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Elucidating the relationship between migraine risk and brain structure using genetic data.
Mitchell, Brittany L; Diaz-Torres, Santiago; Bivol, Svetlana; Cuellar-Partida, Gabriel; Gerring, Zachary F; Martin, Nicholas G; Medland, Sarah E; Grasby, Katrina L; Nyholt, Dale R; Rentería, Miguel E.
Afiliação
  • Mitchell BL; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
  • Diaz-Torres S; School of Biomedical Sciences, Faculty of Health, Centre for Genomics and Personalised Health, Queensland University of Technology (QUT), Brisbane, QLD, Australia.
  • Bivol S; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
  • Cuellar-Partida G; School of Biomedical Sciences, Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia.
  • Gerring ZF; The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.
  • Medland SE; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
  • Grasby KL; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
  • Nyholt DR; School of Biomedical Sciences, Faculty of Health, Centre for Genomics and Personalised Health, Queensland University of Technology (QUT), Brisbane, QLD, Australia.
  • Rentería ME; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Brain ; 145(9): 3214-3224, 2022 09 14.
Article em En | MEDLINE | ID: mdl-35735024
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Transtornos de Enxaqueca Tipo de estudo: Clinical_trials / Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Transtornos de Enxaqueca Tipo de estudo: Clinical_trials / Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article