Characterization of 58 STRs and 94 SNPs with the ForenSeq™ DNA signature prep kit in Mexican-Mestizos from the Monterrey city (Northeast, Mexico) von Aguilar-Velázquez, José Alonso, Duran-Salazar, Miguel Ángel, Córdoba-Mercado, Miranda Fabiola, Coronado-Avila, Carolina Elena, Salas-Salas, Orlando, Martinez-Cortés, Gabriela, Casals, Ferrán, Calafell, Francesc, Ramos-González, Benito, Rangel-Villalobos, Héctor

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Assessment of the gene mosaicism burden in blood and its implications for immune disorders von Solís-Moruno, Manuel, Mensa-Vilaró, Anna, Batlle-Masó, Laura, Lobón, Irene, Bonet, Núria, Marquès-Bonet, Tomàs, Aróstegui, Juan I., Casals, Ferran

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Human Genetic Variation, Shared and Private von Casals, Ferran, Bertranpetit, Jaume

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Publisher Correction: Assessment of the gene mosaicism burden in blood and its implications for immune disorders von Solís-Moruno, Manuel, Mensa-Vilaró, Anna, Batlle-Masó, Laura, Lobón, Irene, Bonet, Núria, Marquès-Bonet, Tomàs, Aróstegui, Juan I., Casals, Ferran

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Severe Autoinflammatory Manifestations and Antibody Deficiency Due to Novel Hypermorphic PLCG2 Mutations von Martín-Nalda, Andrea, Fortuny, Claudia, Rey, Lourdes, Bunney, Tom D., Alsina, Laia, Esteve-Solé, Ana, Bull, Daniel, Anton, Maria Carmen, Basagaña, María, Casals, Ferran, Deyá, Angela, García-Prat, Marina, Gimeno, Ramon, Juan, Manel, Martinez-Banaclocha, Helios, Martinez-Garcia, Juan J, Mensa-Vilaró, Anna, Rabionet, Raquel, Martin-Begue, Nieves, Rudilla, Francesc, Yagüe, Jordi, Estivill, Xavier, García-Patos, Vicente, Pujol, Ramon M., Soler-Palacín, Pere, Katan, Matilda, Pelegrín, Pablo, Colobran, Roger, Vicente, Asun, Arostegui, Juan I.

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Genomic analysis of Andamanese provides insights into ancient human migration into Asia and adaptation von Mondal, Mayukh, Casals, Ferran, Xu, Tina, Dall'Olio, Giovanni M, Pybus, Marc, Netea, Mihai G, Comas, David, Laayouni, Hafid, Li, Qibin, Majumder, Partha P, Bertranpetit, Jaume

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Chimpanzee genomic diversity reveals ancient admixture with bonobos von de Manuel, Marc, Kuhlwilm, Martin, Frandsen, Peter, Sousa, Vitor C., Desai, Tariq, Prado-Martinez, Javier, Hernandez-Rodriguez, Jessica, Dupanloup, Isabelle, Lao, Oscar, Hallast, Pille, Schmidt, Joshua M., Heredia-Genestar, José María, Benazzo, Andrea, Barbujani, Guido, Peter, Benjamin M., Kuderna, Lukas F. K., Casals, Ferran, Angedakin, Samuel, Arandjelovic, Mimi, Boesch, Christophe, Kühl, Hjalmar, Vigilant, Linda, Langergraber, Kevin, Novembre, John, Gut, Marta, Gut, Ivo, Navarro, Arcadi, Carlsen, Frauds, Andres, Aida M., Siegismund, Hans. R., Scally, Aylwyn, Excoffier, Laurent, Tyler-Smith, Chris, Castellano, Sergi, Xue, Yali, Hvilsom, Christina, Marques-Bonet, Tomas

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Case report: Novel compound heterozygous IL1RN mutations as the likely cause of a lethal form of deficiency of interleukin-1 receptor antagonist von Urbaneja, Elena, Bonet, Nuria, Solis-Moruno, Manuel, Mensa-Vilaro, Anna, de Landazuri, Iñaki Ortiz, Tormo, Marc, Lara, Rocio, Plaza, Susana, Fabregat, Virginia, Yagüe, Jordi, Casals, Ferran, Arostegui, Juan I

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Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts von Awadalla, Philip, Gauthier, Julie, Myers, Rachel A., Casals, Ferran, Hamdan, Fadi F., Griffing, Alexander R., Côté, Mélanie, Henrion, Edouard, Spiegelman, Dan, Tarabeux, Julien, Piton, Amélie, Yang, Yan, Boyko, Adam, Bustamante, Carlos, Xiong, Lan, Rapoport, Judith L., Addington, Anjené M., DeLisi, J. Lynn E., Krebs, Marie-Odile, Joober, Ridha, Millet, Bruno, Fombonne, Éric, Mottron, Laurent, Zilversmit, Martine, Keebler, Jon, Daoud, Hussein, Marineau, Claude, Roy-Gagnon, Marie-Hélène, Dubé, Marie-Pierre, Eyre-Walker, Adam, Drapeau, Pierre, Stone, Eric A., Lafrenière, Ronald G., Rouleau, Guy A.

