Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles

par Herrera-Rivero, Marisol, Hochfeld, Lara M., Sivalingam, Sugirthan, Nöthen, Markus M., Heilmann-Heimbach, Stefanie
Publié dans BMC Dermatol (2020)

Expression profiling and bioinformatic analyses suggest new target genes and pathways for human hair follicle related microRNAs

par Hochfeld, Lara M., Anhalt, Thomas, Reinbold, Céline S., Herrera-Rivero, Marisol, Fricker, Nadine, Nöthen, Markus M., Heilmann-Heimbach, Stefanie
Publié dans BMC Dermatol (2017)

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

par Pechlivanis, Sonali, Heilmann-Heimbach, Stefanie, Erbel, Raimund, Mahabadi, Amir A., Hochfeld, Lara M., Jöckel, Karl-Heinz, Nöthen, Markus M., Moebus, Susanne
Publié dans PLoS One (2019)

Associations between SNPs and immune-related circulating proteins in schizophrenia

par Chan, Man K., Cooper, Jason D., Heilmann-Heimbach, Stefanie, Frank, Josef, Witt, Stephanie H., Nöthen, Markus M., Steiner, Johann, Rietschel, Marcella, Bahn, Sabine
Publié dans Sci Rep (2017)

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

par Herrera-Rivero, Marisol, Zhang, Rong, Heilmann-Heimbach, Stefanie, Mueller, Andreas, Bagci, Soyhan, Dresbach, Till, Schröder, Lukas, Holdenrieder, Stefan, Reutter, Heiko M., Kipfmueller, Florian
Publié dans Sci Rep (2018)

Variants of DNMT3A cause transcript-specific DNA methylation patterns and affect hematopoiesis

par Božić, Tanja, Frobel, Joana, Raic, Annamarija, Ticconi, Fabio, Kuo, Chao-Chung, Heilmann-Heimbach, Stefanie, Goecke, Tamme W, Zenke, Martin, Jost, Edgar, Costa, Ivan G, Wagner, Wolfgang
Publié dans Life Sci Alliance (2018)

Sustained Immunoparalysis in Endotoxin-Tolerized Monocytic Cells

par Weisheit, Christina K., Klüners, Alexandra, Wild, Lennart, Casalter, Alexandra, Heilmann-Heimbach, Stefanie, Sivalingam, Sugirthan, Kleiner, Jan L., Ehrentraut, Stefan F., Hoeft, Andreas, Frede, Stilla, Ehrentraut, Heidi
Publié dans Mediators Inflamm (2020)

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

par Schröder, Christopher, Leitão, Elsa, Wallner, Stefan, Schmitz, Gerd, Klein-Hitpass, Ludger, Sinha, Anupam, Jöckel, Karl-Heinz, Heilmann-Heimbach, Stefanie, Hoffmann, Per, Nöthen, Markus M., Steffens, Michael, Ebert, Peter, Rahmann, Sven, Horsthemke, Bernhard
Publié dans Epigenetics Chromatin (2017)

Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4

par Degenhardt, Franziska, Krämer, Laurenz, Frank, Josef, Treutlein, Jens, Heilmann‐Heimbach, Stefanie, Hecker, Julian, Fier, Heide Löhlein, Lang, Maren, Witt, Stephanie H., Koller, Anna C., Mann, Karl, Hoffmann, Sabine, Kiefer, Falk, Spanagel, Rainer, Rietschel, Marcella, Nöthen, Markus M.
Publié dans Alcohol Clin Exp Res (2016)

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

par Czauderna, Carolin, Palestino-Dominguez, Mayrel, Castven, Darko, Becker, Diana, Zanon-Rodriguez, Luis, Hajduk, Jovana, Mahn, Friederike L., Herr, Monika, Strand, Dennis, Strand, Susanne, Heilmann-Heimbach, Stefanie, Gomez-Quiroz, Luis E., Wörns, Marcus A., Galle, Peter R., Marquardt, Jens U.
Publié dans PLoS One (2018)

Acquisition of chromosome 1q duplication in parental and genome‐edited human‐induced pluripotent stem cell‐derived neural stem cells results in their higher proliferation rate in v...

par Mehrjardi, Narges Zare, Molcanyi, Marek, Hatay, Firuze Fulya, Timmer, Marco, Shahbazi, Ebrahim, Ackermann, Justus P., Herms, Stefan, Heilmann‐Heimbach, Stefanie, Wunderlich, Thomas F., Prochnow, Nora, Haghikia, Aiden, Lampert, Angelika, Hescheler, Jürgen, Neugebauer, Edmund A. M., Baharvand, Hossein, Šarić, Tomo
Publié dans Cell Prolif (2020)

