Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Susann Scherag"'
Autor:
André Scherag, Christian Dina, Anke Hinney, Vincent Vatin, Susann Scherag, Carla I G Vogel, Timo D Müller, Harald Grallert, H-Erich Wichmann, Beverley Balkau, Barbara Heude, Marjo-Riitta Jarvelin, Anna-Liisa Hartikainen, Claire Levy-Marchal, Jacques Weill, Jérôme Delplanque, Antje Körner, Wieland Kiess, Peter Kovacs, Nigel W Rayner, Inga Prokopenko, Mark I McCarthy, Helmut Schäfer, Ivonne Jarick, Heiner Boeing, Eva Fisher, Thomas Reinehr, Joachim Heinrich, Peter Rzehak, Dietrich Berdel, Michael Borte, Heike Biebermann, Heiko Krude, Dieter Rosskopf, Christian Rimmbach, Winfried Rief, Tobias Fromme, Martin Klingenspor, Annette Schürmann, Nadja Schulz, Markus M Nöthen, Thomas W Mühleisen, Raimund Erbel, Karl-Heinz Jöckel, Susanne Moebus, Tanja Boes, Thomas Illig, Philippe Froguel, Johannes Hebebrand, David Meyre
Publikováno v:
PLoS Genetics, Vol 6, Iss 4, p 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
Externí odkaz:
https://doaj.org/article/03ae334df6704a48ab2b24253c722f85
Autor:
André Scherag, Ivonne Jarick, Jessica Grothe, Heike Biebermann, Susann Scherag, Anna-Lena Volckmar, Carla Ivane Ganz Vogel, Brandon Greene, Johannes Hebebrand, Anke Hinney
Publikováno v:
PLoS ONE, Vol 5, Iss 11, p e13967 (2010)
BACKGROUND: Independent genome-wide association studies (GWAS) showed an obesogenic effect of two single nucleotide polymorphisms (SNP; rs12970134 and rs17782313) more than 150 kb downstream of the melanocortin 4 receptor gene (MC4R). It is unclear i
Externí odkaz:
https://doaj.org/article/2a0d7b89508b46f889ea7f17bb379b1a
Autor:
Gereon R. Fink, Timo D. Vloet, Kerstin Konrad, Susann Scherag, Susanne Neufang, Beate Herpertz-Dahlmann, Susanne Gilsbach
Publikováno v:
Developmental Cognitive Neuroscience
Highlights ▸ Dopamine is essential for executive functioning. ▸ 7-repeat allele of the DRD4-48 base pair repeat gene leads to sub-sensitive postsynaptic D4 receptor. ▸ We investigated effects of genotype on executive functions with fMRI in chil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5700a4692a694ef3edf11b47d92e3bd1
http://europepmc.org/articles/PMC7005761
http://europepmc.org/articles/PMC7005761
Autor:
Christian Fleischhaker, Ulrike Lehmkuhl, Sandro Sorbi, Timo D. Müller, Fernando Fernández-Aranda, André Scherag, Stefano Erzegovesi, Benedetta Nacmias, Beate Herpertz-Dahlmann, Wolfgang Herzog, Helmut Schäfer, Daniela Di Bella, Valdo Ricca, Johannes Hebebrand, Mònica Gratacòs, Stefan Ehrlich, Brandon Greene, Manfred M. Fichter, Marta Ribasés, Heinz Erich Wichmann, Anke Hinney, Susann Scherag, Maria Cristina Cavallini, Thomas Illig, Xavier Estivill, Harald Grallert, Laura Bellodi, Elena Cellini
Publikováno v:
Obesity Facts. 5:408-419
Objective: The common single nucleotide polymorphism (SNP) rs9939609 in the fat mass and obesity-associated gene (FTO) is associated with obesity. As genetic variants associated with weight regulation might also be implicated in the etiology of eatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ea6925d64811860a532704344bfb885
https://doi.org/10.1159/000340057
https://doi.org/10.1159/000340057
Autor:
Hai-Jun Wang, Susann Scherag, Anke Hinney, André Scherag, Tanja Boes, Carla I. G. Vogel, Johannes Hebebrand, Thomas Reinehr, Michaela Kleber, Christian L. Roth
Publikováno v:
Pediatric Diabetes. 12:435-441
Aims: The G-allele of the single nucleotide polymorphism (SNP) rs10830963 in MTNR1B (melatonin receptor 1B gene) is associated with type 2 diabetes mellitus and glucose levels in adults. The aim of this study was to analyze whether there is an allele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fbb82e6a9d276eec4f0d504c8119d53
https://doi.org/10.1111/j.1399-5448.2010.00738.x
https://doi.org/10.1111/j.1399-5448.2010.00738.x
Autor:
André Scherag, Tanja Boes, Johannes Hebebrand, Susann Scherag, Anke Hinney, Carla I. G. Vogel, Thomas Reinehr, Christian L. Roth
Publikováno v:
