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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2010 4
2011 7
2012 13
2013 7
2014 4
2015 6
2016 1
2017 3
2018 2
2019 2
2020 2
2021 2
2022 1
2023 1
2024 0

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44 results

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Page 1
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. 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.
Genetic predictors of severe intraventricular hemorrhage in extremely low-birthweight infants.
Thornburg CD, Erickson SW, Page GP, Clark EAS, DeAngelis MM, Hartnett ME, Goldstein RF, Dagle JM, Murray JC, Poindexter BB, Das A, Cotten CM; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Thornburg CD, et al. J Perinatol. 2021 Feb;41(2):286-294. doi: 10.1038/s41372-020-00821-w. Epub 2020 Sep 25. J Perinatol. 2021. PMID: 32978526 Free PMC article.
Maternal contributions to preterm delivery.
Boyd HA, Poulsen G, Wohlfahrt J, Murray JC, Feenstra B, Melbye M. Boyd HA, et al. Am J Epidemiol. 2009 Dec 1;170(11):1358-64. doi: 10.1093/aje/kwp324. Epub 2009 Oct 23. Am J Epidemiol. 2009. PMID: 19854807 Free PMC article.
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.
Zhang G, Feenstra B, Bacelis J, Liu X, Muglia LM, Juodakis J, Miller DE, Litterman N, Jiang PP, Russell L, Hinds DA, Hu Y, Weirauch MT, Chen X, Chavan AR, Wagner GP, Pavličev M, Nnamani MC, Maziarz J, Karjalainen MK, Rämet M, Sengpiel V, Geller F, Boyd HA, Palotie A, Momany A, Bedell B, Ryckman KK, Huusko JM, Forney CR, Kottyan LC, Hallman M, Teramo K, Nohr EA, Davey Smith G, Melbye M, Jacobsson B, Muglia LJ. Zhang G, et al. N Engl J Med. 2017 Sep 21;377(12):1156-1167. doi: 10.1056/NEJMoa1612665. Epub 2017 Sep 6. N Engl J Med. 2017. PMID: 28877031 Free PMC article.
Integrated genomic analyses in bronchopulmonary dysplasia.
Ambalavanan N, Cotten CM, Page GP, Carlo WA, Murray JC, Bhattacharya S, Mariani TJ, Cuna AC, Faye-Petersen OM, Kelly D, Higgins RD; Genomics and Cytokine Subcommittees of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Ambalavanan N, et al. J Pediatr. 2015 Mar;166(3):531-7.e13. doi: 10.1016/j.jpeds.2014.09.052. Epub 2014 Nov 6. J Pediatr. 2015. PMID: 25449221 Free PMC article.
Genome-wide association study of sepsis in extremely premature infants.
Srinivasan L, Page G, Kirpalani H, Murray JC, Das A, Higgins RD, Carlo WA, Bell EF, Goldberg RN, Schibler K, Sood BG, Stevenson DK, Stoll BJ, Van Meurs KP, Johnson KJ, Levy J, McDonald SA, Zaterka-Baxter KM, Kennedy KA, Sánchez PJ, Duara S, Walsh MC, Shankaran S, Wynn JL, Cotten CM; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Srinivasan L, et al. Arch Dis Child Fetal Neonatal Ed. 2017 Sep;102(5):F439-F445. doi: 10.1136/archdischild-2016-311545. Epub 2017 Mar 10. Arch Dis Child Fetal Neonatal Ed. 2017. PMID: 28283553 Free PMC article.
Genome-wide association study identifies four loci associated with eruption of permanent teeth.
Geller F, Feenstra B, Zhang H, Shaffer JR, Hansen T, Esserlind AL, Boyd HA, Nohr EA, Timpson NJ, Fatemifar G, Paternoster L, Evans DM, Weyant RJ, Levy SM, Lathrop M, Smith GD, Murray JC, Olesen J, Werge T, Marazita ML, Sørensen TI, Melbye M. Geller F, et al. PLoS Genet. 2011 Sep;7(9):e1002275. doi: 10.1371/journal.pgen.1002275. Epub 2011 Sep 8. PLoS Genet. 2011. PMID: 21931568 Free PMC article.
44 results