Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility von Yin, Xianyong, Low, Hui Qi, Wang, Ling, Li, Yonghong, Ellinghaus, Eva, Han, Jiali, Estivill, Xavier, Sun, Liangdan, Zuo, Xianbo, Shen, Changbing, Zhu, Caihong, Zhang, Anping, Sanchez, Fabio, Padyukov, Leonid, Catanese, Joseph J., Krueger, Gerald G., Duffin, Kristina Callis, Mucha, Sören, Weichenthal, Michael, Weidinger, Stephan, Lieb, Wolfgang, Foo, Jia Nee, Li, Yi, Sim, Karseng, Liany, Herty, Irwan, Ishak, Teo, Yikying, Theng, Colin T. S., Gupta, Rashmi, Bowcock, Anne, De Jager, Philip L., Qureshi, Abrar A., de Bakker, Paul I. W., Seielstad, Mark, Liao, Wilson, Ståhle, Mona, Franke, Andre, Zhang, Xuejun, Liu, Jianjun

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Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies von Estivill, Xavier, Armengol, Lluís

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Circulating miRNAs, isomiRs and small RNA clusters in human plasma and breast milk von Rubio, Mercedes, Bustamante, Mariona, Hernandez-Ferrer, Carles, Fernandez-Orth, Dietmar, Pantano, Lorena, Sarria, Yaris, Piqué-Borras, Maria, Vellve, Kilian, Agramunt, Silvia, Carreras, Ramon, Estivill, Xavier, Gonzalez, Juan R, Mayor, Alfredo

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International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases von Boycott, Kym M., Rath, Ana, Chong, Jessica X., Hartley, Taila, Alkuraya, Fowzan S., Baynam, Gareth, Brookes, Anthony J., Brudno, Michael, Carracedo, Angel, den Dunnen, Johan T., Dyke, Stephanie O.M., Estivill, Xavier, Goldblatt, Jack, Gonthier, Catherine, Groft, Stephen C., Gut, Ivo, Hamosh, Ada, Hieter, Philip, Höhn, Sophie, Hurles, Matthew E., Kaufmann, Petra, Knoppers, Bartha M., Krischer, Jeffrey P., Macek, Milan, Matthijs, Gert, Olry, Annie, Parker, Samantha, Paschall, Justin, Philippakis, Anthony A., Rehm, Heidi L., Robinson, Peter N., Sham, Pak-Chung, Stefanov, Rumen, Taruscio, Domenica, Unni, Divya, Vanstone, Megan R., Zhang, Feng, Brunner, Han, Bamshad, Michael J., Lochmüller, Hanns

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MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function von Miñones-Moyano, Elena, Porta, Sílvia, Escaramís, Georgia, Rabionet, Raquel, Iraola, Susana, Kagerbauer, Birgit, Espinosa-Parrilla, Yolanda, Ferrer, Isidre, Estivill, Xavier, Martí, Eulàlia

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Changes in the stool and oropharyngeal microbiome in obsessive-compulsive disorder von Domènech, Laura, Willis, Jesse, Alemany-Navarro, Maria, Morell, Marta, Real, Eva, Escaramís, Geòrgia, Bertolín, Sara, Sánchez Chinchilla, Daniel, Balcells, Susanna, Segalàs, Cinto, Estivill, Xavier, Menchón, Jose M., Gabaldón, Toni, Alonso, Pino, Rabionet, Raquel

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Multi-omics signatures of the human early life exposome von Maitre, Léa, Bustamante, Mariona, Hernández-Ferrer, Carles, Thiel, Denise, Lau, Chung-Ho E., Siskos, Alexandros P., Vives-Usano, Marta, Ruiz-Arenas, Carlos, Pelegrí-Sisó, Dolors, Robinson, Oliver, Mason, Dan, Wright, John, Cadiou, Solène, Slama, Rémy, Heude, Barbara, Casas, Maribel, Sunyer, Jordi, Papadopoulou, Eleni Z., Gutzkow, Kristine B., Andrusaityte, Sandra, Grazuleviciene, Regina, Vafeiadi, Marina, Chatzi, Leda, Sakhi, Amrit K., Thomsen, Cathrine, Tamayo, Ibon, Nieuwenhuijsen, Mark, Urquiza, Jose, Borràs, Eva, Sabidó, Eduard, Quintela, Inés, Carracedo, Ángel, Estivill, Xavier, Coen, Muireann, González, Juan R., Keun, Hector C., Vrijheid, Martine

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Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis von Rabionet, Raquel, Remesal, Agustín, Mensa-Vilaró, Anna, Murías, Sara, Alcobendas, Rosa, González-Roca, Eva, Ruiz-Ortiz, Estibaliz, Antón, Jordi, Iglesias, Estibaliz, Modesto, Consuelo, Comas, David, Puig, Anna, Drechsel, Oliver, Ossowski, Stephan, Yagüe, Jordi, Merino, Rosa, Estivill, Xavier, Arostegui, Juan I.