Adverse genomic alterations and stemness features are induced by field cancerization in the microenvironment of hepatocellular carcinomas

par Castven, Darko, Fischer, Michael, Becker, Diana, Heinrich, Stefan, Andersen, Jesper B., Strand, Dennis, Sprinzl, Martin F., Strand, Susanne, Czauderna, Carolin, Heilmann-Heimbach, Stefanie, Roessler, Stephanie, Weinmann, Arndt, Wörns, Marcus A., Thorgeirsson, Snorri S., Galle, Peter R., Matter, Matthias S., Lang, Hauke, Marquardt, Jens U.
Publié dans Oncotarget (2017)

Glutamate concentration in the anterior cingulate cortex in alcohol dependence: association with alcohol withdrawal and exploration of contribution from glutamatergic candidate gen...

par Streit, Fabian, Treutlein, Jens, Frischknecht, Ulrich, Hermann, Derik, Mann, Karl, Kiefer, Falk, Sack, Markus, Hall, Alisha S.M., Frank, Josef, Witt, Stephanie H., Foo, Jerome C., Degenhardt, Franziska, Heilmann-Heimbach, Stefanie, Nöthen, Markus M., Sommer, Wolfgang H., Spanagel, Rainer, Rietschel, Marcella, Ende, Gabriele
Publié dans Psychiatr Genet (2018)

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

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

Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

par Ehret, Julia K., Engels, Hartmut, Cremer, Kirsten, Becker, Jessica, Zimmermann, Johannes P., Wohlleber, Eva, Grasshoff, Ute, Rossier, Eva, Bonin, Michael, Mangold, Elisabeth, Bevot, Andrea, Schön, Stefanie, Heilmann-Heimbach, Stefanie, Dennert, Nicola, Mathieu-Dramard, Michèle, Lacaze, Elodie, Plessis, Ghislaine, de Broca, Alain, Jedraszak, Guillaume, Röthlisberger, Benno, Miny, Peter, Filges, Isabel, Dufke, Andreas, Andrieux, Joris, Lee, Jennifer A., Zink, Alexander M.
Publié dans Mol Cytogenet (2015)

Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer

par Neidhardt, Guido, Hauke, Jan, Ramser, Juliane, Groß, Eva, Gehrig, Andrea, Müller, Clemens R., Kahlert, Anne-Karin, Hackmann, Karl, Honisch, Ellen, Niederacher, Dieter, Heilmann-Heimbach, Stefanie, Franke, André, Lieb, Wolfgang, Thiele, Holger, Altmüller, Janine, Nürnberg, Peter, Klaschik, Kristina, Ernst, Corinna, Ditsch, Nina, Jessen, Frank, Ramirez, Alfredo, Wappenschmidt, Barbara, Engel, Christoph, Rhiem, Kerstin, Meindl, Alfons, Schmutzler, Rita K., Hahnen, Eric
Publié dans JAMA Oncol (2016)

Genome-wide significant risk factors on chromosome 19 and the APOE locus

par Moreno-Grau, Sonia, Hernández, Isabel, Heilmann-Heimbach, Stefanie, Ruiz, Susana, Rosende-Roca, Maitée, Mauleón, Ana, Vargas, Liliana, Rodríguez-Gómez, Octavio, Alegret, Montserrat, Espinosa, Ana, Ortega, Gemma, Aguilera, Nuria, Abdelnour, Carla, Neuroimaging Initiative, Alzheimer’s Disease, Gil, Silvia, Maier, Wolfgang, Sotolongo-Grau, Oscar, Tárraga, Lluís, Ramirez, Alfredo, López-Arrrieta, Jesús, Antúnez, Carmen, Serrano-Ríos, Manuel, Boada, Mercè, Ruiz, Agustín
Publié dans Oncotarget (2018)

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

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

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

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

Shared genetic etiology between alcohol dependence and major depressive disorder

par Foo, Jerome C., Streit, Fabian, Treutlein, Jens, Ripke, Stephan, Witt, Stephanie H., Strohmaier, Jana, Degenhardt, Franziska, Forstner, Andreas J., Hoffmann, Per, Soyka, Michael, Dahmen, Norbert, Scherbaum, Norbert, Wodarz, Norbert, Heilmann-Heimbach, Stefanie, Herms, Stefan, Cichon, Sven, Preuss, Ulrich, Gaebel, Wolfgang, Ridinger, Monika, Hoffmann, Sabine, Schulze, Thomas G., Maier, Wolfgang, Zill, Peter, Müller-Myhsok, Bertram, Ising, Marcus, Lucae, Susanne, Nöthen, Markus M., Mann, Karl, Kiefer, Falk, Rietschel, Marcella, Frank, Josef
Publié dans Psychiatr Genet (2018)