{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,24]],"date-time":"2026-09-24T21:04:01Z","timestamp":1790283841173,"version":"4.1.0"},"reference-count":62,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2026,9,1]],"date-time":"2026-09-01T00:00:00Z","timestamp":1788220800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2026,9,1]],"date-time":"2026-09-01T00:00:00Z","timestamp":1788220800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2026,9,13]],"date-time":"2026-09-13T00:00:00Z","timestamp":1789257600000},"content-version":"vor","delay-in-days":12,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100025520","name":"Medical Research Future Fund","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100025520","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["cell.com","clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Trends in Molecular Medicine"],"published-print":{"date-parts":[[2026,9]]},"DOI":"10.1016\/j.molmed.2026.09.002","type":"journal-article","created":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T12:17:23Z","timestamp":1790165843000},"update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["Genomic newborn screening, a healthcare system transformation"],"prefix":"10.1016","author":[{"given":"Lilian","family":"Downie","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8640-1371","authenticated-orcid":false,"given":"Zornitza","family":"Stark","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.molmed.2026.09.002_bb0005","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1186\/s12887-018-1200-1","article-title":"The BabySeq Project: implementing genomic sequencing in newborns","volume":"18","author":"Holm","year":"2018","journal-title":"BMC Pediatr."},{"key":"10.1016\/j.molmed.2026.09.002_bb0010","doi-asserted-by":"crossref","first-page":"755","DOI":"10.1038\/s41576-023-00621-w","article-title":"Genomic newborn screening for rare diseases","volume":"24","author":"Stark","year":"2023","journal-title":"Nat. Rev. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0015","series-title":"Fit for the Future: 10 Year Health Plan for England","author":"Department of Health and Social Care, England","year":"2025"},{"key":"10.1016\/j.molmed.2026.09.002_bb0020","doi-asserted-by":"crossref","first-page":"1823","DOI":"10.1038\/s41591-024-03055-x","article-title":"Exploring the benefits, harms and costs of genomic newborn screening for rare diseases","volume":"30","author":"Baple","year":"2024","journal-title":"Nat. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0025","doi-asserted-by":"crossref","first-page":"2","DOI":"10.3390\/ijns7010002","article-title":"Ethical and psychosocial implications of genomic newborn screening","volume":"7","author":"Levy","year":"2021","journal-title":"Int. J. Neonatal Screen."},{"key":"10.1016\/j.molmed.2026.09.002_bb0030","doi-asserted-by":"crossref","DOI":"10.1001\/jamanetworkopen.2021.14336","article-title":"Principles of genomic newborn screening programs: a systematic review","volume":"4","author":"Downie","year":"2021","journal-title":"JAMA Netw. Open"},{"key":"10.1016\/j.molmed.2026.09.002_bb0035","doi-asserted-by":"crossref","first-page":"232","DOI":"10.1001\/jama.2024.19662","article-title":"Expanded newborn screening using genome sequencing for early actionable conditions","volume":"333","author":"Ziegler","year":"2025","journal-title":"JAMA"},{"key":"10.1016\/j.molmed.2026.09.002_bb0040","doi-asserted-by":"crossref","first-page":"3762","DOI":"10.1038\/s41591-025-03945-8","article-title":"Feasibility and clinical utility of expanded genomic newborn screening in the early check program","volume":"31","author":"Cope","year":"2025","journal-title":"Nat. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0045","doi-asserted-by":"crossref","first-page":"1339","DOI":"10.1038\/s41591-024-03465-x","article-title":"Population-based, first-tier genomic newborn screening in the maternity ward","volume":"31","author":"Boemer","year":"2025","journal-title":"Nat. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0050","doi-asserted-by":"crossref","first-page":"4236","DOI":"10.1038\/s41591-025-03986-z","article-title":"Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study","volume":"31","author":"Lunke","year":"2025","journal-title":"Nat. