K. Heim

发表

Analyzing Illumina Gene Expression Microarray Data from Different Tissues: Methodological Aspects of Data Analysis in the MetaXpress Consortium

C. Gieger, A. Peters, K. Strauch, 2012, PloS one.

Risk gene variants for nicotine dependence in the CHRNA5–CHRNA3–CHRNB4 cluster are associated with cognitive performance

Christian Gieger, Thomas Meitinger, Jürgen Gallinat, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Novel biomarkers for pre-diabetes identified by metabolomics

Christian Gieger, Thomas Meitinger, Monica Campillos, 2012, Molecular systems biology.

META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS

Christian Gieger, Nicholas J Timpson, Manuel A. R. Ferreira, 2011, Nature Genetics.

Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.

C. Gieger, F. Kronenberg, A. Peters, 2010, Atherosclerosis.

Review Process File

Yixue Li, Ying He, Tao Xu, 2012 .

High-density genotyping study identifies four new susceptibility loci for atopic dermatitis

Yusuke Nakamura, Sen Yang, Andre Franke, 2013, Nature Genetics.

Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation.

M. Elstner, T. Meitinger, T. Strom, 2011, American journal of human genetics.

Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood

Christian Gieger, Thomas Meitinger, Uwe Völker, 2012, European Journal of Human Genetics.

Dilution of candidates: the case of iron-related genes in restless legs syndrome

C. Gieger, A. Peters, T. Meitinger, 2012, European Journal of Human Genetics.

Expression analysis of dopaminergic neurons in Parkinson’s disease and aging links transcriptional dysregulation of energy metabolism to cell death

M. Elstner, D. Turnbull, C. Morris, 2011, Acta Neuropathologica.

Impairment of Drosophila Orthologs of the Human Orphan Protein C19orf12 Induces Bang Sensitivity and Neurodegeneration

T. Meitinger, H. Prokisch, O. Sibon, 2014, PloS one.

University of Groningen Impairment of Drosophila orthologs of the human orphan protein C19orf12 induces bang sensitivity and neurodegeneration Iuso,

T. Meitinger, H. Prokisch, O. Sibon, 2014 .

Genome-Wide Association Study Identifies Two Novel Regions at 11p15.5-p13 and 1p31 with Major Impact on Acute-Phase Serum Amyloid A

C. Gieger, M. Waldenberger, T. Spector, 2010, PLoS genetics.

A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1

D. Mehta, H. Prokisch, T. Illig, 2010, Journal of Lipid Research.

A common FADS 2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK 1

D. Mehta, H. Prokisch, T. Illig, 2009 .

Single‐cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene

I. McKeith, M. Elstner, D. Turnbull, 2009, Annals of neurology.

Molecular Systems Biology Peer Review Process File Novel Biomarkers for Pre-diabetes Identified by Metabolomics Transaction Report

C. Gieger, T. Meitinger, T. Pischon, 2022 .

High-density genotyping study identifies four new susceptibility loci for atopic dermatitis

James T. Elder, M. Nöthen, Yusuke Nakamura, 2013, Nature Genetics.