Ding J, Garber JJ, Uchida A, et al. An esophagus cell atlas reveals dynamic rewiring during active eosinophilic esophagitis and remission. Nature communications. 2024;15(1):3344. doi:10.1038/s41467-024-47647-0PubMedGoogle ScholarDOI
Publications
Nievergelt CM, Maihofer AX, Atkinson EG, et al. Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. Nature genetics. 2024. doi:10.1038/s41588-024-01707-9PubMedGoogle ScholarDOI
Leisman DE, Handisides DR, Busse LW, et al. ACE inhibitors and angiotensin receptor blockers differentially alter the response to angiotensin II treatment in vasodilatory shock. Critical care (London, England). 2024;28(1):130. doi:10.1186/s13054-024-04910-6PubMedGoogle ScholarDOI
Kuznetsova KG, Vašíček J, Skiadopoulou D, et al. Bioinformatics pipeline for the systematic mining genomic and proteomic variation linked to rare diseases: The example of monogenic diabetes. PloS one. 2024;19(4):e0300350. doi:10.1371/journal.pone.0300350PubMedGoogle ScholarDOI
Toikumo S, Jennings M V, Pham BK, et al. Multi-ancestry meta-analysis of tobacco use disorder identifies 461 potential risk genes and reveals associations with multiple health outcomes. Nature human behaviour. 2024. doi:10.1038/s41562-024-01851-6PubMedGoogle ScholarDOI
Minikel EV, Painter JL, Dong CC, Nelson MR. Refining the impact of genetic evidence on clinical success. Nature. 2024. doi:10.1038/s41586-024-07316-0PubMedGoogle ScholarDOI
Minikel EV, Painter JL, Dong CC, Nelson MR. Refining the impact of genetic evidence on clinical success. Nature. 2024. doi:10.1038/s41586-024-07316-0PubMedGoogle ScholarDOI
Choi J, Lee EA. Analysis of REST binding sites with canonical and non-canonical motifs in human cell lines. BMC medical genomics. 2024;17(Suppl 1):92. doi:10.1186/s12920-024-01860-4PubMedGoogle ScholarDOI
Roh JD, Castro C, Yu A, et al. Placental senescence pathophysiology is shared between peripartum cardiomyopathy and preeclampsia in mouse and human. Science translational medicine. 2024;16(743):eadi0077. doi:10.1126/scitranslmed.adi0077DOIPubMedGoogle Scholar
Cacheiro P, Lawson S, Van den Veyver IB, et al. Lethal phenotypes in Mendelian disorders. Genetics in medicine : official journal of the American College of Medical Genetics. 2024:101141. doi:10.1016/j.gim.2024.101141PubMedGoogle ScholarDOI