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0055","doi-asserted-by":"crossref","first-page":"1034","DOI":"10.1016\/j.ajhg.2023.05.007","article-title":"Actionability of unanticipated monogenic disease risks in newborn genomic screening: findings from the BabySeq Project","volume":"110","author":"Green","year":"2023","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0060","doi-asserted-by":"crossref","DOI":"10.1038\/s41431-026-02192-w","article-title":"Scaling up genomic newborn screening: implementation lessons from the BabyScreen+ study","author":"Kugenthiran","year":"2026","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0065","doi-asserted-by":"crossref","DOI":"10.1038\/s41431-026-02101-1","article-title":"Revisiting penetrance in an era of genomic screening","author":"Jackson","year":"2026","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0070","doi-asserted-by":"crossref","first-page":"4022","DOI":"10.1038\/s41591-025-04061-3","article-title":"Determining the value of genomics in healthcare","volume":"31","author":"Goranitis","year":"2025","journal-title":"Nat. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0075","doi-asserted-by":"crossref","first-page":"1","DOI":"10.3310\/DJRF1124","article-title":"Evaluating whole genome sequencing for rare diseases in newborn screening: evidence synthesis from a series of systematic reviews","volume":"29","author":"Freeman","year":"2025","journal-title":"Health Technol. Assess."},{"key":"10.1016\/j.molmed.2026.09.002_bb0080","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1136\/jme-2022-108471","article-title":"Storing paediatric genomic data for sequential interrogation across the lifespan","volume":"51","author":"Gyngell","year":"2025","journal-title":"J. Med. Ethics"},{"key":"10.1016\/j.molmed.2026.09.002_bb0085","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1007\/s40258-025-01013-3","article-title":"Data-related and methodological challenges in assessing the cost-effectiveness of traditional and genomic newborn screening programs","volume":"24","author":"Lamsal","year":"2026","journal-title":"Appl. Health Econ. Health Policy"},{"key":"10.1016\/j.molmed.2026.09.002_bb0090","doi-asserted-by":"crossref","DOI":"10.1038\/s41431-026-02136-4","article-title":"Health economic evaluations of genomic newborn screening: approaches by studies within the International Consortium on Newborn Sequencing","author":"Smith","year":"2026","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0095","doi-asserted-by":"crossref","first-page":"40","DOI":"10.3390\/ijns8030040","article-title":"Newborn screening by genomic sequencing: opportunities and challenges","volume":"8","author":"Bick","year":"2022","journal-title":"Int. J. Neonatal Screen."},{"key":"10.1016\/j.molmed.2026.09.002_bb0100","doi-asserted-by":"crossref","first-page":"1605","DOI":"10.1016\/j.ajhg.2022.08.003","article-title":"A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases","volume":"109","author":"Kingsmore","year":"2022","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0105","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1038\/s41525-026-00551-6","article-title":"Supporting decisions about genomic newborn screening at scale in the digital age: the BabyScreen+ study","volume":"11","author":"Downie","year":"2026","journal-title":"NPJ Genom. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0110","doi-asserted-by":"crossref","first-page":"657","DOI":"10.1001\/jama.2017.10289","article-title":"Patient decision aids to engage adults in treatment or screening decisions","volume":"318","author":"Stacey","year":"2017","journal-title":"JAMA"},{"key":"10.1016\/j.molmed.2026.09.002_bb0115","doi-asserted-by":"crossref","first-page":"1086","DOI":"10.1038\/s41436-021-01112-1","article-title":"The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care","volume":"23","author":"Shickh","year":"2021","journal-title":"Genet. