Went M, Sud A, Mills C, et al. Phenome-wide Mendelian randomisation analysis of 378,142 cases reveals risk factors for eight common cancers. Nature communications. 2024;15(1):2637. doi:10.1038/s41467-024-46927-zGoogle ScholarDOIPubMed
Publications
Oh J, Lee M, Park J, et al. Prenatal and postnatal exposure to antibiotics and risk of food allergy in the offspring: A nationwide birth cohort study in South Korea. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology. 2024;35(3):e14114. doi:10.1111/pai.14114Google ScholarDOIPubMed
Weiss J, Raghu VK, Paruchuri K, et al. Deep Learning to Estimate Cardiovascular Risk From Chest Radiographs : A Risk Prediction Study. Annals of internal medicine. 2024. doi:10.7326/M23-1898Google ScholarDOIPubMed
Condic M, Rohr A, Riemann S, et al. Immune Profiling of Vulvar Squamous Cell Cancer Discovers a Macrophage-rich Subtype Associated with Poor Prognosis. Cancer research communications. 2024;4(3):861-875. doi:10.1158/2767-9764.CRC-22-0366Google ScholarDOIPubMed
Spasic M, Ogayo ER, Parsons AM, Mittendorf EA, van Galen P, McAllister SS. Spectral Flow Cytometry Methods and Pipelines for Comprehensive Immunoprofiling of Human Peripheral Blood and Bone Marrow. Cancer research communications. 2024;4(3):895-910. doi:10.1158/2767-9764.CRC-23-0357Google ScholarDOIPubMed
Zhu B, Bai Y, Yeo YY, et al. A Spatial Multi-Modal Dissection of Host-Microbiome Interactions within the Colitis Tissue Microenvironment. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.03.04.583400Google ScholarDOIPubMed
Dondi A, Borgsmüller N, Ferreira PF, et al. De novo detection of somatic variants in long-read single-cell RNA sequencing data. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.03.06.583775Google ScholarDOIPubMed
Nazeen S, Wang X, Zielinski D, et al. Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathies. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.03.03.583145Google ScholarDOIPubMed
Nagarajan P, Winkler TW, Bentley AR, et al. A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.03.07.24303870Google ScholarDOIPubMed
Rohm D, Black JB, McCutcheon SR, et al. Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editing. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.03.03.583177Google ScholarDOIPubMed