EYS mutations and implementation of minigene assay for variant classification in EYS-associated retinitis pigmentosa in northern Sweden

por Westin, Ida Maria, Jonsson, Frida, Österman, Lennart, Holmberg, Monica, Burstedt, Marie, Golovleva, Irina
Publicado en Sci Rep (2021)

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

por Winbo, Annika, Stattin, Eva-Lena, Westin, Ida Maria, Norberg, Anna, Persson, Johan, Jensen, Steen M., Rydberg, Annika
Publicado en BMC Med Genet (2017)

Genetic screening in sudden cardiac death in the young can save future lives

por Stattin, Eva-Lena, Westin, Ida Maria, Cederquist, Kristina, Jonasson, Jenni, Jonsson, Björn-Anders, Mörner, Stellan, Norberg, Anna, Krantz, Peter, Wisten, Aase
Publicado en Int J Legal Med (2015)