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