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Prof. Dr. Anke Hinney

Funktionen

  • Direktor, Institut für Geschlechtersensible Medizin

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

  • Fender, Anke C.; Hinney, Anke
    Biomedical research as collateral damage in a new world Order?
    In: International Journal of Cardiology (IJC) Heart & Vasculature , Jg. 57 2025, 101633
    DOI
  • 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 , Jg. 30 2025, Nr. 5, S. 1836 – 1846
    DOI (Open Access)
  • Hinney, Anke; Jochimsen, Maren; Kindler-Röhrborn, Andrea; Lilienfeld-Toal, Marie
    Geschlechtersensible Medizin : Wie die Beachtung von Diversität die Medizin auf vielen Ebenenbesser machen kann
    In: Unikate: Berichte aus Forschung und Lehre 2025, Nr. 62: Offen(er) im Blick : Diversity Management und Diskriminierungskritik an der Universität, S. 66 – 67
    DOI, Online Volltext (Open Access)
  • Beckord, Jil; Birke, Jennifer; Krakowczyk, Julia Barbara; Hesse, Samira; Hinney, Anke; Dörrie, Nora; Schneider, Johanna Sophie; Komlenac, Nikola; Bäuerle, Alexander; Teufel, Martin
    PTSD and CPTSD in the new ICD-11 : A latent profile analysis
    In: Psychiatry Research , Jg. 344 2025, 116350
    DOI (Open Access)
  • Dinkelbach, Lars; Peters, Triinu; Grasemann, Corinna; Hinney, Anke; Hirtz, Raphael
    The causal role of male pubertal timing for the development of externalizing and internalizing traits : results from Mendelian randomization studies
    In: Psychological Medicine , Jg. 55 2025, e101
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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 , Jg. 29 2024, Nr. 12, S. 3900 – 3914
    DOI (Open Access)
  • 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
    DOI
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • Schmidt, Axel; Casadei, Nicolas; Brand, Fabian; Demidov, German; Vojgani, Elaheh; Abolhassani, Ayda; Aldisi, Rana; Butler-Laporte, Guillaume; Alawathurage, T. Madhusankha; Augustin, Max; Bals, Robert; Bellinghausen, Carla; Berger, Marc Moritz; Bitzer, Michael; Bode, Christian; Boos, Jannik; Brenner, Thorsten; Cornely, Oliver A.; Eggermann, Thomas; Erber, Johanna; Feldt, Torsten; Fuchsberger, Christian; Gagneur, Julien; Göpel, Siri; Haack, Tobias; Häberle, Helene; Hanses, Frank; Heggemann, Julia; Hehr, Ute; Hellmuth, Johannes C.; Herr, Christian; Hinney, Anke; Hoffmann, Per; Illig, Thomas; Jensen, Björn-Erik Ole; Keitel, Verena; Kim-Hellmuth, Sarah; Koehler, Philipp; Kurth, Ingo; Lanz, Anna-Lisa; Latz, Eicke; Lehmann, Clara; Luedde, Tom; Maj, Carlo; Mian, Michael; Miller, Abigail; Muenchhoff, Maximilian; Pink, Isabell; Protzer, Ulrike; Rohn, Hana; Rybniker, Jan; Scaggiante, Federica; Schaffeldt, Anna; Scherer, Clemens; Schieck, Maximilian; Schmidt, Susanne V.; Schommers, Philipp; Spinner, Christoph D.; Vehreschild, Maria J.G.T.; Velavan, Thirumalaisamy P.; Volland, Sonja; Wilfling, Sibylle; Winter, Christof; Richards, J. Brent; Heimbach, André; Becker, Kerstin; Ossowski, Stephan; Schultze, Joachim L.; Nürnberg, Peter; Nöthen, Markus M.; Motameny, Susanne; Nothnagel, Michael; Riess, Olaf; Schulte, Eva C.; Ludwig, Kerstin U.
