Ulla‐Britt Diamant

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Najim Lahrouchi, Rafik Tadros, Lia Crotti et al. · Circulation · 2020 · 141 citations · Full text

Life Sciences, Cardiology, Genetics +15

QT correction using Bazett’s formula remains preferable in long QT syndrome type 1 and 2

Pia Dahlberg, Ulla‐Britt Diamant, Thomas Gilljam et al. · Annals of Noninvasive Electrocardiology · 2020 · 81 citations · Full text

Medicine, Cardiology, Internal Medicine +15

Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden

Annika Winbo, Eva‐Lena Stattin, Ulla‐Britt Diamant et al. · EP Europace · 2012 · 45 citations

Life Sciences, Cardiology, Genetics +17

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 · 37 citations · Full text

Life Sciences, Cardiology, Genetics +15

Origin of the Swedish long QT syndrome Y111C/KCNQ1 founder mutation

Annika Winbo, Ulla‐Britt Diamant, Annika Rydberg et al. · Heart Rhythm · 2010 · 33 citations

Life Sciences, Genetics, Molecular Genetics +9