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The Lancet. Global Health|February 21, 2019
Effect of 10-valent pneumococcal conjugate vaccine on the incidence of radiologically-confirmed pneumonia and clinically-defined pneumonia in Kenyan children: an interrupted time-series analysisMicah Silaba, Michael Ooko, Christian Bottomley, et al.
Scientific Reports|January 14, 2018
FDXR is a biomarker of radiation exposure in vivoGráinne O'Brien, Lourdes Cruz-Garcia, Matthäus Majewski, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 12, 2017
A First-in-Human, Phase I, Dose-Escalation Study of TAK-117, a Selective PI3Kα Isoform Inhibitor, in Patients with Advanced Solid MalignanciesDejan Juric, Johann S de Bono, Patricia M LoRusso, et al.
Epilepsia Open|May 4, 2026
KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severityTrupti Jadhav, Sophie E Bouffler, Emily Innes, et al.
Geroscience|March 17, 2025
3-Monothiopomalidomide, a new immunomodulatory imide drug (IMiD), blunts inflammation and mitigates ischemic stroke in the ratKai-Yun Chen, Shih-Chang Hsueh, Pathik Parekh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2024
A national education program for rapid genomics in pediatric acute care: Building workforce confidence, competence, and capabilityGiulia McCorkell, Amy Nisselle, Donna Halton, et al.
JAMA Oncology|February 4, 2021
Comparison of Multiparametric Magnetic Resonance Imaging-Targeted Biopsy With Systematic Transrectal Ultrasonography Biopsy for Biopsy-Naive Men at Risk for Prostate Cancer: A Phase 3 Randomized Clinical TrialLaurence Klotz, Joseph Chin, Peter C Black, et al.
BMJ Medicine|March 20, 2023
Consistency of covid-19 trial preprints with published reports and impact for decision making: retrospective reviewDena Zeraatkar, Tyler Pitre, Gareth Leung, et al.
Human Mutation|October 31, 2009
OBSL1 mutations in 3-M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levelsCeline Huber, Mélanie Fradin, Thomas Edouard, et al.
American Journal of Human Genetics|November 12, 2018
Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch SyndromeJennifer A Wambach, Daniel J Wegner, Nivedita Patni, et al.
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