Z Kutalik

Summary

Affiliation: University of Lausanne
Country: Switzerland

Publications

  1. pmc Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort
    Armand Valsesia
    Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland
    BMC Genomics 13:241. 2012
  2. pmc Comparative modular analysis of gene expression in vertebrate organs
    Barbara Piasecka
    Department of Ecology and Evolution, University of Lausanne, Biophore, CH 1005 Lausanne, Switzerland
    BMC Genomics 13:124. 2012
  3. ncbi S-system parameter estimation for noisy metabolic profiles using newton-flow analysis
    Z Kutalik
    Department of Medical Genetics, University of Lausanne, Rue de Bugnon 27, Lausanne 1005, Switzerland
    IET Syst Biol 1:174-80. 2007
  4. doi Methods for testing association between uncertain genotypes and quantitative traits
    Zoltan Kutalik
    Department of Medical Genetics, University of Lausanne, Rue du Bugnon 27, 1005 Lausanne, Switzerland
    Biostatistics 12:1-17. 2011
  5. doi Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability
    Zoltan Kutalik
    Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland
    Genet Epidemiol 35:341-9. 2011
  6. pmc Genome-wide association study identifies two loci strongly affecting transferrin glycosylation
    Zoltan Kutalik
    Department of Medical Genetics, University of Lausanne, Lausanne, 1005, Switzerland
    Hum Mol Genet 20:3710-7. 2011

Collaborators

Detail Information

Publications6

  1. pmc Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort
    Armand Valsesia
    Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland
    BMC Genomics 13:241. 2012
    ..Sophisticated algorithms that infer CNVs by combining the intensities from SNP-probes for the two alleles can already be used to extract a partial view of such GSV from existing data sets...
  2. pmc Comparative modular analysis of gene expression in vertebrate organs
    Barbara Piasecka
    Department of Ecology and Evolution, University of Lausanne, Biophore, CH 1005 Lausanne, Switzerland
    BMC Genomics 13:124. 2012
    ..Several recent studies reported some evidence in favor of such conservation. Most studies compute organs' similarity across all orthologous genes, whereas the expression level of many genes are not informative about organ specificity...
  3. ncbi S-system parameter estimation for noisy metabolic profiles using newton-flow analysis
    Z Kutalik
    Department of Medical Genetics, University of Lausanne, Rue de Bugnon 27, Lausanne 1005, Switzerland
    IET Syst Biol 1:174-80. 2007
    ..We show that the performance of this method compares favorably with competing methods for ideal profiles, and that it also allows the determination of parameters for noisy profiles...
  4. doi Methods for testing association between uncertain genotypes and quantitative traits
    Zoltan Kutalik
    Department of Medical Genetics, University of Lausanne, Rue du Bugnon 27, 1005 Lausanne, Switzerland
    Biostatistics 12:1-17. 2011
    ..5 M single nucleotide polymorphisms and 5000 individuals...
  5. doi Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability
    Zoltan Kutalik
    Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland
    Genet Epidemiol 35:341-9. 2011
    ..This methodology also enables us to predict the benefit of future GWA studies that aim to reveal more associated genetic markers via increased sample size...
  6. pmc Genome-wide association study identifies two loci strongly affecting transferrin glycosylation
    Zoltan Kutalik
    Department of Medical Genetics, University of Lausanne, Lausanne, 1005, Switzerland
    Hum Mol Genet 20:3710-7. 2011
    ..8% of the variation in CDT%. These allelic effects are postulated to be caused by variation in availability of glucose-1-phosphate as a precursor of the glycan (PGM1), and variation in transferrin (TF) structure...