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Nature Genetics|March 9, 2023
Pharmacological disruption of mSWI/SNF complex activity restricts SARS-CoV-2 infectionJin Wei, Ajinkya Patil, Clayton K Collings, et al.
Nature Genetics|March 9, 2023
Immune selection determines tumor antigenicity and influences response to checkpoint inhibitorsLuis Zapata, Giulio Caravagna, Marc J Williams, et al.
Nature Genetics|February 16, 2023
Genetics of sexually dimorphic adipose distribution in humansGrace T Hansen, Débora R Sobreira, Zachary T Weber, et al.
Nature Genetics|August 26, 2025
Mutational landscape of triple-negative breast cancer in African American womenSong Yao, Lei Wei, Qiang Hu, et al.
Nature Genetics|May 20, 1998
The impact of L1 retrotransposons on the human genomeH H Kazazian, J V Moran
Nature Genetics|May 20, 1998
Duplication of ATR inhibits MyoD, induces aneuploidy and eliminates radiation-induced G1 arrestL Smith, S J Liu, L Goodrich, et al.
Nature Genetics|May 20, 1998
Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosisD J Shears, H J Vassal, F R Goodman, et al.
Nature Genetics|May 20, 1998
Mutations in the integrin alpha7 gene cause congenital myopathyY K Hayashi, F L Chou, E Engvall, et al.
Nature Genetics|February 16, 2010
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delaySanthosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, et al.
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