Familial aortic disease and a large duplication in chromosome 16p13.1

por Erhart, Philipp, Brandt, Tobias, Straub, Beate K., Hausser, Ingrid, Hentze, Sabine, Böckler, Dittmar, Grond‐Ginsbach, Caspar
Publicado 2018

Insight lectures: top women scientists talk about their work

por Aderin-Pocock, Maggie, Montagnon, Elsa, Muckenthaler, Martina, Hentze, Sabine, Mota, Maria, Rosenthal, Nadia, Verde, Licia, Pauss, Felicitas
Publicado 2009

ESHG PPPC Comments on postmortem use of genetic data for research purposes

por Fellmann, Florence, Rial-Sebbag, Emmanuelle, Patch, Christine, Hentze, Sabine, Stefandottir, Vigdis, Mendes, Álvaro, van El, Carla G., Cornel, Martina C., Forzano, Francesca
Publicado 2019

The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice

por Forzano, Francesca, Antonova, Olga, Clarke, Angus, de Wert, Guido, Hentze, Sabine, Jamshidi, Yalda, Moreau, Yves, Perola, Markus, Prokopenko, Inga, Read, Andrew, Reymond, Alexandre, Stefansdottir, Vigdis, van El, Carla, Genuardi, Maurizio
Publicado 2021

Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice

por Forzano, Francesca, Antonova, Olga, Clarke, Angus, de Wert, Guido, Hentze, Sabine, Jamshidi, Yalda, Moreau, Yves, Perola, Markus, Prokopenko, Inga, Read, Andrew, Reymond, Alexandre, Stefansdottir, Vigdis, van El, Carla, Genuardi, Maurizio
Publicado 2022

Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’

por Forzano, Francesca, Antonova, Olga, Clarke, Angus, de Wert, Guido, Hentze, Sabine, Jamshidi, Yalda, Moreau, Yves, Perola, Markus, Prokopenko, Inga, Read, Andrew, Reymond, Alexandre, Stefansdottir, Vigdis, van El, Carla, Genuardi, Maurizio
Publicado 2022

Correction to: Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’

por Forzano, Francesca, Antonova, Olga, Clarke, Angus, de Wert, Guido, Hentze, Sabine, Jamshidi, Yalda, Moreau, Yves, Perola, Markus, Prokopenko, Inga, Read, Andrew, Reymond, Alexandre, Stefansdottir, Vigdis, van El, Carla, Genuardi, Maurizio
Publicado 2022

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

por de Wert, Guido, Dondorp, Wybo, Clarke, Angus, Dequeker, Elisabeth M. C., Cordier, Christophe, Deans, Zandra, van El, Carla G., Fellmann, Florence, Hastings, Ros, Hentze, Sabine, Howard, Heidi, Macek, Milan, Mendes, Alvaro, Patch, Chris, Rial-Sebbag, Emmanuelle, Stefansdottir, Vigdis, Cornel, Martina C., Forzano, Francesca
Publicado 2020

Is Fetal Hydrops in Turner Syndrome a Risk Factor for the Development of Maternal Mirror Syndrome?

por Bedei, Ivonne Alexandra, Graf, Alexander, Gloning, Karl-Philipp, Meyer-Wittkopf, Matthias, Willner, Daria, Krapp, Martin, Hentze, Sabine, Scharf, Alexander, Degenhardt, Jan, Heling, Kai-Sven, Kozlowski, Peter, Trautmann, Kathrin, Jahns, Kai, Geipel, Anne, Tekesin, Ismail, Elsässer, Michael, Wilhelm, Lucas, Gottschalk, Ingo, Baumüller, Jan-Erik, Birdir, Cahit, Zöllner, Felix, Wolter, Aline, Schenk, Johanna, Gehrke, Tascha, Keil, Corinna, Espinosa, Jimmy, Axt-Fliedner, Roland
Publicado 2022

Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex

por Falb, Ruth J, Müller, Amelie J, Klein, Wolfram, Grimmel, Mona, Grasshoff, Ute, Spranger, Stephanie, Stöbe, Petra, Gauck, Darja, Kuechler, Alma, Dikow, Nicola, Schwaibold, Eva M C, Schmidt, Christoph, Averdunk, Luisa, Buchert, Rebecca, Heinrich, Tilman, Prodan, Natalia, Park, Joohyun, Kehrer, Martin, Sturm, Marc, Kelemen, Olga, Hartmann, Silke, Horn, Denise, Emmerich, Dirk, Hirt, Nina, Neumann, Armin, Kristiansen, Glen, Gembruch, Ulrich, Haen, Susanne, Siebert, Reiner, Hentze, Sabine, Hoopmann, Markus, Ossowski, Stephan, Waldmüller, Stephan, Beck-Wödl, Stefanie, Gläser, Dieter, Tekesin, Ismail, Distelmaier, Felix, Riess, Olaf, Kagan, Karl-Oliver, Dufke, Andreas, Haack, Tobias B
Publicado 2023