Dunlap G, Wagner A, Meednu N, et al. Clonal associations of lymphocyte subsets and functional states revealed by single cell antigen receptor profiling of T and B cells in rheumatoid arthritis synovium. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.18.533282
Publications
Bormes G, Love J, Akeju O, et al. Self-Directed Home-Based Dim-Light Melatonin Onset Collection: The Circadia Pilot Study. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.05.26.23290467
Yin L, Zander M, Huang SSC, et al. Transcription Factor Dynamics in Cross-Regulation of Plant Hormone Signaling Pathways. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.07.531630
Guo MH, Francioli LC, Stenton SL, et al. Inferring compound heterozygosity from large-scale exome sequencing data. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.19.533370
Engal E, Oja KT, Maroofian R, et al. Biallelic loss of function variants in , encoding a spliceosome protein, result in a variable neurodevelopmental delay syndrome. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.19.23291425
Suliman S, Nieto-Caballero VE, Asgari S, et al. History of tuberculosis disease is associated with genetic regulatory variation in Peruvians. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.20.23291558
Hu Y, Ma S, Kartha VK, et al. Single-cell multi-scale footprinting reveals the modular organization of DNA regulatory elements. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.28.533945
Zhang H, Kelly K, Lee J, et al. Self-delivering CRISPR RNAs for AAV Co-delivery and Genome Editing . bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.20.533459
Lee J, Gilliland T, Koyama S, et al. Integrative metabolomics differentiate coronary artery disease, peripheral artery disease, and venous thromboembolism risks. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.21.23291103
Yurkovetskiy L, Egri S, Kurhade C, et al. S:D614G and S:H655Y are gateway mutations that act epistatically to promote SARS-CoV-2 variant fitness. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.30.535005