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STOX2 but not STOX1 is differentially expressed in decidua from pre-eclamptic women: data from the Second Nord-Trondelag Health Study.
Fenstad MH, Johnson MP, Løset M, Mundal SB, Roten LT, Eide IP, Bjørge L, Sande RK, Johansson AK, Dyer TD, Forsmo S, Blangero J, Moses EK, Austgulen R. Fenstad MH, et al. Among authors: loset m. Mol Hum Reprod. 2010 Dec;16(12):960-8. doi: 10.1093/molehr/gaq064. Epub 2010 Jul 19. Mol Hum Reprod. 2010. PMID: 20643876 Free PMC article.
A transcriptional profile of the decidua in preeclampsia.
Løset M, Mundal SB, Johnson MP, Fenstad MH, Freed KA, Lian IA, Eide IP, Bjørge L, Blangero J, Moses EK, Austgulen R. Løset M, et al. Am J Obstet Gynecol. 2011 Jan;204(1):84.e1-27. doi: 10.1016/j.ajog.2010.08.043. Am J Obstet Gynecol. 2011. PMID: 20934677 Free PMC article.
Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22.
Løset M, Johnson MP, Melton PE, Ang W, Huang RC, Mori TA, Beilin LJ, Pennell C, Roten LT, Iversen AC, Austgulen R, East CE, Blangero J, Brennecke SP, Moses EK. Løset M, et al. Pregnancy Hypertens. 2014 Apr;4(2):178-85. doi: 10.1016/j.preghy.2014.03.005. Epub 2014 Mar 22. Pregnancy Hypertens. 2014. PMID: 26104425
OS070. Shared genetic risk factors for preeclampsia and cardiovascular disease.
Løset M, Johnson MP, Pennell C, Huang RC, Mori T, Beilin L, Melton P, Roten LT, Iversen AC, Austgulen R, East C, Blangero J, Brennecke SP, Moses EK. Løset M, et al. Pregnancy Hypertens. 2012 Jul;2(3):214-5. doi: 10.1016/j.preghy.2012.04.071. Epub 2012 Jun 13. Pregnancy Hypertens. 2012. PMID: 26105283
OP004. A SNP associated with susceptibility to preeclampsia near the inhibin, beta B gene, is also associated with cardiovascular disease risk traits.
Løset M, Johnson MP, Melton PE, Ang W, Marsh J, Huang RC, Mori T, Beilin L, Pennell C, Roten LT, Iversen AC, Austgulen R, East CE, Blangero J, Brennecke SP, Moses EK. Løset M, et al. Pregnancy Hypertens. 2013 Apr;3(2):63. doi: 10.1016/j.preghy.2013.04.020. Epub 2013 Jun 6. Pregnancy Hypertens. 2013. PMID: 26105849
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.
Nielsen JB, Rom O, Surakka I, Graham SE, Zhou W, Roychowdhury T, Fritsche LG, Gagliano Taliun SA, Sidore C, Liu Y, Gabrielsen ME, Skogholt AH, Wolford B, Overton W, Zhao Y, Chen J, Zhang H, Hornsby WE, Acheampong A, Grooms A, Schaefer A, Zajac GJM, Villacorta L, Zhang J, Brumpton B, Løset M, Rai V, Lundegaard PR, Olesen MS, Taylor KD, Palmer ND, Chen YD, Choi SH, Lubitz SA, Ellinor PT, Barnes KC, Daya M, Rafaels N, Weiss ST, Lasky-Su J, Tracy RP, Vasan RS, Cupples LA, Mathias RA, Yanek LR, Becker LC, Peyser PA, Bielak LF, Smith JA, Aslibekyan S, Hidalgo BA, Arnett DK, Irvin MR, Wilson JG, Musani SK, Correa A, Rich SS, Guo X, Rotter JI, Konkle BA, Johnsen JM, Ashley-Koch AE, Telen MJ, Sheehan VA, Blangero J, Curran JE, Peralta JM, Montgomery C, Sheu WH, Chung RH, Schwander K, Nouraie SM, Gordeuk VR, Zhang Y, Kooperberg C, Reiner AP, Jackson RD, Bleecker ER, Meyers DA, Li X, Das S, Yu K, LeFaive J, Smith A, Blackwell T, Taliun D, Zollner S, Forer L, Schoenherr S, Fuchsberger C, Pandit A, Zawistowski M, Kheterpal S, Brummett CM, Natarajan P, Schlessinger D, Lee S, Kang HM, Cucca F, Holmen OL, Åsvold BO, Boehnke M, Kathiresan S, Abecasis GR, Chen YE, Willer CJ, Hveem K. Nielsen JB, et al. Among authors: loset m. Nat Commun. 2020 Dec 18;11(1):6417. doi: 10.1038/s41467-020-20086-3. Nat Commun. 2020. PMID: 33339817 Free PMC article.
22 results