Skip to main content

Publications

featured publications

  • Polygenic risk scores across the extended psychosis spectrum.

    Translational psychiatry

    Authors: Lukasz Smigielski, Sergi Papiol, Anastasia Theodoridou, Karsten Heekeren, Miriam Gerstenberg, Diana Wotruba, Roman Buechler, Per Hoffmann, Stefan Herms, Kristina Adorjan, Heike Anderson-Schmidt, Monika Budde, Ashley L Comes, Katrin Gade, Maria Heilbronner, Urs Heilbronner, Janos L Kalman, Farahnaz Klöhn-Saghatolislam, Daniela Reich-Erkelenz, Sabrina K Schaupp, Eva C Schulte, Fanny Senner, Ion-George Anghelescu, Volker Arolt, Bernhard T Baune, Udo Dannlowski, Detlef E Dietrich, Andreas J Fallgatter, Christian Figge, Markus Jäger, Georg Juckel, Carsten Konrad, Vanessa Nieratschker, Jens Reimer, Eva Reininghaus, Max Schmauß, Carsten Spitzer, Martin von Hagen, Jens Wiltfang, Jörg Zimmermann, Anna Gryaznova, Laura Flatau-Nagel, Markus Reitt, Milena Meyers, Barbara Emons, Ida Sybille Haußleiter, Fabian U Lang, Thomas Becker, Moritz E Wigand, Stephanie H Witt, Franziska Degenhardt, Andreas J Forstner, Marcella Rietschel, Markus M Nöthen, Till F M Andlauer, Wulf Rössler, Susanne Walitza, Peter Falkai, Thomas G Schulze, Edna Grünblatt

  • Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history.

    Genetics in medicine : official journal of the American College of Medical Genetics

    Authors: Emadeldin Hassanin, Patrick May, Rana Aldisi, Isabel Spier, Andreas J Forstner, Markus M Nöthen, Stefan Aretz, Peter Krawitz, Dheeraj Reddy Bobbili, Carlo Maj

  • Association of Attention-Deficit/Hyperactivity Disorder and Depression Polygenic Scores with Lithium Response: A Consortium for Lithium Genetics Study.

    Complex psychiatry

    Authors: Brandon J Coombes, Vincent Millischer, Anthony Batzler, Beth Larrabee, Liping Hou, Sergi Papiol, Urs Heilbronner, Mazda Adli, Kazufumi Akiyama, Nirmala Akula, Azmeraw T Amare, Raffaella Ardau, Barbara Arias, Jean-Michel Aubry, Lena Backlund, Michael Bauer, Bernhard T Baune, Frank Bellivier, Antoni Benabarre, Susanne Bengesser, Abesh Kumar Bhattacharjee, Pablo Cervantes, Hsi-Chung Chen, Caterina Chillotti, Sven Cichon, Scott R Clark, Francesc Colom, Cristiana Cruceanu, Piotr M Czerski, Nina Dalkner, Franziska Degenhardt, Maria Del Zompo, J Raymond DePaulo, Bruno Étain, Peter Falkai, Ewa Ferensztajn-Rochowiak, Andreas J Forstner, Louise Frisen, Sébastien Gard, Julie S Garnham, Fernando S Goes, Maria Grigoroiu-Serbanescu, Paul Grof, Ryota Hashimoto, Joanna Hauser, Stefan Herms, Per Hoffmann, Stephane Jamain, Esther Jiménez, Jean-Pierre Kahn, Layla Kassem, Tadafumi Kato, John R Kelsoe, Sarah Kittel-Schneider, Barbara König, Po-Hsiu Kuo, Ichiro Kusumi, Gonzalo Laje, Mikael Landén, Catharina Lavebratt, Marion Leboyer, Susan G Leckband, Mario Maj, Mirko Manchia, Lina Martinsson, Michael J McCarthy, Susan L McElroy, Philip B Mitchell, Marina Mitjans, Francis M Mondimore, Palmiero Monteleone, Caroline M Nievergelt, Markus M Nöthen, Tomas Novák, Claire O'Donovan, Urban Osby, Norio Ozaki, Andrea Pfennig, Claudia Pisanu, James B Potash, Andreas Reif, Eva Reininghaus, Marcella Rietschel, Guy A Rouleau, Janusz K Rybakowski, Martin Schalling, Peter R Schofield, Klaus Oliver Schubert, Barbara W Schweizer, Giovanni Severino, Tatyana Shekhtman, Paul D Shilling, Katzutaka Shimoda, Christian Simhandl, Claire M Slaney, Alessio Squassina, Thomas Stamm, Pavla Stopkova, Alfonso Tortorella, Gustavo Turecki, Eduard Vieta, Stephanie H Witt, Peter P Zandi, Janice M Fullerton, Martin Alda, Mark A Frye, Thomas G Schulze, Francis J McMahon, Joanna M Biernacka

  • Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.

