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Arne Pfeufer

Showing results (41-50 of 82) with videos related to

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Heart Rhythm|November 9, 2010
Lack of replication in polymorphisms reported to be associated with atrial fibrillationMoritz F Sinner, Steven A Lubitz, Arne Pfeufer, et al.
European Journal of Human Genetics : EJHG|September 25, 2014
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonablenessFranziska Severin, Pascal Borry, Martina C Cornel, et al.
The Journal of Clinical Investigation|May 10, 2008
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansHiroshi Watanabe, Tamara T Koopmann, Solena Le Scouarnec, et al.
BMC Neurology|October 29, 2011
Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF featuresFranziska Hopfner, Barbara Schormair, Franziska Knauf, et al.
European Heart Journal|January 21, 2011
Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathyDirk Sibbing, Arne Pfeufer, Tamara Perisic, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN projectFabio Marroni, Arne Pfeufer, Yurii S Aulchenko, et al.
Science (New York, N.Y.)|April 15, 2006
A common genetic variant is associated with adult and childhood obesityAlan Herbert, Norman P Gerry, Matthew B McQueen, et al.
Genetic Epidemiology|January 3, 2013
SNP prioritization using a Bayesian probability of associationJohn R Thompson, Martin Gögele, Christian X Weichenberger, et al.
American Journal of Human Genetics|May 27, 2014
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT intervalAshish Kapoor, Rajesh B Sekar, Nancy F Hansen, et al.
Genetic Epidemiology|January 12, 2013
Importance of different types of prior knowledge in selecting genome-wide findings for follow-upCosetta Minelli, Alessandro De Grandi, Christian X Weichenberger, et al.
Pageof 9

Showing results (41-50 of 82) with videos related to

Sort By:
Pageof 9
Heart Rhythm|November 9, 2010
Lack of replication in polymorphisms reported to be associated with atrial fibrillationMoritz F Sinner, Steven A Lubitz, Arne Pfeufer, et al.
European Journal of Human Genetics : EJHG|September 25, 2014
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonablenessFranziska Severin, Pascal Borry, Martina C Cornel, et al.
The Journal of Clinical Investigation|May 10, 2008
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansHiroshi Watanabe, Tamara T Koopmann, Solena Le Scouarnec, et al.
BMC Neurology|October 29, 2011
Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF featuresFranziska Hopfner, Barbara Schormair, Franziska Knauf, et al.
European Heart Journal|January 21, 2011
Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathyDirk Sibbing, Arne Pfeufer, Tamara Perisic, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN projectFabio Marroni, Arne Pfeufer, Yurii S Aulchenko, et al.
Science (New York, N.Y.)|April 15, 2006
A common genetic variant is associated with adult and childhood obesityAlan Herbert, Norman P Gerry, Matthew B McQueen, et al.
Genetic Epidemiology|January 3, 2013
SNP prioritization using a Bayesian probability of associationJohn R Thompson, Martin Gögele, Christian X Weichenberger, et al.
American Journal of Human Genetics|May 27, 2014
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT intervalAshish Kapoor, Rajesh B Sekar, Nancy F Hansen, et al.
Genetic Epidemiology|January 12, 2013
Importance of different types of prior knowledge in selecting genome-wide findings for follow-upCosetta Minelli, Alessandro De Grandi, Christian X Weichenberger, et al.
Pageof 9