    Systematic assessment of COVID-19 host genetics using whole genome sequencing data
    In: PLoS Pathogens , Jg. 20 2024, Nr. 12, e1012786
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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 , Jg. 57 2024, Nr. 12, S. 2461 – 2468
    DOI (Open Access)
  • 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
    DOI
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • Hirtz, Raphael; Hinney, Anke
    Genetic and epigenetic findings in anorexia nervosa
    In: Medizinische Genetik , Jg. 32 2020, Nr. 1, S. 25 – 29
    DOI (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
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    Assessing Causal links between metabolic traits, inflammation and Schizophrenia : a Univariable and Multivariable Bidirectional Mendelian Randomization Study
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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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    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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    Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with Obesity
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    Genetik und Epigenetik der Adipositas
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  • Liu, Xuanshi; Hinney, Anke; Scholz, Markus; Scherag, Andre; Tönjes, Anke; Stumvoll, Michael; Stadler, Peter F.; Hebebrand, Johannes; Böttcher, Yvonne
    Indications for potential parent-of-origin effects within the FTO gene
    In: PLoS ONE , Jg. 10 2015, Nr. 3, S. e0119206
    DOI (Open Access)
  • Hinney, Anke; Volckmar, Anna-Lena
    Perspektiven der genetischen Forschung bei Essstörungen am Beispiel der Anorexia nervosa
    In: Psychotherapie, Psychosomatik, Medizinische Psychologie (PPmP) , Jg. 65 2015, Nr. 1, S. 8 – 10
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    A genome-wide association study of anorexia nervosa
    In: Molecular Psychiatry , Jg. 19 2014, Nr. 10, S. 1085 – 1094
    DOI (Open Access)
  • Wendt, Laura; Albring, Antje; Benson, Sven; Engler, Harald; Engler, Andrea; Hinney, Anke; Rief, Winfried; Witzke, Oliver; Schedlowski, Manfred
    Catechol-O-Methyltransferase Val158Met Polymorphism Is Associated with Somatosensory Amplification and Nocebo Responses
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  • Reinehr, Thomas; Wolters, Barbara; Roth, Christian L; Hinney, Anke
    FTO Gene : Association to Weight Regain after Lifestyle Intervention in Overweight Children
    In: Hormone Research in Paediatrics , Jg. 81 2014, Nr. 6, S. 391 – 396
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  • Hinney, Anke; Volckmar, Anna-Lena; Antel, Jochen
    Genes and the hypothalamic control of metabolism in humans
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  • Hinney, Anke; Albayrak, Özgür; Antel, Jochen; Volckmar, Anna-Lena; Sims, Rebecca; Chapman, Jade; Harold, Denise; Gerrish, Amy; Heid, Iris M.; Winkler, Thomas W.; Scherag, Andre; Wiltfang, Jens; Williams, Julie; Hebebrand, Johannes
    Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity
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  • Jarick, I.; Volckmar, A.-L.; Pütter, Carolin; Pechlivanis, Sonali; Nguyen. T. T.; Dauvermann, R.; Beck, S.; Albayrak, Özgür; Scherag, S.; Gilsbach, S.; Cichon, S.; Hoffmann, P.; Degenhardt, F.; Nöthen, M. M.; Schreiber, S.; Wichmann, H.-E.; Jöckel, Karl-Heinz; Heinrich, J.; Tiesler, C. M. T.; Faraone, S. V.; Walitza, S.; Sinzig, J.; Freitag, C.; Meyer, J.; Herpertz-Dahlmann, B.; Lehmkuhl, G.; Renner, J.; Warnke, A.; Romanos, M.; Lesch, K.-P.; Reif, A.; Schimmelmann, G.; Hebebrand, Johannes; Scherag, Andre; Hinney, Anke
    Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder
    In: Molecular Psychiatry , Jg. 19 2014, Nr. 1, S. 115 – 121
    DOI (Open Access)
  • Knoll, Nadja; Jarick, Ivonne; Volckmar, Anna-Lena; Klingenspor, Martin; Illig, Thomas; Grallert, Harald; Gieger, Christian; Wichmann, Heinz-Erich; Peters, Annette; Wiegand, Susanna; Biebermann, Heike; Fischer-Posovszky, Pamela; Wabitsch, Martin; Völzke, Henry; Nauck, Matthias; Teumer, Alexander; Rosskopf, Dieter; Rimmbach, Christian; Schreiber, Stefan; Jacobs, Gunnar; Lieb, Wolfgang; Franke, Andre; Hebebrand, Johannes; Hinney, Anke
    Mitochondrial DNA Variants in Obesity
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  • Handke, D.; Kuhnen, P.; Hebebrand, Johannes; Hinney, Anke; Gruters-Kieslich, A.; Krude, H.
