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Identification of regulatory variants associated with genetic susceptibility to meningococcal disease.
Borghini, Lisa; Png, Eileen; Binder, Alexander; Wright, Victoria J; Pinnock, Ellie; de Groot, Ronald; Hazelzet, Jan; Emonts, Marieke; Van der Flier, Michiel; Schlapbach, Luregn J; Anderson, Suzanne; Secka, Fatou; Salas, Antonio; Fink, Colin; Carrol, Enitan D; Pollard, Andrew J; Coin, Lachlan J; Kuijpers, Taco W; Martinon-Torres, Federico; Zenz, Werner; Levin, Michael; Hibberd, Martin L; Davila, Sonia.
Afiliação
  • Borghini L; Human Genetics, Genome Institute of Singapore, Singapore, Singapore. borghini.lisa@gmail.com.
  • Png E; Infectious diseases, Genome Institute of Singapore, Singapore, Singapore. borghini.lisa@gmail.com.
  • Binder A; Infectious diseases, Genome Institute of Singapore, Singapore, Singapore.
  • Wright VJ; Department of General Pediatrics, Medical University of Graz, Graz, Austria.
  • Pinnock E; Section for Paediatrics, Division of Infectious Diseases, Department of Medicine, Imperial College London, London, UK.
  • de Groot R; Micropathology Ltd, University of Warwick, Warwick, UK.
  • Hazelzet J; Department of Pediatrics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Emonts M; Department of Pediatrics, Erasmus Medical Center-Sophia Children's hospital, University Medical Center, Rotterdam, The Netherlands.
  • Van der Flier M; Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Schlapbach LJ; Paediatric Infectious Diseases and Immunology Department, Newcastle upon Tyne Hospitals Foundation Trust, Great North Children's Hospital, Newcastle upon Tyne, United Kingdom.
  • Anderson S; Department of Pediatrics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Secka F; Faculty of Medicine, The University of Queensland, Brisbane, Australia.
  • Salas A; Paediatric Critical Care Research Group, Mater Research Institute, University of Queensland, Brisbane, Australia.
  • Fink C; Paediatric Intensive Care Unit, Lady Cilento Children's Hospital, Brisbane, Australia.
  • Carrol ED; Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
  • Pollard AJ; Medical Research Council Unit Gambia, Banjul, The Gambia.
  • Coin LJ; Medical Research Council Unit Gambia, Banjul, The Gambia.
  • Kuijpers TW; Unidade de Xenética, Departamento de Anatomía Patolóxica e Ciencias Forenses, Instituto de Ciencias Forenses, Facultade de Medicina, Universidade de Santiago de Compostela, and GenPoB Research Group, Instituto de Investigaciones Sanitarias (IDIS), Hospital Clínico Universitario de Santiago, Galicia,
  • Martinon-Torres F; Micropathology Ltd, University of Warwick, Warwick, UK.
  • Zenz W; Institute of Infection and Global Health, University of Liverpool, Liverpool, UK.
  • Levin M; Oxford Vaccine Group, Department of Pediatrics, University of Oxford and the NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Hibberd ML; Institute for Molecular Bioscience, The University of Queensland, St Lucia, Queensland, 4072, Australia.
  • Davila S; Division of Pediatric Hematology, Immunology and Infectious diseases, Emma Children's Hospital Academic Medical Center, Amsterdam, The Netherlands.
Sci Rep ; 9(1): 6966, 2019 05 06.
Article em En | MEDLINE | ID: mdl-31061469
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Hipofaríngeas / Sequências Reguladoras de Ácido Nucleico / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Infecções Meningocócicas / Neisseria meningitidis Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Hipofaríngeas / Sequências Reguladoras de Ácido Nucleico / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Infecções Meningocócicas / Neisseria meningitidis Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article