K. Kontula

发表

Familial and Sporadic Inflammatory Bowel Disease: Comparison of Clinical Features and Serological Markers in a Genetically Homogeneous Population

H. Järvinen, M. Färkkilä, T. Heliö, 2002, Scandinavian journal of gastroenterology.

Melanocortin-3-receptor gene variants in morbid obesity

C. Schalin-Jäntti, K. Kontula, L. Oksanen, 2003, International Journal of Obesity.

Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA

J. Lonnqvist, L. Peltonen, A. Paetau, 1997, Neurology.

Development of Cushing’s disease in a patient with anorexia nervosa

A. Paetau, R. Pelkonen, K. Kontula, 1984, Journal of endocrinological investigation.

Prevalence of familial hypercholesterolemia among young north Karelian patients with coronary heart disease: a study based on diagnosis by polymerase chain reaction.

M. Taskinen, K. Kontula, U. Koivisto, 1993, Journal of Lipid Research.

Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low‐density‐lipoprotein receptor gene and PvuII polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment

K. Kontula, A. Vuorio, M. Tikkanen, 1995, Journal of internal medicine.

A novel polymorphism of apolipoprotein A-IV is the result of an asparagine to serine substitution at residue 127.

M. Taskinen, J. Metso, P. Koskinen, 1992, Biochimica et biophysica acta.

Prevalence of Alzheimer’s disease in very elderly people

J. Hardy, R. Sulkava, K. Kontula, 2001, Neurology.

Lipoproteins and their genetic variation in subjects with and without angiographically verified coronary artery disease.

M. Nieminen, M. Taskinen, M. Jauhiainen, 1992, Arteriosclerosis and thrombosis : a journal of vascular biology.

Glucocorticoid receptors in adrenocorticoid disorders.

L. Andersson, R. Pelkonen, K. Kontula, 1980, The Journal of clinical endocrinology and metabolism.

Clinical Research

M. Viitasalo, L. Toivonen, J. Paavola, 2022 .

A single-base substitution in the proximal Sp1 site of the human low density lipoprotein receptor promoter as a cause of heterozygous familial hypercholesterolemia.

O. Jänne, K. Kontula, J. Palvimo, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Common candidate gene variants are associated with QT interval duration in the general population

V. Salomaa, M. Viitasalo, P. Lahermo, 2009, Journal of internal medicine.

Common Candidate Gene Variants Are Associated with Qt Interval Duration in the General Population from The

L. Peltonen, V. Salomaa, M. Nieminen, 2022 .

Angiotensin converting enzyme gene insertion/deletion polymorphism, angiotensinogen gene polymorphisms, family history of hypertension, and childhood blood pressure.

K. Kontula, M. Uhari, M. Nuutinen, 1999, American journal of hypertension.

Telomere length and cardiovascular risk in hypertensive patients with left ventricular hypertrophy: the LIFE study

R. Devereux, K. Silventoinen, U. Faire, 2011, Journal of Human Hypertension.

Apolipoprotein A-IFin. Dominantly inherited hypoalphalipoproteinemia due to a single base substitution in the apolipoprotein A-I gene.

J. Viikari, L. Paulin, H. Gylling, 1997, Arteriosclerosis, thrombosis, and vascular biology.