Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report. BMC Medical Genetics. 21(1). 87–87. 4 indexed citations

Lauter, Gilbert, Kristiina Tammimies, Hans Matsson, et al.. (2015). X-box promoter motif searches: from C. elegans to humans to novel candidate ciliopathies. HAL (Le Centre pour la Communication Scientifique Directe). 4(S1). 1 indexed citations

Hofmeister, Wolfgang, Daniel Nilsson, Alexandra Topa, et al.. (2014). CTNND2—a candidate gene for reading problems and mild intellectual disability. Journal of Medical Genetics. 52(2). 111–122. 29 indexed citations

Tammimies, Kristiina, Morana Vitezic, Hans Matsson, et al.. (2012). Molecular Networks of DYX1C1 Gene Show Connection to Neuronal Migration Genes and Cytoskeletal Proteins. Biological Psychiatry. 73(6). 583–590. 31 indexed citations

Tammimies, Kristiina, Morana Vitezic, Hans Matsson, et al.. (2012). ISDN2012_0190: The molecular network of the dyslexia candidate gene DYX1C1 shows connection to neuronal migration genes and cytoskeletal proteins. International Journal of Developmental Neuroscience. 30(8). 675–676. 2 indexed citations

Massinen, Satu, Hans Matsson, Kristiina Tammimies, et al.. (2011). Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons. PLoS ONE. 6(6). e20580–e20580. 94 indexed citations

Goumidi, Louisa, Karin Dahlman‐Wright, Isabel Tapia‐Páez, et al.. (2011). Study of Estrogen Receptor-α and Receptor-β Gene Polymorphisms on Alzheimer's Disease. Journal of Alzheimer s Disease. 26(3). 431–439. 15 indexed citations

Massinen, Satu, Kristiina Tammimies, Isabel Tapia‐Páez, et al.. (2009). Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia. Human Molecular Genetics. 18(15). 2802–2812. 48 indexed citations

10.

Dahlqvist, Johanna, et al.. (2009). Multiple epiphyseal dysplasia. Acta Orthopaedica. 80(6). 711–715. 13 indexed citations

11.

Anthoni, Heidi, Marco Zucchelli, Hans Matsson, et al.. (2007). A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Human Molecular Genetics. 16(6). 667–677. 91 indexed citations

12.

Matsson, Hans, Jacqueline Eason, Carol S. Bookwalter, et al.. (2007). Alpha-cardiac actin mutations produce atrial septal defects. Human Molecular Genetics. 17(2). 256–265. 112 indexed citations

13.

Matsson, Hans, Edward J. Davey, Anne-Sophie Fröjmark, et al.. (2006). Erythropoiesis in the Rps19 disrupted mouse: Analysis of erythropoietin response and biochemical markers for Diamond-Blackfan anemia. Blood Cells Molecules and Diseases. 36(2). 259–264. 27 indexed citations

14.

Matsson, Hans, Edward J. Davey, Isao Hamaguchi, et al.. (2004). Targeted Disruption of the Ribosomal Protein S19 Gene Is Lethal Prior to Implantation. Molecular and Cellular Biology. 24(9). 4032–4037. 120 indexed citations

15.

Matsson, Hans, et al.. (1999). Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia. Human Genetics. 105(5). 496–500. 23 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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