Functional evaluation of GUCY1A3 mutations associated with myocardial infarction risk

por Wobst, Jana, Dang, Tan An, Kessler, Thorsten, Ameln, Simon von, Tennstedt, Stephanie, Hengstenberg, Christian, Erdmann, Jeanette, Schunkert, Heribert
Publicado 2015

H-ABC– and dystonia-causing TUBB4A mutations show distinct pathogenic effects

por Krajka, Victor, Vulinovic, Franca, Genova, Mariya, Tanzer, Kerstin, Jijumon, A. S., Bodakuntla, Satish, Tennstedt, Stephanie, Mueller-Fielitz, Helge, Meier, Britta, Janke, Carsten, Klein, Christine, Rakovic, Aleksandar
Publicado 2022

A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family

por Ramzan, Shafaq, Tennstedt, Stephanie, Tariq, Muhammad, Khan, Sheraz, Noor Ul Ayan, Hafiza, Ali, Aamir, Munz, Matthias, Thiele, Holger, Korejo, Asad Aslam, Mughal, Abdul Razzaq, Jamal, Syed Zahid, Nürnberg, Peter, Baig, Shahid Mahmood, Erdmann, Jeanette, Ahmad, Ilyas
Publicado 2021

Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus

por Munz, Matthias, Richter, Gesa M., Loos, Bruno G., Jepsen, Søren, Divaris, Kimon, Offenbacher, Steven, Teumer, Alexander, Holtfreter, Birte, Kocher, Thomas, Bruckmann, Corinna, Jockel-Schneider, Yvonne, Graetz, Christian, Munoz, Loreto, Bhandari, Anita, Tennstedt, Stephanie, Staufenbiel, Ingmar, van der Velde, Nathalie, Uitterlinden, André G., de Groot, Lisette C. P. G. M., Wellmann, Jürgen, Berger, Klaus, Krone, Bastian, Hoffmann, Per, Laudes, Matthias, Lieb, Wolfgang, Franke, Andre, Dommisch, Henrik, Erdmann, Jeanette, Schaefer, Arne S.
Publicado 2018