Atkinson EG, Artomov M, Loboda AA, et al. Discordant calls across genotype discovery approaches elucidate variants with systematic errors. Genome research. 2023. doi:10.1101/gr.277908.123
Publications
Anchan RM, Spies JB, Zhang S, et al. Long-term health-related quality of life and symptom severity following hysterectomy, myomectomy, or uterine artery embolization for the treatment of symptomatic uterine fibroids. American journal of obstetrics and gynecology. 2023. doi:10.1016/j.ajog.2023.05.020
Kartoun U, Fahed AC, Kany S, et al. Exploring the link between Gilbert’s syndrome and atherosclerotic cardiovascular disease: insights from a subpopulation-based analysis of over one million individuals. European heart journal open. 2023;3(3):oead059. doi:10.1093/ehjopen/oead059
Diray-Arce J, Fourati S, Jayavelu ND, et al. Multi-omic longitudinal study reveals immune correlates of clinical course among hospitalized COVID-19 patients. Cell reports. Medicine. 2023:101079. doi:10.1016/j.xcrm.2023.101079
Mattsson J, Ljungars A, Carlsson A, et al. Sequence enrichment profiles enable target-agnostic antibody generation for a broad range of antigens. Cell reports methods. 2023;3(5):100475. doi:10.1016/j.crmeth.2023.100475
Haas BJ, Dobin A, Ghandi M, et al. Targeted characterization of fusion transcripts in tumor and normal tissues via FusionInspector. Cell reports methods. 2023;3(5):100467. doi:10.1016/j.crmeth.2023.100467
Hassan S, Wang T, Shi K, et al. Self-oxygenation of engineered living tissues orchestrates osteogenic commitment of mesenchymal stem cells. Biomaterials. 2023;300:122179. doi:10.1016/j.biomaterials.2023.122179
Fiziev P, McRae J, Ulirsch JC, et al. Rare penetrant mutations confer severe risk of common diseases. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.05.01.23289356
Fiziev P, McRae J, Ulirsch JC, et al. Rare penetrant mutations confer severe risk of common diseases. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.05.01.23289356
Fiziev P, McRae J, Ulirsch JC, et al. Rare penetrant mutations confer severe risk of common diseases. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.05.01.23289356