Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study.

by Sonali Pechlivanis, Stefanie Heilmann-Heimbach, Raimund Erbel, Amir A Mahabadi, Lara M Hochfeld, Karl-Heinz Jöckel, Markus M Nöthen, Susanne Moebus
Published 2019-01-01

Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2

by Azra Fatima, Dina Ivanyuk, Stefan Herms, Stefanie Heilmann-Heimbach, Orla O'Shea, Charlotte Chapman, Zsuszanna Izsvák, Martin Farr, Jürgen Hescheler, Tomo Šarić
Published 2016-03-01

Circulating microRNAs are associated with Pulmonary Hypertension and Development of Chronic Lung Disease in Congenital Diaphragmatic Hernia

by Marisol Herrera-Rivero, Rong Zhang, Stefanie Heilmann-Heimbach, Andreas Mueller, Soyhan Bagci, Till Dresbach, Lukas Schröder, Stefan Holdenrieder, Heiko M. Reutter, Florian Kipfmueller
Published 2018-07-01

Associations between SNPs and immune-related circulating proteins in schizophrenia

by Man K. Chan, Jason D. Cooper, Stefanie Heilmann-Heimbach, Josef Frank, Stephanie H. Witt, Markus M. Nöthen, Johann Steiner, Marcella Rietschel, Sabine Bahn
Published 2017-10-01

Polygenic risk for obsessive-compulsive disorder (OCD) predicts brain response during working memory task in OCD, unaffected relatives, and healthy controls

by Stephan Heinzel, Christian Kaufmann, Rosa Grützmann, Julia Klawohn, Anja Riesel, Katharina Bey, Stefanie Heilmann-Heimbach, Leonie Weinhold, Alfredo Ramirez, Michael Wagner, Norbert Kathmann
Published 2021-09-01

Sustained Immunoparalysis in Endotoxin-Tolerized Monocytic Cells

by Christina K. Weisheit, Alexandra Klüners, Lennart Wild, Alexandra Casalter, Stefanie Heilmann-Heimbach, Sugirthan Sivalingam, Jan L. Kleiner, Stefan F. Ehrentraut, Andreas Hoeft, Stilla Frede, Heidi Ehrentraut
Published 2020-01-01

Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function

by Christopher Schröder, Elsa Leitão, Stefan Wallner, Gerd Schmitz, Ludger Klein-Hitpass, Anupam Sinha, Karl-Heinz Jöckel, Stefanie Heilmann-Heimbach, Per Hoffmann, Markus M. Nöthen, Michael Steffens, Peter Ebert, Sven Rahmann, Bernhard Horsthemke
Published 2017-07-01

Ginkgo biloba induces different gene expression signatures and oncogenic pathways in malignant and non-malignant cells of the liver.

by Carolin Czauderna, Mayrel Palestino-Dominguez, Darko Castven, Diana Becker, Luis Zanon-Rodriguez, Jovana Hajduk, Friederike L Mahn, Monika Herr, Dennis Strand, Susanne Strand, Stefanie Heilmann-Heimbach, Luis E Gomez-Quiroz, Marcus A Wörns, Peter R Galle, Jens U Marquardt
Published 2018-01-01

Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation

by Stephanie H. Witt, Josef Frank, Maria Gilles, Maren Lang, Jens Treutlein, Fabian Streit, Isabell A. C. Wolf, Verena Peus, Barbara Scharnholz, Tabea S. Send, Stefanie Heilmann-Heimbach, Sugirthan Sivalingam, Helene Dukal, Jana Strohmaier, Marc Sütterlin, Janine Arloth, Manfred Laucht, Markus M. Nöthen, Michael Deuschle, Marcella Rietschel
Published 2018-04-01

Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy.

by Markus Draaken, Michael Knapp, Tracie Pennimpede, Johanna M Schmidt, Anne-Karolin Ebert, Wolfgang Rösch, Raimund Stein, Boris Utsch, Karin Hirsch, Thomas M Boemers, Elisabeth Mangold, Stefanie Heilmann, Kerstin U Ludwig, Ekkehart Jenetzky, Nadine Zwink, Susanne Moebus, Bernhard G Herrmann, Manuel Mattheisen, Markus M Nöthen, Michael Ludwig, Heiko Reutter
Published 2015-03-01

Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study

by Axel Krug, Markus Wöhr, Dominik Seffer, Henrike Rippberger, A. Özge Sungur, Bruno Dietsche, Frederike Stein, Sugirthan Sivalingam, Andreas J. Forstner, Stephanie H. Witt, Helene Dukal, Fabian Streit, Anna Maaser, Stefanie Heilmann-Heimbach, Till F. M. Andlauer, Stefan Herms, Per Hoffmann, Marcella Rietschel, Markus M. Nöthen, Martin Lackinger, Gerhard Schratt, Michael Koch, Rainer K. W. Schwarting, Tilo Kircher
Published 2020-06-01

