Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
Esslinger, Ulrike, Garnier, Sophie, Korniat, Agathe, Proust, Carole, Kararigas, Georgios, Müller-Nurasyid, Martina, Empana, Jean-Philippe, Morley, Michael P, Perret, Claire, Stark, Klaus, Bick, Alexander G, Prasad, Sanjay K, Kriebel, Jennifer, Li, Jin, Tiret, Laurence, Strauch, Konstantin, O'Regan, Declan P, Marguiles, Kenneth B, Seidman, Jonathan G, Boutouyrie, Pierre, Lacolley, Patrick, Jouven, Xavier, Hengstenberg, Christian, Komajda, Michel, Hakonarson, Hakon, Isnard, Richard, Arbustini, Eloisa, Grallert, Harald, Cook, Stuart A, Seidman, Christine E, Regitz-Zagrosek, Vera, Cappola, Thomas P, Charron, Philippe, Cambien, François, Villard, Eric
Published in PloS one (14.02.2020)
Published in PloS one (14.02.2020)
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Fifteen Genetic Loci Associated With the Electrocardiographic P Wave
Christophersen, Ingrid E, Magnani, Jared W, Yin, Xiaoyan, Barnard, John, Weng, Lu-Chen, Arking, Dan E, Niemeijer, Maartje N, Lubitz, Steven A, Avery, Christy L, Duan, Qing, Felix, Stephan B, Bis, Joshua C, Kerr, Kathleen F, Isaacs, Aaron, Müller-Nurasyid, Martina, Müller, Christian, North, Kari E, Reiner, Alex P, Tinker, Lesley F, Kors, Jan A, Teumer, Alexander, Petersmann, Astrid, Sinner, Moritz F, Buzkova, Petra, Smith, Jonathan D, Van Wagoner, David R, Völker, Uwe, Waldenberger, Melanie, Peters, Annette, Meitinger, Thomas, Limacher, Marian C, Wilhelmsen, Kirk C, Psaty, Bruce M, Hofman, Albert, Uitterlinden, Andre, Krijthe, Bouwe P, Zhang, Zhu-Ming, Schnabel, Renate B, Kääb, Stefan, van Duijn, Cornelia, Rotter, Jerome I, Sotoodehnia, Nona, Dörr, Marcus, Li, Yun, Chung, Mina K, Soliman, Elsayed Z, Alonso, Alvaro, Whitsel, Eric A, Stricker, Bruno H, Benjamin, Emelia J, Heckbert, Susan R, Ellinor, Patrick T
Published in Circulation. Cardiovascular genetics (01.08.2017)
Published in Circulation. Cardiovascular genetics (01.08.2017)
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Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes
Mandaviya, Pooja R, Joehanes, Roby, Aïssi, Dylan, Kühnel, Brigitte, Marioni, Riccardo E, Truong, Vinh, Stolk, Lisette, Beekman, Marian, Bonder, Marc Jan, Franke, Lude, Gieger, Christian, Huan, Tianxiao, Ikram, M Arfan, Kunze, Sonja, Liang, Liming, Lindemans, Jan, Liu, Chunyu, McRae, Allan F, Mendelson, Michael M, Müller-Nurasyid, Martina, Peters, Annette, Slagboom, P Eline, Starr, John M, Trégouët, David-Alexandre, Uitterlinden, André G, van Greevenbroek, Marleen M J, van Heemst, Diana, van Iterson, Maarten, Wells, Philip S, Yao, Chen, Deary, Ian J, Gagnon, France, Heijmans, Bastiaan T, Levy, Daniel, Morange, Pierre-Emmanuel, Waldenberger, Melanie, Heil, Sandra G, van Meurs, Joyce B J
Published in PloS one (30.10.2017)
Published in PloS one (30.10.2017)
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Genetic variants in RBFOX3 are associated with sleep latency
Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Müller-Myhsok, Bertram, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tõnu, van Mill, Josine G, Mbarek, Hamdi, Watson, Nathaniel F, Melville, Scott A, Del Greco, Fabiola M, Byrne, Enda M, Oole, Edwin, Kolcic, Ivana, Chen, Ting-Hsu, Evans, Daniel S, Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A, Zgaga, Lina, Mihailov, Evelin, Stone, Katie L, Campbell, Harry, Brouwer, Rutger Ww, Demirkan, Ayse, Isaacs, Aaron, Dogas, Zoran, Marciante, Kristin D, Campbell, Susan, Borovecki, Fran, Luik, Annemarie I, Li, Man, Hottenga, Jouke Jan, Huffman, Jennifer E, van den Hout, Mirjam Cgn, Cummings, Steven R, Aulchenko, Yurii S, Gehrman, Philip R, Uitterlinden, André G, Wichmann, Heinz-Erich, Müller-Nurasyid, Martina, Fehrmann, Rudolf Sn, Montgomery, Grant W, Hofman, Albert, Kao, Wen Hong Linda, Oostra, Ben A, Wright, Alan F, Vink, Jacqueline M, Wilson, James F, Pramstaller, Peter P, Hicks, Andrew A, Polasek, Ozren, Punjabi, Naresh M, Redline, Susan, Psaty, Bruce M, Heath, Andrew C, Merrow, Martha, Tranah, Gregory J, Gottlieb, Daniel J, Boomsma, Dorret I, Martin, Nicholas G, Rudan, Igor, Tiemeier, Henning, van IJcken, Wilfred Fj, Penninx, Brenda W, Metspalu, Andres, Meitinger, Thomas, Franke, Lude, Roenneberg, Till, van Duijn, Cornelia M
Published in European journal of human genetics : EJHG (01.10.2016)
Published in European journal of human genetics : EJHG (01.10.2016)
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Deciphering the 8q24.21 association for glioma
Enciso-Mora, Victor, Hosking, Fay J, Kinnersley, Ben, Wang, Yufei, Shete, Sanjay, Zelenika, Diana, Broderick, Peter, Idbaih, Ahmed, Delattre, Jean-Yves, Hoang-Xuan, Khe, Marie, Yannick, Di Stefano, Anna Luisa, Labussière, Marianne, Dobbins, Sara, Boisselier, Blandine, Ciccarino, Pietro, Rossetto, Marta, Armstrong, Georgina, Liu, Yanhong, Gousias, Konstantinos, Schramm, Johannes, Lau, Ching, Hepworth, Sarah J, Strauch, Konstantin, Müller-Nurasyid, Martina, Schreiber, Stefan, Franke, Andre, Moebus, Susanne, Eisele, Lewin, Forsti, Asta, Hemminki, Kari, Tomlinson, Ian P, Swerdlow, Anthony, Lathrop, Mark, Simon, Matthias, Bondy, Melissa, Sanson, Marc, Houlston, Richard S
Published in Human molecular genetics (01.06.2013)
Published in Human molecular genetics (01.06.2013)
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Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium
Weng, Lu-Chen, Lunetta, Kathryn L., Müller-Nurasyid, Martina, Smith, Albert Vernon, Thériault, Sébastien, Weeke, Peter E., Barnard, John, Bis, Joshua C., Lyytikäinen, Leo-Pekka, Kleber, Marcus E., Martinsson, Andreas, Lin, Henry J., Rienstra, Michiel, Trompet, Stella, Krijthe, Bouwe P., Dörr, Marcus, Klarin, Derek, Chasman, Daniel I., Sinner, Moritz F., Waldenberger, Melanie, Launer, Lenore J., Harris, Tamara B., Soliman, Elsayed Z., Alonso, Alvaro, Paré, Guillaume, Teixeira, Pedro L., Denny, Joshua C., Shoemaker, M. Benjamin, Van Wagoner, David R., Smith, Jonathan D., Psaty, Bruce M., Sotoodehnia, Nona, Taylor, Kent D., Kähönen, Mika, Nikus, Kjell, Delgado, Graciela E., Melander, Olle, Engström, Gunnar, Yao, Jie, Guo, Xiuqing, Christophersen, Ingrid E., Ellinor, Patrick T., Geelhoed, Bastiaan, Verweij, Niek, Macfarlane, Peter, Ford, Ian, Heeringa, Jan, Franco, Oscar H., Uitterlinden, André G., Völker, Uwe, Teumer, Alexander, Rose, Lynda M., Kääb, Stefan, Gudnason, Vilmundur, Arking, Dan E., Conen, David, Roden, Dan M., Chung, Mina K., Heckbert, Susan R., Benjamin, Emelia J., Lehtimäki, Terho, März, Winfried, Smith, J. Gustav, Rotter, Jerome I., van der Harst, Pim, Jukema, J. Wouter, Stricker, Bruno H., Felix, Stephan B., Albert, Christine M., Lubitz, Steven A.
