Simon Heath

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Publications in SciGraph latest 50 shown

  • 2018-12 Deciphering the mechanism of action of 089, a compound impairing the fungal cell cycle in SCIENTIFIC REPORTS
  • 2018-06 The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia in NATURE MEDICINE
  • 2017-12 Single-cell transcriptome conservation in cryopreserved cells and tissues in GENOME BIOLOGY
  • 2016-11-29 Increased DNA methylation variability in type 1 diabetes across three immune effector cell types in NATURE COMMUNICATIONS
  • 2016-11-25 Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease in NATURE COMMUNICATIONS
  • 2016-06-27 Saturation analysis for whole-genome bisulfite sequencing data in NATURE BIOTECHNOLOGY
  • 2016-06-27 Information recovery from low coverage whole-genome bisulfite sequencing 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 A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing in NATURE COMMUNICATIONS
  • 2015-07 Whole-genome fingerprint of the DNA methylome during human B cell differentiation in NATURE GENETICS
  • 2015-02 Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2014-12 HMTI-0197. Whole blood transcriptome analysis in migraine with aura patients: a case control study in THE JOURNAL OF HEADACHE AND PAIN
  • 2014-12 Variation in genomic landscape of clear cell renal cell carcinoma across Europe in NATURE COMMUNICATIONS
  • 2014-09 DRD2/ANKK1 Polymorphism Modulates the Effect of Ventral Striatal Activation on Working Memory Performance in NEUROPSYCHOPHARMACOLOGY
  • 2013-12 Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy in NATURE GENETICS
  • 2013-07 Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 in NATURE GENETICS
  • 2012-12 SNP calling by sequencing pooled samples in BMC BIOINFORMATICS
  • 2012-06 A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance in NATURE GENETICS
  • 2012-02 A trans-ethnic genetic study of rheumatoid arthritis identified FCGR2A as a candidate common risk factor in Japanese and European populations in MODERN RHEUMATOLOGY
  • 2011-10 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk in NATURE
  • 2011-10 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure in NATURE GENETICS
  • 2011-08 Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis in NATURE
  • 2011-01 Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3 in NATURE GENETICS
  • 2011 Applications of Second Generation Sequencing Technologies in Complex Disorders in BEHAVIORAL NEUROGENETICS
  • 2009-11 An Association Study of 22 Candidate Genes in Psoriasis Families Reveals Shared Genetic Factors with Other Autoimmune and Skin Disorders in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2009-10 Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease in NATURE GENETICS
  • 2009-06 Genome-wide association study identifies eight loci associated with blood pressure in NATURE GENETICS
  • 2009-05 A common variant on chromosome 11q13 is associated with atopic dermatitis in NATURE GENETICS
  • 2009-02 A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22 in NEUROGENETICS
  • 2008-12 Linkage mapping of CVD risk traits in the isolated Norfolk Island population in HUMAN GENETICS
  • 2008-12 Investigation of the fine structure of European populations with applications to disease association studies in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2008-12 Lung cancer susceptibility locus at 5p15.33 in NATURE GENETICS
  • 2008-04 Linkage disequilibrium analysis in the genetically isolated Norfolk Island population in HEREDITY
  • 2007-10 A genome-wide association study of global gene expression in NATURE GENETICS
  • 2007-10 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 in NATURE GENETICS
  • 2007-07 Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma in NATURE
  • 2007-06 Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2006-04 Associations of the IL2Rα, IL4Rα, IL10Rα, and IFNγR1 cytokine receptor genes with AIDS progression in a French AIDS cohort in IMMUNOGENETICS
  • 2005-12 Single-nucleotide polymorphism versus microsatellite markers in a combined linkage and segregation analysis of a quantitative trait in BMC GENETICS
  • 2005-02 Linkage and mutational analysis of familial thyroid dysgenesis demonstrate genetic heterogeneity implicating novel genes in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2004-04 Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS in IMMUNOGENETICS
  • 2003-09 Genomic analysis of Th1–Th2 cytokine genes in an AIDS cohort: identification of IL4 and IL10 haplotypes associated with the disease progression in GENES & IMMUNITY
  • 2003-07 Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q in MOLECULAR PSYCHIATRY
  • 2003-07 Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q in MOLECULAR PSYCHIATRY
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