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American Journal of Physiology. Lung Cellular and Molecular Physiology|December 20, 2022
Neonatal hyperoxia induces activated pulmonary cellular states and sex-dependent transcriptomic changes in a model of experimental bronchopulmonary dysplasiaSheng Xia, Lisandra Vila Ellis, Konner Winkley, et al.
Biomarker Insights|November 7, 2022
MicroRNA Content of Ewing Sarcoma Derived Extracellular Vesicles Leads to Biomarker Potential and Identification of a Previously Undocumented EWS-FLI1 TranslocationJennifer Crow, Glenson Samuel, Emily Farrow, et al.
Journal of the Pediatric Infectious Diseases Society|January 9, 2018
Prospective Surveillance of Pediatric Invasive Group A Streptococcus InfectionNatasha S Ching, Nigel Crawford, Alissa McMinn, et al.
Vaccine|October 5, 2024
Effective integration of COVID-19 vaccination with routine immunization: A case study from Kinshasa, DRCGuillaume Mwamba, Emily Margaret Gibson, Carla Toko, et al.
Human Mutation|December 17, 2014
Loss of function variants in human PNPLA8 encoding calcium-independent phospholipase A2 γ recapitulate the mitochondriopathy of the homologous null mouseCarol J Saunders, Sung Ho Moon, Xinping Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 2, 2021
ASCL2 reciprocally controls key trophoblast lineage decisions during hemochorial placenta developmentKaela M Varberg, Khursheed Iqbal, Masanaga Muto, et al.
NPJ Genomic Medicine|December 22, 2017
Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, <i>CYP2D6</i>, from whole-genome sequencesGreyson P Twist, Andrea Gaedigk, Neil A Miller, et al.
NPJ Genomic Medicine|December 22, 2017
Erratum: Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, <i>CYP2D6</i>, from whole-genome sequencesGreyson P Twist, Andrea Gaedigk, Neil A Miller, et al.
Nature Metabolism|February 19, 2020
Single-cell analysis of human adipose tissue identifies depot and disease specific cell typesJinchu Vijay, Marie-Frédérique Gauthier, Rebecca L Biswell, et al.
Genome Medicine|October 1, 2015
A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseasesNeil A Miller, Emily G Farrow, Margaret Gibson, et al.
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