Kimmo Kontula

Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia

Päivi J. Laitinen, Kevin M. Brown, Kirsi Piippo et al. · Circulation · 2001 · 734 citations · Full text

Medicine, Cardiology, Genetics +16

Apolipoprotein E, Dementia, and Cortical Deposition of β-Amyloid Protein

Tuomo Polvikoski, Raimo Sulkava, Matti Haltia et al. · New England Journal of Medicine · 1995 · 492 citations

Life Sciences, Genetics, Neurology +17

A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E

Ann‐Christine Syvänen, Katriina Aalto‐Setälä, Leena Harju et al. · Genomics · 1990 · 390 citations

Life Sciences, Genetics, Molecular Genetics +9

Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease

Sun‐Gou Ji, Brian D. Juran, Sören Mucha et al. · Nature Genetics · 2016 · 382 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Sudden Death in Familial Polymorphic Ventricular Tachycardia Associated With Calcium Release Channel (Ryanodine Receptor) Leak

Stephan E. Lehnart, Xander H.T. Wehrens, Päivi J. Laitinen et al. · Circulation · 2004 · 336 citations

Medicine, Cardiology, Physiology +17