A Biobank for Long-term and Sustainable Research in the Field of Congenital Heart Disease in Germany

por Pickardt, Thomas, Niggemeyer, Eva, Bauer, Ulrike M.M., Abdul-Khaliq, Hashim
Publicado 2016

Acquired Comorbidities in Adults with Congenital Heart Disease: An Analysis of the German National Register for Congenital Heart Defects

por Maurer, Susanne J., Bauer, Ulrike M. M., Baumgartner, Helmut, Uebing, Anselm, Walther, Claudia, Tutarel, Oktay
Publicado 2021

Nationwide Registry‐Based Analysis of Infective Endocarditis Risk After Pulmonary Valve Replacement

por Stammnitz, Clara, Huscher, Dörte, Bauer, Ulrike M. M., Urban, Aleksandra, Nordmeyer, Johannes, Schubert, Stephan, Photiadis, Joachim, Berger, Felix, Klaassen, Sabine
Publicado 2022

Transition in Patients with Congenital Heart Disease in Germany: Results of a Nationwide Patient Survey

por Helm, Paul C., Kaemmerer, Harald, Breithardt, Günter, Sticker, Elisabeth J., Keuchen, Roland, Neidenbach, Rhoia, Diller, Gerhard-Paul, Tutarel, Oktay, Bauer, Ulrike M. M.
Publicado 2017

Sex differences in publication volume and quality in congenital heart disease: are women disadvantaged?

por van Doren, Sophie, Brida, Margarita, Gatzoulis, Michael A, Kempny, Aleksander, Babu-Narayan, Sonya V, Bauer, Ulrike M M, Baumgartner, Helmut, Diller, Gerhard Paul
Publicado 2019

RNA expression profiles and regulatory networks in human right ventricular hypertrophy due to high pressure load

por Chouvarine, Philippe, Photiadis, Joachim, Cesnjevar, Robert, Scheewe, Jens, Bauer, Ulrike M.M., Pickardt, Thomas, Kramer, Hans-Heiner, Dittrich, Sven, Berger, Felix, Hansmann, Georg
Publicado 2021

New Insights into the Education of Children with Congenital Heart Disease with and without Trisomy 21

por Schmitt, Katharina R. L., Sievers, Laura K., Hütter, Alina, Abdul-Khaliq, Hashim, Poryo, Martin, Berger, Felix, Bauer, Ulrike M. M., Helm, Paul C., Pfitzer, Constanze
Publicado 2023

Microcephaly is associated with impaired educational development in children with congenital heart disease

por Pfitzer, Constanze, Sievers, Laura K., Hütter, Alina, Khaliq, Hashim-Abdul, Poryo, Martin, Berger, Felix, Bauer, Ulrike M. M., Helm, Paul C., Schmitt, Katharina R. L.
Publicado 2022

Utility of deep learning networks for the generation of artificial cardiac magnetic resonance images in congenital heart disease

por Diller, Gerhard-Paul, Vahle, Julius, Radke, Robert, Vidal, Maria Luisa Benesch, Fischer, Alicia Jeanette, Bauer, Ulrike M. M., Sarikouch, Samir, Berger, Felix, Beerbaum, Philipp, Baumgartner, Helmut, Orwat, Stefan
Publicado 2020

Surgery during pregnancy – results of a German questionnaire

por Fritze-Büttner, Frauke, Toth, Bettina, Bühren, Astrid, Schlosser, Katja, Schierholz, Stefanie, Rumpel, Beatrix, Helm, Paul C., Bauer, Ulrike M. M., Niethard, Maya, Prediger, Sarah, Götzky, Kristina, Jähne, Joachim
Publicado 2020

The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5

por Lessel, Davor, Muhammad, Tariq, Casar Tena, Teresa, Moepps, Barbara, Burkhalter, Martin D., Hitz, Marc-Phillip, Toka, Okan, Rentzsch, Axel, Schubert, Stephan, Schalinski, Adelheid, Bauer, Ulrike M. M., Kubisch, Christian, Ware, Stephanie M., Philipp, Melanie
Publicado 2016

Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genes

por Breuer, Katinka, Riedhammer, Korbinian M., Müller, Nicole, Schaidinger, Birthe, Dombrowsky, Gregor, Dittrich, Sven, Zeidler, Susanne, Bauer, Ulrike M. M., Westphal, Dominik S., Meitinger, Thomas, Dakal, Tikam Chand, Hitz, Marc-Phillip, Breuer, Johannes, Reutter, Heiko, Hilger, Alina C., Hoefele, Julia
Publicado 2022

