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Plos One|March 27, 2015
Modulators of hepatic lipoprotein metabolism identified in a search for small-molecule inducers of tribbles pseudokinase 1 expressionMarek M Nagiec, Adam P Skepner, Joseph Negri, et al.American Journal of Medical Genetics. Part A|August 6, 2021
Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypesAlanna Strong, Cara Skraban, Kevin Meyers, et al.American Journal of Human Genetics|August 5, 2017
Human Germline Genome EditingKelly E Ormond, Douglas P Mortlock, Derek T Scholes, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|April 4, 2015
Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary ArteriesMélissa Beaudoin, Rajat M Gupta, Hong-Hee Won, et al.Cell|January 12, 2022
Engineered virus-like particles for efficient in vivo delivery of therapeutic proteinsSamagya Banskota, Aditya Raguram, Susie Suh, et al.Nature Biotechnology|May 4, 2023
Efficient prime editing in mouse brain, liver and heart with dual AAVsJessie R Davis, Samagya Banskota, Jonathan M Levy, et al.Cytotherapy|July 5, 2025
Advancing gene-editing platforms to improve the viability of rare-disease therapeutics: key insights from a 2024 Scientific Exchange hosted by ARM, ISCT, and DanaherFyodor Urnov, Sadik Kassim, Kiran Musunuru, et al.American Journal of Medical Genetics. Part A|May 7, 2021
A new syndrome of moyamoya disease, kidney dysplasia, aminotransferase elevation, and skin disease associated with de novo variants in RNF213Alanna Strong, Gina O'Grady, Evelyn Shih, et al.Developmental Cell|November 7, 2017
ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear DevelopmentAlex M Rohacek, Thomas W Bebee, Richard K Tilton, et al.Nature Communications|August 20, 2016
Circular non-coding RNA ANRIL modulates ribosomal RNA maturation and atherosclerosis in humansLesca M Holdt, Anika Stahringer, Kristina Sass, et al.Pageof 22