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Pharmacogenetic profiling via genome sequencing in children with medical complexity.
Pan A, Scodellaro S, Khan T, Ushcatz I, Wu W, Curtis M, Cohen E, Cohn RD, Hayeems RZ, Meyn MS, Orkin J, Otal J, Reuter MS, Walker S, Scherer SW, Marshall CR, Cohn I, Costain G. Pan A, et al. Among authors: orkin j. Pediatr Res. 2023 Mar;93(4):905-910. doi: 10.1038/s41390-022-02313-3. Epub 2022 Sep 27. Pediatr Res. 2023. PMID: 36167815 Free PMC article.
De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome.
Costain G, Callewaert B, Gabriel H, Tan TY, Walker S, Christodoulou J, Lazar T, Menten B, Orkin J, Sadedin S, Snell M, Vanlander A, Vergult S, White SM, Scherer SW, Hayeems RZ, Blaser S, Wodak SJ, Chitayat D, Marshall CR, Meyn MS. Costain G, et al. Among authors: orkin j. Genet Med. 2019 Apr;21(4):1021-1026. doi: 10.1038/s41436-018-0323-y. Epub 2018 Oct 8. Genet Med. 2019. PMID: 30293988 Free article.
Family-provider consensus outcomes for children with medical complexity.
Fayed N, Guttmann A, Chiu A, Gardecki M, Orkin J, Hamid JS, Major N, Lim A, Cohen E. Fayed N, et al. Among authors: orkin j. Dev Med Child Neurol. 2019 Sep;61(9):1093-1100. doi: 10.1111/dmcn.14110. Epub 2018 Dec 10. Dev Med Child Neurol. 2019. PMID: 30536803 Free article.
Complex care for kids Ontario: protocol for a mixed-methods randomised controlled trial of a population-level care coordination initiative for children with medical complexity.
Orkin J, Chan CY, Fayed N, Lin JLL, Major N, Lim A, Peebles ER, Moretti ME, Soscia J, Sultan R, Willan AR, Offringa M, Guttmann A, Bartlett L, Kanani R, Culbert E, Hardy-Brown K, Gordon M, Perlmutar M, Cohen E. Orkin J, et al. BMJ Open. 2019 Aug 1;9(8):e028121. doi: 10.1136/bmjopen-2018-028121. BMJ Open. 2019. PMID: 31375613 Free PMC article.
117 results