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Copy-number analysis from genome sequencing data of 11,754 rare-disease parent-child trios: A model for identifying autosomal recessive human gene knockouts including a novel gene for autosomal recessive retinopathy.
Olinger E, Wilson IJ, Orr S, Barroso-Gil M, Neatu R; Genomics England Research Consortium; Atan D, Sayer JA. Olinger E, et al. Among authors: orr s. Genet Med Open. 2024 Feb 29;2:101834. doi: 10.1016/j.gimo.2024.101834. eCollection 2024. Genet Med Open. 2024. PMID: 39669628 Free PMC article.
Altered post-fracture systemic bone loss in a mouse model of osteocyte dysfunction.
Osipov B, Emami AJ, Cunningham HC, Orr S, Lin YY, Jbeily EH, Punati RS, Murugesh DK, Zukowski HM, Loots GG, Carney R, Vargas D, Ferguson VL, Christiansen BA. Osipov B, et al. Among authors: orr s. JBMR Plus. 2024 Nov 1;8(12):ziae135. doi: 10.1093/jbmrpl/ziae135. eCollection 2024 Dec. JBMR Plus. 2024. PMID: 39605879 Free PMC article.
Comparison of autonomic reactivity to trauma and nightmare imagery: A Pilot Study.
McGrory CM, Kram Mendelsohn A, Pineles SL, Lasko NB, Ivkovic V, Moon M, Cetinkaya D, Bazer O, Fortier E, Kelly A, Bragdon LB, Arditte Hall KA, Tanev K, Orr SP, Pace-Schott EF. McGrory CM, et al. Among authors: orr sp. Sleep Adv. 2024 Aug 13;5(1):zpae060. doi: 10.1093/sleepadvances/zpae060. eCollection 2024. Sleep Adv. 2024. PMID: 39246523 Free PMC article.
651 results