Exploring Genetic Associations of Alzheimer’s Disease Loci With Mild Cognitive Impairment Neurocognitive Endophenotypes

by Ana Espinosa, Begoña Hernández-Olasagarre, Sonia Moreno-Grau, Luca Kleineidam, Luca Kleineidam, Luca Kleineidam, Stefanie Heilmann-Heimbach, Stefanie Heilmann-Heimbach, Isabel Hernández, Steffen Wolfsgruber, Steffen Wolfsgruber, Holger Wagner, Maitée Rosende-Roca, Ana Mauleón, Liliana Vargas, Asunción Lafuente, Octavio Rodríguez-Gómez, Carla Abdelnour, Silvia Gil, Marta Marquié, Miguel A. Santos-Santos, Ángela Sanabria, Gemma Ortega, Gemma Monté-Rubio, Alba Pérez, Marta Ibarria, Susana Ruiz, Johannes Kornhuber, Oliver Peters, Lutz Frölich, Michael Hüll, Jens Wiltfang, Tobias Luck, Steffi Riedel-Heller, Laura Montrreal, Pilar Cañabate, Mariola Moreno, Silvia Preckler, Nuria Aguilera, Itziar de Rojas, Adelina Orellana, Montserrat Alegret, Sergi Valero, Markus M. Nöthen, Markus M. Nöthen, Michael Wagner, Michael Wagner, Frank Jessen, Frank Jessen, Frank Jessen, Lluis Tárraga, Mercè Boada, Alfredo Ramírez, Alfredo Ramírez, Agustín Ruiz
Published 2018-10-01

DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning.

by Janine Arloth, Gökcen Eraslan, Till F M Andlauer, Jade Martins, Stella Iurato, Brigitte Kühnel, Melanie Waldenberger, Josef Frank, Ralf Gold, Bernhard Hemmer, Felix Luessi, Sandra Nischwitz, Friedemann Paul, Heinz Wiendl, Christian Gieger, Stefanie Heilmann-Heimbach, Tim Kacprowski, Matthias Laudes, Thomas Meitinger, Annette Peters, Rajesh Rawal, Konstantin Strauch, Susanne Lucae, Bertram Müller-Myhsok, Marcella Rietschel, Fabian J Theis, Elisabeth B Binder, Nikola S Mueller
Published 2020-02-01

Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families

by Jose Guzman-Parra, Fabian Streit, Andreas J. Forstner, Jana Strohmaier, Maria José González, Susana Gil Flores, Francisco J. Cabaleiro Fabeiro, Francisco del Río Noriega, Fermin Perez Perez, Jesus Haro González, Guillermo Orozco Diaz, Yolanda de Diego-Otero, Berta Moreno-Kustner, Georg Auburger, Franziska Degenhardt, Stefanie Heilmann-Heimbach, Stefan Herms, Per Hoffmann, Josef Frank, Jerome C. Foo, Lea Sirignano, Stephanie H. Witt, Sven Cichon, Fabio Rivas, Fermín Mayoral, Markus M. Nöthen, Till F. M. Andlauer, Marcella Rietschel
Published 2021-01-01

Exome sequencing in large, multiplex bipolar disorder families from Cuba.

by Anna Maaser, Andreas J Forstner, Jana Strohmaier, Julian Hecker, Kerstin U Ludwig, Sugirthan Sivalingam, Fabian Streit, Franziska Degenhardt, Stephanie H Witt, Céline S Reinbold, Anna C Koller, Ruth Raff, Stefanie Heilmann-Heimbach, Sascha B Fischer, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Stefan Herms, Per Hoffmann, Holger Thiele, Peter Nürnberg, Heide Löhlein Fier, Guillermo Orozco-Díaz, Deinys Carmenate-Naranjo, Niurka Proenza-Barzaga, Georg W J Auburger, Till F M Andlauer, Sven Cichon, Beatriz Marcheco-Teruel, Ole Mors, Marcella Rietschel, Markus M Nöthen
Published 2018-01-01

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.

