Social camouflaging in females with autism spectrum disorder: A systematic review von Tubío-Fungueiriño, María, Cruz, Sara, Sampaio, Adriana, Carracedo, Angel, Fernández-Prieto, Montse

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UTMOST, a single and cross-tissue TWAS (Transcriptome Wide Association Study), reveals new ASD (Autism Spectrum Disorder) associated genes von Rodriguez-Fontenla, Cristina, Carracedo, Angel

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The human early-life exposome (HELIX): project rationale and design von Vrijheid, Martine, Slama, Rémy, Robinson, Oliver, Chatzi, Leda, Coen, Muireann, van den Hazel, Peter, Thomsen, Cathrine, Wright, John, Athersuch, Toby J, Avellana, Narcis, Basagaña, Xavier, Brochot, Celine, Bucchini, Luca, Bustamante, Mariona, Carracedo, Angel, Casas, Maribel, Estivill, Xavier, Fairley, Lesley, van Gent, Diana, Gonzalez, Juan R, Granum, Berit, Gražulevičienė, Regina, Gutzkow, Kristine B, Julvez, Jordi, Keun, Hector C, Kogevinas, Manolis, McEachan, Rosemary R C, Meltzer, Helle Margrete, Sabidó, Eduard, Schwarze, Per E, Siroux, Valérie, Sunyer, Jordi, Want, Elizabeth J, Zeman, Florence, Nieuwenhuijsen, Mark J

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HLA alleles: important pieces to the COVID-19 puzzle von Castro-Santos, Patricia, Carracedo, Ángel, Díaz-Peña, Roberto

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Straightforward inference of ancestry and admixture proportions through ancestry-informative insertion deletion multiplexing von Pereira, Rui, Phillips, Christopher, Pinto, Nádia, Santos, Carla, dos Santos, Sidney Emanuel Batista, Amorim, António, Carracedo, Ángel, Gusmão, Leonor

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An overview of STRUCTURE: applications, parameter settings, and supporting software von Porras-Hurtado, Liliana, Ruiz, Yarimar, Santos, Carla, Phillips, Christopher, Carracedo, Angel, Lareu, Maria V

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Synaptic, transcriptional and chromatin genes disrupted in autism von De Rubeis, Silvia, He, Xin, Goldberg, Arthur P., Poultney, Christopher S., Samocha, Kaitlin, Ercument Cicek, A., Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarjinder, Klei, Lambertus, Kosmicki, Jack, Fu, Shih-Chen, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F., Brownfeld, Jessica M., Cai, Jinlu, Campbell, Nicholas G., Carracedo, Angel, Chahrour, Maria H., Chiocchetti, Andreas G., Coon, Hilary, Crawford, Emily L., Crooks, Lucy, Curran, Sarah R., Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A., Gallagher, Louise, Geller, Evan, Guter, Stephen J., Sean Hill, R., Ionita-Laza, Iuliana, Jimenez Gonzalez, Patricia, Kilpinen, Helena, Klauck, Sabine M., Kolevzon, Alexander, Lee, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma’ayan, Avi, Marshall, Christian R., McInnes, Alison L., Neale, Benjamin, Owen, Michael J., Ozaki, Norio, Parellada, Mara, Parr, Jeremy R., Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J., Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Wang, Li-San, Weiss, Lauren A., Jeremy Willsey, A., Yu, Timothy W., Yuen, Ryan K. C., Cook, Edwin H., Freitag, Christine M., Gill, Michael, Hultman, Christina M., Lehner, Thomas, Palotie, Aarno, Schellenberg, Gerard D., Sklar, Pamela, State, Matthew W., Sutcliffe, James S., Walsh, Christopher A., Scherer, Stephen W., Zwick, Michael E., Barrett, Jeffrey C., Cutler, David J., Roeder, Kathryn, Devlin, Bernie, Daly, Mark J., Buxbaum, Joseph D.

