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Publications

Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum.

Lee DSM, Cardone KM, Zhang DY, et al. Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.07.16.23292724

Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum.

Lee DSM, Cardone KM, Zhang DY, et al. Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.07.16.23292724

Author Correction: Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations.

Feofanova E V, Brown MR, Alkis T, et al. Author Correction: Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations. Nature communications. 2023;14(1):6611. doi:10.1038/s41467-023-42472-3

Author Correction: A biallelic multiple nucleotide length polymorphism explains functional causality at 5p15.33 prostate cancer risk locus.

Spisák S, Tisza V, Nuzzo PV, et al. Author Correction: A biallelic multiple nucleotide length polymorphism explains functional causality at 5p15.33 prostate cancer risk locus. Nature communications. 2023;14(1):6623. doi:10.1038/s41467-023-42515-9

Clinical utility of polygenic scores for cardiometabolic disease in Arabs.

Shim I, Kuwahara H, Chen N, et al. Clinical utility of polygenic scores for cardiometabolic disease in Arabs. Nature communications. 2023;14(1):6535. doi:10.1038/s41467-023-41985-1

Clinical trial links oncolytic immunoactivation to survival in glioblastoma.

Ling AL, Solomon IH, Landivar AM, et al. Clinical trial links oncolytic immunoactivation to survival in glioblastoma. Nature. 2023. doi:10.1038/s41586-023-06623-2

Author Correction: Efficient C•G-to-G•C base editors developed using CRISPRi screens, target-library analysis, and machine learning.

Koblan LW, Arbab M, Shen MW, et al. Author Correction: Efficient C•G-to-G•C base editors developed using CRISPRi screens, target-library analysis, and machine learning. Nature biotechnology. 2023. doi:10.1038/s41587-023-02028-8

Familial Clonal Hematopoiesis in a Long Telomere Syndrome.

Nakao T, Natarajan P. Familial Clonal Hematopoiesis in a Long Telomere Syndrome. The New England journal of medicine. 2023;389(16):1535. doi:10.1056/NEJMc2309139#sa1

Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression.

Guintivano J, Byrne EM, Kiewa J, et al. Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression. The American journal of psychiatry. 2023:appiajp20230053. doi:10.1176/appi.ajp.20230053

Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression.

Guintivano J, Byrne EM, Kiewa J, et al. Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression. The American journal of psychiatry. 2023:appiajp20230053. doi:10.1176/appi.ajp.20230053