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Nature Genetics|September 22, 2022
SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association testsWei Zhou, Wenjian Bi, Zhangchen Zhao, et al.Nature Genetics|September 29, 2022
Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human geneticsKarthik A Jagadeesh, Kushal K Dey, Daniel T Montoro, et al.Nature Genetics|October 4, 2022
Long-range phasing of dynamic, tissue-specific and allele-specific regulatory elementsSofia Battaglia, Kevin Dong, Jingyi Wu, et al.Nature Genetics|October 4, 2022
Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apneaJanina Sörmann, Marcus Schewe, Peter Proks, et al.Nature Genetics|September 7, 2022
Genetic determinants of chromatin reveal prostate cancer risk mediated by context-dependent gene regulationSylvan C Baca, Cassandra Singler, Soumya Zacharia, et al.Nature Genetics|September 7, 2022
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease preventionZhe Wang, Andrew Emmerich, Nicolas J Pillon, et al.Nature Genetics|October 20, 2022
Genome sequencing reveals evidence of adaptive variation in the genus ZeaLu Chen, Jingyun Luo, Minliang Jin, et al.Nature Genetics|April 1, 1994
The mottled gene is the mouse homologue of the Menkes disease geneB Levinson, C Vulpe, B Elder, et al.Nature Genetics|April 1, 1994
Long-range mapping of gaps and telomeres with RecA-assisted restriction endonuclease (RARE) cleavageL J Ferrin, R D Camerini-OteroNature Genetics|April 1, 1994
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12D Bonnet, A Pelet, L Legeai-Mallet, et al.Pageof 744