Global research landscape, knowledge structure, and emerging trends in adverse childhood experiences and personality disorders: a bibliometric analysis
Adjunctive berberine for schizophrenia with metabolic syndrome: a systematic review and meta-analysis
Shared reading is associated with fewer emotional/behavioral problems and better prosocial behavior in preschool children: a cross-sectional study in western China
Global trends and neurobiological frontiers of manual therapy in sleep disorders: integrating bibliometrics with clinical evidence
Prevalence of depression in patients with advanced cancer receiving palliative care: a meta-analysis of self‐report instruments
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Automated reanalysis of genomic data for rare disease diagnostics at scale
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Talos, a new tool for the automated analysis of genomic data, demonstrates the feasibility and diagnostic utility of systematic reanalyses of data in rare diseases.
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STAT+: Wagering on FDA changes, Regenxbio will submit Duchenne gene therapy for approval
Regenxbio said Wednesday it will apply for accelerated approval for its gene therapy for Duchenne muscular dystrophy — just a month after the company said regulators wanted to see another trial and that it would hold off on an application.
The announcement comes as the Food and Drug Administration seemingly reverses course on a slew of drugs it recently rejected or spurned. On Monday, Regenxbio said the FDA agreed to reconsider a Hunter syndrome gene therapy that it rejected just four months ago, when Marty Makary and Vinay Prasad were still at the agency’s helm. Both officials have left the FDA in recent weeks.
Wednesday’s announcement is unusual, however. In a press release, the company gave no indication reviewers had changed their stance on the company’s Duchenne gene therapy.