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miRTrace reveals the organismal origins of microRNA sequencing data von Kang, Wenjing, Eldfjell, Yrin, Fromm, Bastian, Estivill, Xavier, Biryukova, Inna, Friedländer, Marc R

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Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability von Beckmann, Jacques S., Estivill, Xavier, Antonarakis, Stylianos E.

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SNPassoc: an R package to perform whole genome association studies von González, Juan R., Armengol, Lluís, Solé, Xavier, Guinó, Elisabet, Mercader, Josep M., Estivill, Xavier, Moreno, Víctor

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Targeting CAG repeat RNAs reduces Huntington's disease phenotype independently of huntingtin levels von Rué, Laura, Bañez-Coronel, Mónica, Creus-Muncunill, Jordi, Giralt, Albert, Alcalá-Vida, Rafael, Mentxaka, Gartze, Kagerbauer, Birgit, Zomeño-Abellán, M Teresa, Aranda, Zeus, Venturi, Veronica, Pérez-Navarro, Esther, Estivill, Xavier, Martí, Eulàlia

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A highly expressed miR-101 isomiR is a functional silencing small RNA von Llorens, Franc, Bañez-Coronel, Mónica, Pantano, Lorena, del Río, Jose Antonio, Ferrer, Isidre, Estivill, Xavier, Martí, Eulàlia

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Identification of autosomal cis expression quantitative trait methylation (cis eQTMs) in children's blood von Ruiz-Arenas, Carlos, Hernandez-Ferrer, Carles, Vives-Usano, Marta, Marí, Sergi, Quintela, Ines, Mason, Dan, Cadiou, Solène, Casas, Maribel, Andrusaityte, Sandra, Gutzkow, Kristine Bjerve, Vafeiadi, Marina, Wright, John, Lepeule, Johanna, Grazuleviciene, Regina, Chatzi, Leda, Carracedo, Ángel, Estivill, Xavier, Marti, Eulàlia, Escaramís, Geòrgia, Vrijheid, Martine, González, Juan R, Bustamante, Mariona

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myriad of miRNA variants in control and Huntington's disease brain regions detected by massively parallel sequencing von Martí, Eulàlia, Pantano, Lorena, Bañez-Coronel, Mónica, Llorens, Franc, Miñones-Moyano, Elena, Porta, Sílvia, Sumoy, Lauro, Ferrer, Isidre, Estivill, Xavier

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Genome-wide DNA methylation study in human placenta identifies novel loci associated with maternal smoking during pregnancy von Morales, Eva, Vilahur, Nadia, Salas, Lucas A, Motta, Valeria, Fernandez, Mariana F, Murcia, Mario, Llop, Sabrina, Tardon, Adonina, Fernandez-Tardon, Guillermo, Santa-Marina, Loreto, Gallastegui, Mara, Bollati, Valentina, Estivill, Xavier, Olea, Nicolas, Sunyer, Jordi, Bustamante, Mariona

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Genome sequencing data analysis for rare disease gene discovery von Umlai, Umm-Kulthum Ismail, Bangarusamy, Dhinoth Kumar, Estivill, Xavier, Jithesh, Puthen Veettil

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Association of Irisin with Fat Mass, Resting Energy Expenditure, and Daily Activity in Conditions of Extreme Body Mass Index von Pardo, María, Crujeiras, Ana B., Amil, María, Aguera, Zaida, Jiménez-Murcia, Susana, Baños, Rosa, Botella, Cristina, de la Torre, Rafael, Estivill, Xavier, Fagundo, Ana B., Fernández-Real, Jose M., Fernández-García, José C., Fruhbeck, Gema, Gómez-Ambrosi, Javier, Rodríguez, Roser, Tinahones, Francisco J., Fernández-Aranda, Fernando, Casanueva, Felipe F.

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Tying malaria and microRNAs: from the biology to future diagnostic perspectives von Rubio, Mercedes, Bassat, Quique, Estivill, Xavier, Mayor, Alfredo

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Aneuploidy: From a Physiological Mechanism of Variance to Down Syndrome von Dierssen, Mara, Herault, Yann, Estivill, Xavier

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