Published in Scientific reports (12.09.2017)
Published in Scientific reports (12.09.2017)
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Journal Article
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
Esslinger, Ulrike, Garnier, Sophie, Korniat, Agathe, Proust, Carole, Kararigas, Georgios, Müller-Nurasyid, Martina, Empana, Jean-Philippe, Morley, Michael, Perret, Claire, Stark, Klaus, Bick, Alexander, Prasad, Sanjay, Kriebel, Jennifer, Li, Jin, Tiret, Laurence, Strauch, Konstantin, O'Regan, Declan, Marguiles, Kenneth, Seidman, Jonathan, Boutouyrie, Pierre, Lacolley, Patrick, Jouven, Xavier, Hengstenberg, Christian, Komajda, Michel, Hakonarson, Hakon, Isnard, Richard, Arbustini, Eloisa, Grallert, Harald, Cook, Stuart, Seidman, Christine, Regitz-Zagrosek, Vera, Cappola, Thomas, Charron, Philippe, Cambien, François, Villard, Eric
Published in PloS one (15.03.2017)
Published in PloS one (15.03.2017)
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Journal Article
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
Esslinger, Ulrike, Garnier, Sophie, Proust, Carole, Kararigas, Georgios, Müller-Nurasyid, Martina, Empana, Jean-Philippe, Morley, Michael, Perret, Claire, Stark, Klaus, Bick, Alexander, Prasad, Sanjay, Kriebel, Jennifer, Li, Jin, Tiret, Laurence, Strauch, Konstantin, O'Regan, Declan, Marguiles, Kenneth, Seidman, Jonathan, Boutouyrie, Pierre, Lacolley, Patrick, Jouven, Xavier, Hengstenberg, Christian, Komajda, Michel, Hakonarson, Hakon, Isnard, Richard, Arbustini, Eloisa, Grallert, Harald, Cook, Stuart, Seidman, Christine, Regitz-Zagrosek, Vera, Cappola, Thomas, Charron, Philippe, Cambien, François, Villard, Eric
Published in PloS one (15.03.2017)
Published in PloS one (15.03.2017)
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Journal Article
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
Esslinger, Ulrike, Garnier, Sophie, Korniat, Agathe, Proust, Carole, Kararigas, Georgios, Müller-Nurasyid, Martina, Empana, Jean-Philippe, Morley, Michael, Perret, Claire, Stark, Klaus, Bick, Alexander, Prasad, Sanjay, Kriebel, Jennifer, Li, Jin, Tiret, Laurence, Strauch, Konstantin, O'Regan, Declan, Marguiles, Kenneth, Seidman, Jonathan, Boutouyrie, Pierre, Lacolley, Patrick, Jouven, Xavier, Hengstenberg, Christian, Komajda, Michel, Hakonarson, Hakon, Isnard, Richard, Arbustini, Eloisa, Grallert, Harald, Cook, Stuart, Seidman, Christine, Regitz-Zagrosek, Vera, Cappola, Thomas, Charron, Philippe, Cambien, François, Villard, Eric
Published in PloS one (15.03.2017)
Published in PloS one (15.03.2017)
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Controversial association results for INSIG2 on body mass index may be explained by interactions with age and with MC4R
Malzahn, Dörthe, Müller-Nurasyid, Martina, Heid, Iris M, Wichmann, H-Erich, Bickeböller, Heike
Published in European journal of human genetics : EJHG (01.10.2014)
Published in European journal of human genetics : EJHG (01.10.2014)
