Benyamin, Beben;Esko, Tõnu;Ried, Janina S;Radhakrishnan, Aparna;Vermeulen, Sita H;Traglia, Michela;Gögele, Martin;Anderson, Denise;Broer, Linda;Podmore, Clara;Luan, Jia?an;Kutalik, Zoltan;Sanna, Serena;van der Meer, Peter;Tanaka, Toshiko;Wang, Fudi;Westra, Harm-Jan;Franke, Lude;Mihailov, Evelin;Milani, Lili;Hälldin, Jonas;Winkelmann, Juliane;Meitinger, Thomas;Thiery, Joachim;Peters, Annette;Waldenberger, Melanie;Rendon, Augusto;Jolley, Jennifer;Sambrook, Jennifer;Kiemeney, Lambertus A;Sweep, Fred C;Sala, Cinzia F;Schwienbacher, Christine;Pichler, Irene;Hui, Jennie;Demirkan, Ayse;Isaacs, Aaron;Amin, Najaf;Steri, Maristella;Waeber, Gerard;Verweij, Niek;Powell, Joseph E;Nyholt, Dale R;Heath, Andrew C;Madden, Pamela A F;Visscher, Peter M;Wright, Margaret J;Montgomery, Grant W;Martin, Nicholas G;Hernandez, Dena;Bandinelli, Stefania;van der Harst, Pim;Uda, Manuela;Vollenweider, Peter;Scott, Robert A;Langenberg, Claudia;Wareham, Nicholas J;van Duijn, Cornelia;Beilby, John;Pramstaller, Peter P;Hicks, Andrew A;Ouwehand, Willem H;Oexle, Konrad;Gieger, Christian;Metspalu, Andres;Camaschella, Clara;Toniolo, Daniela;Swinkels, Dorine W;Whitfield, John B
Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
Nat Commun
2015
6
6542

Zech, Michael;Boesch, Sylvia;Jochim, Angela;Graf, Sebastian;Lichtner, Peter;Peters, Annette;Gieger, Christian;Mueller, Joerg;Poewe, Werner;Haslinger, Bernhard;Winkelmann, Juliane
Large-scale TUBB4A mutational screening in isolated dystonia and controls.
Parkinsonism Relat Disord
2015
21
10
1278-81

Stuart, Philip E;Nair, Rajan P;Tsoi, Lam C;Tejasvi, Trilokraj;Das, Sayantan;Kang, Hyun Min;Ellinghaus, Eva;Chandran, Vinod;Callis-Duffin, Kristina;Ike, Robert;Li, Yanming;Wen, Xiaoquan;Enerback, Charlotta;Gudjonsson, Johann E;Kõks, Sulev;Kingo, Külli;Esko, Tõnu;Mrowietz, Ulrich;Reis, André;Wichmann, H Erich;Gieger, Christian;Hoffmann, Per;Nöthen, Markus M;Winkelmann, Juliane;Kunz, Manfred;Moreta, Elvia G;Mease, Philip J;Ritchlin, Christopher T;Bowcock, Anne M;Krueger, Gerald G;Lim, Henry W;Weidinger, Stephan;Weichenthal, Michael;Voorhees, John J;Rahman, Proton;Gregersen, Peter K;Franke, Andre;Gladman, Dafna D;Abecasis, Goncalo R;Elder, James T
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture.
Am J Hum Genet
2015
97
6
816-36

Zech, Michael;Boesch, Sylvia;Sycha, Thomas;Mueller, Joerg;Poewe, Werner;Winkelmann, Juliane
TOR1A, THAP1, and GNAL mutational screening in Austrian patients with primary isolated dystonia.
Mov Disord
2015
30
13
1853-4

Moutsianas, Loukas;Jostins, Luke;Beecham, Ashley H;Dilthey, Alexander T;Xifara, Dionysia K;Ban, Maria;Shah, Tejas S;Patsopoulos, Nikolaos A;Alfredsson, Lars;Anderson, Carl A;Attfield, Katherine E;Baranzini, Sergio E;Barrett, Jeffrey;Binder, Thomas M C;Booth, David;Buck, Dorothea;Celius, Elisabeth G;Cotsapas, Chris;D'Alfonso, Sandra;Dendrou, Calliope A;Donnelly, Peter;Dubois, Bénédicte;Fontaine, Bertrand;Lar Fugger, Lars;Goris, An;Gourraud, Pierre-Antoine;Graetz, Christiane;Hemmer, Bernhard;Hillert, Jan;Kockum, Ingrid;Leslie, Stephen;Lill, Christina M;Martinelli-Boneschi, Filippo;Oksenberg, Jorge R;Olsson, Tomas;Oturai, Annette;Saarela, Janna;Søndergaard, Helle Bach;Spurkland, Anne;Taylor, Bruce;Winkelmann, Juliane;Zipp, Frauke;Haines, Jonathan L;Pericak-Vance, Margaret A;Spencer, Chris C A;Stewart, Graeme;Hafler, David A;Ivinson, Adrian J;Harbo, Hanne F;Hauser, Stephen L;De Jager, Philip L;Compston, Alastair;McCauley, Jacob L;Sawcer, Stephen wcer;McVean, Gil
Class II HLA interactions modulate genetic risk for multiple sclerosis.
Nat Genet
2015
47
10
1107-13

Zech, Michael;Castrop, Florian;Haslinger, Bernhard;Winkelmann, Juliane
Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia.
Mov Disord
2015
30
6
878-9

Trenkwalder, Claudia, C;Winkelmann, Juliane, J;Inoue, Yuichi, Y;Paulus, Walter, W
Restless legs syndrome-current therapies and management of augmentation.
Nat Rev Neurol
2015
11
8
434-45

Schulte, Eva C;Fukumori, Akio;Mollenhauer, Brit;Hor, Hyun;Arzberger, Thomas;Perneczky, Robert;Kurz, Alexander;Diehl-Schmid, Janine;Hüll, Michael;Lichtner, Peter;Eckstein, Gertrud;Zimprich, Alexander;Haubenberger, Dietrich;Pirker, Walter;Brücke, Thomas;Bereznai, Benjamin;Molnar, Maria J;Lorenzo-Betancor, Oswaldo;Pastor, Pau;Peters, Annette;Gieger, Christian;Estivill, Xavier;Meitinger, Thomas;Kretzschmar, Hans A;Trenkwalder, Claudia;Haass, Christian;Winkelmann, Juliane
Rare variants in ?-Amyloid precursor protein (APP) and Parkinson's disease.
Eur J Hum Genet
2015
23
10
1328-33

Zech, Michael;Lam, Daniel D;Francescatto, Ludmila;Schormair, Barbara;Salminen, Aaro V;Jochim, Angela;Wieland, Thomas;Lichtner, Peter;Peters, Annette;Gieger, Christian;Lochmüller, Hanns;Strom, Tim M;Haslinger, Bernhard;Katsanis, Nicholas;Winkelmann, Juliane
Recessive mutations in the ?3 (VI) collagen gene COL6A3 cause early-onset isolated dystonia.
Am J Hum Genet
2015
96
6
883-93