    The Origin of the Obesity Associated Pomc DNA Hypermethylation Variant
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    A novel SP1/SP3 dependent intronic enhancer governing transcription of the UCP3 gene in brown adipocytes
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  • Volckmar, Anna Lena; Pütter, Carolin; Song, Jieyun; Graniger, J.; Knoll, Nadja; Wolters, Barbara; Hebebrand, Johannes; Scherag, Andre; Reinehr, Thomas; Hinney, Anke
    Analyses of Non-Synonymous Obesity Risk Alleles in SH2B1 (rs7498665) and APOB48R (rs180743) in Obese Children and Adolescents Undergoing a 1-year Lifestyle Intervention
    In: Experimental and Clinical Endocrinology & Diabetes , Jg. 121 2013, Nr. 6, S. 334 – 337
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  • Roth, Christian L.; Hinney, Anke; Schur, Ellen A.; Elfers, Clinton T.; Reinehr, Thomas
    Association analyses for dopamine receptor gene polymorphisms and weight status in a longitudinal analysis in obese children before and after lifestyle intervention
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  • Schimmelmann, B.G.; Hinney, Anke; Scherag, Andre; Pütter, Carolin; Pechlivanis, Sonali; Cichon, S.; Jöckel, Karl-Heinz; Schreiber, S.; Wichmann, H.E.; Albayrak, Özgür; Dauvermann, M.; Konrad, K.; Wilhelm, C.; Herpertz-Dahlmann, B.; Lehmkuhl, G.; Sinzig, J.; Renner, T.J.; Romanos, M.; Warnke, A.; Lesch, K.P.; Reif, A.; Hebebrand, Johannes
    Bipolar disorder risk alleles in children with ADHD
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  • Albayrak, Özgür; Pütter, Carolin; Volckmar, Anna-Lena; Cichon, Sven; Hoffmann, Per; Nöthen, Markus M.; Jöckel, Karl-Heinz; Schreiber, Stefan; Wichmann, H-Erich; Faraone, Stephen V.; Neale, Benjamin M.; Herpertz-Dahlmann, Beate; Lehmkuhl, Gerd; Sinzig, Judith; Renner, Tobias J.; Romanos, Marcel; Warnke, Andreas; Lesch, Klaus-Peter; Reif, Andreas; Schimmelmann, Benno G.; Scherag, André; Hebebrand, Johannes; Hinney, Anke
    Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder
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    Gene Set of Nuclear-Encoded Mitochondrial Regulators Is Enriched for Common Inherited Variation in Obesity
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  • Hinney, Anke; Volckmar, Anna-Lena
    Genetics of Eating Disorders
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  • Berndt, Sonja; Gustafsson, Stefan; Magi, Reedik; Ganna, Andrea; Wheeler, Eleanor; Feitosa, Mary; Justice, Anne; Monda, Keri; Croteau-Chonka, Damien; Day, Felix; Pechlivanis, Sonali; Hebebrand, Johannes; Pütter, Carolin; Hinney, Anke; Jöckel, Karl-Heinz; Scherag, Andre
    Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
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  • Groen-Blokhuis, M.; Whitehouse, A.; Tiemeier, H.; Pappa, I.; Jugessur, A.; McGue, M.; Hinney, Anke; St Pourcain, B.; Tiesler, C.; Trzaskowski, M.; Bustamante, M.; Middeldorp, C.; Boomsma, D.