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0120","doi-asserted-by":"crossref","first-page":"1190","DOI":"10.1016\/j.ajhg.2022.05.001","article-title":"Digital health-enabled genomics: opportunities and challenges","volume":"109","author":"Bombard","year":"2022","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0125","doi-asserted-by":"crossref","DOI":"10.1136\/bmjopen-2024-089108","article-title":"Perceptions of genomic newborn screening: a cross-sectional survey conducted with UK medical students","volume":"14","author":"Seed","year":"2024","journal-title":"BMJ Open"},{"key":"10.1016\/j.molmed.2026.09.002_bb0130","doi-asserted-by":"crossref","first-page":"1599","DOI":"10.1038\/s41431-024-01650-7","article-title":"Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the action, actor, context, target, time framework","volume":"32","author":"Tutty","year":"2024","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0135","doi-asserted-by":"crossref","DOI":"10.5694\/mja2.70135","article-title":"Genomic newborn screening: commodity or public good?","volume":"224","author":"Gyngell","year":"2026","journal-title":"Med. J. Aust."},{"key":"10.1016\/j.molmed.2026.09.002_bb0140","series-title":"Principles and Practice of Screening for Disease","author":"Wilson","year":"1968"},{"key":"10.1016\/j.molmed.2026.09.002_bb0145","doi-asserted-by":"crossref","DOI":"10.3389\/fgene.2022.867371","article-title":"Parental attitudes toward standard newborn screening and newborn genomic sequencing: findings from the BabySeq study","volume":"13","author":"Armstrong","year":"2022","journal-title":"Front. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0150","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1186\/s40246-024-00611-x","article-title":"Australian public perspectives on genomic newborn screening: which conditions should be included?","volume":"18","author":"Lynch","year":"2024","journal-title":"Hum. Genomics"},{"key":"10.1016\/j.molmed.2026.09.002_bb0155","doi-asserted-by":"crossref","DOI":"10.1016\/j.gim.2025.101618","article-title":"Operationalizing the Wilson-Jungner principles for the genomics era: consensus recommendations from the International Consortium on Newborn Sequencing","volume":"28","author":"Downie","year":"2026","journal-title":"Genet. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0160","doi-asserted-by":"crossref","DOI":"10.1016\/j.gim.2024.101077","article-title":"Gene selection for genomic newborn screening: moving toward consensus?","volume":"26","author":"Downie","year":"2024","journal-title":"Genet. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0165","doi-asserted-by":"crossref","DOI":"10.1016\/j.gim.2025.101443","article-title":"Data-driven consideration of genetic disorders for global genomic newborn screening programs","volume":"27","author":"Minten","year":"2025","journal-title":"Genet. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0170","doi-asserted-by":"crossref","first-page":"182","DOI":"10.1038\/s41431-024-01677-w","article-title":"Genomic sequencing in newborn screening: balancing consent with the right of the asymptomatic at-risk child to be found","volume":"33","author":"Knoppers","year":"2025","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0175","doi-asserted-by":"crossref","first-page":"501","DOI":"10.1038\/gim.2014.139","article-title":"Parents are interested in newborn genomic testing during the early postpartum period","volume":"17","author":"Waisbren","year":"2015","journal-title":"Genet. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0180","doi-asserted-by":"crossref","first-page":"1012","DOI":"10.1002\/humu.24309","article-title":"Variant interpretation using population databases: lessons from gnomAD","volume":"43","author":"Gudmundsson","year":"2022","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.molmed.2026.09.002_bb0185","doi-asserted-by":"crossref","DOI":"10.1001\/jamanetworkopen.2023.39571","article-title":"Rates and classification of variants of uncertain significance in hereditary disease genetic testing","volume":"6","author":"Chen","year":"2023","journal-title":"JAMA Netw. Open"},{"key":"10.1016\/j.molmed.2026.09.002_bb0190","doi-asserted-by":"crossref","first-page":"350","DOI":"10.1001\/jama.2021.23686","article-title":"Population-based penetrance of deleterious clinical variants","volume":"327","author":"Forrest","year":"2022","journal-title":"JAMA"},{"key":"10.1016\/j.molmed.2026.09.002_bb0195","doi-asserted-by":"crossref","first-page":"275","DOI":"10.1016\/j.ajhg.2018.12.015","article-title":"Assessing