Sequence variants in HECTD1 result in a variable neurodevelopmental disorder von Zerafati-Jahromi, Gazelle, Oxman, Elias, Hoang, Hieu D, Charng, Wu-Lin, Kotla, Tanvitha, Yuan, Weimin, Ishibashi, Keito, Sebaoui, Sonia, Luedtke, Kathryn, Winrow, Bryce, Ganetzky, Rebecca D, Ruiz, Anna, Manso-Basúz, Carmen, Spataro, Nino, Kannu, Peter, Athey, Taryn, Peroutka, Christina, Barnes, Caitlin, Sidlow, Richard, Anadiotis, George, Magnussen, Kari, Valenzuela, Irene, Moles-Fernandez, Alejandro, Berger, Seth, Grant, Christina L, Vilain, Eric, Arnadottir, Gudny A, Sulem, Patrick, Sulem, Telma S, Stefansson, Kari, Massey, Shavonne, Ginn, Natalie, Poduri, Annapurna, D'Gama, Alissa M, Valentine, Rozalia, Trowbridge, Sara K, Murali, Chaya N, Franciskovich, Rachel, Tran, Yen, Webb, Bryn D, Keppler-Noreuil, Kim M, Hall, April L, McGivern, Bobbi, Monaghan, Kristin G, Guillen Sacoto, Maria J, Baldridge, Dustin, Silverman, Gary A, Dahiya, Sonika, Turner, Tychele N, Schedl, Tim, Corbin, Joshua G, Pak, Stephen C, Zohn, Irene E, Gurnett, Christina A

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PSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response von Deb, Wallid, Rosenfelt, Cory, Vignard, Virginie, Papendorf, Jonas Johannes, Möller, Sophie, Wendlandt, Martin, Studencka-Turski, Maja, Cogné, Benjamin, Besnard, Thomas, Ruffier, Léa, Toutain, Bérénice, Poirier, Léa, Cuinat, Silvestre, Kritzer, Amy, Crunk, Amy, diMonda, Janette, Vengoechea, Jaime, Mercier, Sandra, Kleinendorst, Lotte, van Haelst, Mieke M., Zuurbier, Linda, Sulem, Telma, Katrínardóttir, Hildigunnur, Friðriksdóttir, Rún, Sulem, Patrick, Stefansson, Kari, Jonsdottir, Berglind, Zeidler, Shimriet, Sinnema, Margje, Stegmann, Alexander P.A., Naveh, Natali, Skraban, Cara M., Gray, Christopher, Murrell, Jill R., Isikay, Sedat, Pehlivan, Davut, Calame, Daniel G., Posey, Jennifer E., Nizon, Mathilde, McWalter, Kirsty, Lupski, James R., Isidor, Bertrand, Bolduc, François V., Bézieau, Stéphane, Krüger, Elke, Küry, Sébastien, Ebstein, Frédéric

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Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genes von Smal, Noor, Majdoub, Fatma, Janssens, Katrien, Reyniers, Edwin, Meuwissen, Marije E. C., Ceulemans, Berten, Northrup, Hope, Hill, Jeremy B., Liu, Lingying, Errichiello, Edoardo, Gana, Simone, Strong, Alanna, Rohena, Luis, Franciskovich, Rachel, Murali, Chaya N., Huybrechs, An, Sulem, Telma, Fridriksdottir, Run, Sulem, Patrick, Stefansson, Kari, Bai, Yan, Rosenfeld, Jill A., Lalani, Seema R., Streff, Haley, Kooy, R. Frank, Weckhuysen, Sarah

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