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Die folgenden Publikationen sind in der Online-Universitätsbibliographie der Universität Duisburg-Essen verzeichnet. Weitere Informationen finden Sie gegebenenfalls auch auf den persönlichen Webseiten der Person.

    Artikel in Zeitschriften

  • Hebebrand, Johannes; Plieger, Moritz; Milos, Gabriella; Peters, Triinu; Hinney, Anke; Antel, Jochen
    Does hypoleptinemia trigger entrapment in anorexia nervosa? : Etiological and clinical considerations
    In: European Eating Disorders Review Jg. 32 (2024) Nr. 3, S. 557 - 574
  • Lodde, Georg; Zhao, Fang; Herbst, Rudolf; Terheyden, Patrick; Utikal, Jochen; Pföhler, Claudia; Ulrich, Jens; Kreuter, Alexander; Mohr, Peter; Gutzmer, Ralf; Meier, Friedegund; Dippel, Edgar; Weichenthal, Michael; Jansen, Philipp; Kowall, Bernd; Galetzka, Wolfgang; Hörst, Fabian; Kleesiek, Jens; Hellwig, Birte; Rahnenführer, Jörg; Rajcsanyi, Luisa; Peters, Triinu; Hinney, Anke; Placke, Jan-Malte; Sucker, Antje; Paschen, Annette; Becker, Jürgen; Livingstone, Elisabeth; Zimmer, Lisa; Tasdogan, Alpaslan; Rösch, Alexander; Hadaschik, Eva; Schadendorf, Dirk; Griewank, Klaus; Ugurel, Selma
    Early versus late response to PD-1-based immunotherapy in metastatic melanoma
    In: European Journal of Cancer (EJC) Jg. 210 (2024) 114295
  • Käver, Larissa; Hinney, Anke; Rajcsanyi, Luisa Sophie; Maier, Hannah Benedictine; Frieling, Helge; Steiger, Howard; Voelz, Clara; Beyer, Cordian; Trinh, Stefanie; Seitz, Jochen
    Epigenetic alterations in patients with anorexia nervosa : A systematic review
    In: Molecular Psychiatry (2024) in press
  • Giuranna, Johanna; Zheng, Yiran; Brandt, Matthäus; Jall, Sigrid; Mukherjee, Amrita; Shankhwar, Soni; Renner, Simone; Kurapati, Nirup Kumar; May, Caroline; Peters, Triinu; Herpertz-Dahlmann, Beate; Seitz, Jochen; de Zwaan, Martina; Herzog, Wolfgang; Ehrlich, Stefan; Zipfel, Stephan; Giel, Katrin; Egberts, Karin; Burghardt, Roland; Föcker, Manuel; Marcus, Katrin; Keyvani, Kathy; Müller, Timo D.; Schmitz, Frank; Rajcsanyi, Luisa Sophie; Hinney, Anke
    Genetic and functional analyses of CTBP2 in anorexia nervosa and body weight regulation
    In: Molecular Psychiatry (2024) in press
  • Rajcsanyi, Luisa Sophie; Schmidt, Jasmin; Düerkop, Sieglinde; Grote, Lola; Peters, Triinu; Körner, Antje; Fischer-Posovszky, Pamela; Hinney, Anke
    Genetische Ursachen der Adipositas und ihre therapeutischen Implikationen : Erkenntnisse der Forschung
    In: Diabetes Aktuell für die Hausarztpraxis Jg. 22 (2024) Nr. 4, S. 152 - 161
  • Dinkelbach, Lars; Peters, Triinu; Grasemann, Corinna; Hebebrand, Johannes; Hinney, Anke; Hirtz, Raphael
    No evidence for a causal contribution of bioavailable testosterone to ADHD in sex-combined and sex-specific two-sample Mendelian randomization studies
    In: European Child and Adolescent Psychiatry Jg. 33 (2024) Nr. 10, S. 3613 - 3623
  • Hirtz, Raphael; Grasemann, Corinna; Hölling, Heike; Von Holt, Björn-Hergen; Albers, Nicola; Hinney, Anke; Hebebrand, Johannes; Peters, Triinu
    No relationship between male pubertal timing and depression : new insights from epidemiology and Mendelian randomization
    In: Psychological Medicine Jg. 54 (2024) Nr. 9, S. 1975 - 1984
  • Rajcsanyi, Luisa Sophie; Zheng, Yiran; Herpertz-Dahlmann, Beate; Seitz, Jochen; de Zwaan, Martina; Herzog, Wolfgang; Ehrlich, Stefan; Zipfel, Stephan; Giel, Katrin; Egberts, Karin; Burghardt, Roland; Föcker, Manuel; Antel, Jochen; Fischer-Posovszky, Pamela; Hebebrand, Johannes; Hinney, Anke
    Unexpected identification of obesity-associated mutations in LEP and MC4R genes in patients with anorexia nervosa
    In: Scientific Reports Jg. 14 (2024) 7067
  • Hebebrand, Johannes; Antel, Jochen; Conceição, Eva; Matthews, Abigail; Hinney, Anke; Peters, Triinu
    What Amount of Weight Loss Can Entail Anorexia Nervosa or Atypical Anorexia Nervosa After Bariatric Surgery?
    In: International Journal of Eating Disorders (2024) in press
  • Berger, Marc; Brenner, Thorsten; Hinney, Anke; Witzke, Oliver; Konik, Margarethe; The COVID-19 Host Genetics Initiative
    A second update on mapping the human genetic architecture of COVID-19
    In: Nature Jg. 621 (2023) S. E7 - E26
  • Hebebrand, Johannes; Hinney, Anke; Antel, Jochen
    Could leptin substitution therapy potentially terminate entrapment in anorexia nervosa?
    In: Nature Reviews Endocrinology Jg. 19 (2023) Nr. 8, S. 435 - 436
  • Zheng, Yiran; Rajcsanyi, Luisa Sophie; Peters, Triinu; Dempfle, Astrid; Wudy, Stefan A.; Hebebrand, Johannes; Hinney, Anke
    Evaluation of the MC3R gene pertaining to body weight and height regulation and puberty development
    In: Scientific Reports Jg. 13 (2023) Nr. 1, 10419
  • Rajcsanyi, Luisa S.; Hoffmann, Anne; Ghosh, Adhideb; Matrisch-Dinkler, Birgit; Zheng, Yiran; Peters, Triinu; Sun, Wenfei; Dong, Hua; Noé, Falko; Wolfrum, Christian; Herpertz-Dahlmann, Beate; Seitz, Jochen; de Zwaan, Martina; Herzog, Wolfgang; Ehrlich, Stefan; Zipfel, Stephan; Giel, Katrin; Egberts, Karin; Burghardt, Roland; Föcker, Manuel; Tsai, Linus T.; Müller, Timo D.; Blüher, Matthias; Hebebrand, Johannes; Hirtz, Raphael; Hinney, Anke
    Genetic variants in genes involved in creatine biosynthesis in patients with severe obesity or anorexia nervosa
    In: Frontiers in Genetics Jg. 14 (2023) 1128133
  • Zheng, Yiran; Rajcsanyi, Luisa Sophie; Kowalczyk, Manuela; Giuranna, Johanna; Herpertz-Dahlmann, Beate; Seitz, Jochen; de Zwaan, Martina; Herzog, Wolfgang; Ehrlich, Stefan; Zipfel, Stephan; Giel, Katrin; Egberts, Karin; Burghardt, Roland; Föcker, Manuel; Al-Lahham, Saad; Hebebrand, Johannes; Führer, Dagmar; Tan, Susanne; Zwanziger, Denise; Peters, Triinu; Hinney, Anke
    Lipocalin 2 - mutation screen and serum levels in patients with anorexia nervosa or obesity and in lean individuals
    In: Frontiers in Endocrinology Jg. 14 (2023) 1137308
  • Hirtz, Raphael; Libuda, Lars; Hinney, Anke; Föcker, Manuel; Bühlmeier, Judith; Holterhus, Paul-Martin; Kulle, Alexandra; Kiewert, Cordula; Kuhnert, Ronny; Cohrdes, Caroline; Peters, Triinu; Hebebrand, Johannes; Grasemann, Corinna
    Age at menarche relates to depression in adolescent girls : Comparing a clinical sample to the general pediatric population
    In: Journal of Affective Disorders Jg. 318 (2022) S. 103 - 112
  • Hirtz, Raphael; Hars, Christine; Naaresh, Roaa; Laabs, Björn-Hergen; Antel, Jochen; Grasemann, Corinna; Hinney, Anke; Hebebrand, Johannes; Peters, Triinu
    Causal Effect of Age at Menarche on the Risk for Depression : Results From a Two-Sample Multivariable Mendelian Randomization Study
    In: Frontiers in Genetics Jg. 13 (2022) 918584
  • Brenner, Thorsten; Hinney, Anke; Witzke, Oliver; Renieri, A.
    Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
    In: Human Genetics Jg. 141 (2022) Nr. 1, S. 147 - 173
  • Degenhardt, Frauke; Franke, Andre; Hinney, Anke; Berger, Marc; Witzke, Oliver
    Detailed stratified GWAS analysis for severe COVID-19 in four European populations
    In: Human Molecular Genetics Jg. 31 (2022) Nr. 23, S. 3945 - 3966
  • Hirtz, Raphael; Zheng, Yiran; Rajcsanyi, Luisa S.; Libuda, Lars; Antel, Jochen; Peters, Triinu; Hebebrand, Johannes; Hinney, Anke
    Ebenen der genetischen Analyse komplexer Phänotypen am Beispiel der Anorexia nervosa und der Varianz des Körpergewichts
    In: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 50 (2022) Nr. 3, S. 175 - 185
  • Libuda, Lars; Hebebrand, Johannes; Föcker, Manuel; Peters, Triinu; Hinney, Anke
    Ernährungseffekten auf der Spur : Wie die Genetik helfen kann, Zusammenhänge zwischen Ernährung und seelischer Gesundheit aufzudecken
    In: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 50 (2022) Nr. 3, S. 217 - 226
  • Rajcsanyi, Luisa Sophie; Diebels, Inga; Pastoors, Lydia; Kanber, Deniz; Peters, Triinu; Volckmar, Anna-Lena; Zheng, Yiran; Grosse, Martin; Dieterich, Christoph; Hebebrand, Johannes; Kaiser, Frank J.; Horsthemke, Bernhard; Hinney, Anke
    Evidence for correlations between BMI-associated SNPs and circRNAs
    In: Scientific Reports Jg. 12 (2022) Nr. 1, 12643
  • Freff, Jana; Bröker, Lisa; Leite Dantas, Rafael; Schwarte, Kathrin; Bühlmeier, Judith; Kraft, Isabelle; Hinney, Anke; Buhlmann, Ulrike; Arolt, Volker; Dannlowski, Udo; Romer, Georg; Baune, Bernhard T.; Hebebrand, Johannes; Föcker, Manuel; Alferink, Judith
    Expression of CXCR4 on CD4⁺ T cells predicts body composition parameters in female adolescents with anorexia nervosa
    In: Frontiers in Psychiatry Jg. 13 (2022) 960905
  • Zheng, Yiran; Rajcsanyi, Luisa Sophie; Herpertz-Dahlmann, Beate; Seitz, Jochen; de Zwaan, Martina; Herzog, Wolfgang; Ehrlich, Stefan; Zipfel, Stephan; Giel, Katrin; Egberts, Karin; Burghardt, Roland; Föcker, Manuel; Al-Lahham, Saad; Peters, Triinu; Libuda, Lars; Antel, Jochen; Hebebrand, Johannes; Hinney, Anke
    PTBP2 – a gene with relevance for both Anorexia nervosa and body weight regulation
    In: Translational Psychiatry Jg. 12 (2022) Nr. 1, 241
  • Rajcsanyi, Luisa Sophie; Zheng, Yiran; Fischer-Posovszky, Pamela; Wabitsch, Martin; Hebebrand, Johannes; Hinney, Anke
    Prevalence estimates of putatively pathogenic leptin variants in the gnomAD database
    In: PLoS ONE Jg. 17 (2022) Nr. 9, e0266642
  • Antel, Jochen; Tan, Susanne; Grabler, Marvin; Ludwig, Christine; Lohkemper, Dominik; Brandenburg, Tim; Barth, Nikolaus; Hinney, Anke; Libuda, Lars; Remy, Miriam; Milos, Gabriella; Hebebrand, Johannes
    Rapid amelioration of anorexia nervosa in a male adolescent during metreleptin treatment including recovery from hypogonadotropic hypogonadism
    In: European Child and Adolescent Psychiatry Jg. 31 (2022) S. 1573 - 1579
  • Rohlfing, Nico; Bonnet, Udo; Tendolkar, Indira; Hinney, Anke; Scherbaum, Norbert
    Subjective reward processing and catechol-O- methyltransferase Val158Met polymorphism as potential research domain criteria in addiction : A pilot study
    In: Frontiers in Psychiatry Jg. 13 (2022) 992657
  • Hirtz, Raphael; Libuda, Lars; Hinney, Anke; Föcker, Manuel; Bühlmeier, Judith; Holterhus, Paul-Martin; Kulle, Alexandra; Kiewert, Cordula; Hauffa, Berthold; Hebebrand, Johannes; Grasemann, Corinna
    The adrenal steroid profile in adolescent depression : a valuable bio-readout?
    In: Translational Psychiatry Jg. 12 (2022) Nr. 1, 255
  • Hinney, Anke; Körner, Antje; Fischer-Posovszky, Pamela
    The promise of new anti-obesity therapies arising from knowledge of genetic obesity traits
    In: Nature Reviews Endocrinology Jg. 18 (2022) Nr. 10, S. 623 - 637
  • Libuda, Lars; Naaresh, Roaa; Ludwig, Christine; Laabs, Björn-Hergen; Antel, Jochen; Föcker, Manuel; Hebebrand, Johannes; Hinney, Anke; Peters, Triinu
    A mendelian randomization study on causal effects of 25(OH)vitamin D levels on attention deficit/hyperactivity disorder
    In: European Journal of Nutrition Jg. 60 (2021) Nr. 5, S. 2581 - 2591
  • Freff, Jana; Schwarte, Kathrin; Bröker, Lisa; Bühlmeier, Judith; Kraft, Isabelle; Öztürk, Dana; Hinney, Anke; Arolt, Volker; Dannlowski, Udo; Romer, Georg; Baune, Bernhard T.; Hebebrand, Johannes; Föcker, Manuel; Alferink, Judith
    Alterations in B cell subsets correlate with body composition parameters in female adolescents with anorexia nervosa
    In: Scientific Reports Jg. 11 (2021) Nr. 1, S. 1125
  • Föcker, Manuel; Cecil, Alexander; Prehn, Cornelia; Adamski, Jerzy; Albrecht, Muriel; Adams, Frederike; Hinney, Anke; Libuda, Lars; Bühlmeier, Judith; Hebebrand, Johannes; Peters, Triinu; Antel, Jochen
    Evaluation of metabolic profiles of patients with anorexia nervosa at inpatient admission, short-and long-term weight regain : Descriptive and pattern analysis
    In: Metabolites Jg. 11 (2021) Nr. 1, 7
  • Müller, Bernhard W.; Hinney, Anke; Scherbaum, Norbert; Weimar, Christian; Kleinschnitz, Christoph; Peters, Triinu; Hochfeld, Lara; Pechlivanis, Sonali; Stang, Andreas; Jokisch, Martha; Kowall, Bernd
    Klotho KL-VS haplotype does not improve cognition in a population-based sample of adults age 55-87 years
    In: Scientific Reports Jg. 11 (2021) Nr. 1, 13852
  • Hebebrand, Johannes; Antel, Jochen; Tan, Susanne; Wabitsch, Martin; Wiesing, Urban; Barth, Nikolaus; Ludwig, Christine; Bühlmeier, Judith; Libuda, Lars; Milos, Gabriella; Hinney, Anke
    Kurzzeitige Behandlung von Patient_innen mit Anorexia nervosa mit rekombinant hergestelltem Human-Leptin (Metreleptin) : Rasch einsetzende positive Effekte auf Stimmung, Kognition und Verhalten
    In: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 49 (2021) Nr. 1, S. 1 - 5
  • Hirtz, Raphael; Libuda, Lars; Hinney, Anke; Föcker, Manuel; Bühlmeier, Judith; Antel, Jochen; Holterhus, Paul-Martin; Kulle, Alexandra; Kiewert, Cordula; Hebebrand, Johannes; Grasemann, Corinna
    Lack of Evidence for a Relationship Between the Hypothalamus-Pituitary-Adrenal and the Hypothalamus-Pituitary-Thyroid Axis in Adolescent Depression
    In: Frontiers in Endocrinology Jg. 12 (2021) 662243
  • Berger, Marc; Brenner, Thorsten; Hinney, Anke; Witzke, Oliver
    Mapping the human genetic architecture of COVID-19
    In: Nature Jg. 600 (2021) S. 472 - 477
  • Munn‐Chernoff, Melissa A.; Johnson, Emma C.; Chou, Yi‐Ling; Hinney, Anke; Hebebrand, Johannes; et al.
    Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes : Evidence from genome‐wide association studies
    In: Addiction Biology Jg. 26 (2021) Nr. 1, e12880
  • Hirtz, Raphael; Libuda, Lars; Hinney, Anke; Föcker, Manuel; Bühlmeier, Judith; Holterhus, Paul-Martin; Kulle, Alexandra; Kiewert, Cordula; Hebebrand, Johannes; Grasemann, Corinna
    Size Matters: The CAG Repeat Length of the Androgen Receptor Gene, Testosterone, and Male Adolescent Depression Severity
    In: Frontiers in Psychiatry Jg. 12 (2021) 732759
  • Peters, Triinu; Antel, Jochen; Naaresh, Roaa; Laabs, Björn-Hergen; Föcker, Manuel; Albers, Nicola; Bühlmeier, Judith; Hinney, Anke; Libuda, Lars; Hebebrand, Johannes
    Suggestive Evidence for Causal Effect of Leptin Levels on Risk for Anorexia Nervosa : Results of a Mendelian Randomization Study
    In: Frontiers in Genetics Jg. 12 (2021) 733606
  • Yu, Dongmei; Sul, Jae Hoon; Huang, Alden Y.; Darrow, Sabrina M.; Greenberg, Erica; Muller-Vahl, Kirsten R.; Stuhrmann, Manfred; Dion, Yves; Rouleau, Guy A.; Aschauer, Harald; Stamenkovic, Mara; Sandor, Paul; Barr, Cathy L.; Grados, Marco A.; Singer, Harvey S.; Nöthen, Markus M.; Hebebrand, Johannes; Hinney, Anke; King, Robert A.; Fernandez, Thomas V.; Barta, Csaba; Nagy, Peter; Depienne, Christel; Worbe, Yulia; Hartmann, Andreas; Budman, Cathy L.; Rizzo, Renata; Lyon, Gholson J.; McMahon, William M.; Cath, Danielle C.; Malaty, Irene A.; Okun, Michael S.; Berlin, Cheston; Woods, Douglas W.; Lee, Paul C.; Jankovic, Joseph; Robertson, Mary M.; Gilbert, Donald L.; Brown, Lawrence W.; Coffey, Barbara J.; Dietrich, Andrea; Hoekstra, Pieter J.; Kuperman, Samuel; Zinner, Samuel H.; Wagner, Michael; Knowles, James A.; Jeremy Willsey, A.; Tischfield, Jay A.; Heiman, Gary A.; Cox, Nancy J.; Freimer, Nelson B.; Neale, Benjamin M.; Davis, Lea K.; Coppola, Giovanni; Mathews, Carol A.; Scharf, Jeremiah M.; Paschou, Peristera; Barr, Cathy L.; Berlin, Cheston; Budman, Cathy L.; Cath, Danielle C.; Coppola, Giovanni; Cox, Nancy J.; Davis, Lea K.; Dion, Yves; Freimer, Nelson B.; Grados, Marco A.; Greenberg, Erica; Huang, Alden Y.; King, Robert A.; Kurlan, Roger; Leckman, James F.; Lyon, Gholson J.; Malaty, Irene A.; Mathews, Carol A.; McMahon, William M.; Neale, Benjamin M.; Okun, Michael S.; Robertson, Mary M.; Rouleau, Guy A.; Sandor, Paul; Scharf, Jeremiah M.; Singer, Harvey S.; Smit, Jan H.; Sul, Jae Hoon; Yu, Dongmei; Aschauer, Harald Aschauer Harald; Barta, Csaba; Budman, Cathy L.; Cath, Danielle C.; Depienne, Christel; Hartmann, Andreas; Hebebrand, Johannes; Konstantinidis, Anastasios; Mathews, Carol A.; Müller-Vahl, Kirsten; Nagy, Peter; Nöthen, Markus M.; Paschou, Peristera; Rizzo, Renata; Rouleau, Guy A.; Sandor, Paul; Scharf, Jeremiah M.; Stamenkovic, Mara; Stuhrmann, Manfred; Wolanczyk, Tomasz; Worbe, Yulia; Brown, Lawrence; Cheon, Keun-Ah; Coffey, Barbara J.; Dietrich, Andrea; Fernandez, Thomas V.; Garcia-Delgar, Blanca; Gilbert, Donald; Grice, Dorothy E.; Hagstrøm, Julie; Hedderly, Tammy; Heiman, Gary A.; Heyman, Isobel; Hoekstra, Pieter J.; Huyser, Chaim; Kim, Young Key; Kim, Young-Shin; King, Robert A.; Koh, Yun-Joo; Kook, Sodahm; Kuperman, Samuel; Leventhal, Bennett L.; Madruga-Garrido, Marcos; Mir, Pablo; Morer, Astrid; Münchau, Alexander; Plessen, Kerstin J.; Roessner, Veit; Shin, Eun-Young; Song, Dong-Ho; Song, Jungeun; Tischfield, Jay A.; Willsey, A. Jeremy; Zinner, Samuel; Aschauer, Harald; Barr, Cathy L.; Barta, Csaba; Batterson, James R.; Batterson, James R.; Batterson, James R.; Berlin, Cheston; Brown, Lawrence; Budman, Cathy L.; Cath, Danielle C.; Coffey, Barbara J.; Coppola, Giovanni; Cox, Nancy J.; Darrow, Sabrina; Darrow, Sabrina; Davis, Lea K.; Depienne, Christel; Dietrich, Andrea; Dion, Yves; Fernandez, Thomas; Freimer, Nelson B.; Gilbert, Donald; Grados, Marco A.; Greenberg, Erica; Hartmann, Andreas; Hebebrand, Johannes; Heiman, Gary; Hirschtritt, Matthew E.; Hirschtritt, Matthew E.; Hirschtritt, Matthew E.; Hoekstra, Pieter; Huang, Alden Y.; Illmann, Cornelia; Illmann, Cornelia; Illmann, Cornelia; Jankovic, Joseph; King, Robert A.; Kuperman, Samuel; Lee, Paul C.; Lyon, Gholson J.; Malaty, Irene A.; Mathews, Carol A.; McMahon, William M.; Müller-Vahl, Kirsten; Nagy, Peter; Neale, Benjamin M.; Nöthen, Markus M.; Okun, Michael S.; Osiecki, Lisa; Osiecki, Lisa; Osiecki, Lisa; Paschou, Peristera; Rizzo, Renata; Robertson, Mary M.; Rouleau, Guy A.; Sandor, Paul; Scharf, Jeremiah M.; Schlögelhofer, Monika; Schlögelhofer, Monika; Schlögelhofer, Monika; Singer, Harvey S.; Stamenkovic, Mara; Stuhrmann, Manfred; Sul, Jae Hoon; Tarnok, Zsanett; Tarnok, Zsanett; Tarnok, Zsanett; Tischfield, Jay; Tsetsos, Fotis; Tsetsos, Fotis; Tsetsos, Fotis; Willsey, A. Jeremy; Woods, Douglas; Worbe, Yulia; Yu, Dongmei; Zinner, Samuel
    Synaptic processes and immune-related pathways implicated in Tourette syndrome
    In: Translational Psychiatry Jg. 11 (2021) Nr. 1, S. 56
  • Libuda, Lars; Timmesfeld, Nina; Antel, Jochen; Hirtz, Raphael; Bauer, Jens; Führer, Dagmar; Zwanziger, Denise; Öztürk, Dana; Langenbach, Gina; Hahn, Denise; Ring, Stefanie; Peters, Triinu; Hinney, Anke; Bühlmeier, Judith; Hebebrand, Johannes; Grasemann, Corinna; Föcker, Manuel
    Effect of vitamin D deficiency on depressive symptoms in child and adolescent psychiatric patients : results of a randomized controlled trial
    In: European Journal of Nutrition Jg. 59 (2020) Nr. 8, S. 3415 - 3424
  • Hirtz, Raphael; Hinney, Anke
    Genetic and epigenetic findings in anorexia nervosa
    In: Medizinische Genetik Jg. 32 (2020) Nr. 1, S. 25 - 29
  • Hirtz, Raphael; Keesen, Anne; Hölling, Heike; Hauffa, Berthold; Hinney, Anke; Grasemann, Corinna
    No Effect of Thyroid Dysfunction and Autoimmunity on Health-Related Quality of Life and Mental Health in Children and Adolescents : Results From a Nationwide Cross-Sectional Study
    In: Frontiers in Endocrinology Jg. 11 (2020) 454
  • Milos, Gabriella; Antel, Jochen; Kaufmann, Lisa-Katrin; Barth, Nikolaus; Koller, Antonia; Tan, Susanne; Wiesing, Urban; Hinney, Anke; Libuda, Lars; Wabitsch, Martin; von Känel, Roland; Hebebrand, Johannes
    Short-term metreleptin treatment of patients with anorexia nervosa : rapid on-set of beneficial cognitive, emotional, and behavioral effects
    In: Translational Psychiatry Jg. 10 (2020) Nr. 1, 303
  • Peters, Triinu; Nüllig, Lena; Antel, Jochen; Naaresh, Roaa; Laabs, Björn-Hergen; Tegeler, Lisa; Amhaouach, Chaima; Libuda, Lars; Hinney, Anke; Hebebrand, Johannes
    The Role of Genetic Variation of BMI, Body Composition, and Fat Distribution for Mental Traits and Disorders : A Look-Up and Mendelian Randomization Study
