Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas by Kunz, Eva K., Matias‐Guiu, Xavier, Hiort, Olaf, Christiansen, Gudrun, Colomer, Anna, Roth, Jürgen, Heitz, Philipp U., Komminoth, Paul

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Analysis ofRET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas by Kunz, Eva K., Matias-Guiu, Xavier, Hiort, Olaf, Christiansen, Gudrun, Colomer, Anna, Roth, Jürgen, Heitz, Philipp U., Komminoth, Paul

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Structure and assembly of the mitochondrial membrane remodelling GTPase Mgm1 by Faelber, Katja, Dietrich, Lea, Noel, Jeffrey K., Wollweber, Florian, Pfitzner, Anna-Katharina, Mühleip, Alexander, Sánchez, Ricardo, Kudryashev, Misha, Chiaruttini, Nicolas, Lilie, Hauke, Schlegel, Jeanette, Rosenbaum, Eva, Hessenberger, Manuel, Matthaeus, Claudia, Kunz, Séverine, von der Malsburg, Alexander, Noé, Frank, Roux, Aurélien, van der Laan, Martin, Kühlbrandt, Werner, Daumke, Oliver

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Commonwealth Neuroendocrine Tumour Research Collaboration and the North American Neuroendocrine Tumor Society Guidelines for the Diagnosis and Management of Patients With Lung Neur... by Singh, Simron, Bergsland, Emily K., Card, Cynthia M., Hope, Thomas A., Kunz, Pamela L., Laidley, David T., Lawrence, Ben, Leyden, Simone, Metz, David C., Michael, Michael, Modahl, Lucy E., Myrehaug, Sten, Padda, Sukhmani K., Pommier, Rodney F., Ramirez, Robert A., Soulen, Michael, Strosberg, Jonathan, Sung, Arthur, Thawer, Alia, Wei, Benjamin, Xu, Bin, Segelov, Eva

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Soluble CD83 improves and accelerates wound healing by the induction of pro-resolving macrophages by Royzman, Dmytro, Peckert-Maier, Katrin, Stich, Lena, König, Christina, Wild, Andreas B., Tauchi, Miyuki, Ostalecki, Christian, Kiesewetter, Franklin, Seyferth, Stefan, Lee, Geoffrey, Eming, Sabine A., Fuchs, Maximilian, Kunz, Meik, Stürmer, Ewa K., Peters, Eva M. J., Berking, Carola, Zinser, Elisabeth, Steinkasserer, Alexander

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Safety and efficacy of epigallocatechin gallate in multiple system atrophy (PROMESA): a randomised, double-blind, placebo-controlled trial by Levin, Johannes, Maaß, Sylvia, Schuberth, Madeleine, Giese, Armin, Oertel, Wolfgang H, Poewe, Werner, Trenkwalder, Claudia, Wenning, Gregor K, Mansmann, Ulrich, Südmeyer, Martin, Eggert, Karla, Mollenhauer, Brit, Lipp, Axel, Löhle, Matthias, Classen, Joseph, Münchau, Alexander, Kassubek, Jan, Gandor, Florin, Berg, Daniela, Egert-Schwender, Silvia, Eberhardt, Cornelia, Paul, Friedemann, Bötzel, Kai, Ertl-Wagner, Birgit, Huppertz, Hans-Jürgen, Ricard, Ingrid, Höglinger, Günter U, André, Elisabeth, Blankenstein, Christiane, Canelo, Monica, Düring, Marco, Ebentheuer, Jens, Fricke, Christopher, Gerbes, Alexander, Groiss, Stefan, Gruber, Doreen, Hartmann, Christian, Kirchner, Thomas, Kroneberg, Daniel, Kunz, Martin, Lorenzl, Stefan, Moldovan, Alexia, Noda, Anna, Pape, Heidi, Respondek, Gesine, Schäffer, Eva, Schneider, Martina, Schnitzler, Alfons, Schulz-Schaeffer, Walter, Schwarz, Johannes, Skowronek, Cornelia, Storch, Alexander, Tadic, Vera, Vadász, Dávid, Zimmermann, Benno

