Christine Schwienbacher

Center for Biomedicine, European Academy Bozen/Bolzano (EURAC)

Affiliated withEuropean Academy Bozen/Bolzano (EURAC)

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 26	2015

Other Publications

Article	Year
Loss of methylation at chromosome 11p15.5 is common in human adult tumors. Oncogene\| PubMed ID: 11971191	2002
NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15). Blood\| PubMed ID: 11986249	2002
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour. Human molecular genetics\| PubMed ID: 17158821	2007
Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS genetics\| PubMed ID: 19798445	2009
Copy number variation and association over T-cell receptor genes--influence of DNA source. Immunogenetics\| PubMed ID: 20582410	2010
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nature genetics\| PubMed ID: 21076409	2010
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. Human molecular genetics\| PubMed ID: 21149283	2011
Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. Human molecular genetics\| PubMed ID: 21208937	2011
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. American journal of human genetics\| PubMed ID: 22703881	2012
Discovery and fine mapping of serum protein loci through transethnic meta-analysis. American journal of human genetics\| PubMed ID: 23022100	2012
Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genes. Journal of molecular neuroscience : MN\| PubMed ID: 23054586	2013
SNP prioritization using a Bayesian probability of association. Genetic epidemiology\| PubMed ID: 23280596	2013
Importance of different types of prior knowledge in selecting genome-wide findings for follow-up. Genetic epidemiology\| PubMed ID: 23307621	2013
Involvement of proprotein convertase PCSK7 in the regulation of systemic iron homeostasis. Hepatology (Baltimore, Md.)\| PubMed ID: 23504908	2013
Profiling of Parkin-binding partners using tandem affinity purification. PloS one\| PubMed ID: 24244333	2013
The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies. BMC endocrine disorders\| PubMed ID: 24484869	2014
Identification of a set of endogenous reference genes for miRNA expression studies in Parkinson's disease blood samples. BMC research notes\| PubMed ID: 25304816	2014
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature communications\| PubMed ID: 25352340	2014
Overexpression of blood microRNAs 103a, 30b, and 29a in L-dopa-treated patients with PD. Neurology\| PubMed ID: 25596505	2015
Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature communications\| PubMed ID: 25817829	2015