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
Publications
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
Strom NI, Halvorsen MW, Tian C, et al. Genome-wide association study identifies new loci associated with OCD. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.03.06.24303776Google 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
Dice ALE, Lawn RB, Ratanatharathorn A, et al. Childhood maltreatment and health in the UK Biobank: triangulation of outcome-wide and polygenic risk score analyses. BMC medicine. 2024;22(1):135. doi:10.1186/s12916-024-03360-9Google ScholarDOIPubMed
Boßelmann CM, Ivaniuk A, St John M, et al. Healthcare utilization and clinical characteristics of genetic epilepsy in electronic health records. Brain communications. 2024;6(2):fcae090. doi:10.1093/braincomms/fcae090Google ScholarDOIPubMed