Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci
Betz, Regina C, Petukhova, Lynn, Ripke, Stephan, Huang, Hailiang, Menelaou, Androniki, Redler, Silke, Becker, Tim, Heilmann, Stefanie, Yamany, Tarek, Duvic, Madeliene, Hordinsky, Maria, Norris, David, Price, Vera H, Mackay-Wiggan, Julian, de Jong, Annemieke, DeStefano, Gina M, Moebus, Susanne, Böhm, Markus, Blume-Peytavi, Ulrike, Wolff, Hans, Lutz, Gerhard, Kruse, Roland, Bian, Li, Amos, Christopher I, Lee, Annette, Gregersen, Peter K, Blaumeiser, Bettina, Altshuler, David, Clynes, Raphael, de Bakker, Paul I W, Nöthen, Markus M, Daly, Mark J, Christiano, Angela M
Published in Nature communications (22.01.2015)
Published in Nature communications (22.01.2015)
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Journal Article
Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies
Denisova, Evgeniya, Westphal, Dana, Surowy, Harald M, Meier, Friedegund, Hutter, Barbara, Reifenberger, Julia, Rütten, Arno, Schulz, Alexander, Sergon, Mildred, Ziemer, Mirjana, Brors, Benedikt, Betz, Regina C, Redler, Silke
Published in Cancer gene therapy (01.06.2022)
Published in Cancer gene therapy (01.06.2022)
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QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum
Föhrenbach, Melanie, Jamra, Rami Abou, Borkhardt, Arndt, Brozou, Triantafyllia, Muschke, Petra, Popp, Bernt, Rey, Linda K., Schaper, Jörg, Surowy, Harald, Zenker, Martin, Zweier, Christiane, Wieczorek, Dagmar, Redler, Silke
Published in Clinical genetics (01.01.2021)
Published in Clinical genetics (01.01.2021)
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Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology
Heilmann, Stefanie, Kiefer, Amy K., Fricker, Nadine, Drichel, Dmitriy, Hillmer, Axel M., Herold, Christine, Tung, Joyce Y., Eriksson, Nicholas, Redler, Silke, Betz, Regina C., Li, Rui, Kárason, Ari, Nyholt, Dale R., Song, Kijoung, Vermeulen, Sita H., Kanoni, Stavroula, Dedoussis, George, Martin, Nicholas G., Kiemeney, Lambertus A., Mooser, Vincent, Stefansson, Kari, Brent Richards, J., Becker, Tim, Brockschmidt, Felix F., Hinds, David A., Nöthen, Markus M.
Published in Journal of investigative dermatology (01.06.2013)
Published in Journal of investigative dermatology (01.06.2013)
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Journal Article
Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata
Tafazzoli, Aylar, Forstner, Andreas J., Broadley, David, Hofmann, Andrea, Redler, Silke, Petukhova, Lynn, Giehl, Kathrin A., Kruse, Roland, Blaumeiser, Bettina, Böhm, Markus, Bertolini, Marta, Rossi, Alfredo, Garcia Bartels, Natalie, Lutz, Gerhard, Wolff, Hans, Blume-Peytavi, Ulrike, Soreq, Hermona, Christiano, Angela M., Botchkareva, Natalia V., Nöthen, Markus M., Betz, Regina C.
Published in Journal of investigative dermatology (01.03.2018)
Published in Journal of investigative dermatology (01.03.2018)
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Journal Article
Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease
Betz, Regina C., Pforr, Jana, Flaquer, Antonia, Redler, Silke, Hanneken, Sandra, Eigelshoven, Sibylle, Kortüm, Anne-Katrin, Tüting, Thomas, Lambert, Julien, De Weert, Jozef, Hillmer, Axel M., Schmael, Christine, Wienker, Thomas F., Kruse, Roland, Lutz, Gerhard, Blaumeiser, Bettina, Nöthen, Markus M.
Published in Journal of investigative dermatology (01.11.2007)
Published in Journal of investigative dermatology (01.11.2007)
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Journal Article
Parent-of-origin Effect in Alopecia Areata: A Large-scale Pedigree Study
Redler, Silke, Basmanav, F Buket Ü, Blaumeiser, Bettina, Bartels, Natalie Garcia, Lutz, Gerhard, Tafazzoli, Aylar, Kruse, Roland, Wolff, Hans, Böhm, Markus, Blume-Peytavi, Ulrike, Becker, Tim, Nöthen, Markus M, Betz, Regina C
Published in Acta dermato-venereologica (06.07.2017)
Published in Acta dermato-venereologica (06.07.2017)
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Journal Article
Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
Redler, Silke, Dobson, Kathy, Drichel, Dmitriy, Heilmann, Stefanie, Wolf, Sabrina, Brockschmidt, Felix F, Tazi-Ahnini, Rachid, Birch, Pattie, Teßmann, Peter, Giehl, Kathrin A, Kruse, Roland, Lutz, Gerhard, Garcia Bartels, Natalie, Hanneken, Sandra, Wolff, Hans, Böhm, Markus, Becker, Tim, Blume-Peytavi, Ulrike, Nöthen, Markus M, Messenger, Andrew G, Betz, Regina C
Published in Journal of dermatological science (01.11.2013)
Published in Journal of dermatological science (01.11.2013)
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Journal Article
Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
Redler, Silke, MD, Kruse, Roland, MD, Eigelshoven, Sibylle, MD, Hanneken, Sandra, MD, Refke, Melanie, Wen, Yaran, MD, Zhang, Xue, MD, PhD, Cichon, Sven, PhD, Betz, Regina C., MD, Nöthen, Markus M., MD
Published in Journal of the American Academy of Dermatology (01.04.2011)
Published in Journal of the American Academy of Dermatology (01.04.2011)
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Journal Article
Genetics and other factors in the aetiology of female pattern hair loss
Redler, Silke, Messenger, Andrew G., Betz, Regina C.
