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Precision Health Database


Precision Health Database|Search|PHGKB

Last data update: Sep 22, 2023. (Total: 61629 Documents since 2012)
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Records 1 - 26 (of 26 Records)

Query Trace: Whole genome sequencing[original query]>>Evidence Synthesis [Product Type]
Whole genome sequencing diagnostic yield for paediatric patients with suspected genetic disorders: systematic review, meta-analysis, and GRADE assessment.
Mario Cesare Nurchis et al. Arch Public Health 2023 81(1) 93
Meta-analysis of the diagnostic and clinical utility of exome and genome sequencing in pediatric and adult patients with rare diseases across diverse populations.
Claudia Ching Yan Chung et al. Genet Med 2023 100896
The cost-effectiveness of whole genome sequencing in neurodevelopmental disorders.
Hannes Runheim et al. Sci Rep 2023 13(1) 6904
Health technology assessment of whole genome sequencing in the diagnosis of genetic disorders: a scoping review of the literature.
Nurchis Mario Cesare et al. International journal of technology assessment in health care 2022 38(1) e71
Parents’ understanding of genome and exome sequencing for pediatric health conditions: a systematic review
J Gereis et al, EJHG, August 23, 2022
Cost-Effectiveness and Budget Impact of Future Developments With Whole-Genome Sequencing for Patients With Lung Cancer.
Simons Martijn J H G et al. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2022
A systematic review to guide future efforts in the determination of genetic causes of pregnancy loss.
Carey Andrew Z et al. Frontiers in reproductive health 2022 3
Incremental net benefit of whole genome sequencing for newborns and children with suspected genetic disorders: Systematic review and meta-analysis of cost-effectiveness evidence.
Nurchis Mario Cesare et al. Health policy (Amsterdam, Netherlands) 2022
Cost Efficacy of Rapid Whole Genome Sequencing in the Pediatric Intensive Care Unit.
Sanford Kobayashi Erica et al. Frontiers in pediatrics 2022 9809536
Early Cost Effectiveness of Whole-Genome Sequencing as a Clinical Diagnostic Test for Patients with Inoperable Stage IIIB,C/IV Non-squamous Non-small-Cell Lung Cancer.
Simons Martijn J H G et al. PharmacoEconomics 2021
Micro-costing diagnostics in oncology: from single-gene testing to whole genome sequencing.
Pasmans Clémence Tb et al. Expert review of pharmacoeconomics & outcomes research 2021
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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