Christine Schwienbacher

Publications

• Corrigendum: Novel Loci Affecting Iron Homeostasis and Their Effects in Individuals at Risk for Hemochromatosis
  Nature Communications. 2015  |   Pubmed ID: 25817829
• Overexpression of Blood MicroRNAs 103a, 30b, and 29a in L-dopa-treated Patients with PD
  Neurology. Feb, 2015  |   Pubmed ID: 25596505
• Novel Loci Affecting Iron Homeostasis and Their Effects in Individuals at Risk for Hemochromatosis
  Nature Communications. 2014  |   Pubmed ID: 25352340
• 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
• 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
• Profiling of Parkin-binding Partners Using Tandem Affinity Purification
  PloS One. 2013  |   Pubmed ID: 24244333
• Involvement of Proprotein Convertase PCSK7 in the Regulation of Systemic Iron Homeostasis
  Hepatology (Baltimore, Md.). Nov, 2013  |   Pubmed ID: 23504908
• Importance of Different Types of Prior Knowledge in Selecting Genome-wide Findings for Follow-up
  Genetic Epidemiology. Feb, 2013  |   Pubmed ID: 23307621
• SNP Prioritization Using a Bayesian Probability of Association
  Genetic Epidemiology. Feb, 2013  |   Pubmed ID: 23280596
• 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
• Discovery and Fine Mapping of Serum Protein Loci Through Transethnic Meta-analysis
  American Journal of Human Genetics. Oct, 2012  |   Pubmed ID: 23022100
• 活化部分凝血活酶时间、 凝血酶原时间及其基因表达谱和冠状动脉疾病的风险的遗传关联。
  American Journal of Human Genetics. Jul, 2012  |   Pubmed ID: 22703881
• 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
• 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
• 22 位点中的常见变异是与 Qrs 和心脏心室传导相关联。
  Nature Genetics. Dec, 2010  |   Pubmed ID: 21076409
• Copy Number Variation and Association over T-cell Receptor Genes--influence of DNA Source
  Immunogenetics. Aug, 2010  |   Pubmed ID: 20582410
• Genetic Determinants of Circulating Sphingolipid Concentrations in European Populations
  PLoS Genetics. Oct, 2009  |   Pubmed ID: 19798445
• Mechanisms Causing Imprinting Defects in Familial Beckwith-Wiedemann Syndrome with Wilms' Tumour
  Human Molecular Genetics. Feb, 2007  |   Pubmed ID: 17158821
• 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
• Loss of Methylation at Chromosome 11p15.5 is Common in Human Adult Tumors
  Oncogene. Apr, 2002  |   Pubmed ID: 11971191