Matches in SemOpenAlex for { <https://semopenalex.org/work/W4220760094> ?p ?o ?g. }
Showing items 1 to 68 of
68
with 100 items per page.
- W4220760094 endingPage "207" @default.
- W4220760094 startingPage "205" @default.
- W4220760094 abstract "Genomic technologies are transforming health care, with next-generation sequencing providing an important tool that underpins diagnostics, gene discovery, and the mechanistic understanding of disease. 1 Rehm HL Evolving health care through personal genomics. Nat Rev Genet. 2017; 18: 259-267 Google Scholar However, next-generation sequencing has had limited success in bringing the power of genomic medicine to neurological disorders caused by pathogenic repeat expansions. 2 Ashley EA Towards precision medicine. Nat Rev Genet. 2016; 17: 507-522 Google Scholar The development of research tools to identify repeat expansions in next-generation sequencing data has begun to address this deficit. 3 Bahlo M Bennett MF Degorski P Tankard RM Delatycki MB Lockhart PJ Recent advances in the detection of repeat expansions with short-read next-generation sequencing. F1000Res. 2018; 7: 736 Google Scholar In The Lancet Neurology, Kristina Ibañez and colleagues 4 Ibañez K Polke J Hagelstrom RT et al. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study. Lancet Neurol. 2022; 21: 232-243 Google Scholar present compelling evidence of translation to clinical use, showing the utility of genome sequencing to diagnose neurogenetic repeat expansion disorders. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation studyIn our study, whole genome sequencing for the detection of repeat expansions showed high sensitivity and specificity, and it led to identification of neurological repeat expansion disorders in previously undiagnosed patients. These findings support implementation of whole genome sequencing in clinical laboratories for diagnosis of patients who have a neurological presentation consistent with a repeat expansion disorder. Full-Text PDF Open Access" @default.
- W4220760094 created "2022-04-03" @default.
- W4220760094 creator A5003766570 @default.
- W4220760094 date "2022-03-01" @default.
- W4220760094 modified "2023-10-16" @default.
- W4220760094 title "Advancing the diagnosis of repeat expansion disorders" @default.
- W4220760094 cites W2513408092 @default.
- W4220760094 cites W2585888498 @default.
- W4220760094 cites W2783973318 @default.
- W4220760094 cites W2808685112 @default.
- W4220760094 cites W2902005673 @default.
- W4220760094 cites W2949838248 @default.
- W4220760094 cites W2987989159 @default.
- W4220760094 cites W2999873532 @default.
- W4220760094 cites W3147352572 @default.
- W4220760094 cites W4213110991 @default.
- W4220760094 doi "https://doi.org/10.1016/s1474-4422(22)00033-3" @default.
- W4220760094 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35182498" @default.
- W4220760094 hasPublicationYear "2022" @default.
- W4220760094 type Work @default.
- W4220760094 citedByCount "4" @default.
- W4220760094 countsByYear W42207600942022 @default.
- W4220760094 countsByYear W42207600942023 @default.
- W4220760094 crossrefType "journal-article" @default.
- W4220760094 hasAuthorship W4220760094A5003766570 @default.
- W4220760094 hasConcept C104317684 @default.
- W4220760094 hasConcept C118552586 @default.
- W4220760094 hasConcept C141231307 @default.
- W4220760094 hasConcept C16568411 @default.
- W4220760094 hasConcept C189206191 @default.
- W4220760094 hasConcept C24432333 @default.
- W4220760094 hasConcept C51679486 @default.
- W4220760094 hasConcept C54355233 @default.
- W4220760094 hasConcept C70721500 @default.
- W4220760094 hasConcept C71924100 @default.
- W4220760094 hasConcept C86803240 @default.
- W4220760094 hasConceptScore W4220760094C104317684 @default.
- W4220760094 hasConceptScore W4220760094C118552586 @default.
- W4220760094 hasConceptScore W4220760094C141231307 @default.
- W4220760094 hasConceptScore W4220760094C16568411 @default.
- W4220760094 hasConceptScore W4220760094C189206191 @default.
- W4220760094 hasConceptScore W4220760094C24432333 @default.
- W4220760094 hasConceptScore W4220760094C51679486 @default.
- W4220760094 hasConceptScore W4220760094C54355233 @default.
- W4220760094 hasConceptScore W4220760094C70721500 @default.
- W4220760094 hasConceptScore W4220760094C71924100 @default.
- W4220760094 hasConceptScore W4220760094C86803240 @default.
- W4220760094 hasIssue "3" @default.
- W4220760094 hasLocation W42207600941 @default.
- W4220760094 hasLocation W42207600942 @default.
- W4220760094 hasOpenAccess W4220760094 @default.
- W4220760094 hasPrimaryLocation W42207600941 @default.
- W4220760094 hasRelatedWork W1697445709 @default.
- W4220760094 hasRelatedWork W1965856472 @default.
- W4220760094 hasRelatedWork W2061338306 @default.
- W4220760094 hasRelatedWork W2127259414 @default.
- W4220760094 hasRelatedWork W2334303976 @default.
- W4220760094 hasRelatedWork W2412321833 @default.
- W4220760094 hasRelatedWork W2519167944 @default.
- W4220760094 hasRelatedWork W2571509159 @default.
- W4220760094 hasRelatedWork W2984906837 @default.
- W4220760094 hasRelatedWork W3201180633 @default.
- W4220760094 hasVolume "21" @default.
- W4220760094 isParatext "false" @default.
- W4220760094 isRetracted "false" @default.
- W4220760094 workType "article" @default.