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De novo Mutations (DNMs) in Autism Spectrum Disorder (ASD): Pathway and Network Analysis von Alonso-Gonzalez, Aitana, Rodriguez-Fontenla, Cristina, Carracedo, Angel

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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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Executive functioning: A mediator between sensory processing and behaviour in autism spectrum disorder von Fernandez-Prieto, Montse, Moreira, Célia, Cruz, Sara, Campos, Vânia, Martínez-Regueiro, Rocío, Taboada, Maria, Carracedo, Angel, Sampaio, Adriana

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A new multiplex for human identification using insertion/deletion polymorphisms von Pereira, Rui, Phillips, Christopher, Alves, Cíntia, Amorim, António, Carracedo, Ángel, Gusmão, Leonor

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Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder von Lim, Elaine T, Uddin, Mohammed, De Rubeis, Silvia, Chan, Yingleong, Kamumbu, Anne S, Zhang, Xiaochang, D'Gama, Alissa M, Kim, Sonia N, Hill, Robert Sean, Goldberg, Arthur P, Poultney, Christopher, Minshew, Nancy J, Kushima, Itaru, Aleksic, Branko, Ozaki, Norio, Parellada, Mara, Arango, Celso, Penzol, Maria J, Carracedo, Angel, Kolevzon, Alexander, Hultman, Christina M, Weiss, Lauren A, Fromer, Menachem, Chiocchetti, Andreas G, Freitag, Christine M, Church, George M, Scherer, Stephen W, Buxbaum, Joseph D, Walsh, Christopher A

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Forensic genetics and genomics: Much more than just a human affair von Arenas, Miguel, Pereira, Filipe, Oliveira, Manuela, Pinto, Nadia, Lopes, Alexandra M, Gomes, Veronica, Carracedo, Angel, Amorim, Antonio

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SNPs in forensic genetics: a review on SNP typing methodologies von Sobrino, Beatriz, Brión, María, Carracedo, Angel

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Utility of polygenic risk scores to aid in the diagnosis of rheumatic diseases von Santiago-Lamelas, Lucía, Dos Santos-Sobrín, Raquel, Carracedo, Ángel, Castro-Santos, Patricia, Díaz-Peña, Roberto

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Neutrophil to lymphocyte ratio and breast cancer risk: analysis by subtype and potential interactions von Gago-Dominguez, Manuela, Matabuena, Marcos, Redondo, Carmen M., Patel, Sandip Pravin, Carracedo, Angel, Ponte, Sara Miranda, Martínez, María Elena, Castelao, J. Esteban

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Common variants conferring risk of schizophrenia von Stefansson, Hreinn, Ophoff, Roel A., Steinberg, Stacy, Andreassen, Ole A., Cichon, Sven, Rujescu, Dan, Werge, Thomas, Pietiläinen, Olli P. H., Mors, Ole, Mortensen, Preben B., Sigurdsson, Engilbert, Gustafsson, Omar, Nyegaard, Mette, Tuulio-Henriksson, Annamari, Ingason, Andres, Hansen, Thomas, Suvisaari, Jaana, Lonnqvist, Jouko, Paunio, Tiina, Børglum, Anders D., Hartmann, Annette, Fink-Jensen, Anders, Nordentoft, Merete, Hougaard, David, Norgaard-Pedersen, Bent, Böttcher, Yvonne, Olesen, Jes, Breuer, René, Möller, Hans-Jürgen, Giegling, Ina, Rasmussen, Henrik B., Timm, Sally, Mattheisen, Manuel, Bitter, István, Réthelyi, János M., Magnusdottir, Brynja B., Sigmundsson, Thordur, Olason, Pall, Masson, Gisli, Gulcher, Jeffrey R., Haraldsson, Magnus, Fossdal, Ragnheidur, Thorgeirsson, Thorgeir E., Thorsteinsdottir, Unnur, Ruggeri, Mirella, Tosato, Sarah, Franke, Barbara, Strengman, Eric, Kiemeney, Lambertus A., Melle, Ingrid, Djurovic, Srdjan, Abramova, Lilia, Kaleda, Vasily, Sanjuan, Julio, de Frutos, Rosa, Bramon, Elvira, Vassos, Evangelos, Fraser, Gillian, Ettinger, Ulrich, Picchioni, Marco, Walker, Nicholas, Toulopoulou, Timi, Need, Anna C., Ge, Dongliang, Lim Yoon, Joeng, Shianna, Kevin V., Freimer, Nelson B., Cantor, Rita M., Murray, Robin, Kong, Augustine, Golimbet, Vera, Carracedo, Angel, Arango, Celso, Costas, Javier, Jönsson, Erik G., Terenius, Lars, Agartz, Ingrid, Petursson, Hannes, Nöthen, Markus M., Rietschel, Marcella, Matthews, Paul M., Muglia, Pierandrea, Peltonen, Leena, St Clair, David, Goldstein, David B., Stefansson, Kari, Collier, David A.

