Andreas Ziegler

发表

Calibrating random forests for probability estimation

Theresa Dankowski, Andreas Ziegler, A. Ziegler, 2016, Statistics in medicine.

Adaptive linear rank tests for eQTL studies

Silke Szymczak, Andreas Ziegler, Tanja Zeller, 2013, Statistics in medicine.

Data mining, neural nets, trees — Problems 2 and 3 of Genetic Analysis Workshop 15

Xin Li, Jing Li, Dumitru Brinza, 2007, Genetic epidemiology.

AUC-based splitting criteria for random survival forests

Matthias Schmid, Marvin N. Wright, Andreas Ziegler, 2015 .

Probability estimation with machine learning methods for dichotomous and multicategory outcome: Applications

Christian Weimar, Andreas Ziegler, Yufeng Liu, 2014, Biometrical journal. Biometrische Zeitschrift.

Individual characteristics and stated preferences for alternative energy sources and propulsion technologies in vehicles

Andreas Ziegler, Andreas Ziegler, 2010 .

Genotype calling for the Affymetrix platform.

Andreas Ziegler, Arne Schillert, A. Ziegler, 2012, Methods in molecular biology.

Appendix: Algorithms Used in Linkage Analyses

Andreas Ziegler, Inke R. König, 2010 .

Solutions to Study Problems

Andreas Ziegler, Inke R. König, 2010 .

An incremental procedure model for e-learning projects at universities

Michael Bischoff, Andreas Ziegler, Inke R. König, 2006 .

Biostatistical Aspects of Genome‐Wide Association Studies

John R Thompson, Andreas Ziegler, Inke R König, 2008, Biometrical journal. Biometrische Zeitschrift.

Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).

Dietmar Roesner, Andreas Ziegler, Inke R König, 2003, Human molecular genetics.

[Predicted functional outcome 100 days after ischemic strokes: design of a prospective study about the external validation of a prognostic model].

Christian Weimar, Andreas Ziegler, Inke R König, 2003, Zeitschrift fur arztliche Fortbildung und Qualitatssicherung.

Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction

Udo Hoffmann, David M Herrington, Eric Boerwinkle, 2011, Circulation.

Comments on ‘Mendelian randomization: using genes as instruments for making causal inferences in epidemiology’ by Debbie A. Lawlor, R. M. Harbord, J. A. Sterne, N. Timpson and G. Davey Smith, Statistics in Medicine, DOI: 10.1002/sim.3034

Andreas Ziegler, Inke R König, Friedrich Pahlke, 2008, Statistics in Medicine.

The Generalised Estimating Equations: An Annotated Bibliography

C. Kastner, Andreas Ziegler, Maria Blettner, 1998 .

Generalized Estimating Equations

Andreas Ziegler, A. Ziegler, M. Vens, 2011 .

Further evidence for DYX1C1 as a susceptibility factor for dyslexia

Bertram Müller-Myhsok, Andreas Ziegler, Andreas Warnke, 2009, Psychiatric genetics.

Predicting Long-Term Outcome After Acute Ischemic Stroke: A Simple Index Works in Patients From Controlled Clinical Trials

Christian Weimar, Andreas Ziegler, Inke R König, 2008, Stroke.

Reducing sample sizes in genome scans: Group sequential study designs with futility stops

Andreas Ziegler, Helmut Schäfer, Inke R König, 2003, Genetic epidemiology.

Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses

Joseph Beyene, Silke Szymczak, Andreas Ziegler, 2009, BMC proceedings.

Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease

Dietmar Roesner, Andreas Ziegler, Matthias Schreiber, 2002, The Lancet.

Genome-Wide Haplotype Analysis of Cis Expression Quantitative Trait Loci in Monocytes

Andreas Ziegler, Nilesh J. Samani, Panos Deloukas, 2013, PLoS genetics.

A Statistical Approach to Genetic Epidemiology: With Access to E-Learning Platform by Friedrich Pahlke

Andreas Ziegler, Inke R. König, I. König, 2010 .

Genome‐wide association studies: quality control and population‐based measures

Andreas Ziegler, A. Ziegler, 2009, Genetic epidemiology.

