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Ebiomedicine|October 27, 2015
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in EpilepsyCostin Leu, Simona Balestrini, Bridget Maher, et al.
Cardiovascular Research|February 8, 2022
Rapid neutrophil mobilization by VCAM-1+ endothelial cell-derived extracellular vesiclesNaveed Akbar, Adam T Braithwaite, Emma M Corr, et al.
Ebiomedicine|April 16, 2025
Genome-wide association meta-analyses of drug-resistant epilepsyCostin Leu, Andreja Avbersek, Remi Stevelink, et al.
Journal of Medical Genetics|March 11, 2020
Pathogenic variants in <i>TNRC6B</i> cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHDJorge Luis Granadillo, Alexander P A Stegmann, Hui Guo, et al.
European Urology Oncology|May 26, 2026
Update of the EORTC Health-related Quality of Life Modules for Bladder Cancer: Phase 1-2 of the Development ProcessElke Rammant, Louis Fox, Silva De Padova, et al.
Science Translational Medicine|October 5, 2018
Anti-α4β7 therapy targets lymphoid aggregates in the gastrointestinal tract of HIV-1-infected individualsMathieu Uzzan, Minami Tokuyama, Adam K Rosenstein, et al.
The American Journal of Medicine|February 10, 2015
Comorbidities frequency in Takotsubo syndrome: an international collaborative systematic review including 1109 patientsFrancesco Pelliccia, Guido Parodi, Cesare Greco, et al.
Science Translational Medicine|April 20, 2018
CD32 is expressed on cells with transcriptionally active HIV but does not enrich for HIV DNA in resting T cellsMohamed Abdel-Mohsen, Leticia Kuri-Cervantes, Judith Grau-Exposito, et al.
American Journal of Human Genetics|July 30, 2019
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental DisordersBjörn Fischer-Zirnsak, Lara Segebrecht, Max Schubach, et al.
Critical Care Medicine|January 2, 2022
Outcome of Temporary Circulatory Support As a Bridge-to-Left Ventricular Assist Device Strategy in Cardiogenic Shock PatientsAuriane Bidaut, Erwan Flécher, Nicolas Nesseler, et al.
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