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Identification of distinct transcriptome signatures of human adipose tissue from fifteen depots

2020 . John, Dorit | Krause, Kerstin | Wohland, Tobias | Gebhardt, Claudia | Linder, Nicolas | Stumvoll, Michael | Blüher, Matthias | Bechmann, Ingo | Kovacs, Peter | Gericke, Martin | Tönjes, Anke

Identification of disease-causing variants by comprehensive genetic testing with exome sequencing in adults with suspicion of hereditary FSGS

Willingness to donate genomic and other medical data: results from Germany

2020 . Voigt, Torsten | Holtz, Verena | Niemiec, Emilia | Howard, Heidi C. | Middleton, Anna | Prainsack, Barbara

In cis TP53 and RAD51C pathogenic variants may predispose to sebaceous gland carcinomas

2020 . Le Duc, Diana | Hentschel, Julia | Neuser, Sonja | Stiller, Mathias | Meier, Carolin | Jäger, Elisabeth | Abou Jamra, Rami | Platzer, Konrad | Monecke, Astrid | Ziemer, Mirjana | Markovic, Aleksander | Bläker, Hendrik | Lemke, Johannes

First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery

Rare heterozygous GDF6 variants in patients with renal anomalies

Perceptions of genetic testing in patients with hereditary chronic pancreatitis and their families: a qualitative triangulation

2020 . Mueller, Regina | Aghdassi, Ali | Kruse, Judith | Lerch, Markus M. | Simon, Peter | Salloch, Sabine

Secondary research use of personal medical data: attitudes from patient and population surveys in The Netherlands and Germany

2020 . Richter, Gesine | Borzikowsky, Christoph | Lesch, Wiebke | Semler, Sebastian C. | Bunnik, Eline M. | Buyx, Alena | Krawczak, Michael

Evaluation of current genetic testing reports in German-speaking countries with regard to secondary use and future electronic implementation

2020 . Radke, Teja Falk | Patton, Simon J. | Pantazoglou, Elisabeth | Sass, Julian | Thun, Sylvia

Towards a fine-scale picture of European genetic diversity

2020 . Nothnagel, Michael

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