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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Mahajan, Anubha, Wessel, Jennifer, Willems, Sara, Zhao, Wei, Robertson, Neil, Chu, Audrey, Gan, Wei, Kitajima, Hidetoshi, Taliun, Daniel, Rayner, N. William, Guo, Xiuqing, Lu, Yingchang, Li, Man, Jensen, Richard, Hu, Yao, Huo, Shaofeng, Lohman, Kurt, Zhang, Weihua, Cook, James, Prins, Bram Peter, Flannick, Jason, Grarup, Niels, Trubetskoy, Vassily Vladimirovich, Kravic, Jasmina, Kim, Young Jin, Rybin, Denis, Yaghootkar, Hanieh, Müller-Nurasyid, Martina, Meidtner, Karina, Li-Gao, Ruifang, Varga, Tibor, Marten, Jonathan, Li, Jin, Smith, Albert Vernon, An, Ping, Ligthart, Symen, Gustafsson, Stefan, Malerba, Giovanni, Demirkan, Ayse, Tajes, Juan Fernandez, Steinthorsdottir, Valgerdur, Wuttke, Matthias, Lecoeur, Cécile, Preuss, Michael, Bielak, Lawrence, Graff, Marielisa, Highland, Heather, Justice, Anne, Liu, Dajiang, Marouli, Eirini, Peloso, Gina Marie, Warren, Helen, Afaq, Saima, Afzal, Shoaib, Ahlqvist, Emma, Almgren, Peter, Amin, Najaf, Bang, Lia, Bertoni, Alain, Bombieri, Cristina, Bork-Jensen, Jette, Brandslund, Ivan, Brody, Jennifer, Burtt, Noël, Canouil, Mickaël, Chen, Yii-Der Ida, Cho, Yoon Shin, Christensen, Cramer, Eastwood, Sophie, Eckardt, Kai-Uwe, Fischer, Krista, Gambaro, Giovanni, Giedraitis, Vilmantas, Grove, Megan, de Haan, Hugoline, Hackinger, Sophie, Hai, Yang, Han, Sohee, Tybjærg-Hansen, Anne, Hivert, Marie-France, Isomaa, Bo, Jäger, Susanne, Jørgensen, Marit, Jørgensen, Torben, Käräjämäki, Annemari, Kim, Bong-Jo, Kim, Sung Soo, Koistinen, Heikki, Kovacs, Peter, Kriebel, Jennifer, Kronenberg, Florian, Läll, Kristi, Lange, Leslie, Lee, Jung-Jin, Lehne, Benjamin, Li, Huaixing, Lin, Keng-Hung, Linneberg, Allan, Liu, Ching-Ti, Liu, Jun
Published in Nature genetics (09.04.2018)
Published in Nature genetics (09.04.2018)
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A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern
Sinner, Moritz F., MD, MPH, Porthan, Kimmo, MD, PhD, Noseworthy, Peter A., MD, Havulinna, Aki S., DSc(tech), Tikkanen, Jani T., MD, Müller-Nurasyid, Martina, PhD, Peloso, Gina, PhD, Ulivi, Sheila, PhD, Beckmann, Britt Maria, MD, Brockhaus, A. Catharina, MSc, Cooper, Rebecca R., MA, Gasparini, Paolo, MD, Hengstenberg, Christian, MD, Hwang, Shih-Jen, PhD, Iorio, Annamaria, MD, Junttila, M. Juhani, MD, Klopp, Norman, PhD, Kähönen, Mika, MD, PhD, Laaksonen, Maarit A., PhD, Lehtimäki, Terho, MD, PhD, Lichtner, Peter, PhD, Lyytikäinen, Leo-Pekka, MD, Martens, Eimo, MD, Meisinger, Christa, MD, Meitinger, Thomas, MD, MSc, Merchant, Faisal M., MD, Nieminen, Markku S., MD, Peters, Annette, PhD, Pietilä, Arto, MSc, Perz, Siegfried, MSc, Oikarinen, Lasse, MD, PhD, Raitakari, Olli, MD, PhD, Reinhard, Wibke, MD, MBA, Silander, Kaisa, PhD, Thorand, Barbara, PhD, MPH, Wichmann, H.-Erich, MD, PhD, Sinagra, Gianfranco, MD, Viikari, Jorma, MD, PhD, O'Donnell, Christopher J., MD, MPH, Ellinor, Patrick T., MD, PhD, Huikuri, Heikki V., MD, Kääb, Stefan, MD, PhD, Newton-Cheh, Christopher, MD, MPH, Salomaa, Veikko, MD, PhD
Published in Heart rhythm (01.10.2012)
Published in Heart rhythm (01.10.2012)
