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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
Vasquez, Alejandro Arias, Renteria, Miguel E., Agartz, Ingrid, Apostolova, Liana G., Bastin, Mark E., Bauer, Michael, Bearden, Carrie E., Binder, Elisabeth B., Bøen, Erlend, Bowman, Ian J., Brohawn, David G., Buitelaar, Jan, Carless, Melanie A., Ching, Christopher R. K., Conrod, Patricia, Depondt, Chantal, de Zubicaray, Greig I., Djurovic, Srdjan, Duggirala, Ravindranath, Dyer, Thomas D., Ekman, Carl Johan, Emsell, Louise, Fears, Scott, Fedko, Iryna, Fox, Peter T., Francks, Clyde, Frodl, Thomas, Frouin, Vincent, Godlewska, Beata, Haukvik, Unn K., Hickie, Ian B., Hoekstra, Pieter J., Homuth, Georg, Hulshoff Pol, Hilleke E., Hwang, Kristy S., Kim, Sungeun, Kochunov, Peter, Krämer, Bernd, Kwok, John B. J., Laje, Gonzalo, Landman, Bennett A., Lauriello, John, Li, Chiang-shan, Liberg, Benny, Liu, Xinmin, Macciardi, Fabio, Malt, Ulrik F., Mattheisen, Manuel, Meyer-Lindenberg, Andreas, Melle, Ingrid, Mohnke, Sebastian, Morris, Derek W., Mueller, Bryon A., Mühleisen, Thomas W., Müller-Myhsok, Bertram, Nichols, Thomas E., Oosterlaan, Jaap, Pandolfo, Massimo, Papmeyer, Martina, Pausova, Zdenka, Penninx, Brenda W., Peterson, Charles P., Potkin, Steven G., Rasmussen, Jerod, Rijpkema, Mark, Risacher, Shannon L., Roiz-Santiañez, Roberto, Romanczuk-Seiferth, Nina, Rujescu, Dan, Salami, Alireza, Scanlon, Cathy, Schmaal, Lianne, Schnack, Hugo G., Schork, Andrew J., Seidman, Larry, Shen, Li, Smoller, Jordan W., Sponheim, Scott R., Starr, John M., Sussmann, Jessika, Sämann, Philipp G., Teumer, Alexander, Toga, Arthur W., Trabzuni, Daniah, Turner, Jessica, Van den Heuvel, Martijn, van Eijk, Kristel, van Erp, Theo G. M., van Haren, Neeltje E. M., van ‘t Ent, Dennis, van Tol, Marie-Jose, Valdés Hernández, Maria C., Versace, Amelia, Weale, Michael E., Westlye, Lars T., Whelan, Christopher D., Wittfeld, Katharina, Zilles, David, Freimer, Nelson B., Lawrence, Natalia S.
Published in Brain imaging and behavior (01.06.2014)
Published in Brain imaging and behavior (01.06.2014)
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Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Chen, Ming-Huei, Raffield, Laura M., Mousas, Abdou, Sakaue, Saori, Huffman, Jennifer E., Moscati, Arden, Trivedi, Bhavi, Jiang, Tao, Akbari, Parsa, Vuckovic, Dragana, Bao, Erik L., Zhong, Xue, Manansala, Regina, Laplante, Véronique, Chen, Minhui, Lo, Ken Sin, Qian, Huijun, Lareau, Caleb A., Beaudoin, Mélissa, Akiyama, Masato, Ben-Shlomo, Yoav, Beswick, Andrew, Bottinger, Erwin P., Brody, Jennifer A., van Rooij, Frank J.A., Cho, Kelly, Choquet, Hélène, Correa, Adolfo, Di Angelantonio, Emanuele, Dimou, Niki, Ding, Jingzhong, Elliott, Paul, Esko, Tõnu, Evans, Michele K., Floyd, James S., Broer, Linda, Grarup, Niels, Guo, Michael H., Greinacher, Andreas, Haessler, Jeff, Hansen, Torben, Howson, Joanna M.M., Huang, Qin Qin, Huang, Wei, Jorgenson, Eric, Kacprowski, Tim, Kanai, Masahiro, Karthikeyan, Savita, Koskeridis, Fotis, Lange, Leslie A., Lerch, Markus M., Linneberg, Allan, Liu, Yongmei, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Martin, Hilary C., Matsuda, Koichi, Mohlke, Karen L., Mononen, Nina, Murakami, Yoshinori, Nadkarni, Girish N., Nauck, Matthias, Nikus, Kjell, Ouwehand, Willem H., Pankratz, Nathan, Pedersen, Oluf, Preuss, Michael, Psaty, Bruce M., Raitakari, Olli T., Roberts, David J., Rich, Stephen S., Rodriguez, Benjamin A.T., Rosen, Jonathan D., Rotter, Jerome I., Schubert, Petra, Spracklen, Cassandra N., Surendran, Praveen, Tang, Hua, Tardif, Jean-Claude, Trembath, Richard C., Ghanbari, Mohsen, Völker, Uwe, Völzke, Henry, Watkins, Nicholas A., Zonderman, Alan B., Wilson, Peter W.F., Li, Yun, Butterworth, Adam S., Gauchat, Jean-François, Chiang, Charleston W.K., Li, Bingshan, Loos, Ruth J.F., Astle, William J., Evangelou, Evangelos, van Heel, David A., Sankaran, Vijay G., Okada, Yukinori, Johnson, Andrew D., Reiner, Alexander P., Auer, Paul L.
