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How do parents decide on genetic testing in pediatrics?: A systematic review by Doll, Elena Sophia (Author) , Lerch, Seraina Petra (Author) , Schmalenberger, Katja (Author) , Alex, Karla (Author) , Kölker, Stefan (Author) , Brennenstuhl, Heiko (Author) , Pereira, Stacey (Author) , Smith, Hadley S. (Author) , Winkler, Eva C. (Author) , Mahal, Julia (Author) , Ditzen, Beate (Author) ,

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Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet) by Eerde, Albertien van (Author) , Teixeira, Ana (Author) , Galletti, Flavia (Author) , Maternik, Michal (Author) , Capone, Valentina (Author) , Westland, Rik (Author) , Mulder, Jaap (Author) , Halbritter, Jan (Author) , Osterholt, Thomas (Author) , Neukel, Valentina (Author) , Weber, Lutz T. (Author) , Liebau, Max C. (Author) , Schaefer, Franz (Author) , Kohl, Stefan (Author) ,

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Towards genomic newborn screening, part I: Mapping the ethical issues by Settegast, Sascha (Author) , Alex, Karla (Author) , Dikow, Nicola (Author) , Mütze, Ulrike (Author) , Schnabel-Besson, Elena (Author) , Doll, Elena Sophia (Author) , Mahal, Julia (Author) , Neth, Lars (Author) , Ditzen, Beate (Author) , Kölker, Stefan (Author) , Müller-Terpitz, Ralf (Author) , Schaaf, Christian P. (Author) , Winkler, Eva C. (Author) ,

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Author correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findin... by Schmidt, Axel (Author) , Hempel, Maja (Author) , Tibelius, Alexandra (Author) , Schwaibold, Eva (Author) , Schaaf, Christian P. (Author) , Zawada, Michal (Author) , Kaufmann, Lilian (Author) , Hinderhofer, Katrin (Author) , Okun, Pamela M. (Author) , Kotzaeridou, Urania (Author) , Hoffmann, Georg F. (Author) , Choukair, Daniela (Author) , Bettendorf, Markus (Author) ,

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Pathogenic SMAD6 variants in patients with idiopathic and complex congenital heart disease associated pulmonary arterial hypertension by Karl, Sofia (Author) , Grünig, Ekkehard (Author) , Shaukat, Memoona (Author) , Held, Matthias (Author) , Apitz, Christian (Author) , von Scheidt, Fabian (Author) , Geiger, Ralf (Author) , Halank, Michael (Author) , Olsson, Karen M. (Author) , Hoeper, Marius M. (Author) , Kamp, Jan C. (Author) , Kovacs, Gabor (Author) , Olschewski, Horst (Author) , Seyfarth, Hans-Jürgen (Author) , Milger, Katrin (Author) , Ewert, Ralf (Author) , Klose, Hans (Author) , Egenlauf, Benjamin (Author) , Xanthouli, Panagiota (Author) , Hinderhofer, Katrin (Author) , Eichstaedt, Christina (Author) ,

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• Verlag, kostenfrei, Volltext

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings by Schmidt, Axel (Author) , Danyel, Magdalena (Author) , Grundmann-Hauser, Kathrin (Author) , Brunet, Theresa (Author) , Klinkhammer, Hannah (Author) , Hsieh, Tzung-Chien (Author) , Engels, Hartmut (Author) , Schlapakow, Elena (Author) , Hempel, Maja (Author) , Tibelius, Alexandra (Author) , Schwaibold, Eva (Author) , Schaaf, Christian P. (Author) , Zawada, Michal (Author) , Kaufmann, Lilian (Author) , Hinderhofer, Katrin (Author) , Okun, Pamela M. (Author) , Kotzaeridou, Urania (Author) , Hoffmann, Georg F. (Author) , Choukair, Daniela (Author) , Bettendorf, Markus (Author) ,

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• Resolving-System, kostenfrei

Genetic variants in patients with multiple arterial aneurysms by Körfer, Daniel (Author) , Grond-Ginsbach, Caspar (Author) , Peters, Andreas (Author) , Burkart, Sebastian (Author) , Hempel, Maja (Author) , Schaaf, Christian P. (Author) , Böckler, Dittmar (Author) , Erhart, Philipp (Author) ,

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Humangenetische Diagnostik bei onkologischen Erkrankungen: Bedeutung von Tumorrisikosyndromen für Therapie und Prävention by Elbracht, Miriam (Author) , Auber, Bernd (Author) , Kurth, Ingo (Author) , Stenzinger, Albrecht (Author) , Schaaf, Christian P. (Author) , Schroeder, Christopher (Author) ,

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A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children by Friedrich, Ulrike A. (Author) , Bienias, Marc (Author) , Zinke, Claudia (Author) , Prazenicova, Maria (Author) , Lohse, Judith (Author) , Jahn, Arne (Author) , Menzel, Maria (Author) , Langanke, Jonas (Author) , Walter, Carolin (Author) , Wagener, Rabea (Author) , Brozou, Triantafyllia (Author) , Varghese, Julian (Author) , Dugas, Martin (Author) , Erlacher, Miriam (Author) , Schröck, Evelin (Author) , Suttorp, Meinolf (Author) , Borkhardt, Arndt (Author) , Hauer, Julia Christina (Author) , Auer, Franziska (Author) ,