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Simulation of Finnish Population History, Guided by Empirical Genetic Data, to Assess Power of Rare-Variant Tests in Finland
Wang, Sophie R., Agarwala, Vineeta, Flannick, Jason, Chiang, Charleston W.K., Altshuler, David, Flannick, Jason, Manning, Alisa, Hartl, Christopher, Agarwala, Vineeta, Fontanillas, Pierre, Green, Todd, Banks, Eric, DePristo, Mark, Poplin, Ryan, Shakir, Khalid, Fennell, Timothy, Murphy, Jacquelyn, Burtt, Noël, Gabriel, Stacey, Altshuler, David, Fuchsberger, Christian, Kang, Hyun Min, Sim, Xueling, Ma, Clement, Locke, Adam, Blackwell, Thomas, Jackson, Anne, Teslovich, Tanya, Stringham, Heather, Chines, Peter, Kwan, Phoenix, Huyghe, Jeroen, Tan, Adrian, Jun, Goo, Stitzel, Michael, Bergman, Richard N., Bonnycastle, Lori, Tuomilehto, Jaakko, Collins, Francis S., Scott, Laura, Mohlke, Karen, Abecasis, Gonçalo, Boehnke, Michael, Strom, Tim, Gieger, Christian, Müller-Nurasyid, Martina, Grallert, Harald, Kriebel, Jennifer, Ried, Janina, Hrabé de Angelis, Martin, Huth, Cornelia, Meisinger, Christa, Peters, Annette, Rathmann, Wolfgang, Strauch, Konstantin, Meitinger, Thomas, Kravic, Jasmina, Ladenvall, Claes, Toumi, Tiinamaija, Isomaa, Bo, Groop, Leif, Gaulton, Kyle, Moutsianas, Loukas, Rivas, Manny, Pearson, Richard, Mahajan, Anubha, Prokopenko, Inga, Kumar, Ashish, Perry, John, Chen, Jeff, Howie, Bryan, van de Bunt, Martijn, Small, Kerrin, Lindgren, Cecilia, Lunter, Gerton, Robertson, Neil, Rayner, Will, Morris, Andrew, Buck, David, Hattersley, Andrew, Spector, Tim, McVean, Gil, Frayling, Tim, Donnelly, Peter, McCarthy, Mark, Hirschhorn, Joel N.
Published in American journal of human genetics (01.05.2014)
Published in American journal of human genetics (01.05.2014)
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Immunochip analysis identifies association of the RAD 50/ IL 13 region with human longevity
Flachsbart, Friederike, Ellinghaus, David, Gentschew, Liljana, Heinsen, Femke‐Anouska, Caliebe, Amke, Christiansen, Lene, Nygaard, Marianne, Christensen, Kaare, Blanché, Hélène, Deleuze, Jean‐François, Derbois, Céline, Galan, Pilar, Büning, Carsten, Brand, Stephan, Peters, Anette, Strauch, Konstantin, Müller‐Nurasyid, Martina, Hoffmann, Per, Nöthen, Markus M., Lieb, Wolfgang, Franke, Andre, Schreiber, Stefan, Nebel, Almut
Published in Aging cell (01.06.2016)
Published in Aging cell (01.06.2016)
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Large-Scale Candidate Gene Analysis in Whites and African Americans Identifies IL6R Polymorphism in Relation to Atrial Fibrillation: The National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) Project
SCHNABEL, Renate B, KERR, Kathleen F, LUNETTA, Kathryn L, MEHRA, Reena, LEVY, Daniel, FOX, Ervin R, ARKING, Dan E, MOSLEY, Thomas H, MÜLLER-NURASYID, Martina, YOUNG, Taylor R, WICHMANN, H.-Erich, SESHADRI, Sudha, LUBITZ, Steven A, FARLOW, Deborah N, ROTTER, Jerome I, SOLIMAN, Elsayed Z, GLAZER, Nicole L, WILSON, James G, BRETELER, Monique M. B, SOTOODEHNIA, Nona, NEWTON-CHEH, Christonher, KÄÄB, Stefan, ELLINOR, Patrick T, ALKYLBEKOVA, Ermeg L, ALONSO, Alvaro, BENJAMIN, Emelia J, HECKBERT, Susan R, MARCUS, Gregory M, SINNER, Moritz F, MAGNANI, Jared W, WOLF, Philip A, DEO, Rajat, LLOYD-JONES, Donald M
