Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19

por Henne, S. K., Hochfeld, L. M., Maj, C., Nöthen, M. M., Heilmann‐Heimbach, S.
Publicado 2021

072 Covid-19 and male androgenetic alopecia: Systematic investigation of a potential epidemiological and genetic association

por Henne, S.K., Hochfeld, L.M., Maj, C., Nöthen, M.M., Heilmann-Heimbach, S.
Publicado 2021

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

por Herrera-Rivero, Marisol, Hochfeld, Lara M., Sivalingam, Sugirthan, Nöthen, Markus M., Heilmann-Heimbach, Stefanie
Publicado 2020

Genetic prediction of male pattern baldness based on large independent datasets

por Chen, Yan, Hysi, Pirro, Maj, Carlo, Heilmann-Heimbach, Stefanie, Spector, Timothy D., Liu, Fan, Kayser, Manfred
Publicado 2022

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

por Hochfeld, Lara M., Anhalt, Thomas, Reinbold, Céline S., Herrera-Rivero, Marisol, Fricker, Nadine, Nöthen, Markus M., Heilmann-Heimbach, Stefanie
Publicado 2017

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

por Pechlivanis, Sonali, Heilmann-Heimbach, Stefanie, Erbel, Raimund, Mahabadi, Amir A., Hochfeld, Lara M., Jöckel, Karl-Heinz, Nöthen, Markus M., Moebus, Susanne
Publicado 2019

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

por Hochfeld, Lara M., Bertolini, Marta, Broadley, David, Botchkareva, Natalia V., Betz, Regina C., Schoch, Susanne, Nöthen, Markus M., Heilmann-Heimbach, Stefanie
Publicado 2021

Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss

por Henne, Sabrina Katrin, Aldisi, Rana, Sivalingam, Sugirthan, Hochfeld, Lara Maleen, Borisov, Oleg, Krawitz, Peter Michael, Maj, Carlo, Nöthen, Markus Maria, Heilmann-Heimbach, Stefanie
Publicado 2023

Associations between SNPs and immune-related circulating proteins in schizophrenia

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

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

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

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

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

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

por 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
Publicado 2018

Sustained Immunoparalysis in Endotoxin-Tolerized Monocytic Cells

por 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
Publicado 2020

A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels

por Schubert, Maria, Pérez Lanuza, Lina, Wöste, Marius, Dugas, Martin, Carmona, F David, Palomino-Morales, Rogelio J, Rassam, Yousif, Heilmann-Heimbach, Stefanie, Tüttelmann, Frank, Kliesch, Sabine, Gromoll, Jörg
Publicado 2022

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

por 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
Publicado 2017

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

por Heinrich, Maria, Sieg, Miriam, Kruppa, Jochen, Nürnberg, Peter, Schreier, Peter H., Heilmann-Heimbach, Stefanie, Hoffmann, Per, Nöthen, Markus M., Janke, Jürgen, Pischon, Tobias, Slooter, Arjen J. C., Winterer, Georg, Spies, Claudia D.
Publicado 2021

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

por Zillich, Lea, Frank, Josef, Streit, Fabian, Friske, Marion M., Foo, Jerome C., Sirignano, Lea, Heilmann-Heimbach, Stefanie, Dukal, Helene, Degenhardt, Franziska, Hoffmann, Per, Hansson, Anita C., Nöthen, Markus M., Rietschel, Marcella, Spanagel, Rainer, Witt, Stephanie H.
Publicado 2021

Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4

por 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.
Publicado 2016

Association of the Polygenic Risk Score With the Probability of Prodromal Parkinson’s Disease in Older Adults

por Maraki, Maria I., Hatzimanolis, Alexandros, Mourtzi, Niki, Stefanis, Leonidas, Yannakoulia, Mary, Kosmidis, Mary H., Dardiotis, Efthimios, Hadjigeorgiou, Georgios M., Sakka, Paraskevi, Ramirez, Alfredo, Grenier-Boley, Benjamin, Lambert, Jean-Charles, Heilmann-Heimbach, Stefanie, Stamelou, Maria, Scarmeas, Nikolaos, Xiromerisiou, Georgia
Publicado 2021

Acquired Resistance to Antiangiogenic Therapies in Hepatocellular Carcinoma Is Mediated by Yes‐Associated Protein 1 Activation and Transient Expansion of Stem‐Like Cancer Cells

por Castven, Darko, Czauderna, Carolin, Becker, Diana, Pereira, Sharon, Schmitt, Jennifer, Weinmann, Arndt, Shah, Viral, Hajduk, Jovana, Keggenhoff, Friederike, Binder, Harald, Keck, Tobias, Heilmann‐Heimbach, Stefanie, Wörns, Marcus A., Thorgeirsson, Snorri S., Breuhahn, Kai, Galle, Peter R., Marquardt, Jens U.
Publicado 2021