Last Posted: Sep 11, 2019
- Perspectives of US private payers on insurance coverage for pediatric and prenatal exome sequencing: Results of a study from the Program in Prenatal and Pediatric Genomic Sequencing (P3EGS).
Trosman Julia R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Sep - Pharmacogenomic genotypes define genetic ancestry in patients and enable population-specific genomic implementation
W Hernandez et al, The Pharmacogenomics Journal. September 10, 2019 - Regional models of genetic services in the United States
C Kaye et al, Genetics i Medicine, September 2019 - Cost-effectiveness analysis of reflex testing for Lynch syndrome in women with endometrial cancer in the UK setting.
Snowsill Tristan M et al. PloS one 2019 14(8) e0221419 - From Somatic Variants Toward Precision Oncology: An Investigation of Reporting Practice for Next-Generation Sequencing-Based Circulating Tumor DNA Analysis.
Peng Rongxue et al. The oncologist 2019 Aug - Implementation of wide-scale pharmacogenetic testing in primary care.
Natasha Petry et al. Pharmacogenomics 2019 Aug 20(12) 903-913 - Longitudinal exposure of English primary care patients to pharmacogenomic drugs: an analysis to inform design of pre-emptive pharmacogenomic testing.
Kimpton James E et al. British journal of clinical pharmacology 2019 Aug - A novel technology tool to capture the clinical information of patients across rural vision centers in a three-tier eye care network in India using the eyeSmart EMR App.
Kammari Priyanka et al. Rural and remote health 2019 Sep 19(3) 5255 - Bridging the Gaps in Personalized Medicine Value Assessment: A Review of the Need for Outcome Metrics across Stakeholders and Scientific Disciplines.
Bush William S et al. Public health genomics 2019 Aug 1-9 - Leveraging European infrastructures to access 1 million human genomes by 2022.
Saunders Gary et al. Nature reviews. Genetics 2019 Aug
.png)
No hay comentarios:
Publicar un comentario