Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1 von Winkelmann, Juliane, Czamara, Darina, Schormair, Barbara, Knauf, Franziska, Schulte, Eva C, Trenkwalder, Claudia, Dauvilliers, Yves, Polo, Olli, Högl, Birgit, Berger, Klaus, Fuhs, Andrea, Gross, Nadine, Stiasny-Kolster, Karin, Oertel, Wolfgang, Bachmann, Cornelius G, Paulus, Walter, Xiong, Lan, Montplaisir, Jacques, Rouleau, Guy A, Fietze, Ingo, Vávrová, Jana, Kemlink, David, Sonka, Karel, Nevsimalova, Sona, Lin, Siong-Chi, Wszolek, Zbigniew, Vilariño-Güell, Carles, Farrer, Matthew J, Gschliesser, Viola, Frauscher, Birgit, Falkenstetter, Tina, Poewe, Werner, Allen, Richard P, Earley, Christopher J, Ondo, William G, Le, Wei-Dong, Spieler, Derek, Kaffe, Maria, Zimprich, Alexander, Kettunen, Johannes, Perola, Markus, Silander, Kaisa, Cournu-Rebeix, Isabelle, Francavilla, Marcella, Fontenille, Claire, Fontaine, Bertrand, Vodicka, Pavel, Prokisch, Holger, Lichtner, Peter, Peppard, Paul, Faraco, Juliette, Mignot, Emmanuel, Gieger, Christian, Illig, Thomas, Wichmann, H-Erich, Müller-Myhsok, Bertram, Meitinger, Thomas

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Effect of blood pressure-lowering agents on microvascular function in people with small vessel diseases (TREAT-SVDs): a multicentre, open-label, randomised, crossover trial von Kopczak, Anna, Stringer, Michael S, van den Brink, Hilde, Kerkhofs, Danielle, Blair, Gordon W, van Dinther, Maud, Reyes, Carmen Arteaga, Garcia, Daniela Jaime, Onkenhout, Laurien, Wartolowska, Karolina A, Thrippleton, Michael J, Kampaite, Agniete, Duering, Marco, Staals, Julie, Lesnik-Oberstein, Saskia, Muir, Keith W, Middeke, Martin, Norrving, Bo, Bousser, Marie-Germaine, Mansmann, Ulrich, Rothwell, Peter M, Doubal, Fergus N, van Oostenbrugge, Robert, Biessels, Geert Jan, Webb, Alastair J S, Wardlaw, Joanna M, Dichgans, Martin, Kopczak, Anna, Stringer, Michael S., van den Brink, Hilde, Kerkhofs, Danielle, Blair, Gordon W., van Dinther, Maud, Arteaga Reyes, Carmen, Jaime Garcia, Daniela, Onkenhout, Laurien, Wartolowska, Karolina A., Thrippleton, Michael J., Kampaite, Agniete, Duering, Marco, Staals, Julie, Lesnik-Oberstein, Saskia, Muir, Keith, Middeke, Martin, Norrving, Bo, Bousser, Marie-Germaine, Mansmann, Ulrich, Rothwell, Peter M., Doubal, Fergus N., van Oostenbrugge, Robert, Biessels, Geert Jan, Webb, Alastair J.S., Wardlaw, Joanna, Dichgans, Martin, André, Elisabeth, Kääb, Stefan, Anders, Hans-Joachim, Hack, Remco, Kaffe, Maria, Dewenter, Anna, Malik, Rainer

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Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon von Spieler, Derek, Kaffe, Maria, Knauf, Franziska, Bessa, José, Tena, Juan J, Giesert, Florian, Schormair, Barbara, Tilch, Erik, Lee, Heekyoung, Horsch, Marion, Czamara, Darina, Karbalai, Nazanin, von Toerne, Christine, Waldenberger, Melanie, Gieger, Christian, Lichtner, Peter, Claussnitzer, Melina, Naumann, Ronald, Müller-Myhsok, Bertram, Torres, Miguel, Garrett, Lillian, Rozman, Jan, Klingenspor, Martin, Gailus-Durner, Valérie, Fuchs, Helmut, Hrabě de Angelis, Martin, Beckers, Johannes, Hölter, Sabine M, Meitinger, Thomas, Hauck, Stefanie M, Laumen, Helmut, Wurst, Wolfgang, Casares, Fernando, Gómez-Skarmeta, Jose Luis, Winkelmann, Juliane

