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Your search keyword '"Frikke-Schmidt, Ruth"' showing total 9 results
Start Over Author "Frikke-Schmidt, Ruth" Journal circulation: cardiovascular genetics
9 results on '"Frikke-Schmidt, Ruth"'

1. Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies

Author

Murabito, Joanne M., primary, White, Charles C., additional, Kavousi, Maryam, additional, Sun, Yan V., additional, Feitosa, Mary F., additional, Nambi, Vijay, additional, Lamina, Claudia, additional, Schillert, Arne, additional, Coassin, Stefan, additional, Bis, Joshua C., additional, Broer, Linda, additional, Crawford, Dana C., additional, Franceschini, Nora, additional, Frikke-Schmidt, Ruth, additional, Haun, Margot, additional, Holewijn, Suzanne, additional, Huffman, Jennifer E., additional, Hwang, Shih-Jen, additional, Kiechl, Stefan, additional, Kollerits, Barbara, additional, Montasser, May E., additional, Nolte, Ilja M., additional, Rudock, Megan E., additional, Senft, Andrea, additional, Teumer, Alexander, additional, van der Harst, Pim, additional, Vitart, Veronique, additional, Waite, Lindsay L., additional, Wood, Andrew R., additional, Wassel, Christina L., additional, Absher, Devin M., additional, Allison, Matthew A., additional, Amin, Najaf, additional, Arnold, Alice, additional, Asselbergs, Folkert W., additional, Aulchenko, Yurii, additional, Bandinelli, Stefania, additional, Barbalic, Maja, additional, Boban, Mladen, additional, Brown-Gentry, Kristin, additional, Couper, David J., additional, Criqui, Michael H., additional, Dehghan, Abbas, additional, den Heijer, Martin, additional, Dieplinger, Benjamin, additional, Ding, Jingzhong, additional, Dörr, Marcus, additional, Espinola-Klein, Christine, additional, Felix, Stephan B., additional, Ferrucci, Luigi, additional, Folsom, Aaron R., additional, Fraedrich, Gustav, additional, Gibson, Quince, additional, Goodloe, Robert, additional, Gunjaca, Grgo, additional, Haltmayer, Meinhard, additional, Heiss, Gerardo, additional, Hofman, Albert, additional, Kieback, Arne, additional, Kiemeney, Lambertus A., additional, Kolcic, Ivana, additional, Kullo, Iftikhar J., additional, Kritchevsky, Stephen B., additional, Lackner, Karl J., additional, Li, Xiaohui, additional, Lieb, Wolfgang, additional, Lohman, Kurt, additional, Meisinger, Christa, additional, Melzer, David, additional, Mohler, Emile R., additional, Mudnic, Ivana, additional, Mueller, Thomas, additional, Navis, Gerjan, additional, Oberhollenzer, Friedrich, additional, Olin, Jeffrey W., additional, O'Connell, Jeff, additional, O'Donnell, Christopher J., additional, Palmas, Walter, additional, Penninx, Brenda W., additional, Petersmann, Astrid, additional, Polasek, Ozren, additional, Psaty, Bruce M., additional, Rantner, Barbara, additional, Rice, Ken, additional, Rivadeneira, Fernando, additional, Rotter, Jerome I., additional, Seldenrijk, Adrie, additional, Stadler, Marietta, additional, Summerer, Monika, additional, Tanaka, Toshiko, additional, Tybjaerg-Hansen, Anne, additional, Uitterlinden, Andre G., additional, van Gilst, Wiek H., additional, Vermeulen, Sita H., additional, Wild, Sarah H., additional, Wild, Philipp S., additional, Willeit, Johann, additional, Zeller, Tanja, additional, Zemunik, Tatijana, additional, Zgaga, Lina, additional, Assimes, Themistocles L., additional, Blankenberg, Stefan, additional, Boerwinkle, Eric, additional, Campbell, Harry, additional, Cooke, John P., additional, de Graaf, Jacqueline, additional, Herrington, David, additional, Kardia, Sharon L.R., additional, Mitchell, Braxton D., additional, Murray, Anna, additional, Münzel, Thomas, additional, Newman, Anne B., additional, Oostra, Ben A., additional, Rudan, Igor, additional, Shuldiner, Alan R., additional, Snieder, Harold, additional, van Duijn, Cornelia M., additional, Völker, Uwe, additional, Wright, Alan F., additional, Wichmann, H.-Erich, additional, Wilson, James F., additional, Witteman, Jacqueline C.M., additional, Liu, Yongmei, additional, Hayward, Caroline, additional, Borecki, Ingrid B., additional, Ziegler, Andreas, additional, North, Kari E., additional, Cupples, L. Adrienne, additional, and Kronenberg, Florian, additional