    Meta-analysis of genome-wide association studies on ADHD : A dimensional approach
    In: Behavior Genetics , Jg. 43 2013, Nr. 6, S. 520 – 521
  • Hebebrand, Johannes; Hinney, Anke; Knoll, Nadja; Volckmar, Anna-Lena; Scherag, Andre
    Molecular Genetic Aspects of Weight Regulation
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  • Hinney, Anke; Wolters, Barbara; Pütter, Carolin; Grallert, Harald; Illig, Thomas; Hebebrand, Johannes; Reinehr, Thomas
    No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight children
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  • Pott, Wilfried; Albayrak, Özgür; Hinney, Anke; Hebebrand, Johannes; Pauli-Pott, Ursula
    Successful treatment with atomoxetine of an adolescent boy with attention deficit/hyperactivity disorder, extreme obesity, and reduced melanocortin 4 receptor function
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    A genome-wide association meta-analysis identifies new childhood obesity loci
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    Addendum: Genome-wide association study in German patients with attention deficit/hyperactivity disorder
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  • Mueller, HermannL; Enriori, PabloJ; Gebhardt, Ursel; Hinney, Anke; Hebebrandt, Johannes; Reinehr, Thomas; Cowley, Michael; Roth, Christian
    Changes of peripheral alpha LPHA-Melanocortin stimulating hormone (alpha-MSH) in childhood craniopharyngioma patients in comparison with other forms of childhood obesity
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    Common variants at 12q15 and 12q24 are associated with infant head circumference
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    Common variants at 6q22 and 17q21 are associated with intracranial volume
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    Comparison of metabolic profiles of acutely ill and short-term weight recovered patients with anorexia nervosa reveals alterations of 33 out of 163 metabolites
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    DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder
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    Do Common Variants Separate between Obese Melanocortin-4 Receptor Gene Mutation Carriers and Non-Carriers? : The Impact of Cryptic Relatedness
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    Erratum to: Impact of FTO genotypes on BMI and weight in polycystic ovary syndrome : a systematic review and meta-analysis
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    Fat mass and obesity-associated gene (FTO) in eating disorders : Evidence for association of the rs9939609 obesity risk allele with Bulimia nervosa and anorexia nervosa
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    Impact of FTO Genotypes on Weight and Body Mass Index in Polycystic Ovary Syndrome : A Systematic Review and Meta-Analysis
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    Impact of FTO genotypes on BMI and weight in polycystic ovary syndrome : A systematic review and meta-analysis
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    Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants
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    Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-through
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    SDCCAG8 obesity alleles and reduced weight loss after a lifestyle intervention in overweight children and adolescents
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    The fatty acid amide hydrolase (FAAH) gene variant rs324420 AA/AC is not associated with weight loss in a 1-year lifestyle intervention for obese children and adolescents
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    Association of the rs10830963 Polymorphism in MTNR1B with Fasting Glucose Levels in Chinese Children and Adolescents
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    Association study in eating disorders : TPH2 associates with anorexia nervosa and self-induced vomiting
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    Common Variants Near MC4R : Exploring Gender Effects in Overweight and Obese Children and Adolescents Participating in a Lifestyle Intervention
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    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
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    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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    Lack of association of cd36 snps with early onset obesity : A meta-analysis in 9,973 european subjects
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    Relationship between MTNR1B (melatonin receptor 1B gene) polymorphism rs10830963 and glucose levels in overweight children and adolescents
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    Successful methylphenidate treatment of early onset extreme obesity in a child with a melanocortin-4 receptor gene mutation and attention deficit/hyperactivity disorder
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    Where in the Genome Are Significant Single Nucleotide Polymorphisms from Genome-Wide Association Studies Located?