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Intensive heart rhythm monitoring to decrease ischemic stroke and systemic embolism—the Find-AF 2 study—rationale and design von Weber-Krüger, Mark, Laufs, Ulrich, Prettin, Christiane, Michalski, Dominik, Etgen, Thorleif, Schellinger, Peter D., Ertl, Michael, Kallmünzer, Bernd, Althaus, Katharina, Hamann, Gerhard F., Mende, Meinhard, Gröschel, Klaus, Köhrmann, Martin, Gröschel, Sonja, Huber, Charlotte, Pelz, Johann, Michalski, Dominik, Kroneberger, Christian, Lingnau, Michale, Schieffer, Miriam, Schertel, Jill Marie, Heyse, Miriam, Ungerer, Matthias, Milanković-Eberl, Dragana, Höcherl, Constanze, Asch, Eric-Manuel, Braadt, Lino-Dominic, Gabrielyan, Inessa, Stirbulescu, Corina, Burgholte, Friederike, Lüers, Claus, Steiner, Thorsten, Cierpinski, Mari-Carmen, Lichti, Bethke, Florian, Vajda-Medina, Esteban, Essa, Hisham, Frank, Benedikt, Stolte, Benjamin, Milles, Lennart, Dimitriadis, Konstantinos, Steiger, Ignaz, Markmann-Boenke, Silke, Macha, Kosmas, Kossel, Clara-Sophie, Cidlinsky, Peter, Vogl, Christine, Fischer, Thomas, Huttelmaier, Moritz, Nordbeck, Octavian Maniuc Peter, von Hardenberg, Albrecht, Jünemann, Martin, Gerner, Stefan, Omar, AlHaj, Wassenberg, Matthias, Hoffmann, Frank, Schönmuth, Bettine, Hütwohl, Daniela, Krause, Lars Udo, Althaus, Katharina, Schellong, Sebastian, Gerk, Ulrich, Burian, Katja, Angermüller, Veronika, Alhammoud, Tameem, Cakiroglu, Hüsniye, Bach, Ullrich, Müller, Robert, Pallesen, Lars-Peder, Keilitz, Janina, Krämer, Christoffer, Wiemers, Milena, Simon, Micha, Finke, Alexander, Expósito, Alexandra Gómez, Mbroh, Joshua, Ritter, Nicolas, Seibel, Lena, Nägele, Herbert, Sydow, Karsten, Schäfer, Jan Hendrik, Charisse, Daniel, Gruber, Katharina, Petzold, Gabor, Ebrahimi, Taraneh, Beckonert, Niklas, Mahnkopf, Christian, Gelderblom, Mathias, Jensen, Märit, Schlemm, Eckhard, Marquardt, Lars, Berthel, Jörg, Strik, Herwig, Honermann, Martin, Burgstaller, Marian Christoph, Ganai, Ahmad Ajaz, Toluli, Adela, Wollenweber, Frank Arne, Silva, Thais Portugal, Lee, Miri

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Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls von Zech, Michael, Gross, Nadine, Jochim, Angela, Castrop, Florian, Kaffe, Maria, Dresel, Christian, Lichtner, Peter, Peters, Annette, Gieger, Christian, Meitinger, Thomas, Haslinger, Bernhard, Winkelmann, Juliane

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Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome von Wieczorek, Dagmar, Newman, William G., Wieland, Thomas, Berulava, Tea, Kaffe, Maria, Falkenstein, Daniela, Beetz, Christian, Graf, Elisabeth, Schwarzmayr, Thomas, Douzgou, Sofia, Clayton-Smith, Jill, Daly, Sarah B., Williams, Simon G., Bhaskar, Sanjeev S., Urquhart, Jill E., Anderson, Beverley, O’Sullivan, James, Boute, Odile, Gundlach, Jasmin, Czeschik, Johanna Christina, van Essen, Anthonie J., Hazan, Filiz, Park, Sarah, Hing, Anne, Kuechler, Alma, Lohmann, Dietmar R., Ludwig, Kerstin U., Mangold, Elisabeth, Steenpaß, Laura, Zeschnigk, Michael, Lemke, Johannes R., Lourenco, Charles Marques, Hehr, Ute, Prott, Eva-Christina, Waldenberger, Melanie, Böhmer, Anne C., Horsthemke, Bernhard, O’Keefe, Raymond T., Meitinger, Thomas, Burn, John, Lüdecke, Hermann-Josef, Strom, Tim M.