    In: Frontiers in Genetics Jg. 11 (2020) 373
  • Bradfield, Jonathan P.; Vogelezang, Suzanne; Felix, Janine F.; Chesi, Alessandra; Helgeland, Øyvind; Horikoshi, Momoko; Karhunen, Ville; Lowry, Estelle; Cousminer, Diana L.; Ahluwalia, Tarunveer S.; Thiering, Elisabeth; Boh, Eileen Tai-Hui; Zafarmand, Mohammad H.; Vilor-Tejedor, Natalia; Wang, Carol A.; Joro, Raimo; Chen, Zhanghua; Gauderman, William J.; Pitkänen, Niina; Parra, Esteban J.; Fernandez-Rhodes, Lindsay; Alyass, Akram; Monnereau, Claire; Curtin, John A.; Have, Christian T.; McCormack, Shana E.; Hollensted, Mette; Frithioff-Bøjsøe, Christine; Valladares-Salgado, Adan; Peralta-Romero, Jesus; Teo, Yik-Ying; Standl, Marie; Leinonen, Jaakko T.; Holm, Jens-Christian; Peters, Triinu; Vioque, Jesus; Vrijheid, Martine; Simpson, Angela; Custovic, Adnan; Vaudel, Marc; Canouil, Mickaël; Lindi, Virpi; Atalay, Mustafa; Kähönen, Mika; Raitakari, Olli T.; van Schaik, Barbera D C; Berkowitz, Robert I.; Cole, Shelley A.; Voruganti, V Saroja; Wang, Yujie; Highland, Heather M.; Comuzzie, Anthony G.; Butte, Nancy F.; Justice, Anne E.; Gahagan, Sheila; Blanco, Estela; Lehtimäki, Terho; Lakka, Timo A.; Hebebrand, Johannes; Bonnefond, Amélie; Grarup, Niels; Froguel, Philippe; Lyytikäinen, Leo-Pekka; Cruz, Miguel; Kobes, Sayuko; Hanson, Robert L.; Zemel, Babette S.; Hinney, Anke; Teo, Koon K.; Meyre, David; North, Kari E.; Gilliland, Frank D.; Bisgaard, Hans; Bustamante, Mariona; Bonnelykke, Klaus; Pennell, Craig E.; Rivadeneira, Fernando; Uitterlinden, André G; Baier, Leslie J.; Vrijkotte, Tanja G M; Heinrich, Joachim; Sørensen, Thorkild I A; Saw, Seang-Mei; Pedersen, Oluf; Hansen, Torben; Eriksson, Johan; Widén, Elisabeth; McCarthy, Mark I.; Njølstad, Pål R; Power, Christine; Hyppönen, Elina; Sebert, Sylvain; Brown, Christopher D.; Järvelin, Marjo-Riitta; Timpson, Nicholas J.; Johansson, Stefan; Hakonarson, Hakon; Jaddoe, Vincent W V
    A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
    In: Human Molecular Genetics Jg. 28 (2019) Nr. 19, S. 3327 - 3338
  • Lin, Bochao; Alkema, Anne; Zinkstok, Janneke; Lars, Libuda; Hebebrand, Johannes; Antel, Jochen; Hinney, Anke; Cahn, Wiepke; Roger, Adan; Luykx, Jurjen
    Assessing Causal links between metabolic traits, inflammation and Schizophrenia : a Univariable and Multivariable Bidirectional Mendelian Randomization Study
    In: European Neuropsychopharmacology Jg. 29 (2019) S. 211
  • Lin, Bochao D.; Alkema, Anne; Peters, Triinu; Zinkstok, Janneke; Libuda, Lars; Hebebrand, Johannes; Antel, Jochen; Hinney, Anke; Cahn, Wiepke; Adan, Roger; Luykx, Jurjen J.
    Assessing causal links between metabolic traits, inflammation and schizophrenia : a univariable and multivariable, bidirectional Mendelian-randomization study
    In: International Journal of Epidemiology Jg. 48 (2019) Nr. 5, S. 1505 - 1514
  • Föcker, Manuel; Hebebrand, Johannes; Hinney, Anke; Scherag, Andre
    Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders : A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches
    In: Biological Psychiatry Jg. 86 (2019) Nr. 8, S. 577 - 586
  • Qasim, Anila; Mayhew, Alexandra J.; Ehtesham, Sahar; Alyass, Akram; Volckmar, Anna Lena; Herpertz, Stephan; Hinney, Anke; Hebebrand, Johannes; Meyre, David
    Gain-of-function variants in the melanocortin 4 receptor gene confer susceptibility to binge eating disorder in subjects with obesity : a systematic review and meta-analysis
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    Genetic and gene expression analysis in CTBP2 : A gene derived from genome-wide data in anorexia nervosa and body weight regulation
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    Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
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    Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms Across Eight Psychiatric Disorders
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    Interrogating the genetic determinants of Tourette's syndrome and other tiC disorders through genome-wide association studies
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    Melanocortin-4 Receptor and Lipocalin 2 Gene Variants in Spanish Children with Abdominal Obesity : Effects on BMI-SDS After a Lifestyle Intervention
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    The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism : Association study and meta-analysis
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    Vitamin D and the Risk of Depression : A Causal Relationship? Findings from a Mendelian Randomization Study
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    Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa
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    Effect of an vitamin D deficiency on depressive symptoms in child and adolescent psychiatric patients - a randomized controlled trial : study protocol
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    High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation
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    Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa
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    Monogene Adipositas : Neue diagnostische und therapeutische Möglichkeiten
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    Relevance of polymorphisms in MC4R and BDNF in short normal stature.
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    The Effect of SH2B1 Variants on Expression of Leptin- and Insulin-Induced Pathways in Murine Hypothalamus
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    The association of Leptin and Food Addiction in Adolescent Psychiatric Patients
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    The association of serum leptin levels with food addiction is moderated by weight status in adolescent psychiatric inpatients
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    The role of genetic variation of human metabolism for BMI, mental traits and mental disorders
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    Waist-hip ratio related genetic loci are associated with risk of impaired fasting glucose in Chinese children : A case control study
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    A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling
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    Anorexia nervosa and body mass index : combined GWAS and functional ex-vivo studies
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    Estimated prevalence of potentially damaging variants in the leptin gene.