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    Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
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    Association of the MC4R V103I polymorphism with obesity : A chinese case-control study and meta-analysis in 55,195 individuals
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    Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin
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    Child and adolescent psychiatric genetics
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    Chipping away the 'missing heritability': GIANT steps forward in the molecular elucidation of obesity - But still lots to go
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    Eating disorders: the current status of molecular genetic research
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    Estrogen receptor 1 gene (ESR1) is associated with restrictive anorexia nervosa
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    Familiality and molecular genetics of attention networks in ADHD
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    From monogenic to polygenic obesity : Recent advances
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    Genes and lifestyle factors in obesity : Results from 12 462 subjects from MONICA/KORA
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    Genetic findings in anorexia and bulimia nervosa
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    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
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    Genetische Ursachen der Adipositas : Zum Stand der Forschung
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    Investigation of a Genome Wide Association Signal for Obesity : Synthetic Association and Haplotype Analyses at the Melanocortin 4 Receptor Gene Locus
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  • Tan, Susanne; Scherag, Andre; Janßen, Onno Eilard; Hahn, Susanne; Lahner, Harald; Dietz, Tiina; Scherag, Susann; Grallert, Harald; Vogel, Carla I.G.; Kimmig, Rainer; Illig, Thomas; Mann, Klaus; Hebebrand, Johannes; Hinney, Anke
    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)
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  • Müller, Timo D.; Brönner, Günter; Wandolski, Melanie; Carrie, Jophia; Nguyen, Trang T.; Greene, Brandon H.; Scherag, Andre; Grallert, Harald; Vogel, Carla I.G.; Scherag, Susann; Rief, Winfried; Wichmann, Hans-Erich; Illig, Thomas; Schäfer, Helmut; Hebebrand, Johannes; Hinney, Anke
    Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity
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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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  • Conradt, Matthias; Dierk, Jan-Michael; Schlumberger, Pia; Albohn, Christina; Rauh, Elisabeth; Hinney, Anke; Hebebrand, Johannes; Rief, Winfried
    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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  • Le Hellard, S.; Theisen, F.M.; Haberhausen, M.; Raeder, M.B.; Fernø, J.; Gebhardt, S.; Hinney, Anke; Remschmidt, H.; Krieg, J.C.; Mehler-Wex, C.; Nöthen, M.M.; Hebebrand, Johannes; Steen, V.M.
    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?
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  • Gueorguiev, Maria; Lecoeur, Cécile; Meyre, David; Benzinou, Michael; Mein, Charles A.; Hinney, Anke; Vatin, Vincent; Weill, Jacques; Heude, Barbara; Hebebrand, Johannes; Grossman, Ashley B.; Korbonits, Márta; Froguel, Philippe
    Association studies on ghrelin and ghrelin receptor gene polymorphisms with obesity
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  • Hilbert, Anja; Dierk, Jan-Michael; Conradt, Matthias; Schlumberger, Pia; Hinney, Anke; Hebebrand, Johannes; Rief, Winfried
    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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  • von Schimmelmann, Benno; Friedel, S.; Nguyen, T.T.; Sauer, S.; Vogel, C.I. Ganz; Konrad, K.; Wilhelm, C.; Sinzig, J.; Renner, T.J.; Romanos, M.; Palmason, H.; Dempfle, A.; Walitza, S.; Freitag, C.; Meyer, J.; Linder, M.; Schäfer, H.; Warnke, A.; Lesch, K.P.; Herpertz-Dahlman, B.; Hinney, Anke; Hebebrand, Johannes
    Exploring the genetic link between RLS and ADHD
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  • Hammer, Christian; Kapeller, Johannes; Endele, Max; Fischer, Christine; Hebebrand, Johannes; Hinney, Anke; Friedel, Susann; Gratacòs, Mònica; Estivill, Xavier; Fichter, Manfred; Fernández-Aranda, Fernando; Ehrlich, Stefan; Rappold, Gudrun; Niesler, Beate
    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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  • Hughes, David A.; Hinney, Anke; Brumm, Harald; Wermter, Anne-Kathrin; Biebermann, Heike; Hebebrand, Johannes; Stoneking, Mark
    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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  • Wermter, Anne-Kathrin; Scherag, Andre; Hölter, Katja; Reichwald, Kathrin; Lichtner, Peter; Siegfried, Wolfgang; Blundell, John; Lawton, Clare; Whybrow, Stephen; Stubbs, James; Arch, Jonathan R.; Meitinger, Thomas; Platzer, Matthias; Hinney, Anke; Hebebrand, Johannes
    Procolipase gene : no association with early-onset obesity or fat intake
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  • Pauli-Pott, Ursula; Friedl, Susann; Hinney, Anke; Hebebrand, Johannes
    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
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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
    In: Nature Genetics , Jg. 39 2007, Nr. 2, S. 218 – 225
    DOI
  • Herbert, Alan; Gerry, Norman P.; McQueen, Matthew B.; Heid, Iris M.; Pfeufer, Arne; Illig, Thomas; Wichmann, H.-Erich; Meitinger, Thomas; Hunter, David; Hu, Frank B.; Colditz, Graham; Hinney, Anke; Hebebrand, Johannes; Koberwitz, Kerstin; Zhu, Xiaofeng; Cooper, Richard; Ardlie, Kristin; Lyon, Helen; Hirschhorn, Joel N.; Laird, Nan M.; Lenburg, Marc E.; Lange, Christoph; Christman, Michael F.
