Einträge von Mangold, Elisabeth auf dem Publikationsserver

Ishorst, Nina, Henschel, Leonie, Thieme, Frederic, Drichel, Dmitriy, Sivalingam, Sugirthan, Mehrem, Sarah L., Fechtner, Ariane C., Fazaal, Julia, Welzenbach, Julia, Heimbach, André, Maj, Carlo, Borisov, Oleg, Hausen, Jonas, Raff, Ruth, Hoischen, Alexander , Dixon, Michael, Rada‐Iglesias, Alvaro, Bartusel, Michaela, Rojas‐Martinez, Augusto, Aldhorae, Khalid, Braumann, Bert, Kruse, Teresa, Kirschneck, Christian, Spanier, Gerrit, Reutter, Heiko, Nowak, Stefanie, Gölz, Lina, Knapp, Michael, Buness, Andreas, Krawitz, Peter , Nöthen, Markus M., Nothnagel, Michael, Becker, Tim, Ludwig, Kerstin U. und Mangold, Elisabeth (2023) Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores. Molecular Genetics & Genomic Medicine 11 (3). Volltext nicht vorhanden.

Heinrichs, Sophie K. M., Hess, Timo, Becker, Jessica, Hamann, Lutz, Vashist, Yogesh K., Butterbach, Katja, Schmidt, Thomas, Alakus, Hakan, Krasniuk, Iurii, Höblinger, Aksana, Lingohr, Philipp, Ludwig, Monika, Hagel, Alexander F., Schildberg, Claus W., Veits, Lothar, Gyvyte, Ugne, Weise, Katharina, Schüller, Vitalia, Böhmer, Anne C., Schröder, Julia, Gehlen, Jan, Kreuser, Nicole, Hofer, Sebastian, Lang, Hauke, Lordick, Florian, Malfertheiner, Peter, Moehler, Markus, Pech, Oliver, Vassos, Nikolaos, Rodermann, Ernst, Izbicki, Jakob R., Kruschewski, Martin, Ott, Katja, Schumann, Ralf R., Vieth, Michael, Mangold, Elisabeth, Gasenko, Evita, Kupcinskas, Limas, Brenner, Hermann, Grimminger, Peter, Bujanda, Luis, Sopeña, Federico, Espinel, Jesús, Thomson, Concha, Pérez-Aísa, Ángeles, Campo, Rafael, Geijo, Fernando, Collette, Daniela, Bruns, Christiane, Messerle, Katharina, Gockel, Ines, Nöthen, Markus M., Lippert, Hans, Ridwelski, Karsten, Lanas, Angel, Keller, Gisela, Knapp, Michael, Leja, Marcis, Kupcinskas, Juozas, García-González, Maria A., Venerito, Marino und Schumacher, Johannes (2018) Evidence for PTGER4 ,PSCA, and MBOAT7 as risk genes for gastric cancer on the genome and transcriptome level. Cancer Medicine 7 (10), S. 5057-5065. Volltext nicht vorhanden.

Wieczorek, Dagmar, Newman, William G. , Wieland, Thomas, Berulava, Tea, Kaffe, Maria, Falkenstein, Daniela, Beetz, Christian , Graf, Elisabeth, Schwarzmayr, Thomas, Douzgou, Sofia, Clayton-Smith, Jill, Daly, Sarah B., Williams, Simon G. , Bhaskar, Sanjeev S., Urquhart, Jill E. , Anderson, Beverley, O’Sullivan, James, Boute, Odile, Gundlach, Jasmin, Czeschik, Johanna Christina, van Essen, Anthonie J., Hazan, Filiz, Park, Sarah, Hing, Anne, Kuechler, Alma, Lohmann, Dietmar R. , Ludwig, Kerstin U., Mangold, Elisabeth, Steenpaß, Laura, Zeschnigk, Michael, Lemke, Johannes R., Lourenco, Charles Marques, Hehr, Ute, Prott, Eva-Christina, Waldenberger, Melanie, Böhmer, Anne C., Horsthemke, Bernhard, O’Keefe, Raymond T., Meitinger, Thomas , Burn, John, Lüdecke, Hermann-Josef und Strom, Tim M. (2014) Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome. The American Journal of Human Genetics 95 (6), S. 698-707. Volltext nicht vorhanden.

