Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Susann Scherag"'
Autor:
Anke Hinney, Susann Scherag, Claudette Boni, Johannes Hebebrand, Lucia Romo, Audrey Versini, Julien-Daniel Guelfi, Philip Gorwood, Yann Le Strat, Stefan Ehrlich, Nicolas Ramoz
Publikováno v:
Neuropsychopharmacology. 35:1818-1825
Anorexia nervosa (AN) is a highly heritable young-onset psychiatric illness the etiology of which remains unknown. Estrogen alpha and beta receptors, encoded by ESR1 and ESR2 genes, are involved in food intake regulation and eating behavior, and may
Publikováno v:
European Child & Adolescent Psychiatry
European Child & Adolescent Psychiatry, 19, 3, pp. 237-57
European Child and Adolescent Psychiatry
European Child and Adolescent Psychiatry, Springer Verlag (Germany), 2010, 19 (3), pp.237-257. ⟨10.1007/s00787-010-0090-z⟩
European Child & Adolescent Psychiatry, 19, 237-57
European Child & Adolescent Psychiatry, 19, 3, pp. 237-57
European Child and Adolescent Psychiatry
European Child and Adolescent Psychiatry, Springer Verlag (Germany), 2010, 19 (3), pp.237-257. ⟨10.1007/s00787-010-0090-z⟩
European Child & Adolescent Psychiatry, 19, 237-57
Contains fulltext : 89108.pdf (Publisher’s version ) (Closed access) As heritability is high in attention-deficit/hyperactivity disorder (ADHD), genetic factors must play a significant role in the development and course of this disorder. In recent
Autor:
T. T. Nguyen, André Scherag, Klaus-Peter Lesch, Joachim Heinrich, Ivonne Jarick, Markus M. Nöthen, Benno G. Schimmelmann, Johannes Hebebrand, Gerd Lehmkuhl, Karl-Heinz Jöckel, Christine M. Freitag, Sebastian Beck, Carolin Pütter, Franziska Degenhardt, Sonali Pechlivanis, Andreas Reif, Susanne Gilsbach, H-Erich Wichmann, Anna-Lena Volckmar, Beate Herpertz-Dahlmann, Stefan Schreiber, Per Hoffmann, Andreas Warnke, Marcel Romanos, Tobias J. Renner, Carla M. T. Tiesler, Sven Cichon, Judith Sinzig, Stephen V. Faraone, Anke Hinney, Susann Scherag, Susanne Walitza, Jobst Meyer, Özgür Albayrak, Maria R. Dauvermann
Publikováno v:
Molecular Psychiatry, 19(1), 115-121. Nature Publishing Group
Molecular Psychiatry
Jarick, I; Volckmar, A-L; Pütter, C; Pechlivanis, S; Nguyen, T T; Dauvermann, M R; Beck, S; Albayrak, O; Scherag, S; Gilsbach, S; Cichon, S; Hoffmann, P; Degenhardt, F; Nöthen, M M; Schreiber, S; Wichmann, H-E; Jöckel, K-H; Heinrich, J; Tiesler, C M T; Faraone, S V; ... (2014). Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular psychiatry, 19(1), pp. 115-121. Basingstoke: Nature Publishing Group 10.1038/mp.2012.161
Molecular psychiatry 19(1), 115-121 (2012). doi:10.1038/mp.2012.161
Mol. Psychiatry 19, 115–121 (2014)
Molecular Psychiatry
Jarick, I; Volckmar, A-L; Pütter, C; Pechlivanis, S; Nguyen, T T; Dauvermann, M R; Beck, S; Albayrak, O; Scherag, S; Gilsbach, S; Cichon, S; Hoffmann, P; Degenhardt, F; Nöthen, M M; Schreiber, S; Wichmann, H-E; Jöckel, K-H; Heinrich, J; Tiesler, C M T; Faraone, S V; ... (2014). Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular psychiatry, 19(1), pp. 115-121. Basingstoke: Nature Publishing Group 10.1038/mp.2012.161
Molecular psychiatry 19(1), 115-121 (2012). doi:10.1038/mp.2012.161
Mol. Psychiatry 19, 115–121 (2014)
Attention-deficit/hyperactivity disorder (ADHD) is a common, highly heritable neurodevelopmental disorder. Genetic loci have not yet been identified by genome-wide association studies. Rare copy number variations (CNVs), such as chromosomal deletions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4c7700e4c5d4a3b6b2d4ffacd22714a
https://cris.maastrichtuniversity.nl/en/publications/d8e7b4df-ec04-41e4-bd62-b0381415a8aa
