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Nature Ecology & Evolution|November 1, 2017
Genome expansion and lineage-specific genetic innovations in the forest pathogenic fungi ArmillariaGyörgy Sipos, Arun N Prasanna, Mathias C Walter, et al.
Nature Ecology & Evolution|February 11, 2018
Author Correction: Genome expansion and lineage-specific genetic innovations in the forest pathogenic fungi ArmillariaGyörgy Sipos, Arun N Prasanna, Mathias C Walter, et al.
Trials|April 24, 2015
Preconditioning Shields Against Vascular Events in Surgery (SAVES), a multicentre feasibility trial of preconditioning against adverse events in major vascular surgery: study protocol for a randomised control trialDonagh Healy, Mary Clarke-Moloney, Brendan Gaughan, et al.
Medicine|June 16, 2023
The SERPINA5 coding variant E228Q does not contribute to clinicopathologic characteristics in Alzheimer's disease: A cross-sectional studyBillie J Matchett, Sarah J Lincoln, Matt Baker, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 3, 2018
SPOP-Mutated/CHD1-Deleted Lethal Prostate Cancer and Abiraterone SensitivityGunther Boysen, Daniel N Rodrigues, Pasquale Rescigno, et al.
Science (New York, N.Y.)|December 4, 2025
Multispecies grasslands produce more yield from lower nitrogen inputs across a climatic gradientJames O'Malley, John A Finn, Carsten S Malisch, et al.
Tomography (Ann Arbor, Mich.)|March 12, 2019
The Impact of Arterial Input Function Determination Variations on Prostate Dynamic Contrast-Enhanced Magnetic Resonance Imaging Pharmacokinetic Modeling: A Multicenter Data Analysis Challenge, Part IIWei Huang, Yiyi Chen, Andriy Fedorov, et al.
The Lancet. HIV|March 11, 2024
Progress towards the UNAIDS 95-95-95 targets in the Fifth Botswana AIDS Impact Survey (BAIS V 2021): a nationally representative surveyMadisa Mine, Kristen A Stafford, Rebecca L Laws, et al.
PLOS Global Public Health|March 24, 2023
Seroprevalence of SARS-CoV-2 in four states of Nigeria in October 2020: A population-based household surveyRosemary A Audu, Kristen A Stafford, Laura Steinhardt, et al.
American Journal of Human Genetics|March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.
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