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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2013 | 1 |
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2018 | 1 |
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Identification of complement factor H variants that predispose to pre-eclampsia: A genetic and functional study.
BJOG. 2023 Nov;130(12):1473-1482. doi: 10.1111/1471-0528.17529. Epub 2023 May 8.
BJOG. 2023.
PMID: 37156755
Protective Low-Frequency Variants for Preeclampsia in the Fms Related Tyrosine Kinase 1 Gene in the Finnish Population.
Lokki AI, Daly E, Triebwasser M, Kurki MI, Roberson EDO, Häppölä P, Auro K, Perola M, Heinonen S, Kajantie E, Kere J, Kivinen K, Pouta A, Salmon JE, Meri S, Daly M, Atkinson JP, Laivuori H.
Lokki AI, et al.
Hypertension. 2017 Aug;70(2):365-371. doi: 10.1161/HYPERTENSIONAHA.117.09406. Epub 2017 Jun 26.
Hypertension. 2017.
PMID: 28652462
Free PMC article.
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Timing and mechanism of conceptus demise in a complement regulatory membrane protein deficient mouse.
Triebwasser MP, Wu X, Bertram P, Hourcade DE, Nelson DM, Atkinson JP.
Triebwasser MP, et al.
Am J Reprod Immunol. 2018 Oct;80(4):e12997. doi: 10.1111/aji.12997. Epub 2018 Jun 20.
Am J Reprod Immunol. 2018.
PMID: 29924462
Free PMC article.
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Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration.
Triebwasser MP, Roberson ED, Yu Y, Schramm EC, Wagner EK, Raychaudhuri S, Seddon JM, Atkinson JP.
Triebwasser MP, et al.
Invest Ophthalmol Vis Sci. 2015 Oct;56(11):6873-8. doi: 10.1167/iovs.15-17432.
Invest Ophthalmol Vis Sci. 2015.
PMID: 26501415
Free PMC article.
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Mutations in complement regulatory proteins predispose to preeclampsia: a genetic analysis of the PROMISSE cohort.
Salmon JE, Heuser C, Triebwasser M, Liszewski MK, Kavanagh D, Roumenina L, Branch DW, Goodship T, Fremeaux-Bacchi V, Atkinson JP.
Salmon JE, et al.
PLoS Med. 2011 Mar;8(3):e1001013. doi: 10.1371/journal.pmed.1001013. Epub 2011 Mar 22.
PLoS Med. 2011.
PMID: 21445332
Free PMC article.
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Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.
Seddon JM, Yu Y, Miller EC, Reynolds R, Tan PL, Gowrisankar S, Goldstein JI, Triebwasser M, Anderson HE, Zerbib J, Kavanagh D, Souied E, Katsanis N, Daly MJ, Atkinson JP, Raychaudhuri S.
Seddon JM, et al.
Nat Genet. 2013 Nov;45(11):1366-70. doi: 10.1038/ng.2741. Epub 2013 Sep 15.
Nat Genet. 2013.
PMID: 24036952
Free PMC article.
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Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD.
Wagner EK, Raychaudhuri S, Villalonga MB, Java A, Triebwasser MP, Daly MJ, Atkinson JP, Seddon JM.
Wagner EK, et al.
Sci Rep. 2016 Aug 30;6:31531. doi: 10.1038/srep31531.
Sci Rep. 2016.
PMID: 27572114
Free PMC article.
Clinical Trial.
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