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Nature Genetics|January 18, 2022
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustionFederica Marasca, Shruti Sinha, Rebecca Vadalà, et al.Nature Genetics|December 21, 2021
Large uncertainty in individual polygenic risk score estimation impacts PRS-based risk stratificationYi Ding, Kangcheng Hou, Kathryn S Burch, et al.Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.Nature Genetics|January 21, 2022
Multi-ancestry eQTL meta-analysis of human brain identifies candidate causal variants for brain-related traitsBiao Zeng, Jaroslav Bendl, Roman Kosoy, et al.Nature Genetics|March 9, 2021
Genome-wide CRISPR screening identifies TMEM106B as a proviral host factor for SARS-CoV-2Jim Baggen, Leentje Persoons, Els Vanstreels, et al.Nature Genetics|March 9, 2021
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWASWouter J Peyrot, Alkes L PriceNature Genetics|December 3, 2021
Large-scale integration of the plasma proteome with genetics and diseaseEgil Ferkingstad, Patrick Sulem, Bjarni A Atlason, et al.Nature Genetics|November 5, 2021
A generalized linear mixed model association tool for biobank-scale dataLongda Jiang, Zhili Zheng, Hailing Fang, et al.Nature Genetics|October 20, 2022
Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.Nature Genetics|September 19, 2022
The evolutionary dynamics of extrachromosomal DNA in human cancersJoshua T Lange, John C Rose, Celine Y Chen, et al.Pageof 742