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Nature Genetics|March 8, 2019
Author Correction: Origin and evolution of the octoploid strawberry genomePatrick P Edger, Thomas J Poorten, Robert VanBuren, et al.Nature Genetics|February 26, 2021
ArchR is a scalable software package for integrative single-cell chromatin accessibility analysisJeffrey M Granja, M Ryan Corces, Sarah E Pierce, et al.Nature Genetics|March 14, 2017
Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformationsXia Wang, Wu-Lin Charng, Chun-An Chen, et al.Nature Genetics|March 14, 2017
Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humansHsiang-Chih Lu, Qiumin Tan, Maxime W C Rousseaux, et al.Nature Genetics|February 21, 2017
Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell typesSung Chun, Alexandra Casparino, Nikolaos A Patsopoulos, et al.Nature Genetics|February 25, 2017
The creativity of immigrantsNature Genetics|May 20, 1998
A mouse model for Prader-Willi syndrome imprinting-centre mutationsT Yang, T E Adamson, J L Resnick, et al.Nature Genetics|May 20, 1998
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functionsN S Heiss, S W Knight, T J Vulliamy, et al.Nature Genetics|May 20, 1998
Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndromeH Chen, Y Lun, D Ovchinnikov, et al.Nature Genetics|May 20, 1998
Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient miceJ A Rafael, J M Tinsley, A C Potter, et al.Pageof 744