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Kimmo Kontula

Showing results (81-90 of 97) with videos related to

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Circulation. Cardiovascular Genetics|August 18, 2016
Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?Lia Crotti, Annukka M Lahtinen, Carla Spazzolini, et al.
Annals of Medicine|January 23, 2009
High prevalence of four long QT syndrome founder mutations in the Finnish populationAnnukka Marjamaa, Veikko Salomaa, Christopher Newton-Cheh, et al.
The Journal of Clinical Investigation|December 9, 2003
The SLC6A14 gene shows evidence of association with obesityElina Suviolahti, Laura J Oksanen, Miina Ohman, et al.
Pharmacogenetics and Genomics|January 13, 2010
Effect of ACE insertion/deletion and 12 other polymorphisms on clinical outcomes and response to treatment in the LIFE studyBørge G Nordestgaard, Kimmo Kontula, Marianne Benn, et al.
Heart Rhythm|February 21, 2012
A common variant near the KCNJ2 gene is associated with T-peak to T-end intervalAnnukka Marjamaa, Lasse Oikarinen, Kimmo Porthan, et al.
Inflammatory Bowel Diseases|May 23, 2009
PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel diseaseMarco Zucchelli, Leif Torkvist, Francesca Bresso, et al.
Gastroenterology|September 15, 2007
Neuropeptide s receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel diseaseMauro D'Amato, Sara Bruce, Francesca Bresso, et al.
Circulation. Cardiovascular Genetics|July 17, 2013
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndromeSabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Annals of Medicine|April 24, 2015
Helsinki alert of biodiversity and healthLeena von Hertzen, Bruce Beutler, John Bienenstock, et al.
BMC Medical Genetics|January 30, 2009
IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac diseaseElisabet Einarsdottir, Lotta L E Koskinen, Emma Dukes, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
Circulation. Cardiovascular Genetics|August 18, 2016
Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?Lia Crotti, Annukka M Lahtinen, Carla Spazzolini, et al.
Annals of Medicine|January 23, 2009
High prevalence of four long QT syndrome founder mutations in the Finnish populationAnnukka Marjamaa, Veikko Salomaa, Christopher Newton-Cheh, et al.
The Journal of Clinical Investigation|December 9, 2003
The SLC6A14 gene shows evidence of association with obesityElina Suviolahti, Laura J Oksanen, Miina Ohman, et al.
Pharmacogenetics and Genomics|January 13, 2010
Effect of ACE insertion/deletion and 12 other polymorphisms on clinical outcomes and response to treatment in the LIFE studyBørge G Nordestgaard, Kimmo Kontula, Marianne Benn, et al.
Heart Rhythm|February 21, 2012
A common variant near the KCNJ2 gene is associated with T-peak to T-end intervalAnnukka Marjamaa, Lasse Oikarinen, Kimmo Porthan, et al.
Inflammatory Bowel Diseases|May 23, 2009
PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel diseaseMarco Zucchelli, Leif Torkvist, Francesca Bresso, et al.
Gastroenterology|September 15, 2007
Neuropeptide s receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel diseaseMauro D'Amato, Sara Bruce, Francesca Bresso, et al.
Circulation. Cardiovascular Genetics|July 17, 2013
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndromeSabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Annals of Medicine|April 24, 2015
Helsinki alert of biodiversity and healthLeena von Hertzen, Bruce Beutler, John Bienenstock, et al.
BMC Medical Genetics|January 30, 2009
IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac diseaseElisabet Einarsdottir, Lotta L E Koskinen, Emma Dukes, et al.
Pageof 10