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Nature Genetics|July 24, 2019
Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion diseaseJun Sone, Satomi Mitsuhashi, Atsushi Fujita, et al.Nature Genetics|October 24, 2018
Long noncoding RNA MALAT1 suppresses breast cancer metastasisJongchan Kim, Hai-Long Piao, Beom-Jun Kim, et al.Nature Genetics|October 24, 2018
Insights into imprinting from parent-of-origin phased methylomes and transcriptomesFlorian Zink, Droplaug N Magnusdottir, Olafur T Magnusson, et al.Nature Genetics|November 7, 2018
Multiple transmissions of de novo mutations in familiesHákon Jónsson, Patrick Sulem, Gudny A Arnadottir, et al.Nature Genetics|November 8, 2018
Author Correction: Distinguishing genetic correlation from causation across 52 diseases and complex traitsLuke J O'Connor, Alkes L PriceNature Genetics|October 31, 2018
Single-allele chromatin interactions identify regulatory hubs in dynamic compartmentalized domainsA Marieke Oudelaar, James O J Davies, Lars L P Hanssen, et al.Nature Genetics|November 14, 2018
Author Correction: Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumorsHuipeng Li, Elise T Courtois, Debarka Sengupta, et al.Nature Genetics|April 4, 2017
Estimating the selective effects of heterozygous protein-truncating variants from human exome dataChristopher A Cassa, Donate Weghorn, Daniel J Balick, et al.Nature Genetics|April 4, 2017
Immunosequencing identifies signatures of cytomegalovirus exposure history and HLA-mediated effects on the T cell repertoireRyan O Emerson, William S DeWitt, Marissa Vignali, et al.Nature Genetics|October 9, 2019
Publisher Correction: Inferring whole-genome histories in large population datasetsJerome Kelleher, Yan Wong, Anthony W Wohns, et al.Pageof 743