Published in Circulation. Cardiovascular genetics (01.10.2011)
Published in Circulation. Cardiovascular genetics (01.10.2011)
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Risk Scores in ST-Segment Elevation Myocardial Infarction Patients with Refractory Cardiogenic Shock and Veno-Arterial Extracorporeal Membrane Oxygenation
Semaan, Carl, Charbonnier, Arthur, Pasco, Jeremy, Darwiche, Walid, Saint Etienne, Christophe, Bailleul, Xavier, Bourguignon, Thierry, Fauchier, Laurent, Angoulvant, Denis, Ivanes, Fabrice, Genet, Thibaud
Published in Journal of clinical medicine (01.03.2021)
Published in Journal of clinical medicine (01.03.2021)
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Heritability of young- and old-onset ischemic stroke
Bluher, Andrew, Devan, William J., Holliday, Elizabeth G., Nalls, Michael, Parolo, Silvia, Bione, Silvia, Giese, Anne-Katrin, Boncoraglio, Giorgio B., Maguire, Jane M., Müller-Nurasyid, Martina, Gieger, Christian, Meschia, James F., Rosand, Jonathan, Rolfs, Arndt, Kittner, Steven J., Mitchell, Braxton D., O’Connell, Jeffrey R., Cheng, Yu-Ching
Published in European journal of neurology (02.09.2015)
Published in European journal of neurology (02.09.2015)
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Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia
Reiner, Alexander P, Hartiala, Jaana, Zeller, Tanja, Bis, Joshua C, Dupuis, Josée, Fornage, Myriam, Baumert, Jens, Kleber, Marcus E, Wild, Philipp S, Baldus, Stephan, Bielinski, Suzette J, Fontes, João D, Illig, Thomas, Keating, Brendan J, Lange, Leslie A, Ojeda, Francisco, Müller-Nurasyid, Martina, Munzel, Thomas F, Psaty, Bruce M, Rice, Kenneth, Rotter, Jerome I, Schnabel, Renate B, Tang, W H Wilson, Thorand, Barbara, Erdmann, Jeanette, Jacobs, Jr, David R, Wilson, James G, Koenig, Wolfgang, Tracy, Russell P, Blankenberg, Stefan, März, Winfried, Gross, Myron D, Benjamin, Emelia J, Hazen, Stanley L, Allayee, Hooman
Published in Human molecular genetics (15.08.2013)
Published in Human molecular genetics (15.08.2013)
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TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patients
Koumakis, Eugénie, Wipff, Julien, Dieudé, Philippe, Ruiz, Barbara, Bouaziz, Matthieu, Revillod, Lucile, Guedj, Mickaël, Distler, Jörg H W, Matucci-Cerinic, Marco, Humbert, Marc, Riemekasten, Gabriella, Airo, Paolo, Melchers, Inga, Hachulla, Eric, Cusi, Daniele, Wichmann, H- Erich, Hunzelmann, Nicolas, Tiev, Kiet, Caramaschi, Paola, Diot, Elisabeth, Kowal-Bielecka, Otylia, Cuomo, Giovanna, Walker, Ulrich, Czirják, László, Damjanov, Nemanja, Lupoli, Sara, Conti, Costanza, Müller-Nurasyid, Martina, Müller-Ladner, Ulf, Riccieri, Valeria, Cracowski, Jean-Luc, Cozzi, Franco, Bournia, Vasiliki Kalliopi, Vlachoyiannopoulos, P, Chiocchia, Gilles, Boileau, Catherine, Allanore, Yannick
Published in Annals of the rheumatic diseases (01.11.2012)
Published in Annals of the rheumatic diseases (01.11.2012)
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