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Plos Biology|December 15, 2020
A sensitive and affordable multiplex RT-qPCR assay for SARS-CoV-2 detectionMartin A M Reijns, Louise Thompson, Juan Carlos Acosta, et al.
Annals of the Rheumatic Diseases|December 20, 2023
Randomised trial of genetic testing and targeted intervention to prevent the development and progression of Paget's disease of boneJonathan Phillips, Deepak Subedi, Steff C Lewis, et al.
BMJ Public Health|November 3, 2025
Community-based serological screening for Chagas disease in London: a cross-sectional, observational pilot studyNatalie Elkheir, Liliana Sanchez Zelaya, Laura Valderrama Penagos, et al.
Calcified Tissue International|November 8, 2025
Baseline Characteristics of the TOPaZ Study: Randomised Trial of Teriparatide and Zoledronic Acid Compared with Standard Care in Adults with Osteogenesis ImperfectaJannie Dahl Hald, Christopher Weir, Catriona Keerie, et al.
JAMA|May 14, 2026
Teriparatide Plus Zoledronic Acid for Osteogenesis Imperfecta: A Randomized Clinical TrialJannie Dahl Hald, Christopher J Weir, Catriona Keerie, et al.
Nature Biotechnology|April 9, 2020
Efficient production of male Wolbachia-infected Aedes aegypti mosquitoes enables large-scale suppression of wild populationsJacob E Crawford, David W Clarke, Victor Criswell, et al.
Nature Biotechnology|July 26, 2020
Author Correction: Efficient production of male Wolbachia-infected Aedes aegypti mosquitoes enables large-scale suppression of wild populationsJacob E Crawford, David W Clarke, Victor Criswell, et al.
Forensic Science International. Genetics|January 23, 2025
The ReAct project: Analysis of data from 23 different laboratories to characterise DNA recovery given two sets of activity level propositionsPeter Gill, Ane Elida Fonneløp, Tacha Hicks, et al.
Lung Cancer (Amsterdam, Netherlands)|January 10, 2025
A reproducibility study on invasion in small pulmonary adenocarcinoma according to the WHO and a modified classification, supported by biomarkersErik Thunnissen, Hans Blaauwgeers, Federica Filipello, et al.
Nature Communications|July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activityAleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
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