Published in Cell (03.09.2020)
Published in Cell (03.09.2020)
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Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia
Hysi, Pirro G., Choquet, Hélène, Khawaja, Anthony P., Wojciechowski, Robert, Tedja, Milly S., Yin, Jie, Simcoe, Mark J., Patasova, Karina, Mahroo, Omar A., Thai, Khanh K., Cumberland, Phillippa M., Melles, Ronald B., Verhoeven, Virginie J. M., Vitart, Veronique, Segre, Ayellet, Stone, Richard A., Wareham, Nick, Hewitt, Alex W., Mackey, David A., Klaver, Caroline C. W., MacGregor, Stuart, Khaw, Peng T., Foster, Paul J., Guggenheim, Jeremy A., Rahi, Jugnoo S., Jorgenson, Eric, Hammond, Christopher J.
Published in Nature genetics (01.04.2020)
Published in Nature genetics (01.04.2020)
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High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Myers, Candace T., Cossette, Patrick, Lemay, Philippe, Spiegelman, Dan, Laporte, Alexandre Dionne, Nassif, Christina, Diallo, Ousmane, Monlong, Jean, Cadieux-Dion, Maxime, Dobrzeniecka, Sylvia, Meloche, Caroline, Retterer, Kyle, Cho, Megan T., Rosenfeld, Jill A., Bi, Weimin, Massicotte, Christine, Miguet, Marguerite, Brunga, Ledia, Regan, Brigid M., Mo, Kelly, Tam, Cory, Hollingsworth, Georgie, FitzPatrick, David R., Canham, Natalie, Blair, Edward, Kerr, Bronwyn, Fry, Andrew E., Thomas, Rhys H., Shelagh, Joss, Hurst, Jane A., Brittain, Helen, Blyth, Moira, Lebel, Robert Roger, Gerkes, Erica H., Davis-Keppen, Laura, Stein, Quinn, Dorison, Sara J., Benke, Paul J., Fassi, Emily, Corsten-Janssen, Nicole, Kamsteeg, Erik-Jan, Mau-Them, Frederic T., Bruel, Ange-Line, Verloes, Alain, Õunap, Katrin, Wojcik, Monica H., Albert, Dara V.F., Venkateswaran, Sunita, Ware, Tyson, Liu, Yu-Chi, Mohammad, Shekeeb S., Bizargity, Peyman, Bacino, Carlos A., Leuzzi, Vincenzo, Martinelli, Simone, Dallapiccola, Bruno, Tartaglia, Marco, Blumkin, Lubov, Wierenga, Klaas J., Purcarin, Gabriela, O’Byrne, James J., Stockler, Sylvia, Lehman, Anna, Keren, Boris, Nougues, Marie-Christine, Mignot, Cyril, Auvin, Stéphane, Nava, Caroline, Hiatt, Susan M., Bebin, Martina, Shao, Yunru, Scaglia, Fernando, Frye, Richard E., Jarjour, Imad T., Jacques, Stéphanie, Boucher, Renee-Myriam, Riou, Emilie, Srour, Myriam, Carmant, Lionel, Lortie, Anne, Major, Philippe, Diadori, Paola, Dubeau, François, D’Anjou, Guy, Bourque, Guillaume, Berkovic, Samuel F., Sadleir, Lynette G., Campeau, Philippe M., Kibar, Zoha, Lafrenière, Ronald G., Girard, Simon L., Mercimek-Mahmutoglu, Saadet, Boelman, Cyrus, Rouleau, Guy A., Scheffer, Ingrid E., Mefford, Heather C., Andrade, Danielle M., Rossignol, Elsa, Minassian, Berge A., Michaud, Jacques L.