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The p.Arg435His Variation of IgG3 With High Affinity to FcRn Is Associated With Susceptibility for Pemphigus Vulgaris-Analysis of Four Different Ethnic Cohorts by Recke, Andreas, Konitzer, Sarah, Lemcke, Susanne, Freitag, Miriam, Sommer, Nele Maxi, Abdelhady, Mohammad, Amoli, Mahsa M, Benoit, Sandrine, El-Chennawy, Farha, Eldarouti, Mohammad, Eming, Rüdiger, Gläser, Regine, Günther, Claudia, Hadaschik, Eva, Homey, Bernhard, Lieb, Wolfgang, Peitsch, Wiebke K, Pföhler, Claudia, Robati, Reza M, Saeedi, Marjan, Sárdy, Miklós, Sticherling, Michael, Uzun, Soner, Worm, Margitta, Zillikens, Detlef, Ibrahim, Saleh, Vidarsson, Gestur, Schmidt, Enno

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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A by Kasperavičiūtė, Dalia, Catarino, Claudia B., Matarin, Mar, Leu, Costin, Novy, Jan, Tostevin, Anna, Leal, Bárbara, Hessel, Ellen V. S., Hallmann, Kerstin, Hildebrand, Michael S., Dahl, Hans-Henrik M., Ryten, Mina, Trabzuni, Daniah, Ramasamy, Adaikalavan, Alhusaini, Saud, Doherty, Colin P., Dorn, Thomas, Hansen, Jörg, Krämer, Günter, Steinhoff, Bernhard J., Zumsteg, Dominik, Duncan, Susan, Kälviäinen, Reetta K., Eriksson, Kai J., Kantanen, Anne-Mari, Pandolfo, Massimo, Gruber-Sedlmayr, Ursula, Schlachter, Kurt, Reinthaler, Eva M., Stogmann, Elisabeth, Zimprich, Fritz, Théâtre, Emilie, Smith, Colin, O’Brien, Terence J., Meng Tan, K., Petrovski, Slave, Robbiano, Angela, Paravidino, Roberta, Zara, Federico, Striano, Pasquale, Sperling, Michael R., Buono, Russell J., Hakonarson, Hakon, Chaves, João, Costa, Paulo P., Silva, Berta M., da Silva, António M., de Graan, Pierre N. E., Koeleman, Bobby P. C., Becker, Albert, Schoch, Susanne, von Lehe, Marec, Reif, Philipp S., Rosenow, Felix, Becker, Felicitas, Weber, Yvonne, Lerche, Holger, Rössler, Karl, Buchfelder, Michael, Hamer, Hajo M., Kobow, Katja, Coras, Roland, Blumcke, Ingmar, Scheffer, Ingrid E., Berkovic, Samuel F., Weale, Michael E., Delanty, Norman, Depondt, Chantal, Cavalleri, Gianpiero L., Kunz, Wolfram S., Sisodiya, Sanjay M.

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Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study by Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

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The comorbidity profiles and medication issues of patients with multiple system atrophy: a systematic cross-sectional analysis by Ye, Lan, Greten, Stephan, Wegner, Florian, Doll-Lee, Johanna, Krey, Lea, Heine, Johanne, Gandor, Florin, Vogel, Annemarie, Berger, Luise, Gruber, Doreen, Levin, Johannes, Katzdobler, Sabrina, Peters, Oliver, Dashti, Eman, Priller, Josef, Spruth, Eike Jakob, Kühn, Andrea A., Krause, Patricia, Spottke, Annika, Schneider, Anja, Beyle, Aline, Kimmich, Okka, Donix, Markus, Haussmann, Robert, Brandt, Moritz, Dinter, Elisabeth, Wiltfang, Jens, Schott, Björn H., Zerr, Inga, Bähr, Mathias, Buerger, Katharina, Janowitz, Daniel, Perneczky, Robert, Rauchmann, Boris-Stephan, Weidinger, Endy, Düzel, Emrah, Glanz, Wenzel, Teipel, Stefan, Kilimann, Ingo, Wurster, Isabel, Brockmann, Kathrin, Hoffmann, Daniel C., Klockgether, Thomas, Krause, Olaf, Heck, Johannes, Höglinger, Günter U., Klietz, Martin

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Optimised synthesis of monoanionic bis(NHC)-pincer ligand precursors and their Li-complexes by Jürgens, Eva, Buys, Kai N., Schmidt, Anna-Theresa, Furfari, Samantha K., Cole, Marcus L., Moser, Michael, Rominger, Frank, Kunz, Doris

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A systematic classification of death causes in multiple myeloma by Mai, Elias K., Haas, Eva-Maria, Lücke, Stephan, Löpprich, Martin, Kunz, Christina, Pritsch, Maria, Knaup-Gregori, Petra, Raab, Marc S., Schlenzka, Jana, Bertsch, Uta, Hillengass, Jens, Goldschmidt, Hartmut

