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Jessica van Setten

Showing results (41-50 of 98) with videos related to

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Science Advances|May 1, 2023
Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicityAmand F Schmidt, Mimount Bourfiss, Abdulrahman Alasiri, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic PlaquesSander W van der Laan, Marten A Siemelink, Saskia Haitjema, et al.
Human Molecular Genetics|September 15, 2018
Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) UveitisJonas J W Kuiper, Jessica van Setten, Matthew Devall, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 16, 2016
Human Validation of Genes Associated With a Murine Atherosclerotic PhenotypeGerard Pasterkamp, Sander W van der Laan, Saskia Haitjema, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'Patrick Deelen, Androniki Menelaou, Elisabeth M van Leeuwen, et al.
Circulation. Cardiovascular Genetics|March 22, 2017
Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin OrganizationSaskia Haitjema, Claartje A Meddens, Sander W van der Laan, et al.
Journal of the American Society of Nephrology : JASN|April 15, 2018
<i>NPHP1</i> (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRDRozemarijn Snoek, Jessica van Setten, Brendan J Keating, et al.
Human Molecular Genetics|June 25, 2014
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathyJonas J W Kuiper, Jessica Van Setten, Stephan Ripke, et al.
Genome Medicine|September 18, 2023
Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to humanJulia E Niskanen, Åsa Ohlsson, Ingrid Ljungvall, et al.
Human Molecular Genetics|November 16, 2013
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosisAn Goris, Jessica van Setten, Frank Diekstra, et al.
Pageof 10

Showing results (41-50 of 98) with videos related to

Sort By:
Pageof 10
Science Advances|May 1, 2023
Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicityAmand F Schmidt, Mimount Bourfiss, Abdulrahman Alasiri, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic PlaquesSander W van der Laan, Marten A Siemelink, Saskia Haitjema, et al.
Human Molecular Genetics|September 15, 2018
Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) UveitisJonas J W Kuiper, Jessica van Setten, Matthew Devall, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 16, 2016
Human Validation of Genes Associated With a Murine Atherosclerotic PhenotypeGerard Pasterkamp, Sander W van der Laan, Saskia Haitjema, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'Patrick Deelen, Androniki Menelaou, Elisabeth M van Leeuwen, et al.
Circulation. Cardiovascular Genetics|March 22, 2017
Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin OrganizationSaskia Haitjema, Claartje A Meddens, Sander W van der Laan, et al.
Journal of the American Society of Nephrology : JASN|April 15, 2018
<i>NPHP1</i> (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRDRozemarijn Snoek, Jessica van Setten, Brendan J Keating, et al.
Human Molecular Genetics|June 25, 2014
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathyJonas J W Kuiper, Jessica Van Setten, Stephan Ripke, et al.
Genome Medicine|September 18, 2023
Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to humanJulia E Niskanen, Åsa Ohlsson, Ingrid Ljungvall, et al.
Human Molecular Genetics|November 16, 2013
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosisAn Goris, Jessica van Setten, Frank Diekstra, et al.
Pageof 10