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    Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index
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    Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa
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    Food addiction in gambling disorder: Frequency and clinical outcomes
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    Genetische Ursachen der Adipositas
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    Polygene Varianten und Epigenetik bei Adipositas
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    Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity
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    Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa
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    Analysis of genes involved in body weight regulation by targeted re-sequencing
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    Association of common variants identified by recent genome-wide association studies with obesity in Chinese children : A case-control study
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    Cover Image, Volume 171B, Number 6, September 2016
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    Decreased melanocortin-4 receptor function conferred by an infrequent variant at the human melanocortin receptor accessory protein 2 gene
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    Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with Obesity
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    Pathway analysis in attention deficit hyperactivity disorder : An ensemble approach
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    Case–Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder
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    Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity : a systematic review and meta-analysis with evidence from up to 331 175 individuals
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    Fine mapping of a GWAS-derived obesity candidate region on chromosome 16p11.2
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    Genetik und Epigenetik der Adipositas
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    Indications for potential parent-of-origin effects within the FTO gene
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    Perspektiven der genetischen Forschung bei Essstörungen am Beispiel der Anorexia nervosa
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    Catechol-O-Methyltransferase Val158Met Polymorphism Is Associated with Somatosensory Amplification and Nocebo Responses
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    FTO Gene : Association to Weight Regain after Lifestyle Intervention in Overweight Children
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  • Song, Jie-Yun; Wang, Hai-Jun; Ma, Jun; Xu, Zhi-Yuan; Hinney, Anke; Hebebrand, Johannes; Wang, Yan
    Association of the rs10830963 Polymorphism in MTNR1B with Fasting Glucose Levels in Chinese Children and Adolescents
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  • Slof-Op 't Landt, Margarita C.T.; Meulenbelt, Ingrid; Bartels, Meike; Suchiman, Eka; Middeldorp, Christel M.; Houwing-Duistermaat, Jeanine J.; Van Trier, Jan; Onkenhout, E.J.; Vink, Jacqueline M.; Van Beijsterveldt, Catharina Eugenie Maria; Brandys, Marek K.; Sanders, Nicole; Zipfel, Stephan; Herzog, Wolfgang; Herpertz-Dahlmann, Beate; Klampfl, Karin; Fleischhaker, Christian; Zeeck, Almut; De Zwaan, Martina; Herpertz, Stephan; Ehrlich, Stefan; Van Elburg, Annemarie A.; Adan, Roger A.H.; Scherag, Susann; Hinney, Anke; Hebebrand, Johannes; Boomsma, Dorret I.; Van Furth, Eric F.; Slagboom, Pieternella Eline
    Association study in eating disorders : TPH2 associates with anorexia nervosa and self-induced vomiting
    In: Genes, Brain and Behavior Jg. 10 (2011) Nr. 2, S. 236 - 243
  • Vogel, Carla I.G.; Boes, Tanja; Reinehr, Thomas; Roth, Christian L.; Scherag, Susann; Scherag, Andre; Hebebrand, Johannes; Hinney, Anke
    Common Variants Near MC4R : Exploring Gender Effects in Overweight and Obese Children and Adolescents Participating in a Lifestyle Intervention
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  • Winter, Yaroslav; Back, Tobias; Scherag, Andre; Linseisen, Jakob; Rohrmann, Sabine; Lanczik, Oliver; Hinney, Anke; Scherag, Susann; Neumaier, Michael; Ringleb, Peter A; Dodel, Richard; Hebebrand, Johannes
    Evaluation of the obesity genes FTO and MC4R and the type 2 diabetes mellitus gene TCF7L2 for contribution to stroke risk : The Mannheim-Heidelberg Stroke Study
    In: Obesity Facts Jg. 4 (2011) Nr. 4, S. 290 - 296
  • Jiao, Hong; Arner, Peter; Dickson, Suzanne L.; Vidal, Hubert; Mejhert, Niklas; Henegar, Corneliu; Taube, Magdalena; Hansson, Caroline; Hinney, Anke; Galan, Pilar; Simon, Chantal; Silveira, Angela; Benrick, Anna; Jansson, John-Olov; Bouloumié, Anne; Langin, Dominique; Laville, Martine; Debard, Cyrille; Axelsson, Tomas; Rydén, Mikael; Kere, Juha; Dahlman-Wright, Karin; Hamsten, Anders; Clement, Karine; Dahlman, Ingrid
    Genetic association and gene expression analysis identify FGFR1 as a new susceptibility gene for human obesity
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    Genetic variation of the ghrelin activator gene ghrelin O-acyltransferase (GOAT) is associated with anorexia nervosa.
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    Genome-wide association study in German patients with attention deficit/hyperactivity disorder
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  • Choquet, Hélène; Labrune, Yann; De Graeve, Franck; Hinney, Anke; Hebebrand, Johannes; Scherag, Andre; Lecoeur, Cécile; Tauber, Maithé; Balkau, Beverley; Elliot, Paul; Jarvelin, Marjo-Riita; Walley, Andrew J.; Besnard, Philippe; Froguel, Philippe; Meyre, David
    Lack of association of cd36 snps with early onset obesity : A meta-analysis in 9,973 european subjects
    In: Obesity Jg. 19 (2011) Nr. 4, S. 833 - 839
  • Jarick, Ivonne; Vogel, Carla I. G.; Scherag, Susann; Schäfer, Helmut; Hebebrand, Johannes; Hinney, Anke; Scherag, Andre
    Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis
    In: Human Molecular Genetics Jg. 20 (2011) Nr. 4, S. 840 - 852
  • Reinehr, Thomas; Scherag, Andre; Wang, Hai-Jun; Roth, Christian L; Kleber, Michaela; Scherag, Susann; Boes, Tanja; Vogel, Carla; Hebebrand, Johannes; Hinney, Anke
    Relationship between MTNR1B (melatonin receptor 1B gene) polymorphism rs10830963 and glucose levels in overweight children and adolescents
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  • Albayrak, Özgür; Albrecht, Beate; Scherag, Susann; Barth, Nikolaus; Hinney, Anke; Hebebrand, Johannes
    Successful methylphenidate treatment of early onset extreme obesity in a child with a melanocortin-4 receptor gene mutation and attention deficit/hyperactivity disorder
    In: European Journal of Pharmacology Jg. 660 (2011) Nr. 1, S. 165 - 170
  • Günther, Torsten; Schmitt, Armin O.; Bortfeldt, Ralf H.; Hinney, Anke; Hebebrand, Johannes; Brockmann, Gudrun A.
    Where in the Genome Are Significant Single Nucleotide Polymorphisms from Genome-Wide Association Studies Located?
    In: OMICS: A Journal of Integrative Biology Jg. 15 (2011) Nr. 7/8, S. 507 - 512
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    Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
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  • Scherag, Andre; Boes, Tanja; Hinney, Anke; Scherag, Susann; Vogel, Carla I.; Hebebrand, Johannes
    Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
    In: Nature Genetics Jg. 42 (2010) Nr. 11, S. 937 - 948
  • Wang, Du; Ma, Jun; Zhang, Su; Hinney, Anke; Hebebrand, Johannes; Wang, Yan; Wang, Hai-Jun
    Association of the MC4R V103I polymorphism with obesity : A chinese case-control study and meta-analysis in 55,195 individuals
    In: Obesity Jg. 18 (2010) Nr. 3, S. 573 - 579
  • Sauber, Jeannine; Grothe, Jessica; Behm, Maria; Scherag, Andre; Grallert, Harald; Illig, Thomas; Hinney, Anke; Hebebrand, Johannes; Wiegand, Susanna; Grüters, Annette; Krude, Heiko; Biebermann, Heike
    Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin
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  • Roth, Christian Ludwig; Enriori, Pablo J.; Gebhardt, Ursel; Hinney, Anke; Müller, Hermann Lothar; Hebebrand, Johannes; Reinehr, Thomas; Cowley, Michael A.
    Changes of peripheral alpha-melanocyte-stimulating hormone in childhood obesity
    In: Metabolism Jg. 59 (2010) Nr. 2, S. 186 - 194
  • Hebebrand, Johannes; Scherag, Andre; Schimmelmann, Benno G.; Hinney, Anke
    Child and adolescent psychiatric genetics
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  • Hebebrand, Johannes; Volckmar, Anna-Lena; Knoll, Nadja; Hinney, Anke
    Chipping away the 'missing heritability': GIANT steps forward in the molecular elucidation of obesity - But still lots to go
    In: Obesity Facts Jg. 3 (2010) Nr. 5, S. 294 - 303
  • Scherag, Susann; Hebebrand, Johannes; Hinney, Anke
    Eating disorders: the current status of molecular genetic research
    In: European Child & Adolescent Psychiatry Jg. 19 (2010) Nr. 3, S. 211 - 226
  • Versini, Audrey; Ramoz, Nicolas; Le Strat, Yann; Scherag, Susann; Ehrlich, Stefan; Boni, Claudette; Hinney, Anke; Hebebrand, Johannes; Romo, Lucia; Guelfi, Julien-Daniel; Gorwood, Philip
    Estrogen receptor 1 gene (ESR1) is associated with restrictive anorexia nervosa
    In: Neuropsychopharmacology Jg. 35 (2010) Nr. 8, S. 1818 - 1825
  • Konrad, Kerstin; Dempfle, Astrid; Friedel, Susann; Heiser, Philip; Holtkamp, Kristian; Walitza, Susanne; Sauer, Sascha; Warnke, Andreas; Remschmidt, Helmut; Gilsbach, Susanne; Schäfer, Helmut; Hinney, Anke; Hebebrand, Johannes; Herpertz-Dahlmann, Beate
    Familiality and molecular genetics of attention networks in ADHD
    In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 153B (2010) Nr. 1, S. 148 - 158
  • Hinney, Anke; Vogel, Carla I.; Hebebrand, Johannes
    From monogenic to polygenic obesity : Recent advances
    In: European Child & Adolescent Psychiatry Jg. 19 (2010) Nr. 3, S. 297 - 310
  • Holzapfel, Christina; Grallert, Harald; Huth, Cornelia; Wahl, Simone; Fischer, Beate; Döring, Angela; Rückert, Ina Maria; Hinney, Anke; Hebebrand, Johannes; Wichmann, Heinz-Erich; Hauner, Hans; Illig, Thomas; Heid, Iris M.