Published
2012
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5. Genome-Wide Association Analysis of High-Density Lipoprotein Cholesterol in the Population-Based KORA Study Sheds New Light on Intergenic Regions

Author

Heid, Iris M., primary, Boes, Eva, additional, Müller, Martina, additional, Kollerits, Barbara, additional, Lamina, Claudia, additional, Coassin, Stefan, additional, Gieger, Christian, additional, Döring, Angela, additional, Klopp, Norman, additional, Frikke-Schmidt, Ruth, additional, Tybj�rg-Hansen, Anne, additional, Brandstätter, Anita, additional, Luchner, Andreas, additional, Meitinger, Thomas, additional, Wichmann, H.-Erich, additional, and Kronenberg, Florian, additional

Published
2008
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6. Copy Number Variation in Glutathione S-Transferases M1 and T1 and Ischemic Vascular Disease.

Author

Nerskøv, Marianne S., Frikke-Schmidt, Ruth, Loft, Steffen, Sillesen, Henrik, Grande, Peer, Nordestgaard, Børge G., and Tybjærg-Hansen, Anne

Subjects
GLUTATHIONE transferase, ISCHEMIA, MEDICAL genetics, CARDIOVASCULAR diseases, POLYMERASE chain reaction, META-analysis, INFLAMMATION, DISEASE risk factors
Abstract

The article presents studies aimed at testing the hypothesis supposing the ability of the copy number variation (CNV) in glutathione S-transferases (GSTs) T1 (GSTT1) and GSTM1 genes to predict ischemic vascular disease (IVD) risk. The study made use of a real-time polymerase chain reaction technique and carried out meta-analyses. Results indicate the absence of the association of CNV in GSTT1 and GSTM1 genes with IVD risk nor with inflammation markers.

Published
2011
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7. Heterozygosity for R1141X in ABCC6and Risk of Ischemic Vascular Disease

Author

Hornstrup, Louise S., Tybjærg-Hansen, Anne, Haase, Christiane L., Nordestgaard, Børge G., Sillesen, Henrik, Grande, Peer, and Frikke-Schmidt, Ruth

Abstract

Pseudoxanthoma elasticum (PXE) is an autosomal recessive disease caused by loss-of-function mutations in ABCC6 and characterized by elastic calcification leading to dermal, ocular, and ischemic vascular disease. We tested the hypothesis that heterozygosity for R1141X, the most frequent PXE-causing mutation in Caucasians, associated with risk of ischemic vascular disease, as previous studies suggested 4- to 11-fold risk of ischemic heart disease (IHD) in heterozygotes.

Published
2011
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8. Copy Number Variation in Glutathione S-Transferases M1and T1and Ischemic Vascular Disease

Author

Nørskov, Marianne S., Frikke-Schmidt, Ruth, Loft, Steffen, Sillesen, Henrik, Grande, Peer, Nordestgaard, Børge G., and Tybjærg-Hansen, Anne

Abstract

Glutathione S-transferases (GSTs) M1 and T1 detoxify products of oxidative stress and may protect against atherosclerosis and ischemic vascular disease (IVD). We tested the hypothesis that copy number variation (CNV) in GSTM1and GSTT1genes, known to be associated with stepwise decreases in catalytic activity, predict risk of IVD.

Published
2011
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9. Context-Dependent Associations Between Variation in Risk of Ischemic Heart Disease and Variation in the 5′ Promoter Region of the Apolipoprotein EGene in Danish Women

Author

Stengård, Jari H., Dyson, Greg, Frikke-Schmidt, Ruth, Tybjærg-Hansen, Anne, Nordestgaard, Borge G., and Sing, Charles F.

Abstract

Variations in the noncoding single-nucleotide polymorphisms (SNPs) at positions 560 and 832 in the 5′ promoter region of the apolipoprotein Egene define genotypes that distinguish between high and low concentrations of plasma total and high-density lipoprotein cholesterol and triglycerides. We addressed whether these genotypes improve the prediction of ischemic heart disease (IHD) in subsamples of individuals defined by traditional risk factors and the genotypes defined by the 2, 3, and 4alleles in exon 4 of the apolipoprotein Egene.

Published
2010
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