https://cris.maastrichtuniversity.nl/en/publications/d8e7b4df-ec04-41e4-bd62-b0381415a8aa
Autor:
Nadja Knoll, Jerzy Adamski, Özgür Albayrak, Susann Scherag, Christian Fleischhaker, Katharina Bühren, Karsten Suhre, Reinhild Schwarte, Beate Herpertz-Dahlmann, Rui Wang-Sattler, Karin Egberts, Anke Hinney, Johannes Hebebrand, Paula Singmann, Thomas Illig, Nina Timmesfeld, Manuel Föcker
Publikováno v:
Journal of psychiatric research. 46(12)
Starvation represents an extreme physiological state and entails numerous endocrine and metabolic adaptations. The large-scale application of metabolomics to patients with acute anorexia nervosa (AN) should lead to the identification of state markers
We present the case report of a 2 year old boy with early onset extreme obesity (body mass index (BMI) 34.2 kg/m²; body mass index standard deviation score (BMI-SDS) 5.4) who is heterozygous for a non-conservative functionally relevant melanocortin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7eb5b03796ab6cfe0c298ae51450eae5
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=79955935514
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=79955935514
Autor:
Wolfgang Herzog, Johannes Hebebrand, Katharina Bühren, Astrid Dempfle, Christian Fleischhaker, Susann Scherag, Beate Herpertz-Dahlmann, Nina Timmesfeld, Karin Egberts, M. Langkamp, M. de Zwaan, E. M. Sheridan, Manuel Föcker, Stephan Zipfel
Due to their sub-normally low fat mass, leptin levels in patients with acute anorexia nervosa (AN) are well below reference levels for age and sex-matched controls. This hypoleptinemia entails endocrinological and behavioral characteristics observed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b9529425e9d4ffba7cbaf50cfbbd2d6
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=79956201183
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=79956201183
Autor:
Anke Hinney, Barbara Heude, Christian Rimmbach, Ivonne Jarick, Peter Kovacs, Heike Biebermann, Susann Scherag, Vincent Vatin, Marjo-Riitta Järvelin, André Scherag, Inga Prokopenko, Claire Levy-Marchal, Dietrich Berdel, Karl-Heinz Jöckel, Joachim Heinrich, Tanja Boes, Raimund Erbel, Peter Rzehak, Eva Fisher, Wieland Kiess, Tobias Fromme, Jérôme Delplanque, Anna-Liisa Hartikainen, Beverley Balkau, Carla I. G. Vogel, Martin Klingenspor, Christian Dina, Jacques Weill, Markus M. Nöthen, Winfried Rief, Annette Schürmann, Timo D. Müller, Harald Grallert, Philippe Froguel, Nigel W. Rayner, Susanne Moebus, Thomas Illig, Thomas W. Mühleisen, Helmut Schäfer, Johannes Hebebrand, David Meyre, Mark I. McCarthy, Dieter Rosskopf, Michael Borte, Heiner Boeing, Thomas Reinehr, Nadja Schulz, Antje Körner, H.-Erich Wichmann, Heiko Krude
Publikováno v:
PLoS Genetics, Vol 6, Iss 4, p e1000916 (2010)
PLoS Genet. 6:e1000916 (2010)
PLoS Genet. 6:e1000916 (2010)
Meta-analyses of population-based genome-wide association studies (GWAS) in adults have recently led to the detection of new genetic loci for obesity. Here we aimed to discover additional obesity loci in extremely obese children and adolescents. We a
Publikováno v:
European Child and Adolescent Psychiatry
European Child and Adolescent Psychiatry, Springer Verlag (Germany), 2009, 19 (3), pp.211-226. ⟨10.1007/s00787-009-0085-9⟩
European Child & Adolescent Psychiatry
European Child and Adolescent Psychiatry, Springer Verlag (Germany), 2009, 19 (3), pp.211-226. ⟨10.1007/s00787-009-0085-9⟩
European Child & Adolescent Psychiatry
International audience; Anorexia nervosa (AN) and bulimia nervosa (BN) are complex disorders characterized by disordered eating behavior where the patient's attitude towards weight and shape, as well as their perception of body shape, are disturbed.