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MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease von Schormair, Barbara, Plag, Jens, Kaffe, Maria, Groß, Nadine, Czamara, Darina, Samtleben, Walter, Lichtner, Peter, Ströhle, Andreas, Stefanidis, Ioannis, Vainas, Andreas, Dardiotis, Efthimios, Sakkas, George K, Gieger, Christian, Müller-Myhsok, Bertram, Meitinger, Thomas, Heemann, Uwe, Hadjigeorgiou, Georgios M, Oexle, Konrad, Winkelmann, Juliane

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Mutational screening of THAP1 in a German population with primary dystonia von Kaffe, Maria, Gross, Nadine, Castrop, Florian, Dresel, Christian, Gieger, Christian, Lichtner, Peter, Haslinger, Bernhard, Winkelmann, Juliane

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Iron in Restless Legs Syndrome von Schulte, Eva C., Kaffe, Maria, Schormair, Barbara, Winkelmann, Juliane

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MEIS1 and BTBD9 - genetic association with RLS in end-stage renal disease von Schormair, Barbara, Plag, Jens, Kaffe, Maria, Gross, Nadine, Czamara, Darina, Samtleben, Walter, Lichtner, Peter, Ströhle, Andreas, Stefanidis, Ioannis, Vainas, Andreas, Dardiotis, Efthimios, Sakkas, George K, Müller-Mhysok, Bertram, Meitinger, Thomas, Heemann, Uwe, Hadjigeorgiou, Georgios M, Oexle, Konrad, Winkelmann, Juliane, Gieger, Christian

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MEIS 1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease von SCHORMAIR, Barbara, PLAG, Jens, DARDIOTIS, Efthimios, SAKKAS, George K, GIEGER, Christian, MÜLLER-MYHSOK, Bertram, MEITINGER, Thomas, HEEMANN, Uwe, HADJIGEORGIOU, Georgios M, OEXLE, Konrad, WINKELMANN, Juliane, KAFFE, Maria, GRASS, Nadine, CZAMARA, Darina, SAMTLEBEN, Walter, LICHTNER, Peter, STRÖHLE, Andreas, STEFANIDIS, Loannis, VAINAS, Andreas

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Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 von Winkelmann, Juliane, Czamara, Darina, Schormair, Barbara, Knauf, Franziska, Schulte, Eva C., Trenkwalder, Claudia, Dauvilliers, Yves, Polo, Olli, Högl, Birgit, Berger, Klaus, Fuhs, Andrea, Gross, Nadine, Stiasny-Kolster, Karin, Oertel, Wolfgang, Bachmann, Cornelius G., Paulus, Walter, Xiong, Lan, Montplaisir, Jacques, Rouleau, Guy A., Fietze, Ingo, Vávrová, Jana, Kemlink, David, Sonka, Karel, Nevsimalova, Sona, Lin, Siong-Chi, Wszolek, Zbigniew, Vilariño-Güell, Carles, Farrer, Matthew J., Gschliesser, Viola, Frauscher, Birgit, Falkenstetter, Tina, Poewe, Werner, Allen, Richard P., Earley, Christopher J., Ondo, William G., Le, Wei-Dong, Spieler, Derek, Kaffe, Maria, Zimprich, Alexander, Kettunen, Johannes, Perola, Markus, Silander, Kaisa, Cournu-Rebeix, Isabelle, Francavilla, Marcella, Fontenille, Claire, Fontaine, Bertrand, Vodicka, Pavel, Prokisch, Holger, Lichtner, Peter, Peppard, Paul, Faraco, Juliette, Mignot, Emmanuel, Gieger, Christian, Illig, Thomas, Wichmann, H.-Erich, Müller-Myhsok, Bertram, Meitinger, Thomas