by Emma C Johnson, Douglas W Bjelland, Daniel P Howrigan, Abdel Abdellaoui, Gerome Breen, Anders Borglum, Sven Cichon, Franziska Degenhardt, Andreas J Forstner, Josef Frank, Giulio Genovese, Stefanie Heilmann-Heimbach, Stefan Herms, Per Hoffman, Wolfgang Maier, Manuel Mattheisen, Derek Morris, Bryan Mowry, Betram Müller-Mhysok, Benjamin Neale, Igor Nenadic, Markus M Nöthen, Colm O'Dushlaine, Marcella Rietschel, Douglas M Ruderfer, Dan Rujescu, Thomas G Schulze, Matthew A Simonson, Eli Stahl, Jana Strohmaier, Stephanie H Witt, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Patrick F Sullivan, Matthew C Keller
Published 2016-10-01

Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

by Stefanie Heilmann-Heimbach, Christine Herold, Lara M. Hochfeld, Axel M. Hillmer, Dale R. Nyholt, Julian Hecker, Asif Javed, Elaine G. Y. Chew, Sonali Pechlivanis, Dmitriy Drichel, Xiu Ting Heng, Ricardo C. -H. del Rosario, Heide L. Fier, Ralf Paus, Rico Rueedi, Tessel E. Galesloot, Susanne Moebus, Thomas Anhalt, Shyam Prabhakar, Rui Li, Stavroula Kanoni, George Papanikolaou, Zoltán Kutalik, Panos Deloukas, Michael P. Philpott, Gérard Waeber, Tim D. Spector, Peter Vollenweider, Lambertus A. L. M. Kiemeney, George Dedoussis, J. Brent Richards, Michael Nothnagel, Nicholas G. Martin, Tim Becker, David A. Hinds, Markus M. Nöthen
Published 2017-03-01

Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.

by Rui Li, Felix F Brockschmidt, Amy K Kiefer, Hreinn Stefansson, Dale R Nyholt, Kijoung Song, Sita H Vermeulen, Stavroula Kanoni, Daniel Glass, Sarah E Medland, Maria Dimitriou, Dawn Waterworth, Joyce Y Tung, Frank Geller, Stefanie Heilmann, Axel M Hillmer, Veronique Bataille, Sibylle Eigelshoven, Sandra Hanneken, Susanne Moebus, Christine Herold, Martin den Heijer, Grant W Montgomery, Panos Deloukas, Nicholas Eriksson, Andrew C Heath, Tim Becker, Patrick Sulem, Massimo Mangino, Peter Vollenweider, Tim D Spector, George Dedoussis, Nicholas G Martin, Lambertus A Kiemeney, Vincent Mooser, Kari Stefansson, David A Hinds, Markus M Nöthen, J Brent Richards
Published 2012-05-01

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Relat...

by Jens Treutlein, Josef Frank, Fabian Streit, Céline S. Reinbold, Dilafruz Juraeva, Franziska Degenhardt, Liz Rietschel, Stephanie H. Witt, Andreas J. Forstner, Monika Ridinger, Jana Strohmaier, Norbert Wodarz, Helene Dukal, Jerome C. Foo, Per Hoffmann, Stefan Herms, Stefanie Heilmann-Heimbach, Michael Soyka, Wolfgang Maier, Wolfgang Gaebel, Norbert Dahmen, Norbert Scherbaum, Bertram Müller-Myhsok, Susanne Lucae, Marcus Ising, Felix Stickel, Thomas Berg, Ulla Roggenbuck, Karl-Heinz Jöckel, Henrike Scholz, Ulrich S. Zimmermann, Stephan Buch, Wolfgang H. Sommer, Rainer Spanagel, Benedikt Brors, Sven Cichon, Karl Mann, Falk Kiefer, Jochen Hampe, Jonas Rosendahl, Markus M. Nöthen, Marcella Rietschel
Published 2017-07-01

Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

by Jayaram Vijayakrishnan, James Studd, Peter Broderick, Ben Kinnersley, Amy Holroyd, Philip J. Law, Rajiv Kumar, James M. Allan, Christine J. Harrison, Anthony V. Moorman, Ajay Vora, Eve Roman, Sivaramakrishna Rachakonda, Sally E. Kinsey, Eamonn Sheridan, Pamela D. Thompson, Julie A. Irving, Rolf Koehler, Per Hoffmann, Markus M. Nöthen, Stefanie Heilmann-Heimbach, Karl-Heinz Jöckel, Douglas F. Easton, Paul D. P. Pharaoh, Alison M. Dunning, Julian Peto, Frederico Canzian, Anthony Swerdlow, Rosalind A. Eeles, ZSofia Kote-Jarai, Kenneth Muir, Nora Pashayan, The PRACTICAL Consortium, Mel Greaves, Martin Zimmerman, Claus R. Bartram, Martin Schrappe, Martin Stanulla, Kari Hemminki, Richard S. Houlston
Published 2018-04-01