FTO genotype is associated with phenotypic variability of body mass index

Joel Eriksson, Joseph E. Powell, Andres Metspalu, 2012, Nature.

A General Approach for Sample Size and Power Calculations Based on the Haseman–Elston Method

Andreas Ziegler, Friedrich Pahlke, A. Ziegler, 2008, Biometrical journal. Biometrische Zeitschrift.

Association Tests for X-Chromosomal Markers – A Comparison of Different Test Statistics

Andreas Ziegler, Christina Loley, Inke R. König, 2011, Human Heredity.

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.

Thomas Meitinger, Uwe Völker, Reinhold Schmidt, 2009, JAMA.

Removing Batch Effects from Longitudinal Gene Expression - Quantile Normalization Plus ComBat as Best Approach for Microarray Transcriptome Data

Harald Binder, Andreas Ziegler, Karl J. Lackner, 2016, PloS one.

SNP-Based Analysis of Genetic Substructure in the German Population

Thomas Meitinger, Kathryn Roeder, Michael Krawczak, 2006, Human Heredity.

A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk

Martin Vingron, Matthias Heinig, Helge G. Roider, 2010, Nature.

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

Alberto Piazza, William Matthai, Flora Peyvandi, 2009, Nature Genetics.

Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility

Silke Szymczak, Joseph Loscalzo, Andreas Ziegler, 2010, PloS one.

Risk estimation and risk prediction using machine-learning methods

Andreas Ziegler, Jochen Kruppa, Inke R. König, 2012, Human Genetics.

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

Bertram Müller-Myhsok, Andreas Ziegler, Andreas Warnke, 2008, Journal of Neural Transmission.

Deconfounding Microarray Analysis

Dirk Repsilber, Stefan H. E. Kaufmann, Andreas Ziegler, 2006 .

Evaluating diagnostic accuracy of genetic profiles in affected offspring families

Andreas Ziegler, Inke R König, Jörg Hager, 2010, Statistics in medicine.

Group Sequential Study Designs in Genetic-Epidemiological Case-Control Studies

Andreas Ziegler, Inke R. König, I. König, 2003, Human Heredity.

Simulated Classical Tests in the Multiperiod Multinomial Probit Model

Andreas Ziegler, A. Ziegler, 2002 .

What Do We Mean by ‘Replication’ and ‘Validation’ in Genome-Wide Association Studies?

Andreas Ziegler, Inke R. König, I. König, 2008, Human Heredity.

Evaluation of single-nucleotide polymorphism imputation using random forests

Silke Szymczak, Andreas Ziegler, Inke R König, 2009, BMC proceedings.

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

Christian Gieger, Bernhard Hemmer, Mark Mühlau, 2016, Science Advances.

Introduction to genetic analysis workshop 17 summaries

John Blangero, Andreas Ziegler, Saurabh Ghosh, 2011, Genetic epidemiology.

A comprehensive evaluation of collapsing methods using simulated and real data: excellent annotation of functionality and large sample sizes required

Andreas Ziegler, Inke R. König, Mary V. Relling, 2014, Front. Genet..

A point mutation in PTPRC is associated with the development of multiple sclerosis

Bernhard Hemmer, Andreas Ziegler, Wolfgang H. Oertel, 2000, Nature Genetics.

CDKN2A Germline Mutations in Familial Pancreatic Cancer

Matthias Rothmund, Robert Grützmann, Andreas Ziegler, 2002, Annals of surgery.

Novel intronic polymorphisms in the RET proto‐oncogene and their association with Hirschsprung disease

Dietmar Roesner, Andreas Ziegler, Matthias Schreiber, 2003, Human mutation.

No association of three polymorphisms in the alpha-2-macroglobulin and lipoprotein related receptor genes with multiple sclerosis

Bernhard Hemmer, Andreas Ziegler, Wolfgang H. Oertel, 2001, Journal of Neuroimmunology.

New loci associated with kidney function and chronic kidney disease

Uwe Völker, Luigi Ferrucci, Reinhold Schmidt, 2010, Nature Genetics.

