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Equity-Centered Postdischarge Support for Medicaid-Insured People: Protocol for a Type 1 Hybrid Effectiveness-Implementation Stepped Wedge Cluster Randomized Controlled Trial.
Brooks Carthon JM, Brom H, Grantham-Murrillo M, Sliwinski K, Mason A, Roeser M, Miles D, Garcia D, Bennett J, Harhay MO, Flores E, Amenyedor K, Clark R. Brooks Carthon JM, et al. Among authors: bennett j. JMIR Res Protoc. 2024 Mar 26;13:e54211. doi: 10.2196/54211. JMIR Res Protoc. 2024. PMID: 38530349 Free PMC article.
Transitional care innovation for Medicaid-insured individuals: early findings.
Brooks Carthon JM, Brom H, French R, Daus M, Grantham-Murillo M, Bennett J, Ryskina K, Ponietowicz E, Cacchione P. Brooks Carthon JM, et al. Among authors: bennett j. BMJ Open Qual. 2022 Aug;11(3):e001798. doi: 10.1136/bmjoq-2021-001798. BMJ Open Qual. 2022. PMID: 35981741 Free PMC article.
Next-generation IEDB tools: a platform for epitope prediction and analysis.
Yan Z, Kim K, Kim H, Ha B, Gambiez A, Bennett J, de Almeida Mendes MF, Trevizani R, Mahita J, Richardson E, Marrama D, Blazeska N, Koşaloğlu-Yalçın Z, Nielsen M, Sette A, Peters B, Greenbaum JA. Yan Z, et al. Among authors: bennett j. Nucleic Acids Res. 2024 May 23:gkae407. doi: 10.1093/nar/gkae407. Online ahead of print. Nucleic Acids Res. 2024. PMID: 38783079
Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans.
Rael VE, Yano JA, Huizar JP, Slayden LC, Weiss MA, Turcotte EA, Terry JM, Zuo W, Thiffault I, Pastinen T, Farrow EG, Jenkins JL, Becker ML, Wong SC, Stevens AM, Otten C, Allenspach EJ, Bonner DE, Bernstein JA, Wheeler MT, Saxton RA; Undiagnosed Diseases Network; Liu B, Majer O, Barton GM. Rael VE, et al. J Exp Med. 2024 Aug 5;221(8):e20232005. doi: 10.1084/jem.20232005. Epub 2024 May 23. J Exp Med. 2024. PMID: 38780621
Pervasive relaxed selection in termite genomes.
Ewart KM, Ho SYW, Chowdhury AA, Jaya FR, Kinjo Y, Bennett J, Bourguignon T, Rose HA, Lo N. Ewart KM, et al. Among authors: bennett j. Proc Biol Sci. 2024 May;291(2023):20232439. doi: 10.1098/rspb.2023.2439. Epub 2024 May 22. Proc Biol Sci. 2024. PMID: 38772424
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder.
Kohler JN, Legro NR, Baldridge D, Shin J, Bowman A, Ugur B, Jackstadt MM, Shriver LP, Patti GJ, Zhang B, Feng W, McAdow AR, Goddard P, Ungar RA, Jensen T, Smith KS, Fresard L, Alvarez R, Bonner D, Reuter CM, McCormack C, Kravets E, Marwaha S, Holt JM; Undiagnosed Diseases Network; Worthey E, Ashley EA, Montgomery SB, Fisher P, Postlethwait J, De Camilli P, Solnica-Krezel L, Bernstein JA, Wheeler MT. Kohler JN, et al. Genet Med. 2024 May 16:101166. doi: 10.1016/j.gim.2024.101166. Online ahead of print. Genet Med. 2024. PMID: 38767059
5,531 results