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Pediatrics|September 3, 2024
A Coproduced Family Reporting Intervention to Improve Safety Surveillance and Reduce DisparitiesAlisa Khan, Jennifer Baird, Sangeeta Mauskar, et al.
Circulation Research|March 11, 2021
MIR503HG Loss Promotes Endothelial-to-Mesenchymal Transition in Vascular DiseaseJoão P Monteiro, Julie Rodor, Axelle Caudrillier, et al.
Cell Reports. Medicine|October 31, 2025
Identification of therapeutic targets for renal medullary carcinoma via integrated genomic and transcriptomic profilingPavlos Msaouel, Nizar M Tannir, Funda Meric-Bernstam, et al.
ACS Medicinal Chemistry Letters|June 20, 2014
Discovery of MK-4409, a Novel Oxazole FAAH Inhibitor for the Treatment of Inflammatory and Neuropathic PainHarry R Chobanian, Yan Guo, Ping Liu, et al.
Gut|February 15, 2013
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European expertsHans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, et al.
Journal of Biomedical Optics|November 13, 2025
Consensus guidelines for cellular label-free optical metabolic imaging: ensuring accuracy and reproducibility in metabolic profilingIrene Georgakoudi, Melissa C Skala, Kyle P Quinn, et al.
The Journal of Clinical Investigation|September 9, 2025
Antithrombin-binding heparan sulfate is ubiquitously expressed in epithelial cells and suppresses pancreatic tumorigenesisThomas Mandel Clausen, Ryan J Weiss, Jacob R Tremblay, et al.
The Journal of Clinical Endocrinology and Metabolism|January 12, 2023
Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 TrialElizabeth Roof, Cheri L Deal, Shawn E McCandless, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|October 28, 2017
Efficacy and Safety of Digital Single-Operator Cholangioscopy for Difficult Biliary StonesOlaya I Brewer Gutierrez, Noor L H Bekkali, Isaac Raijman, et al.
American Journal of Human Genetics|May 23, 2020
De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and OsteochondromasDara Tolchin, Jessica P Yeager, Priya Prasad, et al.
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