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Balancing Selection Is the Main Force Shaping the Evolution of Innate Immunity Genes von Ferrer-Admetlla, Anna, Bosch, Elena, Sikora, Martin, Marques-Bonet, Tomas, Ramirez-Soriano, Anna, Muntasell, Aura, Navarro, Arcadi, Lazarus, Ross, Calafell, Francesc, Bertranpetit, Jaume, Casals, Ferran

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Genetic diagnosis of autoinflammatory disease patients using clinical exome sequencing von Batlle-Masó, Laura, Mensa-Vilaró, Anna, Solís-Moruno, Manuel, Marquès-Bonet, Tomàs, Arostegui, Juan I., Casals, Ferran

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Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond von de Valles-Ibáñez, Guillem, Esteve-Solé, Ana, Piquer, Mònica, González-Navarro, E Azucena, Hernandez-Rodriguez, Jessica, Laayouni, Hafid, González-Roca, Eva, Plaza-Martin, Ana María, Deyà-Martínez, Ángela, Martín-Nalda, Andrea, Martínez-Gallo, Mónica, García-Prat, Marina, Del Pino-Molina, Lucía, Cuscó, Ivón, Codina-Solà, Marta, Batlle-Masó, Laura, Solís-Moruno, Manuel, Marquès-Bonet, Tomàs, Bosch, Elena, López-Granados, Eduardo, Aróstegui, Juan Ignacio, Soler-Palacín, Pere, Colobran, Roger, Yagüe, Jordi, Alsina, Laia, Juan, Manel, Casals, Ferran

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Natural Selection in the Great Apes von Cagan, Alexander, Theunert, Christoph, Laayouni, Hafid, Santpere, Gabriel, Pybus, Marc, Casals, Ferran, Prüfer, Kay, Navarro, Arcadi, Marques-Bonet, Tomas, Bertranpetit, Jaume, Andrés, Aida M

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FHLdb: A Comprehensive Database on the Molecular Basis of Familial Hemophagocytic Lymphohistiocytosis von Viñas-Giménez, Laura, Padilla, Natàlia, Batlle-Masó, Laura, Casals, Ferran, Rivière, Jacques G, Martínez-Gallo, Mónica, de la Cruz, Xavier, Colobran, Roger

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Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans von Casals, Ferran, Hodgkinson, Alan, Hussin, Julie, Idaghdour, Youssef, Bruat, Vanessa, de Maillard, Thibault, Grenier, Jean-Christophe, Grenier, Jean-Cristophe, Gbeha, Elias, Hamdan, Fadi F, Girard, Simon, Spinella, Jean-François, Larivière, Mathieu, Saillour, Virginie, Healy, Jasmine, Fernández, Isabel, Sinnett, Daniel, Michaud, Jacques L, Rouleau, Guy A, Haddad, Elie, Le Deist, Françoise, Awadalla, Philip

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A transient inflammatory response contributes to oxaliplatin neurotoxicity in mice von Calls, Aina, Torres‐Espin, Abel, Tormo, Marc, Martínez‐Escardó, Laura, Bonet, Núria, Casals, Ferran, Navarro, Xavier, Yuste, Víctor J., Udina, Esther, Bruna, Jordi

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Second GHEP-ISFG exercise for DVI: “DNA-led” victims’ identification in a simulated air crash von Vullo, Carlos M., Catelli, Laura, Ibarra Rodriguez, Adriana A., Papaioannou, Aikaterini, Merino, J. Carlos Álvarez, Lopez-Parra, AM, Gaviria, Aníbal, Baeza-Richer, Carlos, Romanini, Carola, González-Moya, Esperanza, Casals, Ferran, Calafell, Francesc, Berardi, Gabriela, Iannacone, Gian Carlo, Vicuña Giraldo, Gloria C., Zorba, Gulbanu K., Boschi, Ilaria, Olarte, Jane Valdivia, Ruiz Gomez, Juan E., Acierno, Juan Pablo, Soto, Manuel López, Miranda, Manuel Velázquez, García King, Marco D., Marrucci, Maria Alessandra, Porto, Maria J., Piñero, Mariana Herrera, Aler, Mercedes, Stephenson Ojea, Mishel M., Navarrete, Santiago Cobos, Toscanini, Ulises, Saragoni, Victor G., Bozzo, Walter, Posada Posada, Yeny C., Bajunovic, Zlatan, Solla, Lourdes Prieto, Parsons, Thomas

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Recent human evolution has shaped geographical differences in susceptibility to disease von Marigorta, Urko M, Lao, Oscar, Casals, Ferran, Calafell, Francesc, Morcillo-Suárez, Carlos, Faria, Rui, Bosch, Elena, Serra, François, Bertranpetit, Jaume, Dopazo, Hernán, Navarro, Arcadi

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A population genetic approach to mapping neurological disorder genes using deep resequencing von Myers, Rachel A, Casals, Ferran, Gauthier, Julie, Hamdan, Fadi F, Keebler, Jon, Boyko, Adam R, Bustamante, Carlos D, Piton, Amelie M, Spiegelman, Dan, Henrion, Edouard, Zilversmit, Martine, Hussin, Julie, Quinlan, Jacklyn, Yang, Yan, Lafrenière, Ronald G, Griffing, Alexander R, Stone, Eric A, Rouleau, Guy A, Awadalla, Philip

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Y-chromosomal sequences of diverse Indian populations and the ancestry of the Andamanese von Mondal, Mayukh, Bergström, Anders, Xue, Yali, Calafell, Francesc, Laayouni, Hafid, Casals, Ferran, Majumder, Partha P., Tyler-Smith, Chris, Bertranpetit, Jaume

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