    Response to Comments on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity"
    In: Science , Jg. 315 2007, Nr. 5809, S. 187e
    DOI
  • Brumm, H; Bolze, F; Friedel, S; Hinney, Anke; Klingenspor, M; Hebebrand, Johannes; Grüters, A; Biebermann, H
    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
    DOI
  • Young, E.H.; Wareham, N.J.; Farooqi, S.; Hinney, Anke; Hebebrand, Johannes; Scherag, Andre; O'Rahilly, S.; Barroso, I.; Sandhu, M.S.
    The V103I polymorphism of the MC4R gene and obesity: Population based studies and meta-analysis of 29 563 individuals
    In: International Journal of Obesity , Jg. 31 2007, Nr. 9, S. 1437 – 1441
    DOI (Open Access)
  • Lyon, Helen N.; Emilsson, Valur; Hinney, Anke; Heid, Iris M.; Lasky-Su, Jessica; Zhu, Xiaofeng; Thorleifsson, Gudmar; Gunnarsdottir, Steinunn; Walters, G. Bragi; Thorsteinsdottir, Unnur; Kong, Augustine; Gulcher, Jeffrey; Nguyen, Thuy Trang; Scherag, Andre; Pfeufer, Arne; Meitinger, Thomas; Brönner, Günter; Rief, Winfried; Soto-Quiros, Manuel E.; Avila, Lydiana; Klanderman, Barbara; Raby, Benjamin A.; Silverman, Edwin K.; Weiss, Scott T.; Laird, Nan; Ding, Xiao; Groop, Leif; Tuomi, Tiinamaija; Isomaa, Bo; Bengtsson, Kristina; Butler, Johannah L.; Cooper, Richard S.; Fox, Caroline S.; O'Donnell, Christopher J.; Vollmert, Caren; Celedón, Juan C.; Wichmann, H. Erich; Hebebrand, Johannes; Stefansson, Kari; Lange, Christoph; Hirschhorn, Joel N.
    The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts
    In: PLoS Genetics , Jg. 3 2007, Nr. 4, S. 0627 – 0633
    DOI (Open Access)
  • Herbert, Alan; Gerry, Norman P.; McQueen, Matthew B.; Heid, Iris M.; Pfeufer, Arne; Illig, Thomas; Wichmann, H.-Erich; Meitinger, Thomas; Hunter, David; Hu, Frank B.; Colditz, Graham; Hinney, Anke; Hebebrand, Johannes; Koberwitz, Kerstin; Zhu, Xiaofeng; Cooper, Richard; Ardlie, Kristin; Lyon, Helen; Hirschhorn, Joel N.; Laird, Nan M.; Lenburg, Marc E.; Lange, Christoph; Christman, Michael F.
    A common genetic variant is associated with adult and childhood obesity
    In: Science , Jg. 312 2006, Nr. 5771, S. 279 – 283
    DOI
  • Hebebrand, Johannes; Dempfle, A.; Saar, K.; Thiele, H.; Herpertz-Dahlmann, B.; Linder, M.; Kiefl, H.; Remschmidt, H.; Hemminger, U.; Warnke, A.; Knölker, U.; Heiser, P.; Friedel, S.; Hinney, Anke; Schäfer, H.; Nürnberg, P.; Konrad, K.
