Generic Cost-Effectiveness Models: A Proof of Concept of a Tool for Informed Decision-Making for Public Health Precision Medicine. Snyder Susan R et al. Public health genomics 2019 Jun 1-11

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Last Posted: Jun 16, 2019

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• Generic Cost-Effectiveness Models: A Proof of Concept of a Tool for Informed Decision-Making for Public Health Precision Medicine.
  Snyder Susan R et al. Public health genomics 2019 Jun 1-11
• Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy.
  Demos Michelle et al. Frontiers in neurology 2019 10434
• Implementation of an NGS-based sequencing and gene fusion panel for clinical screening of patients with suspected hematologic malignancies.
  Levy Michael A et al. European journal of haematology 2019 Jun
• Molecular biomarkers and precision medicine in colorectal cancer: a systematic review of health economic analyses.
  Henderson Raymond et al. Oncotarget 2019 May 10(36) 3408-3423
• M-SAKHI - mobile health solutions to help community providers promote maternal and infant nutrition and health using a community-based cluster RCT in rural India: A study protocol.
  Patel Archana B et al. Maternal & child nutrition 2019 Jun e12850
• Telemedicine infectious diseases consultations and clinical outcomes: a systematic review and meta-analysis protocol.
  Burnham Jason P et al. Systematic reviews 2019 Jun 8(1) 135
• Long-term economic impacts of exome sequencing for suspected monogenic disorders: diagnosis, management, and reproductive outcomes.
  Schofield Deborah et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 May
• Cost-effectiveness of screening for HLA-B*1502 prior to initiation of carbamazepine in epilepsy patients of Asian ancestry in the United States.
  Choi Hyunmi et al. Epilepsia 2019 Jun
• Effectiveness of a genetic test panel designed for gynecological cancer: an exploratory study.
  Ida Koichi et al. Medical oncology (Northwood, London, England) 2019 May 36(7) 62
• Importance of patient selection criteria in determining diagnostic copy number variations in patients with multiple congenital anomaly/mental retardation.
  Altiner Sule et al. Molecular cytogenetics 2019 1223

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