Jenni Jonasson

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia

Jenni Jonasson, Vesa Juvonen, Pertti Sistonen et al. · European Journal of Human Genetics · 2000 · 65 citations · Full text

Founder Mutation, Mendelian Disorder, Genetic Disorder +5

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

Eva‐Lena Stattin, Ida Maria Westin, Kristina Cederquist et al. · International Journal of Legal Medicine · 2015 · 65 citations · Full text

Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients

Malin Olsson, Urban Hellman, Violaine Planté‐Bordeneuve et al. · Clinical Genetics · 2009 · 45 citations

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

Eva‐Lena Stattin, Ida Maria Boström, Annika Winbo et al. · BMC Cardiovascular Disorders · 2012 · 36 citations · Full text

Expression of ataxin-7 in CNS and non-CNS tissue of normal and SCA7 individuals

Jenni Jonasson, Anna‐Lena Ström, Patricia Hart et al. · Acta Neuropathologica · 2002 · 33 citations

Molecular Neuroscience, Autoimmune Disease, Immunology +6