    A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs
    In: Molecular Psychiatry , Jg. 11 2006, Nr. 2, S. 196 – 205
    DOI (Open Access)
  • Biebermann, Heike; Castañeda, Tamara R.; van Landeghem, Frank; von Deimling, Andreas; Escher, Frederike; Brabant, Georg; Hebebrand, Johannes; Hinney, Anke; Tschöp, Matthias H.; Grüters, Annette; Krude, Heiko
    A role for β-melanocyte-stimulating hormone in human body-weight regulation
    In: Cell Metabolism , Jg. 3 2006, Nr. 2, S. 141 – 146
    DOI (Open Access)
  • Meidtner, K.; Wermter, A.-K.; Hinney, Anke; Remschmidt, H.; Hebebrand, Johannes; Fries, R.
    Association of the melanocortin 4 receptor with feed intake and daily gain in F2 Mangalitsa x Piétrain pigs
    In: Animal Genetics , Jg. 37 2006, Nr. 3, S. 245 – 247
    DOI
  • Cellini, Elena; Nacmias, Benedetta; Brecelj-Anderluh, Maria; Badía-Casanovas, Ana; Bellodi, Laura; Boni, Claudette; Di Bella, Daniela; Estivill, Xavier; Fernandez-Aranda, Fernando; Foulon, Christine; Friedel, Susan; Gabrovsek, Mojca; Gorwood, Philip; Gratacos, Monica; Guelfi, Julien; Hebebrand, Johannes; Hinney, Anke; Holliday, Jo; Hu, Xun; Karwautz, Andreas; Kipman, Amelie; Komel, Radovan; Rotella, Carlo Maria; Ribases, Marta; Ricca, Valdo; Romo, Lucia; Tomori, Martina; Treasure, Janet; Wagner, Gudrun; Collier, David A.; Sorbi, Sandro
    Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa
    In: Psychiatric Genetics , Jg. 16 2006, Nr. 2, S. 51 – 52
    DOI
  • Dempfle, Astrid; Wudy, Stefan A.; Saar, Kathrin; Hagemann, Sandra; Friedel, Susann; Scherag, Andre; Berthold, Lars D.; Alzen, Gerhard; Gortner, Ludwig; Blum, Werner F.; Hinney, Anke; Nürnberg, Peter; Schäfer, Helmut; Hebebrand, Johannes
    Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies
    In: Human Molecular Genetics , Jg. 15 2006, Nr. 18, S. 2772 – 2783
    DOI
  • Dierk, Jan-Michael; Conradt, Matthias; Schlumberger, Pia; Rauh, Elisabeth; Albohn, Christina; Hinney, Anke; Hebebrand, Johannes; Rief, Winfried
    Genetische Aspekte in der Adipositas-Beratung – Auswirkungen auf Körperakzeptanz und subjektives Wohlbefinden
    In: Verhaltenstherapie: Praxis, Forschung, Perspektiven , Jg. 16 2006, Nr. 3, S. 193 – 200
    DOI
  • von Schimmelmann, Benno; Friedel, Susann; Christiansen, Hanna; Dempfle, Astrid; Hinney, Anke; Hebebrand, Johannes
    Genetische Befunde bei der Aufmerksamkeitsdefizit- und Hyperaktivitätsstörung (ADHS)
    In: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie , Jg. 34 2006, Nr. 6, S. 425 – 433
    DOI
  • Marti, Amelia; Ochoa, M. Carmen; Sánchez-Villegas, Almudena; Martínez, J. Alfredo; Martínez-González, Miguel Angel; Hebebrand, Johannes; Hinney, Anke; Vedder, Helmut
    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
    DOI (Open Access)
  • Hinney, Anke; Bettecken, Thomas; Tarnow, Patrick; Brumm, Harald; Reichwald, Kathrin; Lichtner, Peter; Scherag, Andre; Nguyen, Thuy Trang; Schlumberger, Pia; Rief, Winfried; Vollmert, Caren; Illig, Thomas; Wichmann, H.-Erich; Schäfer, Helmut; Platzer, Matthias; Biebermann, Heike; Meitinger, Thomas; Hebebrand, Johannes
    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
    DOI (Open Access)
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI
  • 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
    DOI
  • Hebebrand, Johannes; Wermter, A.-K.; Hinney, Anke
    Adipositas : Genetik und Gen-Umwelt-Interaktionen
    In: Monatsschrift Kinderheilkunde , Jg. 152 2004, Nr. 8, S. 870 – 878
    DOI
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI
  • 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
    DOI

    • 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
    DOI
  • Hinney, Anke; Hebebrand, Johannes
    Three at one swoop!
