Probing the limits of gate-based charge sensing von Gonzalez-Zalba, M. F., Barraud, S., Ferguson, A. J., Betz, A. C.

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Nutrition management for head and neck cancer patients improves clinical outcome and survival von Müller-Richter, Urs, Betz, C., Hartmann, S., Brands, R.C.

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Dimensionality effects on the luminescence properties of hBN von Schué, Léonard, Berini, Bruno, Betz, Andreas C, Plaçais, Bernard, Ducastelle, François, Barjon, Julien, Loiseau, Annick

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Dispersively Detected Pauli Spin-Blockade in a Silicon Nanowire Field-Effect Transistor von Betz, A. C, Wacquez, R, Vinet, M, Jehl, X, Saraiva, A. L, Sanquer, M, Ferguson, A. J, Gonzalez-Zalba, M. F

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Mutations in POGLUT1, Encoding Protein O-Glucosyltransferase 1, Cause Autosomal-Dominant Dowling-Degos Disease von Basmanav, F. Buket, Oprisoreanu, Ana-Maria, Pasternack, Sandra M., Thiele, Holger, Fritz, Günter, Wenzel, Jörg, Größer, Leopold, Wehner, Maria, Wolf, Sabrina, Fagerberg, Christina, Bygum, Anette, Altmüller, Janine, Rütten, Arno, Parmentier, Laurent, El Shabrawi-Caelen, Laila, Hafner, Christian, Nürnberg, Peter, Kruse, Roland, Schoch, Susanne, Hanneken, Sandra, Betz, Regina C.

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis von Adam, Ronja, Spier, Isabel, Zhao, Bixiao, Kloth, Michael, Marquez, Jonathan, Hinrichsen, Inga, Kirfel, Jutta, Tafazzoli, Aylar, Horpaopan, Sukanya, Uhlhaas, Siegfried, Stienen, Dietlinde, Friedrichs, Nicolaus, Altmüller, Janine, Laner, Andreas, Holzapfel, Stefanie, Peters, Sophia, Kayser, Katrin, Thiele, Holger, Holinski-Feder, Elke, Marra, Giancarlo, Kristiansen, Glen, Nöthen, Markus M., Büttner, Reinhard, Möslein, Gabriela, Betz, Regina C., Brieger, Angela, Lifton, Richard P., Aretz, Stefan

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Gate-Sensing Coherent Charge Oscillations in a Silicon Field-Effect Transistor von Gonzalez-Zalba, M. Fernando, Shevchenko, Sergey N, Barraud, Sylvain, Johansson, J. Robert, Ferguson, Andrew J, Nori, Franco, Betz, Andreas C

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The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease von Minnerop, Martina, Weber, Bernd, Schoene-Bake, Jan-Christoph, Roeske, Sandra, Mirbach, Sandra, Anspach, Christian, Schneider-Gold, Christiane, Betz, Regina C., Helmstaedter, Christoph, Tittgemeyer, Marc, Klockgether, Thomas, Kornblum, Cornelia

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Hot electron cooling by acoustic phonons in graphene von Betz, A C, Vialla, F, Brunel, D, Voisin, C, Picher, M, Cavanna, A, Madouri, A, Fève, G, Berroir, J-M, Plaçais, B, Pallecchi, E

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Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex von Romano, Maria-Teresa, Tafazzoli, Aylar, Mattern, Maximilian, Sivalingam, Sugirthan, Wolf, Sabrina, Rupp, Alexander, Thiele, Holger, Altmüller, Janine, Nürnberg, Peter, Ellwanger, Jürgen, Gambon, Reto, Baumer, Alessandra, Kohlschmidt, Nicolai, Metze, Dieter, Holdenrieder, Stefan, Paus, Ralf, Lütjohann, Dieter, Frank, Jorge, Geyer, Matthias, Bertolini, Marta, Kokordelis, Pavlos, Betz, Regina C.

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Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness von Hochfeld, Lara M., Bertolini, Marta, Broadley, David, Botchkareva, Natalia V., Betz, Regina C., Schoch, Susanne, Nothen, Markus M., Heilmann-Heimbach, Stefanie

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Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome von Wang, Huijun, Humbatova, Aytaj, Liu, Yuanxiang, Qin, Wen, Lee, Mingyang, Cesarato, Nicole, Kortüm, Fanny, Kumar, Sheetal, Romano, Maria Teresa, Dai, Shangzhi, Mo, Ran, Sivalingam, Sugirthan, Motameny, Susanne, Wu, Yuan, Wang, Xiaopeng, Niu, Xinwu, Geng, Songmei, Bornholdt, Dorothea, Kroisel, Peter M., Tadini, Gianluca, Walter, Scott D., Hauck, Fabian, Girisha, Katta M., Calza, Anne-Marie, Bottani, Armand, Altmüller, Janine, Buness, Andreas, Yang, Shuxia, Sun, Xiujuan, Ma, Lin, Kutsche, Kerstin, Grzeschik, Karl-Heinz, Betz, Regina C., Lin, Zhimiao

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Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies von 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

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A path through the reticulate pigmentation disorder jungle von Betz, R.C.

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Lysophosphatidic acid receptor LPAR6 supports the tumorigenicity of hepatocellular carcinoma von Mazzocca, Antonio, Dituri, Francesco, De Santis, Flavia, Filannino, Addolorata, Lopane, Chiara, Betz, Regina C, Li, Ying-Yi, Mukaida, Naofumi, Winter, Peter, Tortorella, Cosimo, Giannelli, Gianluigi, Sabbà, Carlo

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Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia von ZHIMIAOLIN, QUANCHEN, RUO XIAO, XUANZHU LIU, LANLAN DAI, XUEJUN ZHU, RUOYU LI, BETZ, Regina C, XUE ZHANG, YONG YANG, LEISHI, MINGYANG LEE, GIEHL, Kathrin A, ZHANLI TANG, HUIJUNWANG, JIEZHANG, JINGHUA YIN, LINGSHEN WU

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Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease von Betz, Regina C., Planko, Laura, Eigelshoven, Sibylle, Hanneken, Sandra, Pasternack, Sandra M., Büssow, Heinrich, Van Den Bogaert, Kris, Wenzel, Joerg, Braun-Falco, Markus, Rütten, Arno, Rogers, Michael A., Ruzicka, Thomas, Nöthen, Markus M., Magin, Thomas M., Kruse, Roland

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Tracking the brain in myotonic dystrophies: A 5-year longitudinal follow-up study von Gliem, Carla, Minnerop, Martina, Roeske, Sandra, Gärtner, Hanna, Schoene-Bake, Jan-Christoph, Adler, Sandra, Witt, Juri-Alexander, Hoffstaedter, Felix, Schneider-Gold, Christiane, Betz, Regina C, Helmstaedter, Christoph, Tittgemeyer, Marc, Amunts, Katrin, Klockgether, Thomas, Weber, Bernd, Kornblum, Cornelia

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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth von Pasternack, Sandra M, Molderings, Gerhard J, Voss, Katrin, Betz, Regina C, Nöthen, Markus M, Aboud, Khalid Al, Lee, Young-Ae, Hillmer, Axel M, Ramirez, Alfredo, Rüschendorf, Franz, Nürnberg, Peter, Franz, Thomas, von Kügelgen, Ivar

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Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature von Begemann, Matthias, Spengler, Sabrina, Gogiel, Magdalena, Grasshoff, Ute, Bonin, Michael, Betz, Regina C, Dufke, Andreas, Spier, Isabel, Eggermann, Thomas

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