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

por Sifrim, Alejandro, Hitz, Marc-Phillip, Wilsdon, Anna, Breckpot, Jeroen, Al Turki, Saeed H., Thienpont, Bernard, McRae, Jeremy, Fitzgerald, Tomas W, Singh, Tarjinder, Swaminathan, Ganesh Jawahar, Prigmore, Elena, Rajan, Diana, Abdul-Khaliq, Hashim, Banka, Siddharth, Bauer, Ulrike M. M., Bentham, Jamie, Berger, Felix, Bhattacharya, Shoumo, Bu'Lock, Frances, Canham, Natalie, Colgiu, Irina-Gabriela, Cosgrove, Catherine, Cox, Helen, Daehnert, Ingo, Daly, Allan, Danesh, John, Fryer, Alan, Gewillig, Marc, Hobson, Emma, Hoff, Kirstin, Homfray, Tessa, Kahlert, Anne-Karin, Ketley, Ami, Kramer, Hans-Heiner, Lachlan, Katherine, Lampe, Anne Katrin, Louw, Jacoba J., Manickara, Ashok Kumar, Manase, Dorin, McCarthy, Karen P., Metcalfe, Kay, Moore, Carmel, Newbury-Ecob, Ruth, Omer, Seham Osman, Ouwehand, Willem H., Park, Soo-Mi, Parker, Michael J., Pickardt, Thomas, Pollard, Martin O., Robert, Leema, Roberts, David J., Sambrook, Jennifer, Setchfield, Kerry, Stiller, Brigitte, Thornborough, Chris, Toka, Okan, Watkins, Hugh, Williams, Denise, Wright, Michael, Mital, Seema, Daubeney, Piers E. F., Keavney, Bernard, Goodship, Judith, Abu-Sulaiman, Riyadh Mahdi, Klaassen, Sabine, Wright, Caroline F., Firth, Helen V., Barrett, Jeffrey C., Devriendt, Koenraad, FitzPatrick, David R., Brook, J. David, Hurles, Matthew
Publicado 2016

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

por Škorić-Milosavljević, Doris, Tadros, Rafik, Bosada, Fernanda M., Tessadori, Federico, van Weerd, Jan Hendrik, Woudstra, Odilia I., Tjong, Fleur V.Y., Lahrouchi, Najim, Bajolle, Fanny, Cordell, Heather J., Agopian, A.J., Blue, Gillian M., Barge-Schaapveld, Daniela Q.C.M., Gewillig, Marc, Preuss, Christoph, Lodder, Elisabeth M., Barnett, Phil, Ilgun, Aho, Beekman, Leander, van Duijvenboden, Karel, Bokenkamp, Regina, Müller-Nurasyid, Martina, Vliegen, Hubert W., Konings, Thelma C., van Melle, Joost P., van Dijk, Arie P.J., van Kimmenade, Roland R.J., Roos-Hesselink, Jolien W., Sieswerda, Gertjan T., Meijboom, Folkert, Abdul-Khaliq, Hashim, Berger, Felix, Dittrich, Sven, Hitz, Marc-Phillip, Moosmann, Julia, Riede, Frank-Thomas, Schubert, Stephan, Galan, Pilar, Lathrop, Mark, Munter, Hans M., Al-Chalabi, Ammar, Shaw, Christopher E., Shaw, Pamela J., Morrison, Karen E., Veldink, Jan H., van den Berg, Leonard H., Evans, Sylvia, Nobrega, Marcelo A., Aneas, Ivy, Radivojkov-Blagojević, Milena, Meitinger, Thomas, Oechslin, Erwin, Mondal, Tapas, Bergin, Lynn, Smythe, John F., Altamirano-Diaz, Luis, Lougheed, Jane, Bouma, Berto J., Chaix, Marie-A., Kline, Jennie, Bassett, Anne S., Andelfinger, Gregor, van der Palen, Roel L.F., Bouvagnet, Patrice, Clur, Sally-Ann B., Breckpot, Jeroen, Kerstjens-Frederikse, Wilhelmina S., Winlaw, David S., Bauer, Ulrike M.M., Mital, Seema, Goldmuntz, Elizabeth, Keavney, Bernard, Bonnet, Damien, Mulder, Barbara J., Tanck, Michael W.T., Bakkers, Jeroen, Christoffels, Vincent M., Boogerd, Cornelis J., Postma, Alex V., Bezzina, Connie R.
Publicado 2021