Sequential Designs for Genetic Epidemiological Linkage or Association Studies A Review of the Literature

Andreas Ziegler, Inke Böddeker, 2001 .

The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol

Paul R. Burton, Andreas Ziegler, Nilesh J. Samani, 2008, Journal of Molecular Medicine.

GEE approaches to marginal regression models for medical diagnostic tests

Jost B Jonas, Andreas Ziegler, Peter Martus, 2004, Statistics in medicine.

Genetic Predisposition to Higher Blood Pressure Increases Coronary Artery Disease Risk

Michael J Pencina, Eric Boerwinkle, Themistocles L Assimes, 2013, Hypertension.

Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees

Joseph Beyene, Nathan L Tintle, Andreas Ziegler, 2014, BMC Proceedings.

Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9 p 21 . 3 and Coronary Artery Disease

Ludwig A Hothorn, Nilesh J Samani, Andreas Ziegler, 2008 .

Discovery and fine mapping of serum protein loci through transethnic meta-analysis.

Christian Gieger, Yusuke Nakamura, Luigi Ferrucci, 2012, American journal of human genetics.

Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

Jie Huang, Uwe Völker, Ming-Huei Chen, 2017, The Journal of clinical investigation.

Multiple censored data in dentistry: A new statistical model for analyzing lesion size in randomized controlled trials

Marvin N. Wright, Andreas Ziegler, Marvin N Wright, 2015, Biometrical journal. Biometrische Zeitschrift.

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.

Andreas Ziegler, Andreas Warnke, Sven Cichon, 2006, American journal of human genetics.

Identification of genetic association of multiple rare variants using collapsing methods

Andreas Ziegler, Yan V. Sun, Nathan Tintle, 2011, Genetic epidemiology.

Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts

Christian Gieger, Thomas Meitinger, Uwe Völker, 2015, BMC Medical Genomics.

BiomarCaRE: rationale and design of the European BiomarCaRE project including 300,000 participants from 13 European countries

Frank Kee, Uwe Siebert, Kari Kuulasmaa, 2014, European Journal of Epidemiology.

A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease

Olli Saarela, Frank Kee, Kaisa Silander, 2011, Circulation. Cardiovascular genetics.

Candidate biomarkers for discrimination between infection and disease caused by Mycobacterium tuberculosis

Dirk Repsilber, Stefan H. E. Kaufmann, Andreas Ziegler, 2007, Journal of Molecular Medicine.

Statistical analysis of rare sequence variants: an overview of collapsing methods

Claudia Hemmelmann, Andreas Ziegler, A. Ziegler, 2011, Genetic epidemiology.

Applied Missing Data Analysis in the Health Sciences. X.‐H. Zhou, C. Zhou, D. Liu, and X. Ding (2014). Hoboken: John Wiley & Sons. 256 pages, ISBN: 978‐0‐470‐52381‐0 (hardback); ISBN: 978‐1‐118‐57364‐8 (eBook).

Andreas Ziegler, Henry Mwambi, A. Ziegler, 2015 .

A pooled analysis of melanocytic nevus phenotype and the risk of cutaneous melanoma at different latitudes

Andreas Ziegler, Victor Siskind, Marianne Berwick, 2009, International journal of cancer.

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

John Spertus, Markus Perola, Eric Boerwinkle, 2012, The Lancet.

Comparison of pre-processing methods for multiplex bead-based immunoassays

Andreas Ziegler, Peter Schulz-Knappe, Arne Schillert, 2016, BMC Genomics.

How to Include Chromosome X in Your Genome‐Wide Association Study

Andreas Ziegler, Jeanette Erdmann, Christina Loley, 2014, Genetic epidemiology.

Developmental Dyslexia – Recurrence Risk Estimates from a German Bi-Center Study Using the Single Proband Sib Pair Design

Bertram Müller-Myhsok, Andreas Ziegler, Andreas Warnke, 2005, Human Heredity.

Photodynamic diagnosis in non-muscle-invasive bladder cancer: a systematic review and cumulative analysis of prospective studies.

Dieter Jocham, Patrice Jichlinski, Andreas Ziegler, 2010, European urology.