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G3 (Bethesda, Md.)|August 30, 2020
High-Quality Assemblies for Three Invasive Social Wasps from the <i>Vespula</i> GenusThomas W R Harrop, Joseph Guhlin, Gemma M McLaughlin, et al.
Journal of Lipid Research|October 10, 2013
CDKN2B expression in adipose tissue of familial combined hyperlipidemia patientsStuart D Horswell, Lee G D Fryer, Claire E Hutchison, et al.
Cell Reports. Medicine|April 4, 2024
Synaptic injury in the inner plexiform layer of the retina is associated with progression in multiple sclerosisChristian Cordano, Sebastian Werneburg, Ahmed Abdelhak, et al.
Anesthesia and Analgesia|October 6, 2023
Development and Pilot Testing of a Programmatic System for Competency Assessment in US Anesthesiology Residency TrainingGlenn E Woodworth, Zachary T Goldstein, Aditee P Ambardekar, et al.
Science (New York, N.Y.)|February 12, 2026
Myelin sheaths in the central nervous system can withstand damage and dynamically remodelDonia Arafa, Julia van de Korput, Philipp N Braaker, et al.
Iscience|March 9, 2026
Operationalizing systemic multi-hazard and multi-risk assessment: Lessons from the MYRIAD-EU frameworkStefan Hochrainer-Stigler, Robert Šakić Trogrlić, Karina Reiter, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Nature|April 1, 2026
DNA damage burden causes selective CUX2 neuron loss in neuroinflammationLaura Morcom, Wenlong Xia, Zhaoyang Xu, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|June 19, 2025
Acute and Long-Term Immune-Treatment Strategies in Anti-LGI1 Antibody-Mediated Encephalitis: A Multicenter Cohort StudyNabil Seery, Robb Wesselingh, Paul Beech, et al.
Human Molecular Genetics|January 27, 2018
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomaliesMarie-France Portnoi, Marie-Charlotte Dumargne, Sandra Rojo, et al.
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