Identification of common genetic risk variants for autism spectrum disorder
Year: 2026
Type: article
Study design: Observational Study
DOI: 10.17615/8pwf-jq42
Authors: Dellenvall, Karin, Xu, Xinyi, Hansen, Christine S., Pedersen, Marianne Giørtz, Martin, Joanna, Børglum, Anders D., Bettella, Francesco, Hougaard, David M., Als, Thomas D., Werge, Thomas, Hultman, Christina M., Nordentoft, Merete, Roussos, Panos, Stefansson, Hreinn, Won, Hyejung, Moran, Jennifer L., Sullivan, Patrick F., Roeder, Kathryn, Mortensen, Preben Bo, Djurovic, Srdjan, Davey Smith, George, Goldstein, Jacqueline I., Steinberg, Stacy, Hauberg, Mads Engel, Pourcain, Beate St, Awashti, Swapnil, Huang, Hailiang, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Chambert, Kimberly, Howrigan, Daniel P., De Rubeis, Silvia, Palmer, Duncan S., Ripke, Stephan, Mattheisen, Manuel, Martin, Alicia R., Palotie, Aarno, Pallesen, Jonatan, Dumont, Ashley L., Belliveau, Rich, Anney, Richard, Poulsen, Jesper Buchhave, Walters, G. Bragi, Grove, Jakob, Daly, Mark J., Demontis, Ditte, Hollegaard, Mads V., Qvist, Per, Nærland, Terje, Walters, Raymond K., Christensen, Jane H., Saemundsen, Evald, Klei, Lambertus, Reichenberg, Abraham, Agerbo, Esben, Nyegaard, Mette, Satterstrom, F. Kyle, Devlin, Bernie, Maller, Julian, Andreassen, Ole A., Hope, Sigrun, Neale, Benjamin M., Reichert, Jennifer, Geschwind, Daniel H., Stefansson, Kari, Stevens, Christine R., Cerrato, Felecia, Mors, Ole, Sandin, Sven, Rehnström, Karola, Pedersen, Carsten Bøcker, dPoterba, Timothy, Churchhouse, Claire, Buxbaum, Joseph D., Turley, Patrick, Robinson, Elise B.
Institution: University of North Carolina at Chapel Hill
Subfield: Cognitive Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W7128511743
FWCI:
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