    Genes and lifestyle factors in obesity : Results from 12 462 subjects from MONICA/KORA
    In: International Journal of Obesity Jg. 34 (2010) Nr. 10, S. 1538 - 1545
  • Hinney, Anke; Scherag, Susann; Hebebrand, Johannes
    Genetic findings in anorexia and bulimia nervosa
    In: Progress in Molecular Biology and Translational Science Jg. 94 (2010) S. 241 - 270
  • Linsel-Nitschke, Patrick; Heeren, Jörg; Aherrahrou, Zouhair; Bruse, Petra; Gieger, Christian; Illig, Thomas; Prokisch, Holger; Heim, Katharina; Doering, Angela; Peters, Annette; Meitinger, Thomas; Wichmann, H.-Erich; Hinney, Anke; Reinehr, Thomas; Roth, Christian; Ortlepp, Jan. R.; Soufi, Mouhidien; Sattler, Alexander M.; Schaefer, Jürgen; Stark, Klaus; Hengstenberg, Christian; Schaefer, Arne; Schreiber, Stefan; Kronenberg, Florian; Samani, Nilesh J.; Schunkert, Heribert; Erdmann, Jeanette
    Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease
    In: Atherosclerosis Jg. 208 (2010) Nr. 1, S. 183 - 189
  • Hebebrand, Johannes; Bammann, K.; Hinney, Anke
    Genetische Ursachen der Adipositas : Zum Stand der Forschung
    In: Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz Jg. 53 (2010) Nr. 7, S. 674 - 680
  • Scherag, André; Jarick, Ivonne; Grothe, Jessica; Biebermann, Heike; Scherag, Susann; Volckmar, Anna-Lena; Vogel, Carla Ivane Ganz; Greene, Brandon; Hebebrand, Johannes; Hinney, Anke
    Investigation of a Genome Wide Association Signal for Obesity : Synthetic Association and Haplotype Analyses at the Melanocortin 4 Receptor Gene Locus
    In: PLoS ONE Jg. 5 (2010) Nr. 11, S. e13967
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    Large effects on body mass index and insulin resistance of fat mass and obesity associated gene (FTO) variants in patients with polycystic ovary syndrome (PCOS)
    In: BMC Medical Genetics Jg. 11 (2010) 12
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    Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity
    In: BMC Medical Genetics Jg. 11 (2010) S. 2
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    Role of the neurotrophin network in eating disorders' subphenotypes : Body mass index and age at onset of the disease
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  • Sayk, Friedhelm; Heutling, Dennis; Dodt, Christoph; Iwen, K. Alexander; Wellhoner, J. Peter; Scherag, Susann; Hinney, Anke; Hebebrand, Johannes; Lehnert, Hendrik
    Sympathetic function in human carriers of melanocortin-4 receptor gene mutations
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    Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups
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    A consultation with genetic information about obesity decreases self-blame about eating and leads to realistic weight loss goals in obese individuals
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    Adipositas/Übergewicht
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    Aggravating effect of INSIG2 and FTO on overweight reduction in a one-year lifestyle intervention
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    Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients : Perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?
    In: Molecular Psychiatry Jg. 14 (2009) Nr. 3, S. 308 - 317
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    Association studies on ghrelin and ghrelin receptor gene polymorphisms with obesity
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    Causal attributions of obese men and women in genetic testing: Implications of genetic/biological attributions
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    Environmental and Genetic Risk Factors in Obesity
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    Exploring the genetic link between RLS and ADHD
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    Functional variants of the serotonin receptor type 3A and B gene are associated with eating disorders
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    Gastric inhibitory polypeptide receptor : Association analyses for obesity of several polymorphisms in large study groups
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    Increased constraints on MC4R during primate and human evolution
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    Lifestyle intervention in obese children with variations in the melanocortin 4 receptor gene
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    Meta-analysis of the INSIG2 association with obesity including 74,345 individuals : Does heterogeneity of estimates relate to study design?
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    Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry
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    Procolipase gene : no association with early-onset obesity or fat intake
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    Serotonin transporter gene polymorphism (5-HTTLPR), environmental conditions, and developing negative emotionality and fear in early childhood
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    'Fat mass and obesity associated' gene (FTO): No significant association of variant rs9939609 with weight loss in a lifestyle intervention and lipid metabolism markers in German obese children and adolescents
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    Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders
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    Association of the MC4R V103I polymorphism with the metabolic syndrome: The KORA study
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    Common variants near MC4R are associated with fat mass, weight and risk of obesity
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    Evidence for an influence of TCF7L2 polymorphism rs7903146 on insulin resistance and sensitivity indices in overweight children and adolescents during a lifestyle intervention
    In: International Journal of Obesity Jg. 32 (2008) Nr. 10, S. 1521 - 1524
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    Evidence of an influence of a polymorphism near the INSIG2 on weight loss during a lifestyle intervention in obese children and adolescents
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    Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa
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    Meta-analysis of Genome-Wide Linkage Scans of Attention Deficit Hyperactivity Disorder
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    Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children : First evidence of polar overdominance in humans
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    Transmission disequilibrium studies in early onset of obsessive-compulsive disorder for polymorphisms in genes of the dopaminergic system
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    Val103Ile polymorphism of the melanocortin-4 receptor gene (MC4R) in cancer cachexia
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    A novel mutation Thr162Arg of the melanocortin 4 receptor gene in a Spanish children and adolescent population
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    Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents
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    Association and linkage of allelic variants of the dopamine transporter gene in ADHD
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    Definable Somatic Disorders in Overweight Children and Adolescents
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    Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample
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    Genome Wide Association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants
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    Is information on genetic determinants of obesity helpful or harmful for obese people? : A randomized clinical trial
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    Mutation screen and association studies in the Diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13
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    No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in Germans
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    No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents
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    No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD
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    Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution
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    Response to Comments on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity"
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    Restoration of signalling capabilities in total loss of function MC4R mutations
    In: Experimental and Clinical Endocrinology & Diabetes Jg. 115 (2007) Nr. S 1, P02_065
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    The V103I polymorphism of the MC4R gene and obesity: Population based studies and meta-analysis of 29 563 individuals
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    The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts
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    A common genetic variant is associated with adult and childhood obesity
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    A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs
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    A role for β-melanocyte-stimulating hormone in human body-weight regulation
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    Association of the melanocortin 4 receptor with feed intake and daily gain in F2 Mangalitsa x Piétrain pigs
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    Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa
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    Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies
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    Genetische Aspekte in der Adipositas-Beratung – Auswirkungen auf Körperakzeptanz und subjektives Wohlbefinden
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    Genetische Befunde bei der Aufmerksamkeitsdefizit- und Hyperaktivitätsstörung (ADHS)
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    Meta-analysis on the effect of the N363S polymorphism of the glucocorticoid receptor gene (GRL) on human obesity
    In: BMC Medical Genetics Jg. 7 (2006)
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    Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany
    In: The Journal of Clinical Endocrinology & Metabolism (JCEM) Jg. 91 (2006) Nr. 5, S. 1761 - 1769
  • Brönner, Günter; Sattler, Alexander M.; Hinney, Anke; Soufi, Muhidien; Geller, Frank; Schäfer, Helmut; Maisch, Bernhard; Hebebrand, Johannes; Schaefer, Juergen R.
    Rapid communication : The 103I variant of the melanocortin 4 receptor is associated with low serum triglyceride levels
    In: The Journal of Clinical Endocrinology & Metabolism (JCEM) Jg. 91 (2006) Nr. 2, S. 535 - 538
  • Wang, C.L.; Liang, L.; Wang, H.J.; Fu, J. Fen; Hebebrand, Johannes; Hinney, Anke
    Several mutations in the melanocortin 4 receptor gene are associated with obesity in Chinese children and adolescents
    In: Journal of Endocrinological Investigation Jg. 29 (2006) Nr. 10, S. 894 - 898
  • Mössner, Rainald; Walitza, Susanne; Geller, Frank; Scherag, Andre; Gutknecht, Lise; Jacob, Christian; Bogusch, Lisa; Remschmidt, Helmut; Simons, Michael; Herpertz-Dahlmann, Beate; Fleischhaker, Christian; Schulz, Eberhard; Warnke, Andreas; Hinney, Anke; Wewetzer, Christoph; Lesch, Klaus-Peter
    Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder
    In: The International Journal of Neuropsychopharmacology Jg. 9 (2006) Nr. 4, S. 437 - 442
  • Ribasés, Marta; Gratacòs, Mònica; Fernández-Aranda, Fernando; Bellodi, Laura; Boni, Claudette; Anderluh, Marija; Cavallini, Maria Cristina; Cellini, Elena; Di Bella, Daniela; Erzegovesi, Stefano; Foulon, Christine; Gabrovsek, Mojca; Gorwood, Philip; Hebebrand, Johannes; Hinney, Anke; Holliday, Jo; Hu, Xun; Karwautz, Andreas; Kipman, Amélie; Komel, Radovan; Nacmias, Benedetta; Remschmidt, Helmut; Ricca, Valdo; Sorbi, Sandro; Tomori, Martina; Wagner, Gudrun; Treasure, Janet; Collier, David A.; Estivill, Xavier
    Association of BDNF with restricting anorexia nervosa and minimum body mass index : A family-based association study of eight European populations
    In: European Journal of Human Genetics Jg. 13 (2005) Nr. 4, S. 428 - 434
  • Heid, I.M.; Vollmert, C.; Hinney, Anke; Döring, A.; Geller, F.; Löwel, H.; Wichmann, H-E; Illig, T.; Hebebrand, Johannes; Kronenberg, F.
    Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys
    In: Journal of medical genetics Jg. 42 (2005) Nr. 4, S. e21
  • Mössner, Rainald; Walitza, Susanne; Lesch, Klaus-Peter; Geller, Frank; Barth, Nikolaus; Remschmidt, Helmut; Hahn, Freya; Herpertz-Dahlmann, Beate; Fleischhaker, Christian; Schulz, Eberhard; Warnke, Andreas; Hinney, Anke; Wewetzer, Christoph
    Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessive-compulsive disorder
    In: The International Journal of Neuropsychopharmacology Jg. 8 (2005) Nr. 1, S. 133 - 136
  • Schäuble, Nadine; Reichwald, Kathrin; Grassl, Wolfgang; Bechstein, Helen; Müller, Hans-Christian; Scherag, Andre; Geller, Frank; Utting, Michael; Siegfried, Wolfgang; Goldschmidt, Hanspeter; Blundell, John; Lawton, Clare; Alam, Rahul; Whybrow, Stephen; Stubbs, James; Platzer, Matthias; Hebebrand, Johannes; Hinney, Anke
    Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity
    In: Journal of Nutrition Jg. 135 (2005) Nr. 6, S. 1387 - 1392
  • Swarbrick, Michael M.; Waldenmaier, Björn; Pennacchio, Len A.; Lind, Denise L.; Cavazos, Martha M.; Geller, Frank; Merriman, Raphael; Ustaszewska, Anna; Malloy, Mary; Scherag, André; Hsueh, Wen-Chi; Rief, Winfried; Mauvais-Jarvis, Franck; Pullinger, Clive R.; Kane, John P.; Dent, Robert; McPherson, Ruth; Kwok, Pui-Yan; Hinney, Anke; Hebebrand, Johannes; Vaisse, Christian
    Lack of support for the association between GAD2 polymorphisms and severe human obesity
    In: PLoS Biology Jg. 3 (2005) Nr. 9, e315
  • Wermter, Anne-Kathrin; Reichwald, Kathrin; Büch, Thomas; Geller, Frank; Platzer, Cornelia; Huse, Klaus; Hess, Claudia; Remschmidt, Helmut; Gudermann, Thomas; Preibisch, Gerald; Siegfried, Wolfgang; Goldschmidt, Hans-Peter; Li, Wei-Dong; Price, R. Arlen; Biebermann, Heike; Krude, Heiko; Vollmert, Caren; Wichmann, H.-Erich; Illig, Thomas; Sørensen, Thorkild I.A.; Astrup, Arne; Larsen, Lesli Hingstrup; Pedersen, Oluf; Eberlé, Delphine; Clément, Karine; Blundell, John; Wabitsch, Martin; Schäfer, Helmut; Platzer, Matthias; Hinney, Anke; Hebebrand, Johannes
    Mutation analysis of the MCHR1 gene in human obesity
    In: European Journal of Endocrinology Jg. 152 (2005) Nr. 6, S. 851 - 862
  • Friedel, S.; Horro, F. Fontenla; Wermter, A.K.; Geller, F.; Dempfle, A.; Reichwald, K.; Smidt, J.; Brönner, G.; Konrad, K.; Herpertz-Dahlmann, B.; Warnke, A.; Hemminger, U.; Linder, M.; Kiefl, H.; Goldschmidt, H.P.; Siegfried, W.; Remschmldt, H.; Hinney, Anke; Hebebrand, Johannes
    Mutation screen of the brain derived neurotrophic factor gene (BDNF) : Identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder
    In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 132B (2005) Nr. 1, S. 96 - 99
  • Zakel, U.A.; Wudy, S.A.; Heinzel-Gutenbrunner, M.; Görg, T.; Schäfer, H.; Gortner, L.; Blum, W.F.; Hebebrand, Johannes; Hinney, Anke
    Prävalenz von Melanocortin-4-Rezeptor(MC4R)-Mutationen und Polymorphismen bei adipösen Kindern und Jugendlichen in einer konsekutiven pädiatrischen Inanspruchnahmepopulation
    In: Klinische Pädiatrie Jg. 217 (2005) Nr. 4, S. 244 - 249
  • Hebebrand, Johannes; Wermter, A.-K.; Hinney, Anke
    Adipositas : Genetik und Gen-Umwelt-Interaktionen
    In: Monatsschrift Kinderheilkunde Jg. 152 (2004) Nr. 8, S. 870 - 878
  • Ribasés, Marta; Gratacòs, Mònica; Fernández-Aranda, Fernando; Bellodi, Laura; Boni, Claudette; Anderluh, Marija; Cavallini, Maria Cristina; Cellini, Elena; Di Bella, Daniela; Erzegovesi, Stefano; Foulon, Christine; Gabrovsek, Mojca; Gorwood, Philip; Hebebrand, Johannes; Hinney, Anke; Holliday, Jo; Hu, Xun; Karwautz, Andreas; Kipman, Amélie; Komel, Radovan; Nacmias, Benedetta; Remschmidt, Helmut; Ricca, Valdo; Sorbi, Sandro; Wagner, Gudrun; Treasure, Janet; Collier, David A.; Estivill, Xavier
    Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations
    In: Human Molecular Genetics Jg. 13 (2004) Nr. 12, S. 1205 - 1212
  • Hebebrand, Johannes; Geller, F.; Dempfle, A.; Heinzel-Gutenbrunner, M.; Raab, M.; Gerber, G.; Wermter, A.-K.; Horro, F.F.; Blundell, J.; Schäfer, H.; Remschmidt, H.; Herpertz, S.; Hinney, Anke
    Binge-eating episodes are not characteristic of carriers of melanocortin-4 receptor gene mutations
    In: Molecular Psychiatry Jg. 9 (2004) Nr. 8, S. 796 - 800
  • Gabrovsek, M.; Brecelj-Anderluh, M.; Bellodi, L.; Cellini, E.; Di Bella, D.; Estivill, X.; Fernandez-Aranda, F.; Freeman, B.; Geller, F.; Gratacos, M.; Haigh, R.; Hebebrand, Johannes; Hinney, Anke; Holliday, J.; Hu, X.; Karwautz, A.; Nacmias, B.; Ribases, M.; Remschmidt, H.; Komel, R.; Sorbi, S.; Tomori, M.; Treasure, J.; Wagner, G.; Zhao, J.; Collier, D.A.
    Combined Family Trio and Case-Control Analysis of the COMT Val158Met Polymorphism in European Patients with Anorexia Nervosa
    In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 124 B (2004) Nr. 1, S. 68 - 72
  • Hinney, Anke; Friedel, Susann; Remschmidt, Helmut; Hebebrand, Johannes
    Genetic risk factors in eating disorders
    In: American Journal of PharmacoGenomics Jg. 4 (2004) Nr. 4, S. 209 - 223
  • Wang, Hai-Jun; Geller, Frank; Dempfle, Astrid; Schäuble, Nadine; Friedel, Susann; Lichtner, Peter; Fontenla-Horro, Francisco; Wudy, Stefan; Hagemann, Sandra; Gortner, Ludwig; Huse, Klaus; Remschmidt, Helmut; Bettecken, Thomas; Meitinger, Thomas; Schäfer, Helmut; Hebebrand, Johannes; Hinney, Anke
    Ghrelin Receptor Gene : Identification of Several Sequence Variants in Extremely Obese Children and Adolescents, Healthy Normal-Weight and Underweight Students, and Children with Short Normal Stature
    In: The Journal of Clinical Endocrinology & Metabolism (JCEM) Jg. 89 (2004) Nr. 1, S. 157 - 162
  • Dempfle, A.; Hinney, Anke; Heinzel-Gutenbrunner, M.; Raab, M.; Geller, F.; Gudermann, T.; Schäfer, H.; Hebebrand, Johannes
    Large quantitative effect of melanocortin-4 receptor gene mutations on body mass index
    In: Journal of Medical Genetics (eJMG) Jg. 41 (2004) Nr. 10, S. 795 - 800
  • Geller, Frank; Reichwald, Kathrin; Dempfle, Astrid; Illig, Thomas; Vollmert, Caren; Herpertz, Stephan; Siffert, Winfried; Platzer, Matthias; Hess, Claudia; Gudermann, Thomas; Biebermann, Heike; Wichmann, H.-Erich; Schäfer, Helmut; Hinney, Anke; Hebebrand, Johannes
    Melanocortin-4 Receptor Gene Variant I103 Is Negatively Associated with Obesity
    In: American Journal of Human Genetics Jg. 74 (2004) Nr. 3, S. 572 - 581
  • Walitza, S.; Wewetzer, C.; Gerlach, M.; Klampfl, K.; Geller, F.; Barth, Nikolaus; Hahn, E.; Herpertz-Dahlmann, B.; Gössler, M.; Fleischhaker, C.; Schulz, E.; Hebebrand, Johannes; Warnke, A.; Hinney, Anke
    Transmission disequilibrium studies in children and adolescents with obsessive-compulsive disorders pertaining to polymorphisms of genes of the serotonergic pathway
    In: Journal of Neural Transmission Jg. 111 (2004) Nr. 7, S. 817 - 825
  • Tafel, J.; Branscheid, I.; Skwarna, B.; Schlimme, M.; Morcos, M.; Algenstaedt, P.; Hinney, Anke; Hebebrand, Johannes; Nawroth, P.; Hamann, Andreas
    Variants in the human β₁-, β₂- and β ₃-adrenergic receptor genes are not associated with morbid obesity in children and adolescents
    In: Diabetes, Obesity and Metabolism Jg. 6 (2004) Nr. 6, S. 452 - 455
  • Vorworte / Nachworte

  • Hinney, Anke; Seitz, Jochen
    Genetik in der Kinder- und Jugendpsychiatrie
    In: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 50 (2022) Nr. 3, S. 171 - 173
  • Hinney, Anke; Hebebrand, Johannes
    Three at one swoop!