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Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 von Juliane Winkelmann, Darina Czamara, Barbara Schormair, Franziska Knauf, Eva C. Schulte, Claudia Trenkwalder, Yves Dauvilliers, Olli Polo, Birgit Högl, Klaus Berger, Andrea Fuhs, Nadine Gross, Karin Stiasny-Kolster, Wolfgang Oertel, Cornelius G. Bachmann, Walter Paulus, Lan Xiong, Jacques Montplaisir, Guy A. Rouleau, Ingo Fietze, Jana Vávrová, David Kemlink, Karel Sonka, Sona Nevsimalova, Siong-Chi Lin, Zbigniew Wszolek, Carles Vilariño-Güell, Matthew J. Farrer, Viola Gschliesser, Birgit Frauscher, Tina Falkenstetter, Werner Poewe, Richard P. Allen, Christopher J. Earley, William G. Ondo, Wei-Dong Le, Derek Spieler, Maria Kaffe, Alexander Zimprich, Johannes Kettunen, Markus Perola, Kaisa Silander, Isabelle Cournu-Rebeix, Marcella Francavilla, Claire Fontenille, Bertrand Fontaine, Pavel Vodicka, Holger Prokisch, Peter Lichtner, Paul Peppard, Juliette Faraco, Emmanuel Mignot, Christian Gieger, Thomas Illig, H.-Erich Wichmann, Bertram Müller-Myhsok, Thomas Meitinger

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Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1: e1002171 von Winkelmann, Juliane, Czamara, Darina, Schormair, Barbara, Knauf, Franziska, Schulte, Eva C, Trenkwalder, Claudia, Dauvilliers, Yves, Polo, Olli, Högl, Birgit, Berger, Klaus, Fuhs, Andrea, Gross, Nadine, Stiasny-Kolster, Karin, Oertel, Wolfgang, Bachmann, Cornelius G, Paulus, Walter, Xiong, Lan, Montplaisir, Jacques, Rouleau, Guy A, Fietze, Ingo, Vávrová, Jana, Kemlink, David, Sonka, Karel, Nevsimalova, Sona, Lin, Siong-Chi, Wszolek, Zbigniew, Vilariño-Güell, Carles, Farrer, Matthew J, Gschliesser, Viola, Frauscher, Birgit, Falkenstetter, Tina, Poewe, Werner, Allen, Richard P, Earley, Christopher J, Ondo, William G, Le, Wei-Dong, Spieler, Derek, Kaffe, Maria, Zimprich, Alexander, Kettunen, Johannes, Perola, Markus, Silander, Kaisa, Cournu-Rebeix, Isabelle, Francavilla, Marcella, Fontenille, Claire, Fontaine, Bertrand, Vodicka, Pavel, Prokisch, Holger, Lichtner, Peter, Peppard, Paul, Faraco, Juliette, Mignot, Emmanuel, Gieger, Christian, Illig, Thomas, Wichmann, H-Erich, Müller-Myhsok, Bertram, Meitinger, Thomas

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Intensive heart rhythm monitoring to decrease ischemic stroke and systemic embolism—the Find-AF 2 study—rationale and design von Uhe, Tobias, Laufs, Ulrich, Gelbrich, Götz, Schellinger, Peter D, Grond, Martin, Hamann, Gerhard F, Mende, Meinhard, Wachter, Rolf, Hahn, Marianne, Kitsiou, Alkisti, Huber, Charlotte, Wartenberg, Katja, Goschenhofer, Anna, Hussain, Rabia-Basari, Sparenberg, Paul, Berberich, Anne, Bauer, Gregor, Reichardt, Christine, Ebel, Bernhard, Asch, Eric-Manuel, Braadt, Lino-Dominic, Kermer, Pawel, Kaste, Matthias, Anter, Ahmed, Meleshchenco, Nataliia, Burgholte, Friederike, Mari-Carmen, Lichti, Probst, Mareike, Essa, Hisham, Frank, Benedikt, Dimitriadis, Konstantinos, Kopczak, Anna, Kaffe, Maria, Clauß, Sebastian, Janowitz, Daniel, Jenniges, Simone, Wiemer, Marcus, Häusler, Georg, Hametner, Christian, Fischer, Thomas, Huttelmaier, Moritz, Nordbeck, Octavian Maniuc Peter, von Hardenberg, Albrecht, Braun, Tobias, Gerner, Stefan, Omar, AlHaj, Wassenberg, Matthias, Langguth, Niklas, Baumgart, Romy, Diel, Norma, Weber, Lorenz, Hütwohl, Daniela, Schellong, Sebastian, Brudzinski, Mirko, Schmitz, Bettina, Crome, Olaf, Dimitrijeski, Boris, Müller, Robert, Hartmann, Christian, Berrouschot, Jörg, Stoll, Anett, Keilitz, Janina, Klunk, Dietrich, Voigt, Roman, Kastrup, Andreas, Schröter, Andreas, Schmucker, Johannes, Krämer, Christoffer, Wiemers, Milena, Bley-Renning, Karen, Mengel, Annerose, Expósito, Alexandra Gómez, Mbroh, Joshua, Ketzler, Rebecca, Kurka, Natalia, Kohlhase, Konstantin, Lieschke, Franziska, Operhalski, Felix, Stösser, Sebastian, Beckonert, Niklas, Jochmann, Svenja, Benesch, Sonka, Butz, Steffi, Forkmann, Mathias, Deb-Chatterji, Milani, Cheng, Bastian, Hoppe, Julia, Schell, Maximilian, Marquardt, Lars, Hötzer, Kai, Neumann-Haefelin, Tobias, Alijaj, Lirim, Niethammer, Margit, Szöllösi, Géza-Attila, Obermann, Marc, Lenz, Arne, Honermann, Martin, Rahban, Laya, Silva, Thais Portugal, Minnerup, Jens

