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Biorxiv : the Preprint Server for Biology|April 17, 2023
A single-cell transcriptional timelapse of mouse embryonic development, from gastrula to pupChengxiang Qiu, Beth K Martin, Ian C Welsh, et al.Nature|February 14, 2024
A single-cell time-lapse of mouse prenatal development from gastrula to birthChengxiang Qiu, Beth K Martin, Ian C Welsh, et al.Biorxiv : the Preprint Server for Biology|November 24, 2025
Large-scale discovery of neural enhancers for cis-regulation therapiesTroy A McDiarmid, Nicholas F Page, Florence M Chardon, et al.MMWR. Morbidity and Mortality Weekly Report|June 5, 2020
Evidence for Limited Early Spread of COVID-19 Within the United States, January-February 2020, Michelle A Jorden, Sarah L Rudman, et al.Science (New York, N.Y.)|November 20, 2012
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disordersBrian J O'Roak, Laura Vives, Wenqing Fu, et al.The Journal of Clinical Investigation|February 9, 2016
FOXE3 mutations predispose to thoracic aortic aneurysms and dissectionsShao-Qing Kuang, Olga Medina-Martinez, Dong-Chuan Guo, et al.Neurology|March 14, 2014
GABRA1 and STXBP1: novel genetic causes of Dravet syndromeGemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, et al.American Journal of Human Genetics|January 7, 2014
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86Atteeq U Rehman, Regie Lyn P Santos-Cortez, Robert J Morell, et al.Nature Genetics|July 10, 2012
TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndromeCatherine Boileau, Dong-Chuan Guo, Nadine Hanna, et al.BMJ Open|October 9, 2020
The Seattle Flu Study: a multiarm community-based prospective study protocol for assessing influenza prevalence, transmission and genomic epidemiologyHelen Y Chu, Michael Boeckh, Janet A Englund, et al.Pageof 43