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Spontaneous premature birth as a target of genomic research.
Hallman M, Haapalainen A, Huusko JM, Karjalainen MK, Zhang G, Muglia LJ, Rämet M. Hallman M, et al. Among authors: karjalainen mk. Pediatr Res. 2019 Mar;85(4):422-431. doi: 10.1038/s41390-018-0180-z. Epub 2018 Sep 18. Pediatr Res. 2019. PMID: 30353040 Review.
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: karjalainen mk. PLoS Genet. 2011 Feb 3;7(2):e1001293. doi: 10.1371/journal.pgen.1001293. PLoS Genet. 2011. PMID: 21304894 Free PMC article.
The genomics of preterm birth: from animal models to human studies.
Bezold KY, Karjalainen MK, Hallman M, Teramo K, Muglia LJ. Bezold KY, et al. Among authors: karjalainen mk. Genome Med. 2013 Apr 29;5(4):34. doi: 10.1186/gm438. eCollection 2013. Genome Med. 2013. PMID: 23673148 Free PMC article. Review.
A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia.
Huusko JM, Karjalainen MK, Mahlman M, Haataja R, Kari MA, Andersson S, Toldi G, Tammela O, Rämet M, Lavoie PM, Hallman M; Gen-BPD Study Group. Huusko JM, et al. Among authors: karjalainen mk. BMC Med Genet. 2014 Nov 1;15:120. doi: 10.1186/s12881-014-0120-7. BMC Med Genet. 2014. PMID: 25409741 Free PMC article.
49 results