Satu Massinen

521 total citations
9 papers, 384 citations indexed

About

Satu Massinen is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Satu Massinen has authored 9 papers receiving a total of 384 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Satu Massinen's work include Reading and Literacy Development (3 papers), Cognitive and developmental aspects of mathematical skills (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Satu Massinen is often cited by papers focused on Reading and Literacy Development (3 papers), Cognitive and developmental aspects of mathematical skills (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Satu Massinen collaborates with scholars based in Sweden, Finland and United States. Satu Massinen's co-authors include Juha Kere, Isabel Tapia‐Páez, Kristiina Tammimies, Hans Matsson, Jaana Nopola‐Hemmi, Myriam Peyrard‐Janvid, Ananda L. Roy, Eero Ċastrén, Riitta Hari and Satu Lamminmäki and has published in prestigious journals such as Journal of Neuroscience, The Journal of Immunology and PLoS ONE.

In The Last Decade

Satu Massinen

9 papers receiving 377 citations

Peers

Satu Massinen

GENET

DEP

MB

CN

SP

Nadine Kluck Germany

F.F. Brockschmidt Germany

Mark Lathrop France

Yixun Li China

Avinash M. Veerappa India

Diana J. Slater United States

D. Curtis Jamison United States

Carol Mayne Australia

Lou Ann Barnett United States

She Min Zeng United States

Nadine Kluck Germany

Satu Massinen

166 ×0.8

GENET

140 ×0.8

DEP

94 ×0.6

MB

44 ×1.0

CN

53 ×1.2

SP

Citations per year, relative to Satu Massinen Satu Massinen (= 1×) peers Nadine Kluck

Countries citing papers authored by Satu Massinen

Since Specialization

Citations

This map shows the geographic impact of Satu Massinen'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 Satu Massinen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Satu Massinen more than expected).

Fields of papers citing papers by Satu Massinen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Satu Massinen. 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 Satu Massinen. The network helps show where Satu Massinen may publish in the future.

Co-authorship network of co-authors of Satu Massinen

This figure shows the co-authorship network connecting the top 25 collaborators of Satu Massinen. A scholar is included among the top collaborators of Satu Massinen 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 Satu Massinen. Satu Massinen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

1.

Massinen, Satu, et al.. (2016). Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1. Journal of Neurodevelopmental Disorders. 8(1). 4–4. 8 indexed citations

2.

Darki, Fahimeh, Satu Massinen, Elina Salmela, et al.. (2016). Human ROBO1 regulates white matter structure in corpus callosum. Brain Structure and Function. 222(2). 707–716. 4 indexed citations

3.

Hannula‐Jouppi, Katariina, Satu Massinen, Tuula Siljander, et al.. (2013). Genetic Susceptibility to Non-Necrotizing Erysipelas/Cellulitis. PLoS ONE. 8(2). e56225–e56225. 10 indexed citations

4.

Lamminmäki, Satu, Satu Massinen, Jaana Nopola‐Hemmi, Juha Kere, & Riitta Hari. (2012). HumanROBO1Regulates Interaural Interaction in Auditory Pathways. Journal of Neuroscience. 32(3). 966–971. 39 indexed citations

5.

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

6.

Haapasalo, Karita, Jaana Vuopio, Jaana Syrjänen, et al.. (2011). Acquisition of Complement Factor H Is Important for Pathogenesis of Streptococcus pyogenes Infections: Evidence from Bacterial In Vitro Survival and Human Genetic Association. The Journal of Immunology. 188(1). 426–435. 31 indexed citations

7.

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

8.

Tapia‐Páez, Isabel, Kristiina Tammimies, Satu Massinen, Ananda L. Roy, & Juha Kere. (2008). The complex of TFII‐I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia. The FASEB Journal. 22(8). 3001–3009. 59 indexed citations

9.

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

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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