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Plos Genetics|March 31, 2025
Human genetic evidence enriched for side effects of approved drugsEric Vallabh Minikel, Matthew R NelsonNeuron|October 21, 2016
Publicly Available Data Provide Evidence against NR1H3 R415Q Causing Multiple SclerosisEric Vallabh Minikel, Daniel G MacArthurScientific Reports|October 22, 2022
Disease stages and therapeutic hypotheses in two decades of neurodegenerative disease clinical trialsMeredith A Mortberg, Sonia M Vallabh, Eric Vallabh MinikelHarvard Review of Psychiatry|March 12, 2014
Autism spectrum disorder genetics: diverse genes with diverse clinical outcomesMichael E Talkowski, Eric Vallabh Minikel, James F GusellaPlos Pathogens|August 22, 2022
Analysis of non-human primate models for evaluating prion disease therapeutic efficacyMeredith A Mortberg, Eric Vallabh Minikel, Sonia M VallabhThe Lancet. Neurology|March 22, 2020
Towards a treatment for genetic prion disease: trials and biomarkersSonia M Vallabh, Eric Vallabh Minikel, Stuart L Schreiber, et al.Nature|April 17, 2024
Refining the impact of genetic evidence on clinical successEric Vallabh Minikel, Jeffery L Painter, Coco Chengliang Dong, et al.Medrxiv : the Preprint Server for Health Sciences|November 19, 2025
Mortality of individuals with antemortem genetic testing for PRNP variants in the United States, 1998-2024Yuan Lian, Keisi Kotobelli, Kathleen Glisic, et al.The Journal of Biological Chemistry|July 13, 2024
Modulation of prion protein expression through cryptic splice site manipulationJuliana E Gentile, Taylor L Corridon, Meredith A Mortberg, et al.Biorxiv : the Preprint Server for Biology|January 8, 2024
Modulation of prion protein expression through cryptic splice site manipulationJuliana E Gentile, Taylor L Corridon, Meredith A Mortberg, et al.Pageof 5