Christian Fuchsberger

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Publications in SciGraph latest 50 shown

  • 2017-12-19 Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-12 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function in SCIENTIFIC REPORTS
  • 2017-12 Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity in NATURE COMMUNICATIONS
  • 2016-11 Reference-based phasing using the Haplotype Reference Consortium panel in NATURE GENETICS
  • 2016-10 Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19 in BMC PROCEEDINGS
  • 2016-10 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci in NATURE GENETICS
  • 2016-10 Independent test assessment using the extreme value distribution theory in BMC PROCEEDINGS
  • 2016-10 A reference panel of 64,976 haplotypes for genotype imputation in NATURE GENETICS
  • 2016-10 Next-generation genotype imputation service and methods in NATURE GENETICS
  • 2016-08 The genetic architecture of type 2 diabetes in NATURE
  • 2016-06-30 Prosaposin is a regulator of progranulin levels and oligomerization in NATURE COMMUNICATIONS
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-12 The Cooperative Health Research in South Tyrol (CHRIS) study: rationale, objectives, and preliminary results in JOURNAL OF TRANSLATIONAL MEDICINE
  • 2015-11 Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers in NATURE GENETICS
  • 2015-10 A global reference for human genetic variation in NATURE
  • 2015-08 Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity in NATURE GENETICS
  • 2014-12 Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel in NATURE COMMUNICATIONS
  • 2014-08 Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization in NATURE GENETICS
  • 2014-06 Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees in BMC PROCEEDINGS
  • 2014-04 Loss-of-function mutations in SLC30A8 protect against type 2 diabetes in NATURE GENETICS
  • 2013-06 Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders in NATURE GENETICS
  • 2013-03 Fine-Mapping of Restless Legs Locus 4 (RLS4) Identifies a Haplotype over the SPATS2L and KCTD18 Genes in JOURNAL OF MOLECULAR NEUROSCIENCE
  • 2013-02 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion in NATURE GENETICS
  • 2012-08 Fast and accurate genotype imputation in genome-wide association studies through pre-phasing in NATURE GENETICS
  • 2010-12 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction in NATURE GENETICS
  • 2010-11 Genes predict village of origin in rural Europe in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-08 Copy number variation and association over T-cell receptor genes—influence of DNA source in IMMUNOGENETICS
  • 2010-05 New loci associated with kidney function and chronic kidney disease in NATURE GENETICS
  • 2010-04 Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-04 Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-04 Common variants at ten loci modulate the QT interval duration in the QTSCD Study in NATURE GENETICS
  • 2007-12 Genetic association studies for gene expressions: permutation-based mutual information in a comparison with standard ANOVA and as a novel approach for feature selection in BMC PROCEEDINGS
  • 2007-12 The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives in BMC MEDICAL GENETICS
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