Entries of Wieland, Thomas on the publication server
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Number of items: 7.
2017
Kuechler, Alma, Czeschik, Johanna Christina, Graf, Elisabeth, Grasshoff, Ute, Hüffmeier, Ulrike, Busa, Tiffany, Beck-Woedl, Stefanie, Faivre, Laurence, Rivière, Jean-Baptiste, Bader, Ingrid, Koch, Johannes, Reis, André 
, Hehr, Ute, Rittinger, Olaf, Sperl, Wolfgang, Haack, Tobias B., Wieland, Thomas, Engels, Hartmut, Prokisch, Holger , Strom, Tim M., Lüdecke, Hermann-Josef and Wieczorek, Dagmar
(2017)
Bainbridge–Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition.
European Journal of Human Genetics 25 (2), pp. 183-191.
Fulltext not available.
, Hehr, Ute, Rittinger, Olaf, Sperl, Wolfgang, Haack, Tobias B., Wieland, Thomas, Engels, Hartmut, Prokisch, Holger , Strom, Tim M., Lüdecke, Hermann-Josef and Wieczorek, Dagmar
(2017)
Bainbridge–Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition.
European Journal of Human Genetics 25 (2), pp. 183-191.
Fulltext not available.
Dewenter, Matthias, Neef, Stefan, Vettel, Christiane, Lämmle, Simon, Beushausen, Christina, Zelarayan, Laura C. , Katz, Sylvia, von der Lieth, Albert, Meyer-Roxlau, Stefanie, Weber, Silvio, Wieland, Thomas , Sossalla, Samuel, Backs, Johannes, Brown, Joan H., Maier, Lars S. and El-Armouche, Ali
(2017)
Calcium/Calmodulin-Dependent Protein Kinase II Activity Persists During Chronic β-Adrenoceptor Blockade in Experimental and Human Heart Failure.
Circulation: Heart Failure 10 (5).
Fulltext not available.
, Katz, Sylvia, von der Lieth, Albert, Meyer-Roxlau, Stefanie, Weber, Silvio, Wieland, Thomas , Sossalla, Samuel, Backs, Johannes, Brown, Joan H., Maier, Lars S. and El-Armouche, Ali
(2017)
Calcium/Calmodulin-Dependent Protein Kinase II Activity Persists During Chronic β-Adrenoceptor Blockade in Experimental and Human Heart Failure.
Circulation: Heart Failure 10 (5).
Fulltext not available.
2016
Brænne, Ingrid, Kleinecke, Mariana, Reiz, Benedikt , Graf, Elisabeth, Strom, Tim, Wieland, Thomas, Fischer, Marcus, Kessler, Thorsten , Hengstenberg, Christian, Meitinger, Thomas , Erdmann, Jeanette and Schunkert, Heribert
(2016)
Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction.
European Journal of Human Genetics 24 (2), pp. 191-197.
Fulltext not available.
, Graf, Elisabeth, Strom, Tim, Wieland, Thomas, Fischer, Marcus, Kessler, Thorsten , Hengstenberg, Christian, Meitinger, Thomas , Erdmann, Jeanette and Schunkert, Heribert
(2016)
Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction.
European Journal of Human Genetics 24 (2), pp. 191-197.
Fulltext not available.
2014
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 and 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), pp. 698-707.
Fulltext not available.
, 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 and 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), pp. 698-707.
Fulltext not available.
2013
Chen, Wen, Oberwinkler, Heike, Werner, Franziska, Gaßner, Birgit, Nakagawa, Hitoshi, Feil, Robert , Hofmann, Franz, Schlossmann, Jens , Dietrich, Alexander , Gudermann, Thomas, Nishida, Motohiro , Del Galdo, Sabrina, Wieland, Thomas and Kuhn, Michaela
(2013)
Atrial Natriuretic Peptide–Mediated Inhibition of Microcirculatory Endothelial Ca 2+ and Permeability Response to Histamine Involves cGMP-Dependent Protein Kinase I and TRPC6 Channels.
Arteriosclerosis, Thrombosis, and Vascular Biology 33 (9), pp. 2121-2129.
Fulltext not available.
, Hofmann, Franz, Schlossmann, Jens , Dietrich, Alexander , Gudermann, Thomas, Nishida, Motohiro , Del Galdo, Sabrina, Wieland, Thomas and Kuhn, Michaela
(2013)
Atrial Natriuretic Peptide–Mediated Inhibition of Microcirculatory Endothelial Ca 2+ and Permeability Response to Histamine Involves cGMP-Dependent Protein Kinase I and TRPC6 Channels.
Arteriosclerosis, Thrombosis, and Vascular Biology 33 (9), pp. 2121-2129.
Fulltext not available.
Beuschlein, Felix , Boulkroun, Sheerazed , Osswald, Andrea, Wieland, Thomas, Nielsen, Hang N, Lichtenauer, Urs D, Penton, David, Schack, Vivien R, Amar, Laurence , Fischer, Evelyn, Walther, Anett, Tauber, Philipp, Schwarzmayr, Thomas, Diener, Susanne, Graf, Elisabeth, Allolio, Bruno, Samson-Couterie, Benoit, Benecke, Arndt, Quinkler, Marcus, Fallo, Francesco, Plouin, Pierre-Francois, Mantero, Franco, Meitinger, Thomas , Mulatero, Paolo, Jeunemaitre, Xavier, Warth, Richard , Vilsen, Bente , Zennaro, Maria-Christina , Strom, Tim M and Reincke, Martin
(2013)
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension.
Nature Genetics 45 (4), pp. 440-444.
Fulltext not available.
, Boulkroun, Sheerazed , Osswald, Andrea, Wieland, Thomas, Nielsen, Hang N, Lichtenauer, Urs D, Penton, David, Schack, Vivien R, Amar, Laurence , Fischer, Evelyn, Walther, Anett, Tauber, Philipp, Schwarzmayr, Thomas, Diener, Susanne, Graf, Elisabeth, Allolio, Bruno, Samson-Couterie, Benoit, Benecke, Arndt, Quinkler, Marcus, Fallo, Francesco, Plouin, Pierre-Francois, Mantero, Franco, Meitinger, Thomas , Mulatero, Paolo, Jeunemaitre, Xavier, Warth, Richard , Vilsen, Bente , Zennaro, Maria-Christina , Strom, Tim M and Reincke, Martin
(2013)
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension.
Nature Genetics 45 (4), pp. 440-444.
Fulltext not available.
2005
Wieland, Thomas, Liebold, Andreas, Jagiello, Magda, Retzl, Gerald and Birnbaum, Dietrich E.
(2005)
Superiority of voriconazole over amphotericin B in the treatment of invasive aspergillosis after heart transplantation.
The Journal of Heart and Lung Transplantation 24 (1), pp. 102-104.
Fulltext not available.