Inger Fosdal

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

Mette Nyegaard, Michael T. Overgaard, Mads T. Søndergaard et al. · The American Journal of Human Genetics · 2012 · 391 citations · Full text

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene

Lars Allan Larsen, Inger Fosdal, Paal Skytt Andersen et al. · European Journal of Human Genetics · 1999 · 73 citations

Kvlqt1 Gene, Mendelian Disorder, Genetic Disorder +11

Mutations in the HERG K+-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

Michael Christiansen, Niels Tønder, Lars Allan Larsen et al. · The American Journal of Cardiology · 2005 · 62 citations

Long Qt Syndrome, Channelopathies, Signal Transduction +7

Analysis of short stature homeobox-containing gene ( SHOX ) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity

Giedré Grigelioniené, Jacqueline Schoumans, Lo Neumeyer et al. · Human Genetics · 2001 · 60 citations

Developmental Biology, Bone Morphogenic Protein, Genetic Disorder +9

Third Trimester Fetal Heart Rate Predicts Phenotype and Mutation Burden in the Type 1 Long QT Syndrome

Annika Winbo, Inger Fosdal, Maria Lindh et al. · Circulation Arrhythmia and Electrophysiology · 2015 · 27 citations