Josefin Johansson

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 3

Top Topics

High Fat Diet Induced

Gene Expression

Hypertrophic Cardiomyopathy

Top Venues

American journal of medical genetics. Part A

Scientific reports

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Josefin Johansson, Sarah Lidéus, Carina Frykholm, Cecilia Gunnarsson, Filip Mihalič, Sanna Gudmundsson, Sara Ekvall, Anna-Maja Molin, Mai Pham, Mauno Vihinen, Kristina Lagerstedt-Robinson, Ann Nordgren, Per Jemth, Adam Ameur, Göran Annerén, Maria Wilbe, Marie-Louise Bondeson
Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3 domain interactions. European journal of human genetics : EJHG (2023)
Josefin Johansson, Carina Frykholm, Katharina Ericson, Kalliopi Kazamia, Amanda Lindberg, Nancy Mulaiese, Geir Falck, Per-Erik Gustafsson, Sarah Lidéus, Sanna Gudmundsson, Adam Ameur, Marie-Louise Bondeson, Maria Wilbe
Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosis. American journal of medical genetics. Part A 188 (6) (2022)
Sanna Gudmundsson, Maria Wilbe, Beata Filipek-Górniok, Anna-Maja Molin, Sara Ekvall, Josefin Johansson, Amin Allalou, Hans Gylje, Vera M Kalscheuer, Johan Ledin, Göran Annerén, Marie-Louise Bondeson
TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish. Scientific reports 9 (1) (2019)