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Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
A genome-wide deletion map in 125,730 individuals for novel rare disease gene and variant discoveryAnthony McGuigan, Alistair T Pagnamenta, Laura E Covill, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 6, 2020
DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degenerationAnjali Vig, James A Poulter, Daniele Ottaviani, et al.
BMJ Global Health|March 24, 2023
Surgery for rheumatic heart disease in the Northern Territory, Australia, 1997-2016: what have we gained?James Doran, David Canty, Karen Dempsey, et al.
Journal of Medical Internet Research|December 6, 2022
Assessment of Clinical Information Quality in Digital Health Technologies: International eDelphi StudyKayode Philip Fadahunsi, Petra A Wark, Nikolaos Mastellos, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
APMAT analysis reveals the association between CD8 T cell receptors, cognate antigen, and T cell phenotype and persistenceJingyi Xie, Daniel G Chen, William Chour, et al.
Nature Communications|February 6, 2025
APMAT analysis reveals the association between CD8 T cell receptors, cognate antigen, and T cell phenotype and persistenceJingyi Xie, Daniel G Chen, William Chour, et al.
Advances in Health Information Science and Practice|December 3, 2025
Clinician Time Savings and Financial Value of Workstation Single Sign-On and Access Management in the United Kingdom and IrelandGeorge A Gellert, Daniel Johnston, Andrew Wilcox, et al.
Regenerative Medicine|November 30, 2018
Science-based assessment of source materials for cell-based medicines: report of a stakeholders workshopGlyn Stacey, Peter Andrews, Curtis Asante, et al.
Nature Communications|May 12, 2026
Whole-protein screening and multi-modal profiling of antigen-specific CD4<sup>+</sup> T cells at single-cell resolutionRongyu Zhang, Jingqi Qi, Michaela McKasson, et al.
The British Journal of Ophthalmology|July 30, 2024
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre studyAustin D Igelman, Elizabeth White, Alaa Tayyib, et al.
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