Published in American journal of human genetics (02.11.2017)
Published in American journal of human genetics (02.11.2017)
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Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
de Lange, Katrina M, Moutsianas, Loukas, Lee, James C, Lamb, Christopher A, Luo, Yang, Kennedy, Nicholas A, Jostins, Luke, Rice, Daniel L, Gutierrez-Achury, Javier, Ji, Sun-Gou, Heap, Graham, Nimmo, Elaine R, Edwards, Cathryn, Henderson, Paul, Mowat, Craig, Sanderson, Jeremy, Satsangi, Jack, Simmons, Alison, Wilson, David C, Tremelling, Mark, Hart, Ailsa, Mathew, Christopher G, Newman, William G, Parkes, Miles, Lees, Charlie W, Uhlig, Holm, Hawkey, Chris, Prescott, Natalie J, Ahmad, Tariq, Mansfield, John C, Anderson, Carl A, Barrett, Jeffrey C
Published in Nature genetics (01.02.2017)
Published in Nature genetics (01.02.2017)
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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
C Yuen, Ryan K, Merico, Daniele, Bookman, Matt, L Howe, Jennifer, Thiruvahindrapuram, Bhooma, Patel, Rohan V, Whitney, Joe, Deflaux, Nicole, Bingham, Jonathan, Wang, Zhuozhi, Pellecchia, Giovanna, Buchanan, Janet A, Walker, Susan, Marshall, Christian R, Uddin, Mohammed, Zarrei, Mehdi, Deneault, Eric, D'Abate, Lia, Chan, Ada J S, Koyanagi, Stephanie, Paton, Tara, Pereira, Sergio L, Hoang, Ny, Engchuan, Worrawat, Higginbotham, Edward J, Ho, Karen, Lamoureux, Sylvia, Li, Weili, MacDonald, Jeffrey R, Nalpathamkalam, Thomas, Sung, Wilson W L, Tsoi, Fiona J, Wei, John, Xu, Lizhen, Tasse, Anne-Marie, Kirby, Emily, Van Etten, William, Twigger, Simon, Roberts, Wendy, Drmic, Irene, Jilderda, Sanne, Modi, Bonnie MacKinnon, Kellam, Barbara, Szego, Michael, Cytrynbaum, Cheryl, Weksberg, Rosanna, Zwaigenbaum, Lonnie, Woodbury-Smith, Marc, Brian, Jessica, Senman, Lili, Iaboni, Alana, Doyle-Thomas, Krissy, Thompson, Ann, Chrysler, Christina, Leef, Jonathan, Savion-Lemieux, Tal, Smith, Isabel M, Liu, Xudong, Nicolson, Rob, Seifer, Vicki, Fedele, Angie, Cook, Edwin H, Dager, Stephen, Estes, Annette, Gallagher, Louise, Malow, Beth A, Parr, Jeremy R, Spence, Sarah J, Vorstman, Jacob, Frey, Brendan J, Robinson, James T, Strug, Lisa J, Fernandez, Bridget A, Elsabbagh, Mayada, Carter, Melissa T, Hallmayer, Joachim, Knoppers, Bartha M, Anagnostou, Evdokia, Szatmari, Peter, Ring, Robert H, Glazer, David, Pletcher, Mathew T, Scherer, Stephen W
Published in Nature neuroscience (01.04.2017)
Published in Nature neuroscience (01.04.2017)
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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
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.
