Salla M Rusanen (Salla Rusanen, Salla Välipakka)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 3

Top Topics

Dna Methylation

Genome Wide Identification

Muscular Dystrophy

Top Venues

Neurology. Genetics

Annals of clinical and translational neurology

Samfundet Folkhälsan

University of Helsinki (MSC)

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

Affiliation History

Samfundet Folkhälsan Dec 01 2017

Finland

PhD student :: Folkhälsan Research Center

Education History

University of Helsinki Aug 01 2015 - Jun 14 2017

Finland

MSC :: Faculty of Biological and Environmental Sciences

University of Helsinki Aug 01 2012 - May 25 2015

Finland

BSC :: Faculty of Biological and Environmental Sciences

Publications

Mridul Johari, George Papadimas, Constantinos Papadopoulos, Sophia Xirou, Aikaterini Kanavaki, Margarita Chrysanthou-Piterou, Salla M Rusanen, Marco Savarese, Peter Hackman, Bjarne Udd
Adult-onset dominant muscular dystrophy in Greek families caused by Annexin A11. Annals of clinical and translational neurology 9 (10) (2022)
Peter Hackman, Salla M Rusanen, Mridul Johari, Anna Vihola, Per Harald Jonson, Jaakko Sarparanta, Kati Donner, Päivi Lahermo, Sampo Koivunen, Helena Luque, Merja Soininen, Ibrahim Mahjneh, Mari Auranen, Meharji Arumilli, Marco Savarese, Bjarne Udd
Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene. Neurology. Genetics 7 (6) (2021)
Manu Jokela, Giorgio Tasca, Anna Vihola, Eugenio Mercuri, Per Harald Jonson, Sara Lehtinen, Salla M Rusanen, Marika Pane, Maria Donati, Mridul Johari, Marco Savarese, Sanna Huovinen, Pirjo Isohanni, Johanna Palmio, Päivi Hartikainen, Bjarne Udd
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild calf-predominant myopathy. Neurology 92 (14) (2019)