Vanea C, Džigurski J, Rukins V, et al. Mapping cell-to-tissue graphs across human placenta histology whole slide images using deep learning with HAPPY. Nature communications. 2024;15(1):2710. doi:10.1038/s41467-024-46986-2Google ScholarDOIPubMed
Publications
Hayes TK, Aquilanti E, Persky NS, et al. Comprehensive mutational scanning of EGFR reveals TKI sensitivities of extracellular domain mutants. Nature communications. 2024;15(1):2742. doi:10.1038/s41467-024-45594-4Google ScholarDOIPubMed
Yu Z, Coorens THH, Uddin MM, Ardlie KG, Lennon N, Natarajan P. Genetic variation across and within individuals. Nature reviews. Genetics. 2024. doi:10.1038/s41576-024-00709-xGoogle ScholarDOIPubMed
Hujoel MLA, Handsaker RE, Sherman MA, et al. Protein-altering variants at copy number-variable regions influence diverse human phenotypes. Nature genetics. 2024. doi:10.1038/s41588-024-01684-zGoogle ScholarDOIPubMed
Trinh MN, Pournamdari A, Small AM, Peloso GM, Patel AP, Natarajan P. Lipoprotein(a) Concentrations Are Independent of Polygenic Score for Coronary Artery Disease. JACC. Advances. 2024;3(2). doi:10.1016/j.jacadv.2023.100800Google ScholarDOIPubMed
Hantel A, Walsh TP, Marron JM, et al. Perspectives of Oncologists on the Ethical Implications of Using Artificial Intelligence for Cancer Care. JAMA network open. 2024;7(3):e244077. doi:10.1001/jamanetworkopen.2024.4077Google ScholarDOIPubMed
Jobanputra V, Schroeder B, Rehm HL, et al. Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action. NPJ genomic medicine. 2024;9(1):23. doi:10.1038/s41525-024-00410-2Google ScholarDOIPubMed
James LM, Strickland Z, Lopez N, Whited JL, Maden M, Lewis J. Identification and Analysis of Axolotl Homologs for Proteins Implicated in Human Neurodegenerative Proteinopathies. Genes. 2024;15(3). doi:10.3390/genes15030310Google ScholarDOIPubMed
Marchant RG, Bryen SJ, Bahlo M, et al. Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing alone. Annals of clinical and translational neurology. 2024. doi:10.1002/acn3.52041Google ScholarDOIPubMed
de Smith AJ, Wahlster L, Jeon S, et al. A noncoding regulatory variant in IKZF1 increases acute lymphoblastic leukemia risk in Hispanic/Latino children. Cell genomics. 2024:100526. doi:10.1016/j.xgen.2024.100526Google ScholarDOIPubMed