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Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies by Lal, Dennis, Ruppert, Ann-Kathrin, Trucks, Holger, Schulz, Herbert, de Kovel, Carolien G, Kasteleijn-Nolst Trenité, Dorothée, Sonsma, Anja C M, Koeleman, Bobby P, Lindhout, Dick, Weber, Yvonne G, Lerche, Holger, Kapser, Claudia, Schankin, Christoph J, Kunz, Wolfram S, Surges, Rainer, Elger, Christian E, Gaus, Verena, Schmitz, Bettina, Helbig, Ingo, Muhle, Hiltrud, Stephani, Ulrich, Klein, Karl M, Rosenow, Felix, Neubauer, Bernd A, Reinthaler, Eva M, Zimprich, Fritz, Feucht, Martha, Møller, Rikke S, Hjalgrim, Helle, De Jonghe, Peter, Suls, Arvid, Lieb, Wolfgang, Franke, Andre, Strauch, Konstantin, Gieger, Christian, Schurmann, Claudia, Schminke, Ulf, Nürnberg, Peter, Sander, Thomas

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Polymorphisms in the mitochondrially encoded ATP synthase 8 gene are associated with susceptibility to bullous pemphigoid in the German population by Hirose, Misa, Schilf, Paul, Benoit, Sandrine, Eming, Rüdiger, Gläser, Regine, Homey, Bernhard, Kunz, Manfred, Nebel, Almut, Peitsch, Wiebke K., Pföhler, Claudia, Sárdy, Miklós, Schreiber, Stefan, Zillikens, Detlef, Schmidt, Enno, Ibrahim, Saleh M.

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Optimised synthesis of monoanionic bis(NHC)-pincer ligand precursors and their Li-complexesElectronic supplementary information (ESI) available: CIF files providing experimental an... by Jürgens, Eva, Buys, Kai N, Schmidt, Anna-Theresa, Furfari, Samantha K, Cole, Marcus L, Moser, Michael, Rominger, Frank, Kunz, Doris

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Warfarin Impairs the Bone Marrow Microenvironment and Hematopoiesis Via the Periostin/Integrin β3 Pathway by Verma, Divij, Fulzele, Keertik, Rahul, Kumar, Karantanou, Christina, Pereira, Raquel, Kunz, Kathrin, Hoelper, Soraya, Weissenberger, Eva, Ziegler, Paul K., Chahabi, Sara Zia, Fontenay, Michaela, Pajevic, Paola Divieti, Krause, Daniela S.

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Investigation of GRIN2A in common epilepsy phenotypes by Lal, Dennis, Steinbrücker, Sandra, Schubert, Julian, Sander, Thomas, Becker, Felicitas, Weber, Yvonne, Lerche, Holger, Thiele, Holger, Krause, Roland, Lehesjoki, Anna-Elina, Nürnberg, Peter, Palotie, Aarno, Neubauer, Bernd A, Muhle, Hiltrud, Stephani, Ulrich, Helbig, Ingo, Becker, Albert J, Schoch, Susanne, Hansen, Jörg, Dorn, Thomas, Hohl, Christin, Lüscher, Nicole, von Spiczak, Sarah, Lemke, Johannes R

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Normalization of serum free light chains during therapy in the MM5 trial predicts prolonged progression free survival and overall survival by Haas, Eva-Maria, Salwender, Hans J., Mai, Elias K., Dürig, Jan, Weisel, Katja, Tichy, Diana, Benner, Axel, Kunz, Christina, Hielscher, Thomas, Bertsch, Uta, Besemer, Britta, Merz, Maximilian, Munder, Markus, Lindemann, Hans-Walter, Hügle-Dörr, Barbara, Giessen, Nicola, Hose, Dirk, Seckinger, Anja, Huhn, Stefanie, Luntz, Steffen, Jauch, Anna, Elmaagacli, Ahmet, Rabold, Bernhard, Fuhrmann, Stephan, Brossart, Peter, Goerner, Martin, Bernhard, Helga, Hoffmann, Martin, Hillengass, Jens, Raab, Marc S., Blau, Igor Wolfgang, Haenel, Mathias, Scheid, Christof, Goldschmidt, Hartmut

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Identification of genes expressed in tumor-associated macrophages by Gottfried, Eva, Faust, Stefan, Fritsche, Jana, Kunz-Schughart, Leoni A., Andreesen, Reinhard, Miyake, Kensuke, Kreutz, Marina

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Predicting Psychotherapy Utilization for Patients With Borderline Personality Disorder by Löffler-Stastka, H., Voracek, M., Leithner, K., Fischer-Kern, M., Presslich, E., Kunz, C., Meissel, T.

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