Cargando…

Systematic Testing of Literature Reported Genetic Variation Associated with Coronary Restenosis: Results of the GENDER Study

BACKGROUND: Coronary restenosis after percutaneous coronary intervention still remains a significant problem, despite all medical advances. Unraveling the mechanisms leading to restenosis development remains challenging. Many studies have identified genetic markers associated with restenosis, but co...

Descripción completa

Detalles Bibliográficos
Autores principales:	Verschuren, Jeffrey J. W., Trompet, Stella, Postmus, Iris, Sampietro, M. Lourdes, Heijmans, Bastiaan T., Houwing-Duistermaat, Jeanine J., Slagboom, P. Eline, Jukema, J. Wouter
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2012
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411750/ https://www.ncbi.nlm.nih.gov/pubmed/22879966 http://dx.doi.org/10.1371/journal.pone.0042401

Ejemplares similares

Pathway Analysis Using Genome-Wide Association Study Data for Coronary Restenosis – A Potential Role for the PARVB Gene
por: Verschuren, Jeffrey J. W., et al.
Publicado: (2013)

Non-Homologous End-Joining Pathway Associated with Occurrence of Myocardial Infarction: Gene Set Analysis of Genome-Wide Association Study Data
por: Verschuren, Jeffrey J. W., et al.
Publicado: (2013)

Lipoprotein Particle Profiles Mark Familial and Sporadic Human Longevity
por: Heijmans, Bastiaan T, et al.
Publicado: (2006)

Secondary phenotype analysis in ascertained family designs: application to the Leiden longevity study
por: Tissier, Renaud, et al.
Publicado: (2017)

Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers
por: Deelen, Joris, et al.
Publicado: (2014)

Matrix Metalloproteinases 2 and 3 Gene Polymorphisms and the Risk of Target Vessel Revascularization after Percutaneous Coronary Intervention: Is There Still Room for Determining Genetic Variation of MMPs for Assessment of an Increased Risk of Restenosis?
por: Verschuren, J.J.W., et al.
Publicado: (2010)

Replication of LDL GWAs hits in PROSPER/PHASE as validation for future (pharmaco)genetic analyses
por: Trompet, Stella, et al.
Publicado: (2011)

Longevity Around the Turn of the 20th Century: Life-Long Sustained Survival Advantage for Parents of Today’s Nonagenarians
por: van den Berg, Niels, et al.
Publicado: (2018)

Maternal and child cytokine relationship in early life is not altered by cytokine gene polymorphisms
por: Djuardi, Y, et al.
Publicado: (2016)

Subclass-specific IgG glycosylation is associated with markers of inflammation and metabolic health
por: Plomp, Rosina, et al.
Publicado: (2017)

Powerful testing via hierarchical linkage disequilibrium in haplotype association studies
por: Balliu, Brunilda, et al.
Publicado: (2019)

Classification for Longevity Potential: The Use of Novel Biomarkers
por: Beekman, Marian, et al.
Publicado: (2016)

Combining evidence for association from transmission disequilibrium and case-control studies using single-nucleotide polymorphisms
por: Putter, Hein, et al.
Publicado: (2005)

Methods to test for association between a disease and a multi-allelic marker applied to a candidate region
por: El Galta, Rachid, et al.
Publicado: (2005)

Does pathway analysis make it easier for common variants to tag rare ones?
por: Uh, Hae-Won, et al.
Publicado: (2011)

Pathway analysis for family data using nested random-effects models
por: Houwing-Duistermaat, Jeanine J, et al.
Publicado: (2011)

Association analysis of insulin-like growth factor-1 axis parameters with survival and functional status in nonagenarians of the Leiden Longevity Study
por: van der Spoel, Evie, et al.
Publicado: (2015)

Coronary restenosis
Publicado: (1993)

Improving stability of prediction models based on correlated omics data by using network approaches
por: Tissier, Renaud, et al.
Publicado: (2018)

Lipidomics of familial longevity
por: Gonzalez-Covarrubias, Vanessa, et al.
Publicado: (2013)

Exploring the possible causal effects of cardiac blood biomarkers in dementia and cognitive performance: a Mendelian randomization study
por: Zonneveld, Michelle H., et al.
Publicado: (2023)

Non-response to (statin) therapy: the importance of distinguishing non-responders from non-adherers in pharmacogenetic studies
por: Trompet, S., et al.
Publicado: (2015)

A new score statistic to test for association given linkage in affected sibling pair-control designs
por: Houwing-Duistermaat, Jeanine J, et al.
Publicado: (2007)

New score tests for age-at-onset linkage analysis in general pedigrees
por: Callegaro, Andrea, et al.
Publicado: (2009)

Genotype-Based Score Test for Association Testing in Families
por: Uh, Hae-Won, et al.
Publicado: (2015)

Genome-wide analysis in multiple-case families: assessing the relationship between triglyceride and methylation
por: Fuady, Angga M., et al.
Publicado: (2018)

Decreased Levels of Bisecting GlcNAc Glycoforms of IgG Are Associated with Human Longevity
por: Ruhaak, L. Renee, et al.
Publicado: (2010)

Factor VII Activating Protease Polymorphism (G534E) Is Associated with Increased Risk for Stroke and Mortality
por: Trompet, Stella, et al.
Publicado: (2011)

Prenatal Famine and Genetic Variation Are Independently and Additively Associated with DNA Methylation at Regulatory Loci within IGF2/H19
por: Tobi, Elmar W., et al.
Publicado: (2012)

Evaluation of regression methods when immunological measurements are constrained by detection limits
por: Uh, Hae-Won, et al.
Publicado: (2008)

Testing for genetic association taking into account phenotypic information of relatives
por: Uh, Hae-Won, et al.
Publicado: (2009)

The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction
por: Trompet, Stella, et al.
Publicado: (2022)

Age-related DNA methylation changes are tissue-specific with ELOVL2 promoter methylation as exception
por: Slieker, Roderick C., et al.
Publicado: (2018)

Influence of genotyping error in linkage mapping for complex traits – an analytic study
por: Lebrec, Jérémie JP, et al.
Publicado: (2008)

How to quantify information loss due to phase ambiguity in haplotype case-control studies
por: Uh, Hae-Won, et al.
Publicado: (2005)

Assessment of global phase uncertainty in case-control studies
por: Uh, Hae-Won, et al.
Publicado: (2009)

The mixed model for the analysis of a repeated‐measurement multivariate count data
por: Martin, Ivonne, et al.
Publicado: (2019)

Estimating Constraints for Protection Factors from HDX-MS Data
por: Skinner, Simon P., et al.
Publicado: (2019)

Targeted Biomarker Discovery by High Throughput Glycosylation Profiling of Human Plasma Alpha1-Antitrypsin and Immunoglobulin A
por: Ruhaak, L. Renee, et al.
Publicado: (2013)

Epigenetic variation during the adult lifespan: cross-sectional and longitudinal data on monozygotic twin pairs
por: Talens, Rudolf P, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_ldjmjh3gakms0pm9q9rpaglnbq