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Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Last data update: Apr 13, 2021. (Total: 39547 Documents since 2012)
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Records 1-15 (of 15 Record(s))
Query Trace: Whole genome sequencing[original query]>>Evidence Synthesis[Product Type]
Publication
Impacts of genomics on the health and social costs of intellectual disability.
Doble Brett et al. Journal of medical genetics 2020 Jan
Methodological Issues in Assessing the Economic Value of Next-Generation Sequencing Tests: Many Challenges and Not Enough Solutions.
Phillips Kathryn A et al. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2018 21(9) 1033-1042
What People Want to Know About Their Genes: A Critical Review of the Literature on Large-Scale Genome Sequencing Studies.
Scherr Courtney L et al. Healthcare (Basel, Switzerland) 2018 Aug 6(3)
Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases.
Clark Michelle M, et al. NPJ genomic medicine 2018 0 0. 16
Effects of Single Nucleotide Polymorphisms on Surgical and Postsurgical Opioid Requirements: A Systematic Review and Meta-Analysis.
Choi Siu-Wai et al. The Clinical journal of pain 2017 Dec 33(12) 1117-1130
Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature.
Schwarze Katharina et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Feb
Do Public Involvement Activities in Biomedical Research and Innovation Recruit Representatively? A Systematic Qualitative Review.
Lander Jonas et al. Public health genomics 2016 19(4) 193-202
A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder.
Tsiplova Kate et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 May
Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Mackley Michael P et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Mar 19(3) 283-293
Is the $1000 Genome as Near as We Think? A Cost Analysis of Next-Generation Sequencing.
van Nimwegen Kirsten J M et al. Clinical chemistry 2016 Nov 62(11) 1458-1464
Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study.
Warren-Gash Charlotte et al. Hereditary cancer in clinical practice 2016 1412
Economic evidence on identifying clinically actionable findings with whole-genome sequencing: a scoping review.
Douglas Michael P et al. Genet. Med. 2015 May 21.
Deep sequencing in pre- and clinical vaccine research.
Diagnostic cancer genome sequencing and the contribution of germline variants.
American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing.
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