Published in Brain (London, England : 1878) (01.10.2013)
Published in Brain (London, England : 1878) (01.10.2013)
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Genome-wide mapping of 5-hydroxymethylcytosines in circulating cell-free DNA as a non-invasive approach for early detection of hepatocellular carcinoma
Cai, Jiabin, Chen, Lei, Zhang, Zhou, Zhang, Xinyu, Lu, Xingyu, Liu, Weiwei, Shi, Guoming, Ge, Yang, Gao, Pingting, Yang, Yuan, Ke, Aiwu, Xiao, Linlin, Dong, Ruizhao, Zhu, Yanjing, Yang, Xuan, Wang, Jiefei, Zhu, Tongyu, Yang, Deping, Huang, Xiaowu, Sui, Chengjun, Qiu, Shuangjian, Shen, Feng, Sun, Huichuan, Zhou, Weiping, Zhou, Jian, Nie, Ji, Zeng, Chang, Stroup, Emily Kunce, Zhang, Xu, Chiu, Brian C-H, Lau, Wan Yee, He, Chuan, Wang, Hongyang, Zhang, Wei, Fan, Jia
Published in Gut (01.12.2019)
Published in Gut (01.12.2019)
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COEXPEDIA: exploring biomedical hypotheses via co-expressions associated with medical subject headings (MeSH)
Yang, Sunmo, Kim, Chan Yeong, Hwang, Sohyun, Kim, Eiru, Kim, Hyojin, Shim, Hongseok, Lee, Insuk
Published in Nucleic acids research (04.01.2017)
Published in Nucleic acids research (04.01.2017)
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Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Ferreira, Manuel A, Vonk, Judith M, Baurecht, Hansjörg, Marenholz, Ingo, Tian, Chao, Hoffman, Joshua D, Helmer, Quinta, Tillander, Annika, Ullemar, Vilhelmina, van Dongen, Jenny, Lu, Yi, Rüschendorf, Franz, Esparza-Gordillo, Jorge, Medway, Chris W, Mountjoy, Edward, Burrows, Kimberley, Hummel, Oliver, Grosche, Sarah, Brumpton, Ben M, Witte, John S, Hottenga, Jouke-Jan, Willemsen, Gonneke, Zheng, Jie, Rodríguez, Elke, Hotze, Melanie, Franke, Andre, Revez, Joana A, Beesley, Jonathan, Matheson, Melanie C, Dharmage, Shyamali C, Bain, Lisa M, Fritsche, Lars G, Gabrielsen, Maiken E, Balliu, Brunilda, Nielsen, Jonas B, Zhou, Wei, Hveem, Kristian, Langhammer, Arnulf, Holmen, Oddgeir L, Løset, Mari, Abecasis, Gonçalo R, Willer, Cristen J, Arnold, Andreas, Homuth, Georg, Schmidt, Carsten O, Thompson, Philip J, Martin, Nicholas G, Duffy, David L, Novak, Natalija, Schulz, Holger, Karrasch, Stefan, Gieger, Christian, Strauch, Konstantin, Melles, Ronald B, Hinds, David A, Hübner, Norbert, Weidinger, Stephan, Magnusson, Patrik K E, Jansen, Rick, Jorgenson, Eric, Lee, Young-Ae, Boomsma, Dorret I, Almqvist, Catarina, Karlsson, Robert, Koppelman, Gerard H, Paternoster, Lavinia
Published in Nature genetics (01.12.2017)
Published in Nature genetics (01.12.2017)
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Characterizing the Genetic Architecture of Parkinson's Disease in Latinos
Loesch, Douglas P., Horimoto, Andrea R. V. R., Heilbron, Karl, Sarihan, Elif I., Inca‐Martinez, Miguel, Mason, Emily, Cornejo‐Olivas, Mario, Torres, Luis, Mazzetti, Pilar, Cosentino, Carlos, Sarapura‐Castro, Elison, Rivera‐Valdivia, Andrea, Medina, Angel C., Dieguez, Elena, Raggio, Victor, Lescano, Andres, Tumas, Vitor, Borges, Vanderci, Ferraz, Henrique B., Rieder, Carlos R., Schumacher‐Schuh, Artur, Santos‐Lobato, Bruno L., Velez‐Pardo, Carlos, Jimenez‐Del‐Rio, Marlene, Lopera, Francisco, Moreno, Sonia, Chana‐Cuevas, Pedro, Fernandez, William, Arboleda, Gonzalo, Arboleda, Humberto, Arboleda‐Bustos, Carlos E., Yearout, Dora, Zabetian, Cyrus P., Cannon, Paul, Thornton, Timothy A., O'Connor, Timothy D., Mata, Ignacio F.
Published in Annals of neurology (01.09.2021)
Published in Annals of neurology (01.09.2021)
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The impact of non-additive genetic associations on age-related complex diseases
Guindo-Martínez, Marta, Amela, Ramon, Bonàs-Guarch, Silvia, Puiggròs, Montserrat, Salvoro, Cecilia, Miguel-Escalada, Irene, Carey, Caitlin E., Cole, Joanne B., Rüeger, Sina, Atkinson, Elizabeth, Leong, Aaron, Sanchez, Friman, Ramon-Cortes, Cristian, Ejarque, Jorge, Palmer, Duncan S., Kurki, Mitja, Aragam, Krishna, Florez, Jose C., Badia, Rosa M., Mercader, Josep M., Torrents, David
Published in Nature communications (23.04.2021)
Published in Nature communications (23.04.2021)
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Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome
Porcu, Eleonora, Sadler, Marie C., Lepik, Kaido, Auwerx, Chiara, Wood, Andrew R., Weihs, Antoine, Sleiman, Maroun S. Bou, Ribeiro, Diogo M., Bandinelli, Stefania, Tanaka, Toshiko, Nauck, Matthias, Völker, Uwe, Delaneau, Olivier, Metspalu, Andres, Teumer, Alexander, Frayling, Timothy, Santoni, Federico A., Reymond, Alexandre, Kutalik, Zoltán
Published in Nature communications (24.09.2021)
Published in Nature communications (24.09.2021)
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The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium
Srinivasan, Shylaja, Chen, Ling, Todd, Jennifer, Divers, Jasmin, Gidding, Samuel, Chernausek, Steven, Gubitosi-Klug, Rose A., Kelsey, Megan M., Shah, Rachana, Black, Mary Helen, Wagenknecht, Lynne E., Manning, Alisa, Flannick, Jason, Imperatore, Giuseppina, Mercader, Josep M., Dabelea, Dana, Florez, Jose C.
