Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3. Kühnisch Jirko et al. Clinical genetics 2019 Sep

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Last Posted: Oct 03, 2019

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• Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3.
  Kühnisch Jirko et al. Clinical genetics 2019 Sep
• Genetics of Unexplained Sudden Cardiac Death in Adult Caucasian and African American Individuals Living in the State of Maryland
  L Guo et al, MedRXIV, September 24, 2019
• Clinical utility of exome sequencing in infantile heart failure.
  Ritter Alyssa et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Sep
• The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy.
  Lahrouchi Najim et al. European journal of human genetics : EJHG 2019 Sep
• Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy.
  Robyns Tomas et al. European journal of medical genetics 2019 Sep 103754
• Importance of Genetic Testing in Dilated Cardiomyopathy: Applications and Challenges in Clinical Practice.
  Lamounier Júnior Arsonval et al. Arquivos brasileiros de cardiologia 2019 Sep 113(2) 274-281
• The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communication.
  Harris Stephanie et al. Molecular genetics & genomic medicine 2019 Sep e940
• Post mortem genetic test, the clinical diagnosis is not fade with the death of the patient.
  Ribeiro Sílvia et al. Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology 2019 Sep
• Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy
  M Gigli et al. JACC, September 2019
• Lessons learned from testing cardiac channelopathy and cardiomyopathy genes in individuals who died suddenly: A two-year prospective study in a large medical examiner's office with an in-house molecular genetics laboratory and genetic counseling services.
  Williams Nori et al. Journal of genetic counseling 2019 Aug

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