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Improving sudden cardiac death risk stratification in hypertrophic cardiomyopathy using established clinical variables and genetic information by Amr, Ali (Author) , Kölemen, Jan (Author) , Reich, Christoph (Author) , Sedaghat-Hamedani, Farbod (Author) , Kayvanpour, Elham (Author) , Haas, Jan (Author) , Frese, Karen S. (Author) , Lehmann, David Hermann (Author) , Katus, Hugo (Author) , Frey, Norbert (Author) , Meder, Benjamin (Author) ,

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Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome by Christiansen, Morten Krogh (Author) , Kjær-Sørensen, Kasper (Author) , Clavsen, Natacha C. (Author) , Dittmann, Sven (Author) , Jensen, Maja Fuhlendorff (Author) , Guldbrandsen, Halvor Østerby (Author) , Pedersen, Lisbeth Nørum (Author) , Sørensen, Rikke Hasle (Author) , Lildballe, Dorte Launholt (Author) , Müller, Klara (Author) , Müller, Patrick (Author) , Vogel, Kira (Author) , Rudic, Boris (Author) , Borggrefe, Martin (Author) , Oxvig, Claus (Author) , Aalkjær, Christian (Author) , Schulze-Bahr, Eric (Author) , Matchkov, Vladimir (Author) , Bundgaard, Henning (Author) , Jensen, Henrik Kjærulf (Author) ,

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Conseil génétique et dépistage de l’hypertension artérielle pulmonaire: consensus du Consortium international pour les études génétiques dans l’HTAP - version française... by Montani, David (Author) , Eichstaedt, Christina (Author) , Belge, C. (Author) , Chung, W. K. (Author) , Gräf, S. (Author) , Grünig, Ekkehard (Author) , Humbert, M. (Author) , Quarck, R. (Author) , Tenorio-Castano, J. A. (Author) , Soubrier, F. (Author) , Trembath, R. C. (Author) , Morrell, N. W. (Author) ,

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Gene panel diagnostics reveals new pathogenic variants in pulmonary arterial hypertension by Eichstaedt, Christina (Author) , Saßmannshausen, Zoe (Author) , Shaukat, Memoona (Author) , Cao, Ding (Author) , Xanthouli, Panagiota (Author) , Gall, Henning (Author) , Sommer, Natascha (Author) , Ghofrani, Hossein-Ardeschir (Author) , Seyfarth, Hans-Jürgen (Author) , Lerche, Marianne (Author) , Halank, Michael (Author) , Kleymann, Janina (Author) , Benjamin, Nicola (Author) , Harutyunova, Satenik (Author) , Egenlauf, Benjamin (Author) , Milger, Katrin (Author) , Rosenkranz, Stephan (Author) , Ewert, Ralf (Author) , Klose, Hans (Author) , Hoeper, Marius M. (Author) , Olsson, Karen M. (Author) , Lankeit, Mareike (Author) , Lange, Tobias J. (Author) , Hinderhofer, Katrin (Author) , Grünig, Ekkehard (Author) ,

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Final results of the southwest German pilot study on cystic fibrosis newborn screening: evaluation of an IRT/PAP protocol with IRT-dependent safety net by Sommerburg, Olaf (Author) , Stahl, Mirjam (Author) , Hämmerling, Susanne Hedwig (Author) , Gramer, Gwendolyn (Author) , Muckenthaler, Martina (Author) , Okun, Jürgen G. (Author) , Kohlmüller, Dirk (Author) , Happich, Margit (Author) , Kulozik, Andreas (Author) , Mall, Marcus A. (Author) , Hoffmann, Georg F. (Author) ,

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Genetische Grundlagen bei Varianten der Geschlechtsentwicklung by Rehnitz, Julia (Author)

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Das sogenannte Recht auf Nichtwissen: normatives Fundament und anwendungspraktische Geltungskraft

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Familial breast cancer: genetic counseling over time, including patients´ expectations and initiators considering the Angelina Jolie effect by Evers, Christina (Author) , Fischer, Christine (Author) , Dikow, Nicola (Author) , Schott, Sarah (Author) ,

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Precision medicine approach to genetic cardiomyopathy by Filonenko, Kateryna (Author) , Katus, Hugo (Author) , Meder, Benjamin (Author) ,

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Genomanalysen als Informationseingriff: ethische, juristische und ökonomische Analysen zum prädiktiven Potential der Genomsequenzierung by Tanner, Klaus (Author) , Kirchhof, Paul (Author) , Schulenburg, Johann-Matthias von der (Author) , Wolfrum, Rüdiger (Author) , Gantner, Gösta (Author) , Molnár-Gábor, Fruzsina (Author) , Frank, Martin (Author) , Plöthner, Marika Anne (Author) ,

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Genomanalysen als Informationseingriff: ethische, juristische und ökonomische Analysen zum prädiktiven Potential der Genomsequenzierung by Tanner, Klaus (Author) , Schulenburg, Johann-Matthias von der (Author) , Wolfrum, Rüdiger (Author) , Kirchhof, Paul (Author) , Gantner, Gösta (Author) , Molnár-Gábor, Fruzsina (Author) , Frank, Martin (Author) , Plöthner, Marika Anne (Author) ,

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