Obesity Facts. 4:67-75
Objective: Association with obesity and increased insulin levels have been reported for two variants (rs17782313 and rs12970134) located downstream of the melanocortin-4 receptor gene (MC4R). Methods: We investigated whether these variants have sex-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e5f1114e2032cf14129d58513be1bb3
https://doi.org/10.1159/000324557
https://doi.org/10.1159/000324557
Autor:
Johannes Hebebrand, Carla I. G. Vogel, Ivonne Jarick, Helmut Schäfer, André Scherag, Susann Scherag, Anke Hinney
Publikováno v:
Human Molecular Genetics
Heritability of obesity is substantial and recent meta-analyses of genome-wide association studies (GWASs) have been successful in detecting several robustly associated genomic regions for obesity using single-nucleotide polymorphisms (SNPs). However
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1f682e65beefb2a670ba507c9e4d7ae
http://europepmc.org/articles/PMC3024044
http://europepmc.org/articles/PMC3024044
Autor:
A. A. van Elburg, Stephan Herpertz, Jacqueline M. Vink, Susann Scherag, Christel M. Middeldorp, Anke Hinney, Stephan Zipfel, C.E.M. van Beijsterveldt, Nicole Sanders, Beate Herpertz-Dahlmann, Ingrid Meulenbelt, Jeanine J. Houwing-Duistermaat, J. van Trier, K. Klampfl, Marek K. Brandys, E. F. van Furth, Stefan Ehrlich, Almut Zeeck, M. C. T. Slof-Op 't Landt, M. de Zwaan, Johannes Hebebrand, Dorret I. Boomsma, Meike Bartels, Christian Fleischhaker, Roger A.H. Adan, Wolfgang Herzog, E. J. Onkenhout, E. Suchiman, P.E. Slagboom
Publikováno v:
Genes, Brain and Behavior
Slof-Op 't Landt, M C T, Meulenbelt, I, Bartels, M, Suchiman, E, Middeldorp, C M, Houwing-Duistermaat, J J, van Trier, J, Onkenhout, E J, Vink, J M, van Beijsterveldt, C E M, Brandys, M K, Sanders, N, Zipfel, S, Herzog, W, Herpertz-Dahlmann, B, Klampfl, K, Fleischhaker, C, Zeeck, A, Zwaan, M, Herpertz, S, Ehrlich, S, van Elburg, A A, Adan, R A H, Scherag, S, Hinney, A, Hebebrand, J, Boomsma, D I, van Furth, E F & Slagboom, P E 2011, ' Association study in eating disorders: TPH2 associates with anorexia nervosa and self induced vomiting ', Genes, Brain and Behavior, vol. 10, no. 2, pp. 236-243 . https://doi.org/10.1111/j.1601-183X.2010.00660.x
Genes, Brain and Behavior, 10(2), 236-243
Genes, brain, and behavior, 10(2), 236-243. Wiley-Blackwell
Genes, Brain and Behavior, 10(2), 236-243. Wiley-Blackwell Publishing
Slof-Op 't Landt, M C T, Meulenbelt, I, Bartels, M, Suchiman, E, Middeldorp, C M, Houwing-Duistermaat, J J, van Trier, J, Onkenhout, E J, Vink, J M, van Beijsterveldt, C E M, Brandys, M K, Sanders, N, Zipfel, S, Herzog, W, Herpertz-Dahlmann, B, Klampfl, K, Fleischhaker, C, Zeeck, A, Zwaan, M, Herpertz, S, Ehrlich, S, van Elburg, A A, Adan, R A H, Scherag, S, Hinney, A, Hebebrand, J, Boomsma, D I, van Furth, E F & Slagboom, P E 2011, ' Association study in eating disorders: TPH2 associates with anorexia nervosa and self induced vomiting ', Genes, Brain and Behavior, vol. 10, no. 2, pp. 236-243 . https://doi.org/10.1111/j.1601-183X.2010.00660.x
Genes, Brain and Behavior, 10(2), 236-243
Genes, brain, and behavior, 10(2), 236-243. Wiley-Blackwell
Genes, Brain and Behavior, 10(2), 236-243. Wiley-Blackwell Publishing
Twin studies suggest that genetic factors play a substantial role in anorexia nervosa (AN) and self-induced vomiting (SV), a key symptom that is shared among different types of eating disorders (EDs). We investigated the association of 25 single nucl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cfa718a075e3e1f0546c208bad9a023
https://doi.org/10.1111/j.1601-183x.2010.00660.x
https://doi.org/10.1111/j.1601-183x.2010.00660.x
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6d3374fda3ed77ac948ebb9fff3109c
https://doi.org/10.1038/npp.2010.49
https://doi.org/10.1038/npp.2010.49
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b7fb4d5a1c8304771b44e013b2583d9
https://doi.org/10.1007/s00787-010-0090-z
https://doi.org/10.1007/s00787-010-0090-z