    In: Obesity Facts Jg. 2 (2009) Nr. 1, S. 3 - 6
  • Abstracts

  • Hirtz, Raphael; Grasemann, Corinna; Dinkelbach, Lars; Hinney, Anke; Hebebrand, Johannes; Peters, Triinu
    No Relationship Between Thyroid Function and ADHD : Results From a Nationwide Prospective Epidemiological Study and Mendelian Randomization
    In: Hormone Research in Paediatrics Jg. 96 (2023) Nr. Suppl. 4, S. 121 - 122
  • Hirtz, Raphael; Hars, Christine; Naaresh, Roaa; Laabs, Bjoern Hergen; Antel, Jochen; Grasemann, Corinna; Hinney, Anke; Hebebrand, Johannes; Peters, Triinu
    Causal Effect of Age at Menarche on the Risk for Depression: Results from a Two-Sample Multivariable Mendelian Randomization Study
    In: Hormone Research in Paediatrics Jg. 95 (2022) Nr. Suppl. 2, S. 346 - 346
  • Hirtz, R.; Libuda, Lars; Hinney, Anke; Föcker, Manuel; Buhlmeier, Judith; Antel, Jochen; Holterhus, Paul-Martin; Kulle, Alexandra; Kiewert, Cordula; Hebebrand, Johannes; Grasemann, Corinna
    Size Matters: CAG Repeat Length of the Androgen Receptor Gene, Testosterone, and Male Adolescent Depression Severity
    In: Hormone Research in Paediatrics Jg. 94 (2021) Nr. Suppl. 1, S. 364
  • Hinney, Anke; Volckmar, A.; Kesselmeier, M.; Antel, Jochen; Heid, I. M.; Herpertz-Dahlmann, B.; Bulik, C.; Collier, D.; Scherag, Andre; Hebebrand, Johannes;
    Genetic variation at three genetic loci involved in anorexia nervosa are associated with body weight regulation
    16th International Congress of ESCAP European Society for Child and Adolescent Psychiatry 20–24 June 2015, Madrid, Spain,
    In: European Child and Adolescent Psychiatry Jg. 24 (2015) Nr. Suppl. 1, S. 64
  • Hebebrand, Johannes; Herpertz-Dahlmann, B.; Konrad, K.; Falissard, B.; Tchanturia, K.; Hinney, Anke;
    The complexity of eating disorders : insight into recent research venues in molecular genetics, neuropsychology, neuroimaging, and social sciences
    16th International Congress of ESCAP European Society for Child and Adolescent Psychiatry 20–24 June 2015, Madrid, Spain,
    In: European Child and Adolescent Psychiatry Jg. 24 (2015) Nr. Suppl. 1, S. S63 - S64
  • Scherag, Andre; Jarick, I.; Pütter, Carolin; Hinney, Anke; Horsthemke, Bernhard; Jöckel, Karl-Heinz; Hebebrand, Johannes;
    Addressing Genomic Imprinting in a Family-based Genome-wide Association Study
    nineteenth annual meeting of the International Genetic Epidemiology Society,
    In: Genetic Epidemiology Jg. 34 (2010) Nr. 8, S. 943 - 943
  • Müller, Hermann L.; Gebhardt, Ursel; Enriori, Pablo J.; Hinney, Anke; Hebebrand, Johannes; Schroder, Sabine; Kolb, Reinhardt; Reinehr, Thomas; Cowley, Micheal A.; Roth, Christian L.;
    Changes of Peripheral Alpha-Melanocyte-Stimulating Hormone in Childhood Craniopharyngioma
    42nd Congress of the International Society of Pediatric Oncology (SIOP), October 21-24, 2010, Boston, USA,
    In: Pediatric Blood and Cancer Jg. 55 (2010) Nr. 5, S. 791 - 791
  • Rief, Winfried; Hebebrand, Johannes; Hinney, Anke;
    Consultation including Genetic information in People with increades risk for Obesity and MC4R-Mutations
    11th International Congress of Behavioral Medicine,
    In: International Journal of Behavioral Medicine Jg. 17 (2010) Nr. Suppl. 1, S. 118
  • Hinney, Anke; Scherag, Andre; Hebebrand, Johannes
    Genetics of obesity
    In: European Neuropsychopharmacology Jg. 20 (2010) Nr. Suppl. 3, S. S190
  • Pahl, R; Nguyen, TT; Hinney, Anke; Greene, B; Hebebrand, Johannes; Schafer, H
    Bias-Corrected Effect Estimators for Genome-Wide Association Studies
    In: Genetic Epidemiology Jg. 32 (2008) Nr. 7, S. 676
  • Dempfle, A; Wudy, SA; Saar, K; Hagemann, S; Friedel, S; Scherag, Andre; Berthold, LD; Alzen, G; Gortner, L; Hinney, Anke; Hebebrand, Johannes
    Linkage genome scan and subsequent association studies show involvement of the vitamin D receptor gene in idiopathic short stature
    In: Genetic Epidemiology Jg. 31 (2007) Nr. 5, S. 450 - 513
  • Heid, IM; Vollmert, C; Kronenberg, F; Huth, C; Ankerst, D; Luchner, A; Hinney, Anke; Bronner, G; Lowell, H; Wichmann, HE; Doring, A; Hebebrand, Johannes
    The MC4R 1031 allele is associated with features of the metabolic syndrome in the population-based KORA study
    In: Genetic Epidemiology Jg. 31 (2007) Nr. 5, S. 475
  • Rettenbacher, E.; Biebermann, H.; Hinney, Anke; Hebebrand, Johannes; Tarnow, P.; Brumm, H.; Prayer, D.
    A novel missense mutation in the melanocortin-4 receptor gene (MC4R) in an Austrian 2-year-old girl with extreme obesity and an asymmetry of the amygdaloid nuclei
    In: International Journal of Obesity Jg. 29 (2005) Nr. S2, S. S155
  • Beiträge in Sammelwerken und Tagungsbänden

  • Frieling, Helge; Hinney, Anke; Bleich, Stefan
    Genetic aspects of obesity
    In: Handbook of Eating Disorders and Obesity / Herpertz, Stephan; de Zwaan, Martina; Zipfel, Stephan (Hrsg.) 2024, S. 445 - 450
  • Hinney, Anke; Giuranna, Johanna
    Genetics of eating and weight disorders
    In: Eating Disorders and Obesity in Children and Adolescents / Hebebrand, Johannes; Herpertz-Dahlmann, Beate (Hrsg.) 2018, S. 67 - 71
  • Hinney, Anke; Giuranna, Johanna
    Polygenic obesity
    In: Pediatric Obesity: Etiology, Pathogenesis and Treatment / Freemark, Michael S. (Hrsg.) 2018, S. 183 - 202
  • Hinney, Anke; Volckmar, Anna-Lena; Knoll, Nadja
    Melanocortin-4 Receptor in Energy Homeostasis and Obesity Pathogenesis
    In: G Protein-Coupled Receptors in Energy Homeostasis and Obesity Pathogenesis / Tao, Ya-Xiong (Hrsg.) 2013, S. 147 - 191
  • Hinney, Anke; Hebebrand, Johannes
    Association and linkage studies in caucasians
    In: Obesity: Genomics and Postgenomics 2008, S. 255 - 263
  • Bücher/Sammelwerke/Tagungsbände

  • Hinney, Anke
    Genetische Mechanismen der Gewichtsregulation
    Duisburg, Essen (2008) CD