the pathogenicity, penetrance, and expressivity of putative disease-causing variants in a population setting","volume":"104","author":"Wright","year":"2019","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0200","doi-asserted-by":"crossref","first-page":"1438","DOI":"10.1111\/jpc.70131","article-title":"Genomic Screening Consortium for Australian Newborns (GenSCAN)","volume":"61","author":"Taylor","year":"2025","journal-title":"J. Paediatr. Child Health"},{"key":"10.1016\/j.molmed.2026.09.002_bb0205","doi-asserted-by":"crossref","first-page":"1132","DOI":"10.1001\/jamapediatrics.2021.2829","article-title":"Psychosocial effect of newborn genomic sequencing on families in the BabySeq Project: a randomized clinical trial","volume":"175","author":"Pereira","year":"2021","journal-title":"JAMA Pediatr."},{"key":"10.1016\/j.molmed.2026.09.002_bb0210","doi-asserted-by":"crossref","DOI":"10.1038\/s41431-026-02036-7","article-title":"Parental experiences of receiving genomic newborn screening results: findings from the BabyScreen+ study","author":"Tutty","year":"2026","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0215","doi-asserted-by":"crossref","DOI":"10.3389\/fgene.2025.1704364","article-title":"Perspectives of parents receiving normal results from genomic newborn screening: a mixed-methods evaluation from the early check program","volume":"16","author":"Gwaltney","year":"2025","journal-title":"Front. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0220","doi-asserted-by":"crossref","first-page":"6","DOI":"10.3390\/ijns10010006","article-title":"Australian public perspectives on genomic newborn screening: risks, benefits, and preferences for implementation","volume":"10","author":"Lynch","year":"2024","journal-title":"Int. J. Neonatal Screen."},{"key":"10.1016\/j.molmed.2026.09.002_bb0225","first-page":"507","article-title":"Psychosocial impact of false-positive newborn screening results: a scoping review","volume":"11","author":"Chudleigh","year":"2024","journal-title":"Children (Basel)"},{"key":"10.1016\/j.molmed.2026.09.002_bb0230","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1038\/s41431-025-02009-2","article-title":"Unexpected genotypes associated with severe paediatric conditions identified in a healthy population cohort","volume":"34","author":"Bylstra","year":"2026","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0235","doi-asserted-by":"crossref","first-page":"S14","DOI":"10.1002\/hast.877","article-title":"Are parents really obligated to learn as much as possible about their children\u2019s genomes?","volume":"48","author":"Johnston","year":"2018","journal-title":"Hastings Cent. Rep."},{"key":"10.1016\/j.molmed.2026.09.002_bb0240","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1038\/s41431-017-0084-0","article-title":"Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study","volume":"26","author":"Halliday","year":"2018","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0245","doi-asserted-by":"crossref","first-page":"1320","DOI":"10.1038\/s41390-024-03668-5","article-title":"Early Intervention services in the era of genomic medicine: setting a research agenda","volume":"97","author":"MacDuffie","year":"2025","journal-title":"Pediatr. Res."},{"key":"10.1016\/j.molmed.2026.09.002_bb0250","doi-asserted-by":"crossref","DOI":"10.1177\/21501319231186500","article-title":"Unveiling the significance and challenges of integrating prevention levels in healthcare practice","volume":"14","author":"AbdulRaheem","year":"2023","journal-title":"J. Prim. Care Community Health"},{"key":"10.1016\/j.molmed.2026.09.002_bb0255","doi-asserted-by":"crossref","first-page":"108","DOI":"10.1186\/s13073-016-0362-4","article-title":"Integrating precision cancer medicine into healthcare-policy, practice, and research challenges","volume":"8","author":"Bertier","year":"2016","journal-title":"Genome Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0260","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1186\/s13073-021-00911-0","article-title":"Advancing precision public health using human genomics: examples from the field