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Nature Genetics|October 22, 2026
Genome-wide detection of genotype-environment interactions at biobank scale with fastGxEChao Ning, Xiang ZhouNature Genetics|November 2, 2026
A catalog of transcriptome genetic regulation in a consanguineous Middle Eastern biobankHaroon Naeem, Ilhame Diboun, Zenab Siddig, et al.Nature Genetics|November 3, 2026
A framework for genome-wide characterization of DNA methylation and variant effect predictionWeiguang Mao, Kathleen M Chen, Christopher Y Park, et al.Nature Genetics|September 18, 2001
Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern VenezuelaM A Sözen, K Suzuki, M M Tolarova, et al.Nature Genetics|October 5, 2001
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxinM C Moreira, C Barbot, N Tachi, et al.Nature Genetics|October 5, 2001
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn diseaseJ D Rioux, M J Daly, M S Silverberg, et al.Nature Genetics|October 5, 2001
High-resolution haplotype structure in the human genomeM J Daly, J D Rioux, S F Schaffner, et al.Nature Genetics|April 28, 2001
A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndromeM Meguro, A Kashiwagi, K Mitsuya, et al.Nature Genetics|April 28, 2001
Susceptibility to mouse cytomegalovirus is associated with deletion of an activating natural killer cell receptor of the C-type lectin superfamilyS H Lee, S Girard, D Macina, et al.Nature Genetics|April 28, 2001
Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiencyT Lübke, T Marquardt, A Etzioni, et al.Pageof 744