These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
211 related articles for article (PubMed ID: 35317923)
1. 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 MC; Riccardi MT; Radio FC; Chillemi G; Bertini ES; Tartaglia M; Cicchetti A; Dallapiccola B; Damiani G Health Policy; 2022 Apr; 126(4):337-345. PubMed ID: 35317923 [TBL] [Abstract][Full Text] [Related]
2. Bayesian cost-effectiveness analysis of Whole genome sequencing versus Whole exome sequencing in a pediatric population with suspected genetic disorders. Nurchis MC; Radio FC; Salmasi L; Heidar Alizadeh A; Raspolini GM; Altamura G; Tartaglia M; Dallapiccola B; Damiani G Eur J Health Econ; 2024 Aug; 25(6):999-1011. PubMed ID: 37975990 [TBL] [Abstract][Full Text] [Related]
3. Cost-Effectiveness of Whole-Genome vs Whole-Exome Sequencing Among Children With Suspected Genetic Disorders. Nurchis MC; Radio FC; Salmasi L; Heidar Alizadeh A; Raspolini GM; Altamura G; Tartaglia M; Dallapiccola B; Pizzo E; Gianino MM; Damiani G JAMA Netw Open; 2024 Jan; 7(1):e2353514. PubMed ID: 38277144 [TBL] [Abstract][Full Text] [Related]
4. Incremental yield of whole-genome sequencing over chromosomal microarray analysis and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta-analysis. Shreeve N; Sproule C; Choy KW; Dong Z; Gajewska-Knapik K; Kilby MD; Mone F Ultrasound Obstet Gynecol; 2024 Jan; 63(1):15-23. PubMed ID: 37725747 [TBL] [Abstract][Full Text] [Related]
5. Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing. Zhou J; Yang Z; Sun J; Liu L; Zhou X; Liu F; Xing Y; Cui S; Xiong S; Liu X; Yang Y; Wei X; Zou G; Wang Z; Wei X; Wang Y; Zhang Y; Yan S; Wu F; Zeng F; Wang J; Duan T; Peng Z; Sun L Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33800913 [TBL] [Abstract][Full Text] [Related]
6. Whole genome sequencing diagnostic yield for paediatric patients with suspected genetic disorders: systematic review, meta-analysis, and GRADE assessment. Nurchis MC; Altamura G; Riccardi MT; Radio FC; Chillemi G; Bertini ES; Garlasco J; Tartaglia M; Dallapiccola B; Damiani G Arch Public Health; 2023 May; 81(1):93. PubMed ID: 37231492 [TBL] [Abstract][Full Text] [Related]
8. Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature. Schwarze K; Buchanan J; Taylor JC; Wordsworth S Genet Med; 2018 Oct; 20(10):1122-1130. PubMed ID: 29446766 [TBL] [Abstract][Full Text] [Related]
9. Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases. Clark MM; Stark Z; Farnaes L; Tan TY; White SM; Dimmock D; Kingsmore SF NPJ Genom Med; 2018; 3():16. PubMed ID: 30002876 [TBL] [Abstract][Full Text] [Related]
10. Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis. Ewans LJ; Minoche AE; Schofield D; Shrestha R; Puttick C; Zhu Y; Drew A; Gayevskiy V; Elakis G; Walsh C; Adès LC; Colley A; Ellaway C; Evans CA; Freckmann ML; Goodwin L; Hackett A; Kamien B; Kirk EP; Lipke M; Mowat D; Palmer E; Rajagopalan S; Ronan A; Sachdev R; Stevenson W; Turner A; Wilson M; Worgan L; Morel-Kopp MC; Field M; Buckley MF; Cowley MJ; Dinger ME; Roscioli T Eur J Hum Genet; 2022 Oct; 30(10):1121-1131. PubMed ID: 35970915 [TBL] [Abstract][Full Text] [Related]
11. Organizational Aspects of the Implementation and Use of Whole Genome Sequencing and Whole Exome Sequencing in the Pediatric Population in Italy: Results of a Survey. Nurchis MC; Raspolini GM; Heidar Alizadeh A; Altamura G; Radio FC; Tartaglia M; Dallapiccola B; Damiani G J Pers Med; 2023 May; 13(6):. PubMed ID: 37373888 [TBL] [Abstract][Full Text] [Related]
12. Using molecular testing and whole-genome sequencing for tuberculosis diagnosis in a low-burden setting: a cost-effectiveness analysis using transmission-dynamic modelling. Mugwagwa T; Abubakar I; White PJ Thorax; 2021 Mar; 76(3):281-291. PubMed ID: 33542086 [TBL] [Abstract][Full Text] [Related]
13. Using the Sankey diagram to visualize article features on the topics of whole-exome sequencing (WES) and whole-genome sequencing (WGS) since 2012: Bibliometric analysis. Li MJ; Chien TW; Liao KW; Lai FJ Medicine (Baltimore); 2022 Sep; 101(38):e30682. PubMed ID: 36197161 [TBL] [Abstract][Full Text] [Related]