Kontula K - Search Results

1

Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings.

Perola M, Kainulainen K, Pajukanta P, Terwilliger JD, Hiekkalinna T, Ellonen P, Kaprio J, Koskenvuo M, Kontula K, Peltonen L. Perola M, et al. Among authors: kontula k. J Hypertens. 2000 Nov;18(11):1579-85. doi: 10.1097/00004872-200018110-00008. J Hypertens. 2000. PMID: 11081770

2

Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension.

Kainulainen K, Perola M, Terwilliger J, Kaprio J, Koskenvuo M, Syvänen AC, Vartiainen E, Peltonen L, Kontula K. Kainulainen K, et al. Among authors: kontula k. Hypertension. 1999 Mar;33(3):844-9. doi: 10.1161/01.hyp.33.3.844. Hypertension. 1999. PMID: 10082497

3

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

Taittonen L, Uhari M, Kontula K, Kainulainen K, Miettinen H, Turtinen J, Nuutinen M. Taittonen L, et al. Among authors: kontula k. Am J Hypertens. 1999 Sep;12(9 Pt 1):858-66. doi: 10.1016/s0895-7061(99)00060-6. Am J Hypertens. 1999. PMID: 10509542

4

Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24.

Ohman M, Oksanen L, Kaprio J, Koskenvuo M, Mustajoki P, Rissanen A, Salmi J, Kontula K, Peltonen L. Ohman M, et al. Among authors: kontula k. J Clin Endocrinol Metab. 2000 Sep;85(9):3183-90. doi: 10.1210/jcem.85.9.6797. J Clin Endocrinol Metab. 2000. PMID: 10999806 Clinical Trial.

5

A blood pressure genetic risk score is a significant predictor of incident cardiovascular events in 32,669 individuals.

Havulinna AS, Kettunen J, Ukkola O, Osmond C, Eriksson JG, Kesäniemi YA, Jula A, Peltonen L, Kontula K, Salomaa V, Newton-Cheh C. Havulinna AS, et al. Among authors: kontula k. Hypertension. 2013 May;61(5):987-94. doi: 10.1161/HYPERTENSIONAHA.111.00649. Epub 2013 Mar 18. Hypertension. 2013. PMID: 23509078 Free PMC article.

6

Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene.

Kainulainen K, Swan H, Miettinen H, Viitasalo M, Rovamo L, Toivonen L, Kontula K. Kainulainen K, et al. Among authors: kontula k. Hum Genet. 1995 Oct;96(4):395-400. doi: 10.1007/BF00191795. Hum Genet. 1995. PMID: 7557959

7

Markers for the gene ob and serum leptin levels in human morbid obesity.

Oksanen L, Ohman M, Heiman M, Kainulainen K, Kaprio J, Mustajoki P, Koivisto V, Koskenvuo M, Jänne OA, Peltonen L, Kontula K. Oksanen L, et al. Among authors: kontula k. Hum Genet. 1997 May;99(5):559-64. doi: 10.1007/s004390050406. Hum Genet. 1997. PMID: 9150718

8

Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs.

Ohman M, Oksanen L, Kainulainen K, Jänne OA, Kaprio J, Koskenvuo M, Mustajoki P, Kontula K, Peltonen L. Ohman M, et al. Among authors: kontula k. Eur J Hum Genet. 1999 Feb-Mar;7(2):117-24. doi: 10.1038/sj.ejhg.5200256. Eur J Hum Genet. 1999. PMID: 10196693

9

Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21.

Paavola P, Heliö T, Kiuru M, Halme L, Turunen U, Terwilliger J, Karvonen AL, Julkunen R, Niemelä S, Nurmi H, Färkkilä M, Kontula K. Paavola P, et al. Among authors: kontula k. Eur J Hum Genet. 2001 May;9(5):328-34. doi: 10.1038/sj.ejhg.5200626. Eur J Hum Genet. 2001. PMID: 11378820

10

The SLC6A14 gene shows evidence of association with obesity.

Suviolahti E, Oksanen LJ, Ohman M, Cantor RM, Ridderstrale M, Tuomi T, Kaprio J, Rissanen A, Mustajoki P, Jousilahti P, Vartiainen E, Silander K, Kilpikari R, Salomaa V, Groop L, Kontula K, Peltonen L, Pajukanta P. Suviolahti E, et al. Among authors: kontula k. J Clin Invest. 2003 Dec;112(11):1762-72. doi: 10.1172/JCI17491. J Clin Invest. 2003. PMID: 14660752 Free PMC article.

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