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Peerj|April 28, 2020
CoproID predicts the source of coprolites and paleofeces using microbiome composition and host DNA contentMaxime Borry, Bryan Cordova, Angela Perri, et al.
Environmental and Molecular Mutagenesis|August 27, 2010
New and emerging technologies for genetic toxicity testingAnthony M Lynch, Jennifer C Sasaki, Rosalie Elespuru, et al.
Open Forum Infectious Diseases|December 24, 2025
Case Report and Epidemiological Investigation of Healthcare-associated <i>Plasmodium falciparum</i> Malaria Transmission in Westchester County, New York-2023Jennifer L White, Karen Southwick, Susan Madison-Antenucci, et al.
Regulatory Toxicology and Pharmacology : RTP|August 1, 2014
Recommendations from a global cross-company data sharing initiative on the incorporation of recovery phase animals in safety assessment studies to support first-in-human clinical trialsFiona Sewell, Kathryn Chapman, Paul Baldrick, et al.
Nature Reviews. Drug Discovery|June 2, 2010
Voluntary exploratory data submissions to the US FDA and the EMA: experience and impactFederico M Goodsaid, Shashi Amur, Jiri Aubrecht, et al.
Lancet Regional Health. Americas|July 4, 2025
Genetic characterization of <i>Plasmodium vivax</i> linked to autochthonous malaria transmission in the US (2023) using Illumina AmpliSeq technology: a genetic epidemiology studyJoel L N Barratt, David Jacobson, Edwin Pierre-Louis, et al.
Nature Biotechnology|May 12, 2010
Towards consensus practices to qualify safety biomarkers for use in early drug developmentFrank D Sistare, Frank Dieterle, Sean Troth, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|February 19, 2008
Interlaboratory evaluation of genomic signatures for predicting carcinogenicity in the ratMark R Fielden, Alex Nie, Michael McMillian, et al.
Nature Biotechnology|May 12, 2010
Renal biomarker qualification submission: a dialog between the FDA-EMEA and Predictive Safety Testing ConsortiumFrank Dieterle, Frank Sistare, Federico Goodsaid, et al.
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