Search Results - Brennecke, S.

Genetic approaches in preeclampsia by Yong, H., Murthi, P., Brennecke, S., Moses, Eric

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Inherited thrombophilias and adverse pregnancy outcomes: A case-control study in an Australian population by Said, J., Higgins, J., Moses, Eric, Walker, S., Monagle, P., Brennecke, S.

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In reply by Said, J., Higgins, J., Moses, Eric, Walker, S., Borg, A., Monagle, P., Brennecke, S.

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Inherited thrombophilia polymorphisms and pregnancy outcomes in nulliparous women by Said, J., Higgins, J., Moses, Eric, Walker, S., Borg, A., Monagle, P., Brennecke, S.

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Increased decidual mRNA expression levels of candidate maternal pre-eclampsia susceptibility genes are associated with clinical severity by Yong, H., Murthi, P., Borg, A., Kalionis, B., Moses, Eric, Brennecke, S., Keogh, R.

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Genetic association of the activin A receptor gene (ACVR2A) and pre-eclampsia by Fitzpatrick, E., Johnson, M., Dyer, T., Forrest, S., Elliott, K., Blangero, J., Brennecke, S., Moses, Eric

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Molecular markers of preterm labor in the choriodecidua by Shankar, R., Johnson, M., Williamson, N., Cullinane, F., Purcell, A., Moses, Eric, Brennecke, S.

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The PAI-1 4G/5G polymorphism is not associated with an increased risk of adverse pregnancy outcome in asymptomatic nulliparous women by Said, J., Tsui, R., Borg, A., Higgins, J., Moses, Eric, Walker, S., Monagle, P., Brennecke, S.

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Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study) by Roten, L., Johnson, M., Forsmo, S., Fitzpatrick, E., Dyer, T., Brennecke, S., Blangero, J., Moses, Eric, Austgulen, R.

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The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations by Johnson, M., Roten, L., Dyer, T., East, C., Forsmo, S., Blangero, J., Brennecke, S., Austgulen, R., Moses, Eric

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The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population by Said, J., Brennecke, S., Moses, Eric, Walker, S., Monagle, P., Campbell, J., Bryant, V., Borg, A., Higgins, J.

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Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genes by Yong, H., Melton, P., Johnson, M., Freed, K., Kalionis, B., Murthi, P., Brennecke, S., Keogh, R., Moses, Eric

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Genetic association of preeclampsia to the inflammatory response gene SEPS1 by Moses, Eric, Johnson, M., Tømmerdal, L., Forsmo, S., Curran, J., Abraham, L., Charlesworth, J., Brennecke, S., Blangero, J., Austgulen, R.

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The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia by Thomsen, L., Mccarthy, N., Melton, P., Cadby, G., Austgulen, R., Nygård, O., Johnson, M., Brennecke, S., Moses, Eric, Bjørge, L., Iversen, A.

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Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13q by Fenstad, M., Johnson, M., Roten, L., Aas, P., Forsmo, S., Klepper, K., East, C., Abraham, L., Blangero, J., Brennecke, S., Austgulen, R., Moses, Eric

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Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes by Melton, Phillip, Johnson, M., Gokhale-Agashe, D., Rea, A., Ariff, A., Cadby, G., Peralta, J., Mcnab, T., Allcock, R., Abraham, L., Blangero, J., Brennecke, S., Moses, E.

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Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22 by Løset, M., Johnson, M., Melton, P., Ang, W., Huang, R., Mori, T., Beilin, L., Pennell, C., Roten, L., Iversen, A., Austgulen, R., East, C., Blangero, J., Brennecke, S., Moses, Eric

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Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes by Kaartokallio, T., Lokki, A., Peterson, H., Kivinen, K., Hiltunen, L., Salmela, E., Lappalainen, T., Maanselkä, P., Heino, S., Knuutila, S., Sayed, A., Poston, L., Brennecke, S., Johnson, M., Morgan, L., Moses, Eric, Kere, J., Laivuori, H.

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Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene by Johnson, M., Brennecke, S., East, C., Göring, H., Kent, J., Dyer, T., Said, J., Roten, L., Iversen, A., Abraham, L., Heinonen, S., Kajantie, E., Kere, J., Kivinen, K., Pouta, A., Laivuori, H., Austgulen, R., Blangero, J., Moses, Eric

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Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease by Johnson, M., Brennecke, S., East, C., Dyer, T., Roten, L., Proffitt, J., Melton, P., Fenstad, M., Aalto-Viljakainen, T., Mäkikallio, K., Heinonen, S., Kajantie, E., Kere, J., Laivuori, H., Austgulen, R., Blangero, J., Moses, Eric, Pouta, A., Kivinen, K., Ekholm, E., Hietala, R., Sainio, S., Saisto, T., Uotila, J., Klemetti, M., Lokki, A., Georgiadis, L.

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