    In: Obesity Facts , Jg. 2 2009, Nr. 1, S. 3 – 6
    DOI (Open Access)

    • Interviews

  • Hinney, Anke; Kindler-Röhrborn, Andrea (Interviewpartner); Beaufays, Sandra (Interviewer)
    Gendermedizin als Emerging Field: Institutsgründung an der Universität Duisburg-Essen
    In: blog interdisziplinäre geschlechterforschung / Kortendiek, Beate / Koordinations- und Forschungsstelle Netzwerk Frauen- und Geschlechterforschung NRW (Hrsg.) 2024
    DOI, Online Volltext (Open Access)

    • Abstracts

  • Leven, A. S.; Peters, T.; Rajcsanyi, L.S.; Tasdogan, Alpaslan; Placke, Jan-Malte; Lodde, Georg; Zimmer, Lisa; Livingstone, Elisabeth; Schadendorf, Dirk; Rösch, Alexander; Hinney, Anke; Ugurel, Selma
    Analysis of gender-specific Differences in Response to First-line Treatment with Immunotherapy or targeted Therapy in Melanoma Patients with metastatic Stage IV Melanoma : An ADO/DeCOG Study of 2032 Patients from the prospective, multicenter Skin Cancer Registry ADOREG
    In: Journal der Deutschen Dermatologischen Gesellschaft (JDDG) , Jg. 22 2024, Nr. Suppl. 4, S. 16 – 17
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • Hinney, Anke; Scherag, Andre; Hebebrand, Johannes
    Genetics of obesity
    In: European Neuropsychopharmacology , Jg. 20 2010, Nr. Suppl. 3, S. S190
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI

    • 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
    DOI
  • 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
    DOI
  • Hinney, Anke; Giuranna, Johanna
    Polygenic obesity
    In: Pediatric Obesity: Etiology, Pathogenesis and Treatment / Freemark, Michael S. (Hrsg.) 2018, S. 183 – 202
    DOI
  • 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
    DOI
  • 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

    • Poster / Posterbeiträge

  • Rajcsanyi, Luisa; Düerkop, Sieglinde; Zheng, Yiran; Seitz, Jochen; Antel, Jochen; Hebebrand, Johannes; Hinney, Anke; et al.
    Analysis of the leptin gene in patients with anorexia nervosa
    57th European Society of Human Genetics (ESHG) Conference, June 1-4, 2024, Berlin, Germany,
    In: European Journal of Human Genetics , Jg. 32 2024, Nr. Suppl. 2, S. 1505 – 1506
    (Open Access)
  • Peters, Triinu; Hirtz, Raphael; Hinney, Anke; Antel, Jochen; Grasemann, Corinna; Hölling, Heike; von Holt, Björn-Hergen; Hebebrand, Johannes; Albers, Nicola; Hars, Christine
    Causal Effect of puberty time on the Risk for Depression in females, but not in males : Results From a Two Sample Multivariable Mendelian Randomization Study
    57th Annual European Human Genetics Conference, June 1-4, 2024, Berlin, Germany,
    In: European Journal of Human Genetics , Jg. 32 2024, Nr. Suppl. 2, S. 1701
    (Open Access)