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Publications

Spectral Flow Cytometry Methods and Pipelines for Comprehensive Immunoprofiling of Human Peripheral Blood and Bone Marrow.

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-23-0357

A Spatial Multi-Modal Dissection of Host-Microbiome Interactions within the Colitis Tissue Microenvironment.

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:10.1101/2024.03.04.583400

De novo detection of somatic variants in long-read single-cell RNA sequencing data.

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:10.1101/2024.03.06.583775

Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathies.

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:10.1101/2024.03.03.583145

A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations.

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:10.1101/2024.03.07.24303870

Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editing.

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:10.1101/2024.03.03.583177

Genome-wide association study identifies new loci associated with OCD.

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:10.1101/2024.03.06.24303776

Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editing.

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:10.1101/2024.03.03.583177

Childhood maltreatment and health in the UK Biobank: triangulation of outcome-wide and polygenic risk score analyses.

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/s12916-024-03360-9

Healthcare utilization and clinical characteristics of genetic epilepsy in electronic health records.

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/fcae090