Anderson JA, Lin D, Lea AJ, et al. DNA methylation signatures of early life adversity are exposure-dependent in wild baboons. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.06.05.542485
Publications
Weisburd B, Tiao G, Rehm HL. Insights from a genome-wide truth set of tandem repeat variation. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.05.05.539588
Cartagena AJ, Taylor KL, Smith JT, et al. The carbapenem inoculum effect provides insight into the molecular mechanisms underlying carbapenem resistance in . bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.05.23.541813
Reiner AP, Roberts MB, Honigberg MC, et al. Association of Clonal Hematopoiesis of Indeterminate Potential with Incident Heart Failure with Preserved Ejection Fraction. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.07.23291038
Zekavat SM, Jorshery SD, Shweikh Y, et al. Insights into human health from phenome- and genome-wide analyses of UK Biobank retinal optical coherence tomography phenotypes. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.05.16.23290063
Yan Z, Tang AA, Eshed A, et al. Rapid and Multiplexed Nucleic Acid Detection using Programmable Aptamer-Based RNA Switches. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.02.23290873
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
Chen S, Neale BM, Berkovic SF, . Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.02.22.23286310
Miller-Fleming TW, Allos A, Gantz E, et al. Developing a Phenotype Risk Score for Tic Disorders in a Large, Clinical Biobank. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.02.21.23286253
Vessels T, Strayer N, Choi KW, et al. Identifying modifiable comorbidities of schizophrenia by integrating electronic health records and polygenic risk. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.01.23290057