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Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction.
Saw, Jacqueline; Yang, Min-Lee; Trinder, Mark; Tcheandjieu, Catherine; Xu, Chang; Starovoytov, Andrew; Birt, Isabelle; Mathis, Michael R; Hunker, Kristina L; Schmidt, Ellen M; Jackson, Linda; Fendrikova-Mahlay, Natalia; Zawistowski, Matthew; Brummett, Chad M; Zoellner, Sebastian; Katz, Alexander; Coleman, Dawn M; Swan, Kirby; O'Donnell, Christopher J; Zhou, Xiang; Li, Jun Z; Gornik, Heather L; Assimes, Themistocles L; Stanley, James C; Brunham, Liam R; Ganesh, Santhi K.
Afiliação
  • Saw J; Vancouver General Hospital, Division of Cardiology, University of British Columbia, Vancouver, BC, Canada. jsaw@mail.ubc.ca.
  • Yang ML; Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Trinder M; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Tcheandjieu C; Vancouver General Hospital, Division of Cardiology, University of British Columbia, Vancouver, BC, Canada.
  • Xu C; Centre for Heart Lung Innovation, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Starovoytov A; VA Palo Alto Health Care System, Palo Alto, CA, USA.
  • Birt I; Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.
  • Mathis MR; Department of Pediatrics, Division of Pediatric Cardiology, Stanford University School of Medicine, Stanford, CA, USA.
  • Hunker KL; Department of Biostatistics and Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor, MI, USA.
  • Schmidt EM; Vancouver General Hospital, Division of Cardiology, University of British Columbia, Vancouver, BC, Canada.
  • Jackson L; Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Fendrikova-Mahlay N; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Zawistowski M; Department of Anesthesiology, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.
  • Brummett CM; Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Zoellner S; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Katz A; Department of Biostatistics and Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor, MI, USA.
  • Coleman DM; Centre for Heart Lung Innovation, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Swan K; Heart and Vascular Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.
  • O'Donnell CJ; Department of Biostatistics and Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor, MI, USA.
  • Zhou X; Department of Biostatistics and Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor, MI, USA.
  • Li JZ; Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Gornik HL; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Assimes TL; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
  • Stanley JC; Vascular Surgery Section, Department of Surgery, Michigan Medicine, University of Michigan, Ann Arbor, MI, 48109, USA.
  • Brunham LR; Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Ganesh SK; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
Nat Commun ; 11(1): 4432, 2020 09 04.
Article em En | MEDLINE | ID: mdl-32887874

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Anomalias dos Vasos Coronários / Genes Neoplásicos / Infarto do Miocárdio Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Male Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Anomalias dos Vasos Coronários / Genes Neoplásicos / Infarto do Miocárdio Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Male Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá País de publicação: Reino Unido