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Cell|July 8, 2014
Disruptive CHD8 mutations define a subtype of autism early in developmentRaphael Bernier, Christelle Golzio, Bo Xiong, et al.Biorxiv : the Preprint Server for Biology|June 9, 2020
SwabExpress: An end-to-end protocol for extraction-free COVID-19 testingSanjay Srivatsan, Sarah Heidl, Brian Pfau, et al.Nature Genetics|May 28, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, et al.Genome Biology|September 16, 2011
Mutation discovery in mice by whole exome sequencingHeather Fairfield, Griffith J Gilbert, Mary Barter, et al.Nature Genetics|March 7, 2017
Single-molecule sequencing and chromatin conformation capture enable de novo reference assembly of the domestic goat genomeDerek M Bickhart, Benjamin D Rosen, Sergey Koren, et al.Cell Systems|June 19, 2021
Benchmarked approaches for reconstruction of in vitro cell lineages and in silico models of C. elegans and M. musculus developmental treesWuming Gong, Alejandro A Granados, Jingyuan Hu, et al.Clinical Chemistry|July 21, 2021
SwabExpress: An End-to-End Protocol for Extraction-Free COVID-19 TestingSanjay Srivatsan, Sarah Heidl, Brian Pfau, et al.Molecular Cell|July 7, 2023
Spatial and temporal organization of the genome: Current state and future aims of the 4D nucleome projectJob Dekker, Frank Alber, Sarah Aufmkolk, et al.Nature Neuroscience|November 24, 2022
Multiregion transcriptomic profiling of the primate brain reveals signatures of aging and the social environmentKenneth L Chiou, Alex R DeCasien, Katherina P Rees, et al.Cell|June 11, 2024
Modulation of FGF pathway signaling and vascular differentiation using designed oligomeric assembliesNatasha I Edman, Ashish Phal, Rachel L Redler, et al.Pageof 43