The scientist’s investigation covers issues in Internal medicine, Endocrinology, Genetics, Allele and Apolipoprotein E. His Internal medicine research includes themes of Genotype, Locus and Cardiology. His Endocrinology study incorporates themes from Receptor, Ryanodine receptor 2, Ryanodine receptor and QT interval.
Kimmo Kontula focuses mostly in the field of Genetics, narrowing it down to matters related to Long QT syndrome and, in some cases, Sotalol and Torsades de pointes. His Allele research is multidisciplinary, incorporating elements of SNP, Single-nucleotide polymorphism and Familial hypercholesterolemia. The concepts of his Apolipoprotein E study are interwoven with issues in Dementia and Age of onset.
His main research concerns Internal medicine, Endocrinology, Genetics, Cardiology and Long QT syndrome. His study explores the link between Internal medicine and topics such as Allele that cross with problems in Single-nucleotide polymorphism. He has included themes like Receptor, Ryanodine receptor 2 and Genotype in his Endocrinology study.
His research integrates issues of Minor allele frequency and Left ventricular hypertrophy in his study of Cardiology. His Long QT syndrome research is multidisciplinary, relying on both hERG and Asymptomatic. His research in Catecholaminergic polymorphic ventricular tachycardia intersects with topics in Ventricular tachycardia and Tachycardia.
Kimmo Kontula mainly focuses on Internal medicine, Cardiology, Genome-wide association study, Long QT syndrome and Blood pressure. Many of his studies involve connections with topics such as Endocrinology and Internal medicine. His Endocrinology research integrates issues from Mutation and Catecholaminergic polymorphic ventricular tachycardia.
Kimmo Kontula interconnects Minor allele frequency and Cohort study in the investigation of issues within Cardiology. He combines subjects such as Essential hypertension, Allele and Locus with his study of Genome-wide association study. His work carried out in the field of Long QT syndrome brings together such families of science as Psychiatry, Asymptomatic, Potassium channel and Mutation.
Kimmo Kontula focuses on Internal medicine, Genome-wide association study, Pharmacology, Long QT syndrome and Genetics. His study in Internal medicine is interdisciplinary in nature, drawing from both Endocrinology, Genetic association, MEDLINE and Cardiology. His studies in Endocrinology integrate themes in fields like Ryanodine receptor 2, Catecholaminergic polymorphic ventricular tachycardia, Ryanodine receptor and Tachycardia.
His Genome-wide association study research is multidisciplinary, incorporating perspectives in Pharmacogenomics, Blood pressure and Locus. The various areas that Kimmo Kontula examines in his Long QT syndrome study include Sudden cardiac death and Potassium channel. His biological study deals with issues like Candidate gene, which deal with fields such as QRS complex.
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Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia
Päivi J. Laitinen;Kevin M. Brown;Kirsi Piippo;Heikki Swan.
A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E.
Ann-Christine Syvänen;Katriina Aalto-Setälä;Leena Harju;Kimmo Kontula.
Apolipoprotein E, dementia, and cortical deposition of beta-amyloid protein.
Tuomo Polvikoski;Raimo Sulkava;Matti Haltia;Katariina Kainulainen.
The New England Journal of Medicine (1995)
Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts.
Heikki Swan;Kirsi Piippo;Matti Viitasalo;Päivi Heikkilä.
Journal of the American College of Cardiology (1999)
CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn’s disease
T Heliö;L Halme;M Lappalainen;H Fodstad.
Family and twin studies in inflammatory bowel disease
Leena Halme;Paulina Paavola-Sakki;Ulla Turunen;Maarit Lappalainen.
World Journal of Gastroenterology (2006)
Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture.
Anna L. Lahti;Ville J. Kujala;Hugh Chapman;Ari-Pekka Koivisto.
Disease Models & Mechanisms (2012)
Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.
Andrew R. Marks;Silvia Priori;Mirella Memmi;Kimmo Kontula.
Journal of Cellular Physiology (2002)
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Dan E. Arking;Sara L. Pulit;Sara L. Pulit;Sara L. Pulit;Lia Crotti;Pim Van Der Harst.
Nature Genetics (2014)
Primary structure of human insulin-like growth factor-binding protein/placental protein 12 and tissue-specific expression of its mRNA
M. Julkunen;R. Koistinen;K. Aalto-Setala;M. Seppala.
FEBS Letters (1988)
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