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American Journal of Human Genetics|November 26, 2018
MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon GuidanceWilliam B Dobyns, Kimberly A Aldinger, Gisele E Ishak, et al.Science (New York, N.Y.)|September 30, 2020
Viral epitope profiling of COVID-19 patients reveals cross-reactivity and correlates of severityEllen Shrock, Eric Fujimura, Tomasz Kula, et al.Nature Communications|September 19, 2024
Shared neutrophil and T cell dysfunction is accompanied by a distinct interferon signature during severe febrile illnesses in childrenHarsita Patel, Michael J Carter, Heather Jackson, et al.JAMA Oncology|October 22, 2016
Association of Distinct Mutational Signatures With Correlates of Increased Immune Activity in Pancreatic Ductal AdenocarcinomaAshton A Connor, Robert E Denroche, Gun Ho Jang, et al.The New England Journal of Medicine|May 9, 2023
Randomized Trial of Early Detection and Treatment of Postpartum HemorrhageIoannis Gallos, Adam Devall, James Martin, et al.Nature Medicine|October 9, 2019
Genome-wide germline correlates of the epigenetic landscape of prostate cancerKathleen E Houlahan, Yu-Jia Shiah, Alexander Gusev, et al.JAMA Neurology|May 10, 2016
Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary MosaicismGhayda M Mirzaa, Catarina D Campbell, Nadia Solovieff, et al.American Journal of Human Genetics|September 3, 2019
Redefining the Etiologic Landscape of Cerebellar MalformationsKimberly A Aldinger, Andrew E Timms, Zachary Thomson, et al.Nature|October 13, 2016
A renewed model of pancreatic cancer evolution based on genomic rearrangement patternsFaiyaz Notta, Michelle Chan-Seng-Yue, Mathieu Lemire, et al.JCI Insight|September 16, 2016
<i>PIK3CA</i>-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distributionGhayda Mirzaa, Andrew E Timms, Valerio Conti, et al.Pageof 140