    Nature communications

    Authors: Sarah Grosche, Ingo Marenholz, Jorge Esparza-Gordillo, Aleix Arnau-Soler, Erola Pairo-Castineira, Franz Rüschendorf, Tarunveer S Ahluwalia, Catarina Almqvist, Andreas Arnold, Hansjörg Baurecht, Hans Bisgaard, Klaus Bønnelykke, Sara J Brown, Mariona Bustamante, John A Curtin, Adnan Custovic, Shyamali C Dharmage, Ana Esplugues, Mario Falchi, Dietmar Fernandez-Orth, Manuel A R Ferreira, Andre Franke, Sascha Gerdes, Christian Gieger, Hakon Hakonarson, Patrick G Holt, Georg Homuth, Norbert Hubner, Pirro G Hysi, Marjo-Riitta Jarvelin, Robert Karlsson, Gerard H Koppelman, Susanne Lau, Manuel Lutz, Patrik K E Magnusson, Guy B Marks, Martina Müller-Nurasyid, Markus M Nöthen, Lavinia Paternoster, Craig E Pennell, Annette Peters, Konrad Rawlik, Colin F Robertson, Elke Rodriguez, Sylvain Sebert, Angela Simpson, Patrick M A Sleiman, Marie Standl, Dora Stölzl, Konstantin Strauch, Agnieszka Szwajda, Albert Tenesa, Philip J Thompson, Vilhelmina Ullemar, Alessia Visconti, Judith M Vonk, Carol A Wang, Stephan Weidinger, Matthias Wielscher, Catherine L Worth, Chen-Jian Xu, Young-Ae Lee

  • Genome-wide interaction study with major depression identifies novel variants associated with cognitive function.

    Molecular psychiatry

    Authors: Anbupalam Thalamuthu, Natalie T Mills, Klaus Berger, Heike Minnerup, Dominik Grotegerd, Udo Dannlowski, Susanne Meinert, Nils Opel, Jonathan Repple, Marius Gruber, Igor Nenadić, Frederike Stein, Katharina Brosch, Tina Meller, Julia-Katharina Pfarr, Andreas J Forstner, Per Hoffmann, Markus M Nöthen, Stephanie Witt, Marcella Rietschel, Tilo Kircher, Mark Adams, Andrew M McIntosh, David J Porteous, Ian J Deary, Caroline Hayward, Archie Campbell, Hans Jörgen Grabe, Alexander Teumer, Georg Homuth, Sandra van der Auwera-Palitschka, K Oliver Schubert, Bernhard T Baune

  • Epigenome-wide association study of alcohol use disorder in five brain regions.

    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology

    Authors: Lea Zillich, Josef Frank, Fabian Streit, Marion M Friske, Jerome C Foo, Lea Sirignano, Stefanie Heilmann-Heimbach, Helene Dukal, Franziska Degenhardt, Per Hoffmann, Anita C Hansson, Markus M Nöthen, Marcella Rietschel, Rainer Spanagel, Stephanie H Witt

  • Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients.

    BMC medical genomics

    Authors: Maria Heinrich, Miriam Sieg, Jochen Kruppa, Peter Nürnberg, Peter H Schreier, Stefanie Heilmann-Heimbach, Per Hoffmann, Markus M Nöthen, Jürgen Janke, Tobias Pischon, Arjen J C Slooter, Georg Winterer, Claudia D Spies

  • Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection.

    BJPsych open

    Authors: Urs Heilbronner, Fabian Streit, Thomas Vogl, Fanny Senner, Sabrina K Schaupp, Daniela Reich-Erkelenz, Sergi Papiol, Mojtaba Oraki Kohshour, Farahnaz Klöhn-Saghatolislam, Janos L Kalman, Maria Heilbronner, Katrin Gade, Ashley L Comes, Monika Budde, Till F M Andlauer, Heike Anderson-Schmidt, Kristina Adorjan, Til Stürmer, Adrian Loerbroks, Manfred Amelang, Eric Poisel, Jerome Foo, Stefanie Heilmann-Heimbach, Andreas J Forstner, Franziska Degenhardt, Jörg Zimmermann, Jens Wiltfang, Martin von Hagen, Carsten Spitzer, Max Schmauss, Eva Reininghaus, Jens Reimer, Carsten Konrad, Georg Juckel, Fabian U Lang, Markus Jäger, Christian Figge, Andreas J Fallgatter, Detlef E Dietrich, Udo Dannlowski, Bernhardt T Baune, Volker Arolt, Ion-George Anghelescu, Markus M Nöthen, Stephanie H Witt, Ole A Andreassen, Chi-Hua Chen, Peter Falkai, Marcella Rietschel, Thomas G Schulze, Eva C Schulte

  • Genetic risk for psychiatric illness is associated with the number of hospitalizations of bipolar disorder patients.

    Journal of affective disorders

    Authors: Janos L Kalman, Sergi Papiol, Maria Grigoroiu-Serbanescu, Kristina Adorjan, Heike Anderson-Schmidt, Katharina Brosch, Monika Budde, Ashley L Comes, Katrin Gade, Andreas Forstner, Dominik Grotegerd, Tim Hahn, Maria Heilbronner, Urs Heilbronner, Stefanie Heilmann-Heimbach, Farah Klöhn-Saghatolislam, Mojtaba Oraki Kohshour, Susanne Meinert, Tina Meller, Niamh Mullins, Igor Nenadić, Markus M Nöthen, Julia-Katharina Pfarr, Daniela Reich-Erkelenz, Marcella Rietschel, Kai G Ringwald, Sabrina Schaupp, Eva C Schulte, Fanny Senner, Frederike Stein, Fabian Streit, Thomas Vogl, Peter Falkai, Udo Dannlowski, Tilo Kircher, Thomas G Schulze, Till F M Andlauer

  • Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness.

    PloS one

    Authors: Lara M Hochfeld, Marta Bertolini, David Broadley, Natalia V Botchkareva, Regina C Betz, Susanne Schoch, Markus M Nöthen, Stefanie Heilmann-Heimbach