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The copy number variation and stroke (CaNVAS) risk and outcome study.

John W ColeTaiwo AdigunRufus AkinyemiOnoja Matthew AkpaSteven BellBowang ChenJordi Jimenez CondeUxue LazcanoIsrael FernandezMyriam FornageCristina Gallego-FabregaChristina JernMichael KrawczakArne LindgrenHugh S MarkusOlle MelanderMayowa OwolabiKristina SchlichtMartin SöderholmVinodh SrinivasasainagendraCarolina Soriano TárragaMartin StenmanHemant TiwariMargaret CorasanitiNatalie FecteauBeth GuizzardiHaley LopezKevin NguyenBrady J GaynorTimothy O'ConnorO Colin StineSteven J KittnerPatrick McArdleBraxton D MitchellHuichun XuCaspar Grond-Ginsbach
Published in: PloS one (2021)
The CaNVAS study will cost-effectively leverage the numerous advantages of using existing case-control data sets, exploring the relationships between CNV and IS and its subtypes, and outcome at 3 months, in both men and women, in those of African and European-Caucasian descent, this, across the entire adult-age spectrum.
Keyphrases
  • copy number
  • mitochondrial dna
  • case control
  • atrial fibrillation
  • dna methylation
  • gene expression
  • machine learning
  • electronic health record