David Kavanagh

Ontology type: schema:Person     

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Publications in SciGraph latest 50 shown

  • 2019-03 C3 glomerulopathy — understanding a rare complement-driven renal disease in NATURE REVIEWS NEPHROLOGY
  • 2018-12 Complement receptor CD46 co-stimulates optimal human CD8+ T cell effector function via fatty acid metabolism in NATURE COMMUNICATIONS
  • 2018-01 Diseases of complement dysregulation—an overview in SEMINARS IN IMMUNOPATHOLOGY
  • 2018-01 Introduction to complement in health and disease: novel aspects and insights in SEMINARS IN IMMUNOPATHOLOGY
  • 2017-03-21 Genetic correlation between amyotrophic lateral sclerosis and schizophrenia in NATURE COMMUNICATIONS
  • 2017-01 Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects in NATURE GENETICS
  • 2016-11 Gene expression elucidates functional impact of polygenic risk for schizophrenia in NATURE NEUROSCIENCE
  • 2016-10 Patterns of genic intolerance of rare copy number variation in 59,898 human exomes in NATURE GENETICS
  • 2015-12 Plasma resistant atypical hemolytic uremic syndrome associated with a CFH mutation treated with eculizumab: a case report in JOURNAL OF MEDICAL CASE REPORTS
  • 2015-02 Schizophrenia genetics: emerging themes for a complex disorder in MOLECULAR PSYCHIATRY
  • 2015-01 Structural basis for sialic acid–mediated self-recognition by complement factor H in NATURE CHEMICAL BIOLOGY
  • 2014-08 Copy number variants and therapeutic response to antidepressant medication in major depressive disorder in THE PHARMACOGENOMICS JOURNAL
  • 2014-07 Biological insights from 108 schizophrenia-associated genetic loci in NATURE
  • 2013-11 Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration in NATURE GENETICS
  • 2013-05 The ENCODE project: implications for psychiatric genetics in MOLECULAR PSYCHIATRY
  • 2012-01 Interpretation of genetic variants of uncertain significance in atypical hemolytic uremic syndrome in KIDNEY INTERNATIONAL
  • 2011-04 Structural basis for engagement by complement factor H of C3b on a self surface in NATURE STRUCTURAL & MOLECULAR BIOLOGY
  • 2010-12 Genetics and complement in atypical HUS in PEDIATRIC NEPHROLOGY
  • 2007-09 C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy in NATURE GENETICS
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