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Functional analysis of the RLS-associated MEIS1 intronic locus von Kaffe, Maria

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MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease von Schormair, Barbara, Plag, Jens, Kaffe, Maria, Gross, Nadine, Czamara, Darina, Samtleben, Walter, Lichtner, Peter, Ströhle, Andreas, Stefanidis, Ioannis, Vainas, Andreas, Dardiotis, Efthimios, Sakkas, George K, Gieger, Christian, Müller-Myhsok, Bertram, Meitinger, Thomas, Heemann, Uwe, Hadjigeorgiou, Georgios M, Oexle, Konrad, Winkelmann, Juliane

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Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 von Winkelmann, Juliane, Czamara, Darina, Schormair, Barbara, Knauf, Franziska, Schulte, Eva C, Trenkwalder, Claudia, Dauvilliers, Yves, Polo, Olli, Hoegl, Birgit, Berger, Klaus, Fuhs, Andrea, Gross, Nadine, Stiasny-Kolster, Karin, Oertel, Wolfgang, Bachmann, Cornelius G, Paulus, Walter, Xiong, Lan, Montplaisir, Jacques, Rouleau, Guy A, Fietze, Ingo, Vavrova, Jana, Kemlink, David, Sonka, Karel, Nevsimalova, Sona, Lin, Siong-Chi, Wszolek, Zbigniew, Vilarino-Gueell, Carles, Farrer, Matthew J, Gschliesser, Viola, Frauscher, Birgit, Falkenstetter, Tina, Poewe, Werner, Allen, Richard P, Earley, Christopher J, Ondo, William G, Le, Wei-Dong, Spieler, Derek, Kaffe, Maria, Zimprich, Alexander, Kettunen, Johannes, Perola, Markus, Silander, Kaisa, Cournu-Rebeix, Isabelle, Francavilla, Marcella, Fontenille, Claire, Fontaine, Bertrand, Vodicka, Pavel, Prokisch, Holger, Lichtner, Peter, Peppard, Paul, Faraco, Juliette, Mignot, Emmanuel, Gieger, Christian, Illig, Thomas, Wichmann, Heinz-Erich, Mueller-Myhsok, Bertram, Meitinger, Thomas

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Nicotinamide enhances myelin production after demyelination through reduction of astrogliosis and microgliosis von Kaplanis, Stefanos Ioannis, Kaffe, Despoina, Ktena, Niki, Lygeraki, Andriani, Kolliniati, Ourania, Savvaki, Maria, Karagogeos, Domna

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MAP3K8 Regulates Cox-2–Mediated Prostaglandin E2 Production in the Lung and Suppresses Pulmonary Inflammation and Fibrosis von Zannikou, Markella, Barbayianni, Ilianna, Fanidis, Dionysios, Grigorakaki, Theodora, Vlachopoulou, Evlalia, Konstantopoulos, Dimitris, Fousteri, Maria, Nikitopoulou, Ioanna, Kotanidou, Anastasia, Kaffe, Eleanna, Aidinis, Vassilis

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