Published in Experimental dermatology (01.06.2017)
Published in Experimental dermatology (01.06.2017)
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De Novo Missense Variations of ATP8B2 Impair Its Phosphatidylcholine Flippase Activity
Takatsu, Hiroyuki, Nishimura, Narumi, Kosugi, Yusuke, Ogawa, Haruo, Nakayama, Kazuhisa, Colin, Estelle, Platzer, Konrad, Abou Jamra, Rami, Redler, Silke, Prouteau, Clément, Ziegler, Alban, Shin, Hye-Won
Published in Molecular and cellular biology (02.09.2024)
Published in Molecular and cellular biology (02.09.2024)
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80 AGE OF ONSET OF SURVEILLANCE COLONOSCOPY FOR MSH6 MUTATION CARRIERS
Hüneburg, Robert, Bucksch, Karolin, Heling, Dominik, Aretz, Stefan, Büttner, Reinhard, Holinski-Feder, Elke, Möslein, Gabriela, Kloor, Matthias, von Knebel Doeberitz, Magnus, Redler, Silke, Löffler, Markus, Vangala, Deepak, Steinke-Lange, Verena, Weitz, Jürgen, Strassburg, Christian P., Nattermann, Jacob, Engel, Christoph
Published in Gastroenterology (New York, N.Y. 1943) (01.05.2021)
Published in Gastroenterology (New York, N.Y. 1943) (01.05.2021)
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Primary cutaneous adenoid cystic carcinoma mimicking dermal cylindroma: histology of the complete surgical excision as the key to diagnosis
Rütten, Arno, Hegenbarth, Wolfgang, Kohl, Peter K, Hillen, Uwe, Redler, Silke
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.08.2018)
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.08.2018)
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Journal Article
Follow-Up Study of the First Genome-Wide Association Scan in Alopecia Areata: IL13 and KIAA0350 as Susceptibility Loci Supported with Genome-Wide Significance
Jagielska, Dagny, Redler, Silke, Brockschmidt, Felix F., Herold, Christine, Pasternack, Sandra M., Garcia Bartels, Natalie, Hanneken, Sandra, Eigelshoven, Sibylle, Refke, Melanie, Barth, Sandra, Giehl, Kathrin A., Kruse, Roland, Lutz, Gerhard, Wolff, Hans, Blaumeiser, Bettina, Böhm, Markus, Blume-Peytavi, Ulrike, Becker, Tim, Nöthen, Markus M., Betz, Regina C.
Published in Journal of investigative dermatology (01.09.2012)
Published in Journal of investigative dermatology (01.09.2012)
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Adenoma and colorectal cancer risks in Lynch syndrome, Lynch‐like syndrome and familial colorectal cancer type X
Bucksch, Karolin, Zachariae, Silke, Ahadova, Aysel, Aretz, Stefan, Büttner, Reinhard, Görgens, Heike, Holinski‐Feder, Elke, Hüneburg, Robert, Kloor, Matthias, Knebel Doeberitz, Magnus, Ladigan‐Badura, Swetlana, Moeslein, Gabriela, Morak, Monika, Nattermann, Jacob, Nguyen, Huu Phuc, Perne, Claudia, Redler, Silke, Schmetz, Ariane, Steinke‐Lange, Verena, Surowy, Harald, Vangala, Deepak B., Weitz, Jürgen, Loeffler, Markus, Engel, Christoph
Published in International journal of cancer (01.01.2022)
Published in International journal of cancer (01.01.2022)
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Journal Article
Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID
Redler, Silke, Strom, Tim M, Wieland, Thomas, Cremer, Kirsten, Engels, Hartmut, Distelmaier, Felix, Schaper, Jörg, Küchler, Alma, Lemke, Johannes R, Jeschke, Stephanie, Schreyer, Nicole, Sticht, Heinrich, Koch, Margarete, Lüdecke, Hermann-Josef, Wieczorek, Dagmar
Published in European journal of human genetics : EJHG (01.06.2017)
Published in European journal of human genetics : EJHG (01.06.2017)
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Gene expression profiling in porocarcinoma indicates heterogeneous tumor development and substantiates poromas as precursor lesions
Holst, Svenja, Weber, Anna K., Meier, Friedegund, Otte, Jörg, Petzsch, Patrick, Reifenberger, Julia, Wachtmeister, Thorsten, Westphal, Dana, Ziemer, Mirjana, Wruck, Wasco, Adjaye, James, Betz, Regina C., Rütten, Arno, Surowy, Harald M., Redler, Silke
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.08.2024)
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.08.2024)
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Journal Article
Phenotype diversity associated with TP63 mutations
Schmetz, Ariane, Xiong, Xing, Cesarato, Nicole, Basmanav, Fitnat Buket, Gierthmuehlen, Petra, Schaper, Jörg, Schlieper, Daniel, Wehner, Maria, Thiele, Holger, Frank, Jorge, Betz, Regina C., Redler, Silke
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.06.2022)
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.06.2022)
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Journal Article
Phänotypische Vielfalt bei Varianten im TP63‐Gen
Schmetz, Ariane, Xiong, Xing, Cesarato, Nicole, Basmanav, Fitnat Buket, Gierthmuehlen, Petra, Schaper, Jörg, Schlieper, Daniel, Wehner, Maria, Thiele, Holger, Frank, Jorge, Betz, Regina C., Redler, Silke
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.06.2022)
Published in Journal der Deutschen Dermatologischen Gesellschaft (01.06.2022)
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