Reutter, Heiko, Draaken, Markus , Pennimpede, Tracie, Wittler, Lars, Brockschmidt, Felix F., Ebert, Anne-Karolin, Bartels, Enrika, Rösch, Wolfgang, Boemers, Thomas M., Hirsch, Karin, Schmiedeke, Eberhard, Meesters, Christian, Becker, Tim, Stein, Raimund, Utsch, Boris, Mangold, Elisabeth, Nordenskjöld, Agneta, Barker, Gillian, Kockum, Christina Clementsson, Zwink, Nadine, Holmdahl, Gundula, Läckgren, Göran, Jenetzky, Ekkehart, Feitz, Wouter F.J., Marcelis, Carlo, Wijers, Charlotte H.W., Van Rooij, Iris A.L.M., Gearhart, John P., Herrmann, Bernhard G., Ludwig, Michael, Boyadjiev, Simeon A., Nöthen, Markus M. und Mattheisen, Manuel (2014) Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder. Human Molecular Genetics 23 (20), S. 5536-5544. Volltext nicht vorhanden.

Esparza-Gordillo, Jorge, Schaarschmidt, Heidi, Liang, Liming, Cookson, William, Bauerfeind, Anja, Lee-Kirsch, Min-Ae, Nemat, Katja, Henderson, John, Paternoster, Lavinia , Harper, John I., Mangold, Elisabeth, Nothen, Markus M. , Rüschendorf, Franz, Kerscher, Tamara, Marenholz, Ingo, Matanovic, Anja, Lau, Susanne, Keil, Thomas, Bauer, Carl-Peter, Kurek, Michael, Ciechanowicz, Andrzej , Macek, Milan, Franke, Andre , Kabesch, Michael, Hubner, Norbert, Abecasis, Gonçalo , Weidinger, Stephan , Moffatt, Miriam und Lee, Young-Ae (2013) A functional IL-6 receptor (IL6R) variant is a risk factor for persistent atopic dermatitis. Journal of Allergy and Clinical Immunology 132 (2), S. 371-377. Volltext nicht vorhanden.

Krüger, Stefan, Engel, Christoph , Bier, Andrea, Silber, Ann-Sophie, Görgens, Heike, Mangold, Elisabeth, Pagenstecher, Constanze, Holinski-Feder, Elke, von Knebel Doeberitz, Magnus, Royer-Pokora, Brigitte, Dechant, Stefan, Pox, Christian, Rahner, Nils, Müller, Annegret und Schackert, Hans K. (2007) The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1. Cancer Letters 252 (1), S. 55-64. Volltext nicht vorhanden.

Goecke, Timm, Schulmann, Karsten, Engel, Christoph , Holinski-Feder, Elke, Pagenstecher, Constanze, Schackert, Hans K., Kloor, Matthias, Kunstmann, Erdmute, Vogelsang, Holger, Keller, Gisela, Dietmaier, Wolfgang, Mangold, Elisabeth, Friedrichs, Nicolaus, Propping, Peter, Krüger, Stefan, Gebert, Johannes, Schmiegel, Wolff, Rueschoff, Josef, Loeffler, Markus und Moeslein, Gabriela (2006) Genotype-Phenotype Comparison of German MLH1 and MSH2 Mutation Carriers Clinically Affected With Lynch Syndrome: A Report by the German HNPCC Consortium. Journal of Clinical Oncology 24 (26), S. 4285-4292. Volltext nicht vorhanden.

Engel, Christoph , Forberg, Jochen, Holinski‐Feder, Elke, Pagenstecher, Constanze, Plaschke, Jens, Kloor, Matthias, Poremba, Christopher, Pox, Christian P., Rüschoff, Josef, Keller, Gisela, Dietmaier, Wolfgang, Rümmele, Petra, Friedrichs, Nicolaus, Mangold, Elisabeth, Buettner, Reinhard, Schackert, Hans K., Kienle, Peter, Stemmler, Susanne, Moeslein, Gabriela und Loeffler, Markus (2006) Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer. International Journal of Cancer 118 (1), S. 115-122. Volltext nicht vorhanden.

Krüger, Stefan, Silber, Ann-Sophie, Engel, Christoph , Görgens, Heike, Mangold, Elisabeth, Pagenstecher, Constanze, Holinski-Feder, Elke, von Knebel Doeberitz, Magnus, Moeslein, Gabriela, Dietmaier, Wolfgang, Stemmler, Susanne, Friedl, Waltraut, Rüschoff, Josef und Schackert, Hans K (2005) Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study. The Lancet Oncology 6 (8), S. 566-572. Volltext nicht vorhanden.