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Cell|January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of AutismF Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2012
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autismPatrícia B S Celestino-Soper, Sara Violante, Emily L Crawford, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
Global Change Biology|June 1, 2018
Dominance-diversity relationships in ant communities differ with invasionXavier Arnan, Alan N Andersen, Heloise Gibb, et al.
Physical Review Letters|August 7, 2007
Production of mesons and baryons at high rapidity and high p(T) in proton-proton collisions at square root[s] = 200 GeVI Arsene, I G Bearden, D Beavis, et al.
Cell|June 17, 2025
Adaptive radiation and social evolution of the antsJoel Vizueta, Zijun Xiong, Guo Ding, et al.
Biorxiv : the Preprint Server for Biology|September 18, 2025
Human-specific features of the cerebellum and ZP2-regulated synapse developmentSuel-Kee Kim, Adriana Cherskov, Aastha Sindhwani, et al.
American Journal of Human Genetics|August 18, 2023
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomaliesChelsea Lowther, Elise Valkanas, Jessica L Giordano, et al.
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