Christine Schwienbacher

Loss of methylation at chromosome 11p15.5 is common in human adult tumors.

NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15).

Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.

Genetic determinants of circulating sphingolipid concentrations in European populations.

Copy number variation and association over T-cell receptor genes--influence of DNA source.

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.

Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.

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

Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genes.

SNP prioritization using a Bayesian probability of association.

Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.

Involvement of proprotein convertase PCSK7 in the regulation of systemic iron homeostasis.

Profiling of Parkin-binding partners using tandem affinity purification.

The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies.

Identification of a set of endogenous reference genes for miRNA expression studies in Parkinson's disease blood samples.

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.

Overexpression of blood microRNAs 103a, 30b, and 29a in L-dopa-treated patients with PD.

Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.