His primary scientific interests are in Genetics, Genome-wide association study, Internal medicine, Single-nucleotide polymorphism and Locus. Genetics is a component of his Gene, Allele, Allele frequency, Haplotype and Genotype studies. The concepts of his Genome-wide association study study are interwoven with issues in Bioinformatics, Genetic epidemiology, Quantitative trait locus, Expression quantitative trait loci and Genetic association.
In his research on the topic of Internal medicine, Mutation is strongly related with Endocrinology. His Single-nucleotide polymorphism study integrates concerns from other disciplines, such as Odds ratio, Coronary artery disease, Myocardial infarction, Cardiology and Disease. Andreas Ziegler interconnects Genetic variability, Case-control study and FTO gene in the investigation of issues within Locus.
Andreas Ziegler focuses on Genetics, Internal medicine, Statistics, Single-nucleotide polymorphism and Gene. His works in Genome-wide association study, Locus, Genetic association, Haplotype and Allele are all subjects of inquiry into Genetics. His research integrates issues of Endocrinology, Oncology and Allele frequency in his study of Internal medicine.
His Statistics study frequently links to adjacent areas such as Econometrics. Andreas Ziegler works in the field of Single-nucleotide polymorphism, namely SNP.
His primary areas of investigation include Genetics, Calcite, Statistics, Genome-wide association study and Single-nucleotide polymorphism. Andreas Ziegler combines topics linked to Evolutionary biology with his work on Genetics. His Calcite study combines topics in areas such as Electron backscatter diffraction, Gelatin, Aggregate and Diagenesis.
The study incorporates disciplines such as Random forest and Econometrics in addition to Statistics. His Genome-wide association study study frequently draws connections between related disciplines such as Quantitative trait locus. His research investigates the link between Single-nucleotide polymorphism and topics such as Gene expression that cross with problems in Phenotype and Bioinformatics.
Andreas Ziegler spends much of his time researching Genetics, Genome-wide association study, Internal medicine, Random forest and Single-nucleotide polymorphism. Genetics and Evolutionary biology are frequently intertwined in his study. He combines subjects such as Quantitative trait locus, Genetic association, Genetic variation, Major histocompatibility complex and Candidate gene with his study of Genome-wide association study.
As part of one scientific family, Andreas Ziegler deals mainly with the area of Internal medicine, narrowing it down to issues related to the Oncology, and often Parkin, Clinical trial, Omics, PINK1 and Clinical endpoint. His studies in Random forest integrate themes in fields like Statistics, Clustering high-dimensional data and Computational science. His Single-nucleotide polymorphism study combines topics from a wide range of disciplines, such as Inflammasome, Genetic predisposition, Immunology and Gene isoform.
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Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
Nature (2010)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda.
Nature Genetics (2010)
Genomewide association analysis of coronary artery disease.
Nilesh J. Samani;Jeanette Erdmann;Alistair S. Hall;Christian Hengstenberg.
The New England Journal of Medicine (2007)
Perzentile für den Body-mass-Index für das Kindes- und Jugendalter unter Heranziehung verschiedener deutscher Stichproben
Katrin Kromeyer-Hauschild;M. Wabitsch;D. Kunze;F. Geller.
Monatsschrift Kinderheilkunde (2001)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Nature (2010)
Plasma HDL cholesterol and risk of myocardial infarction: A mendelian randomisation study
Benjamin F. Voight;Benjamin F. Voight;Benjamin F. Voight;Gina M. Peloso;Gina M. Peloso;Marju Orho-Melander;Ruth Frikke-Schmidt.
web science (2012)
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Heribert Schunkert;Inke R. König;Sekar Kathiresan;Muredach P. Reilly.
Nature Genetics (2011)
Large-scale association analysis identifies new risk loci for coronary artery disease
Panos Deloukas;Stavroula Kanoni;Christina Willenborg;Martin Farrall.
Nature Genetics (2013)
Gene map of the extended human MHC
Roger Horton;Laurens Wilming;Vikki Rand;Ruth C. Lovering.
Nature Reviews Genetics (2004)
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Sekar Kathiresan;Benjamin F Voight;Shaun Purcell;Kiran Musunuru.
Nature Genetics (2009)
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