Published in Diabetes (New York, N.Y.) (01.04.2021)
Published in Diabetes (New York, N.Y.) (01.04.2021)
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Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
O'Dushlaine, C., Rossin, L., Lee P., H., Duncan, L., Parikshak N., N., Newhouse, S., Ripke, S., Neale B., M., Purcell S., M., Posthuma, D., Nurnberger J., I., Lee S., H., Faraone S., V., Perlis R., H., Mowry B., J., Thapar, A., Goddard M., E., Witte J., S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen O., A., Anjorin, A., Anney, R., Anttila, V., Arking D., E., Asherson, P., Azevedo M., H., Backlund, L., Badner J., A., Bailey A., J., Banaschewski, T., Barchas J., D., Barnes M., R., Barrett T., B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen S., E., Berrettini, W., Betancur, Catalina, Bettecken, T., Biederman, J., Binder E., B., Black D., W., Blackwood D., H., Bloss C., S., Boehnke, M., Boomsma D., I., Breuer, R., Bruggeman, R., Cormican, P., Buccola N., G., Buitelaar J., K., Bunney W., E., Buxbaum J., D., Byerley W., F., Byrne E., M., Caesar, S., Cahn, W., Cantor R., M., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Mattheisen, M., Cloninger C., R., Collier D., A., Cook E., H., Coon, H., Cormand, B., Corvin, A., Coryell W., H., Craig D., W., Craig I., W., Crosbie, J., Cuccaro M., L., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., de Geus E., J., Degenhardt, F., Djurovic, S., Donohoe G., J., Doyle A., E., Duan, J., Dudbridge, F., Duketis, E., Ebstein R., P., Edenberg H., J., Elia, J., Ennis, S., Etain, B., Fanous, F.
Published in Nature neuroscience (01.02.2015)
Published in Nature neuroscience (01.02.2015)
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Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels
Emdin, Connor A., Khera, Amit V., Natarajan, Pradeep, Klarin, Derek, Won, Hong-Hee, Peloso, Gina M., Stitziel, Nathan O., Nomura, Akihiro, Zekavat, Seyedeh M., Bick, Alexander G., Gupta, Namrata, Asselta, Rosanna, Duga, Stefano, Merlini, Piera Angelica, Correa, Adolfo, Kessler, Thorsten, Wilson, James G., Bown, Matthew J., Hall, Alistair S., Braund, Peter S., Samani, Nilesh J., Schunkert, Heribert, Marrugat, Jaume, Elosua, Roberto, McPherson, Ruth, Farrall, Martin, Watkins, Hugh, Willer, Cristen, Abecasis, Gonçalo R., Felix, Janine F., Vasan, Ramachandran S., Lander, Eric, Rader, Daniel J., Danesh, John, Ardissino, Diego, Gabriel, Stacey, Saleheen, Danish, Kathiresan, Sekar
Published in Journal of the American College of Cardiology (27.12.2016)
Published in Journal of the American College of Cardiology (27.12.2016)
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Nasal DNA methylation profiling of asthma and rhinitis
Qi, Cancan, Jiang, Yale, Yang, Ivana V., Forno, Erick, Wang, Ting, Vonk, Judith M., Gehring, Ulrike, Smit, Henriëtte A., Milanzi, Edith B., Carpaij, Orestes A., Berg, Marijn, Hesse, Laura, Brouwer, Sharon, Cardwell, Jonathan, Vermeulen, Cornelis J., Acosta-Pérez, Edna, Canino, Glorisa, Boutaoui, Nadia, van den Berge, Maarten, Teichmann, Sarah A., Nawijn, Martijn C., Chen, Wei, Celedón, Juan C., Xu, Cheng-Jian, Koppelman, Gerard H.
Published in Journal of allergy and clinical immunology (01.06.2020)
Published in Journal of allergy and clinical immunology (01.06.2020)
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