Rezultati pretrage - Anika Götz
- Prikaz rezultata 1 – 2 od 2
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1
Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation Study od Patrick Linsel‐Nitschke, Anika Götz, Jeanette Erdmann, Ingrid Brænne, Peter S. Braund, Christian Hengstenberg, Klaus Stark, Marcus Fischer, Stefan Schreiber, Nour Eddine El Mokhtari, Arne S. Schäefer, Jürgen Schrezenmeier, Deborah C. Rubin, Anke Hinney, Thomas Reinehr, Christian Roth, Jan R. Ortlepp, Peter Hanrath, Alistair S. Hall, Massimo Mangino, Wolfgang Lieb, Claudia Lamina, Iris M. Heid, Angela Doering, Christian Gieger, Annette Peters, Thomas Meitinger, H.‐Erich Wichmann, Inke R. König, Andreas Ziegler, Florian Kronenberg, Nilesh J. Samani, Heribert Schunkert
Izdano 2008Artigo -
2
Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease od Heribert Schunkert, Anika Götz, Peter S. Braund, Ralph McGinnis, David‐Alexandre Trégouët, Massimo Mangino, Patrick Linsel‐Nitschke, François Cambien, Christian Hengstenberg, Klaus Stark, Stefan Blankenberg, Laurence Tiret, Pierre Ducimetière, Andrew Keniry, Mohammed J. R. Ghori, Stefan Schreiber, Nour Eddine El Mokhtari, Alistair S. Hall, Richard J. Dixon, Alison H. Goodall, Henrike Liptau, Helen Perlstein Pollard, Dániel Schwarz, Ludwig A. Hothorn, H.‐Erich Wichmann, Inke R. König, Marcus Fischer, Christa Meisinger, Willem H. Ouwehand, Panos Deloukas, John R. Thompson, Jeanette Erdmann, Andreas Ziegler, Nilesh J. Samani
Izdano 2008Revisão
Alati za pretragu:
Povezani predmeti
Allele
Biology
Coronary artery disease
Gene
Genetics
Genotype
Internal medicine
Locus (genetics)
Medicine
Odds ratio
Single-nucleotide polymorphism
Allele frequency
Case-control study
Cholesterol
Confidence interval
Endocrinology
Familial hypercholesterolemia
Gastroenterology
Genetic association
Genome-wide association study
Genotyping
Haplotype
LDL receptor
Lipoprotein
Meta-analysis
Minor allele frequency
Oncology
PCSK9
SNP