and future research opportunities","volume":"13","author":"Roberts","year":"2021","journal-title":"Genome Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0265","doi-asserted-by":"crossref","first-page":"S50","DOI":"10.1097\/CCM.0b013e3181921349","article-title":"Toward theragnostics","volume":"37","author":"Pene","year":"2009","journal-title":"Crit. Care Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0270","doi-asserted-by":"crossref","DOI":"10.1111\/cts.70246","article-title":"Frequency and implications of high-risk pharmacogenomic phenotypes identified in a diverse Australian pediatric oncology cohort","volume":"18","author":"Moore","year":"2025","journal-title":"Clin. Transl. Sci."},{"key":"10.1016\/j.molmed.2026.09.002_bb0275","doi-asserted-by":"crossref","first-page":"769","DOI":"10.1038\/s41436-018-0391-z","article-title":"Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG)","volume":"21","author":"David","year":"2019","journal-title":"Genet. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0280","doi-asserted-by":"crossref","first-page":"2991","DOI":"10.1038\/s41591-026-04477-5","article-title":"Automated reanalysis of genomic data for rare disease diagnostics at scale","volume":"32","author":"Welland","year":"2026","journal-title":"Nat. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0285","doi-asserted-by":"crossref","first-page":"e93","DOI":"10.1016\/S2589-7500(22)00195-9","article-title":"Secondary data for global health digitalisation","volume":"5","author":"Naher","year":"2023","journal-title":"Lancet Digit. Health"},{"key":"10.1016\/j.molmed.2026.09.002_bb0290","doi-asserted-by":"crossref","first-page":"142","DOI":"10.1038\/s41431-021-00990-y","article-title":"Rapid genomic testing for critically ill children: time to become standard of care?","volume":"30","author":"Stark","year":"2022","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.molmed.2026.09.002_bb0295","doi-asserted-by":"crossref","DOI":"10.1126\/science.aaf7000","article-title":"Genetic identification of familial hypercholesterolemia within a single U.S. health care system","volume":"354","author":"Abul-Husn","year":"2016","journal-title":"Science"},{"key":"10.1016\/j.molmed.2026.09.002_bb0300","doi-asserted-by":"crossref","DOI":"10.1001\/jamanetworkopen.2018.2140","article-title":"Exome sequencing-based screening for BRCA1\/2 expected pathogenic variants among adult biobank participants","volume":"1","author":"Manickam","year":"2018","journal-title":"JAMA Netw. Open"},{"key":"10.1016\/j.molmed.2026.09.002_bb0305","doi-asserted-by":"crossref","first-page":"1877","DOI":"10.1056\/NEJMoa2314768","article-title":"Nationwide, couple-based genetic carrier screening","volume":"391","author":"Kirk","year":"2024","journal-title":"N. Engl. J. Med."},{"key":"10.1016\/j.molmed.2026.09.002_bb0310","doi-asserted-by":"crossref","first-page":"419","DOI":"10.1016\/j.ajhg.2023.01.018","article-title":"Australian Genomics: outcomes of a 5-year national program to accelerate the integration of genomics in healthcare","volume":"110","author":"Stark","year":"2023","journal-title":"Am. J. Hum. Genet."}],"container-title":["Trends in Molecular Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1471491426002182?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1471491426002182?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,9,24]],"date-time":"2026-09-24T20:32:20Z","timestamp":1790281940000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1471491426002182"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,9]]},"references-count":62,"alternative-id":["S1471491426002182"],"URL":"https:\/\/doi.org\/10.1016\/j.molmed.2026.09.002","relation":{},"ISSN":["1471-4914"],"issn-type":[{"value":"1471-4914","type":"print"}],"subject":[],"published":{"date-parts":[[2026,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genomic newborn screening, a healthcare system transformation","name":"articletitle","label":"Article Title"},{"value":"Trends in Molecular Medicine","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.molmed.2026.09.002","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2026 The Authors. Published by Elsevier Ltd.","name":"copyright","label":"Copyright"}]}}