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The Journal of Cell Biology|August 10, 2019
Chromatin compartment dynamics in a haploinsufficient model of cardiac laminopathyAlessandro Bertero, Paul A Fields, Alec S T Smith, et al.Nature Genetics|September 25, 2012
Estimating the human mutation rate using autozygosity in a founder populationCatarina D Campbell, Jessica X Chong, Maika Malig, et al.Cell|November 10, 2023
Proteostasis governs differential temperature sensitivity across embryonic cell typesMichael W Dorrity, Lauren M Saunders, Madeleine Duran, et al.Biorxiv : the Preprint Server for Biology|July 3, 2023
Multiplex single-cell chemical genomics reveals the kinase dependence of the response to targeted therapyJosé L McFaline-Figueroa, Sanjay Srivatsan, Andrew J Hill, et al.Nature|December 4, 2012
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variantsWenqing Fu, Timothy D O'Connor, Goo Jun, et al.American Journal of Medical Genetics. Part A|August 3, 2016
SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset featuresPatricia G Wheeler, Bobby G Ng, Laura Sanford, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|July 9, 2013
Germline missense variants in the BTNL2 gene are associated with prostate cancer susceptibilityLiesel M Fitzgerald, Akash Kumar, Evan A Boyle, et al.Molecular Metabolism|February 8, 2020
Single-cell ATAC-Seq in human pancreatic islets and deep learning upscaling of rare cells reveals cell-specific type 2 diabetes regulatory signaturesVivek Rai, Daniel X Quang, Michael R Erdos, et al.Nature Methods|October 16, 2007
Multiplex amplification of large sets of human exonsGregory J Porreca, Kun Zhang, Jin Billy Li, et al.Cell|July 3, 2007
A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system developmentIvan P G Moskowitz, Jae B Kim, Meredith L Moore, et al.Pageof 43