ӳ��ý

Publications

Examining the role of common variants in rare neurodevelopmental conditions.

Huang QQ, Wigdor EM, Malawsky DS, et al. Examining the role of common variants in rare neurodevelopmental conditions. Nature. 2024. doi:10.1038/s41586-024-08217-y

Spatial multiomic landscape of the human placenta at molecular resolution.

Ounadjela JR, Zhang K, Kobayashi-Kirschvink KJ, et al. Spatial multiomic landscape of the human placenta at molecular resolution. Nature medicine. 2024. doi:10.1038/s41591-024-03073-9

Spatially resolved single-cell atlas unveils a distinct cellular signature of fatal lung COVID-19 in a Malawian population.

Nyirenda J, Hardy OM, Filho JDS, et al. Spatially resolved single-cell atlas unveils a distinct cellular signature of fatal lung COVID-19 in a Malawian population. Nature medicine. 2024. doi:10.1038/s41591-024-03354-3

Author Correction: Brca1 haploinsufficiency promotes early tumor onset and epigenetic alterations in a mouse model of hereditary breast cancer.

Li CMC, Cordes A, Oliphant MUJ, et al. Author Correction: Brca1 haploinsufficiency promotes early tumor onset and epigenetic alterations in a mouse model of hereditary breast cancer. Nature genetics. 2024. doi:10.1038/s41588-024-02034-9

Genetic and phenotypic architecture of human myocardial trabeculation.

McGurk KA, Qiao M, Zheng SL, et al. Genetic and phenotypic architecture of human myocardial trabeculation. Nature cardiovascular research. 2024. doi:10.1038/s44161-024-00564-3

Author Correction: Single-cell transcriptomics stratifies organoid models of metabolic dysfunction-associated steatotic liver disease.

Hess A, Gentile SD, Ben Saad A, et al. Author Correction: Single-cell transcriptomics stratifies organoid models of metabolic dysfunction-associated steatotic liver disease. The EMBO journal. 2024. doi:10.1038/s44318-024-00308-w

Pathogenic PDE12 variants impair mitochondrial RNA processing causing neonatal mitochondrial disease.

Van Haute L, Páleníková P, Tang JX, et al. Pathogenic PDE12 variants impair mitochondrial RNA processing causing neonatal mitochondrial disease. EMBO molecular medicine. 2024. doi:10.1038/s44321-024-00172-5

Long-Term Health Outcomes of Individuals With Pseudodeficiency Alleles in IDUA May Inform Newborn Screening Practices for Mucopolysaccharidosis Type I.

Grady LO, Zoltick ES, Zouk H, et al. Long-Term Health Outcomes of Individuals With Pseudodeficiency Alleles in IDUA May Inform Newborn Screening Practices for Mucopolysaccharidosis Type I. American journal of medical genetics. Part A. 2024:e63940. doi:10.1002/ajmg.a.63940

Long-Term Health Outcomes of Individuals With Pseudodeficiency Alleles in IDUA May Inform Newborn Screening Practices for Mucopolysaccharidosis Type I.

Grady LO, Zoltick ES, Zouk H, et al. Long-Term Health Outcomes of Individuals With Pseudodeficiency Alleles in IDUA May Inform Newborn Screening Practices for Mucopolysaccharidosis Type I. American journal of medical genetics. Part A. 2024:e63940. doi:10.1002/ajmg.a.63940

Comparative genomics reveals putative copper tolerance genes in a Fusarium oxysporum strain.

Ragasa LRP, Cuomo CA, Del Rosario RCH, Velarde MC. Comparative genomics reveals putative copper tolerance genes in a Fusarium oxysporum strain. G3 (Bethesda, Md.). 2024. doi:10.1093/g3journal/jkae272