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Genes and environment in neonatal intraventricular hemorrhage.
Ment LR, Ådén U, Bauer CR, Bada HS, Carlo WA, Kaiser JR, Lin A, Cotten CM, Murray J, Page G, Hallman M, Lifton RP, Zhang H; Gene Targets for IVH Study Group and the Neonatal Research Network. Ment LR, et al. Among authors: hallman m. Semin Perinatol. 2015 Dec;39(8):592-603. doi: 10.1053/j.semperi.2015.09.006. Epub 2015 Oct 26. Semin Perinatol. 2015. PMID: 26516117 Free PMC article. Review.
Candidate gene analysis: severe intraventricular hemorrhage in inborn preterm neonates.
Adén U, Lin A, Carlo W, Leviton A, Murray JC, Hallman M, Lifton RP, Zhang H, Ment LR; Gene Targets for Intraventricular Hemorrhage Study Group. Adén U, et al. Among authors: hallman m. J Pediatr. 2013 Nov;163(5):1503-6.e1. doi: 10.1016/j.jpeds.2013.06.025. Epub 2013 Jul 26. J Pediatr. 2013. PMID: 23896193 Free PMC article.
Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study.
Kim J, Stirling KJ, Cooper ME, Ascoli M, Momany AM, McDonald EL, Ryckman KK, Rhea L, Schaa KL, Cosentino V, Gadow E, Saleme C, Shi M, Hallman M, Plunkett J, Teramo KA, Muglia LJ, Feenstra B, Geller F, Boyd HA, Melbye M, Marazita ML, Dagle JM, Murray JC. Kim J, et al. Among authors: hallman m. BMC Med Genet. 2013 Jul 26;14:77. doi: 10.1186/1471-2350-14-77. BMC Med Genet. 2013. PMID: 23889750 Free PMC article.
Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.
Haataja R, Karjalainen MK, Luukkonen A, Teramo K, Puttonen H, Ojaniemi M, Varilo T, Chaudhari BP, Plunkett J, Murray JC, McCarroll SA, Peltonen L, Muglia LJ, Palotie A, Hallman M. Haataja R, et al. Among authors: hallman m. PLoS Genet. 2011 Feb 3;7(2):e1001293. doi: 10.1371/journal.pgen.1001293. PLoS Genet. 2011. PMID: 21304894 Free PMC article.
Safety and pharmacokinetics of multiple dose myo-inositol in preterm infants.
Phelps DL, Ward RM, Williams RL, Nolen TL, Watterberg KL, Oh W, Goedecke M, Ehrenkranz RA, Fennell T, Poindexter BB, Cotten CM, Hallman M, Frantz ID 3rd, Faix RG, Zaterka-Baxter KM, Das A, Ball MB, Lacy CB, Walsh MC, Carlo WA, Sánchez PJ, Bell EF, Shankaran S, Carlton DP, Chess PR, Higgins RD. Phelps DL, et al. Among authors: hallman m. Pediatr Res. 2016 Aug;80(2):209-17. doi: 10.1038/pr.2016.97. Epub 2016 Apr 13. Pediatr Res. 2016. PMID: 27074126 Free PMC article. Clinical Trial.
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Huusko JM, Karjalainen MK, Graham BE, Zhang G, Farrow EG, Miller NA, Jacobsson B, Eidem HR, Murray JC, Bedell B, Breheny P, Brown NW, Bødker FL, Litterman NK, Jiang PP, Russell L, Hinds DA, Hu Y; 23andMe Research Team; Rokas A, Teramo K, Christensen K, Williams SM, Rämet M, Kingsmore SF, Ryckman KK, Hallman M, Muglia LJ. Huusko JM, et al. Among authors: hallman m. PLoS Genet. 2018 Jul 12;14(7):e1007394. doi: 10.1371/journal.pgen.1007394. eCollection 2018 Jul. PLoS Genet. 2018. PMID: 30001343 Free PMC article.
545 results