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The impact of genetic variations in the serotonergic system on symptom severity and clinical outcome in functional neurological disorders von Weber, Samantha, Rey Álvarez, Lucía Trinidad, Ansede-Bermejo, Juan, Cruz, Raquel, del Real, Álvaro, Bühler, Janine, Carracedo, Ángel, Aybek, Selma

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Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice von Keller, Annika, Westenberger, Ana, Sobrido, Maria J, García-Murias, Maria, Domingo, Aloysius, Sears, Renee L, Lemos, Roberta R, Ordoñez-Ugalde, Andres, Nicolas, Gael, da Cunha, José E Gomes, Rushing, Elisabeth J, Hugelshofer, Michael, Wurnig, Moritz C, Kaech, Andres, Reimann, Regina, Lohmann, Katja, Dobričić, Valerija, Carracedo, Angel, Petrović, Igor, Miyasaki, Janis M, Abakumova, Irina, Mäe, Maarja Andaloussi, Raschperger, Elisabeth, Zatz, Mayana, Zschiedrich, Katja, Klepper, Jörg, Spiteri, Elizabeth, Prieto, Jose M, Navas, Inmaculada, Preuss, Michael, Dering, Carmen, Janković, Milena, Paucar, Martin, Svenningsson, Per, Saliminejad, Kioomars, Khorshid, Hamid R K, Novaković, Ivana, Aguzzi, Adriano, Boss, Andreas, Le Ber, Isabelle, Defer, Gilles, Hannequin, Didier, Kostić, Vladimir S, Campion, Dominique, Geschwind, Daniel H, Coppola, Giovanni, Betsholtz, Christer, Klein, Christine, Oliveira, Joao R M

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Examining the independent and joint effects of molecular genetic liability and environmental exposures in schizophrenia: results from the EUGEI study von Guloksuz, Sinan, Pries, Lotta‐Katrin, Delespaul, Philippe, Kenis, Gunter, Luykx, Jurjen J., Lin, Bochao D., Richards, Alexander L., Akdede, Berna, Binbay, Tolga, Altınyazar, Vesile, Yalınçetin, Berna, Gümüş‐Akay, Güvem, Cihan, Burçin, Soygür, Haldun, Ulaş, Halis, Cankurtaran, EylemŞahin, Kaymak, Semra Ulusoy, Mihaljevic, Marina M., Petrovic, Sanja Andric, Mirjanic, Tijana, Bernardo, Miguel, Cabrera, Bibiana, Bobes, Julio, Saiz, Pilar A., García‐Portilla, María Paz, Sanjuan, Julio, Aguilar, Eduardo J., Santos, José Luis, Jiménez‐López, Estela, Arrojo, Manuel, Carracedo, Angel, López, Gonzalo, González‐Peñas, Javier, Parellada, Mara, Maric, Nadja P., Atbaşog˘lu, Cem, Ucok, Alp, Alptekin, Köksal, Saka, Meram Can, Arango, Celso, O'Donovan, Michael, Rutten, Bart P.F., van Os, Jim, Alizadeh, Behrooz Z., van Amelsvoort, Therese, van Beveren, Nico J., Bruggeman, Richard, Cahn, Wiepke, de Haan, Lieuwe, Delespaul, Philippe, Luykx, Jurjen J., Myin‐Germeys, Inez, van Winkel, Ruud, van Os, Jim

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