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Biological Psychiatry|June 11, 2013
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous traitPauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Biological Psychiatry|December 24, 2014
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Pauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 17, 2025
Cell-type-informed genotyping of mosaic focal epilepsies reveals cell-autonomous and non-cell-autonomous disease-associated transcriptional programsSara Bizzotto, Maya Talukdar, Edward A Stronge, et al.
Nature|May 14, 2025
Spatial transcriptomics reveals human cortical layer and area specificationXuyu Qian, Kyle Coleman, Shunzhou Jiang, et al.
Brain, Behavior, and Immunity|March 29, 2024
CSMD1 regulates brain complement activity and circuit developmentMatthew L Baum, Daniel K Wilton, Rachel G Fox, et al.
Nature Genetics|November 5, 2022
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinismMatthew N Wakeling, Nick D L Owens, Jessica R Hopkinson, et al.
Cell Reports|July 26, 2018
The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular VesiclesMichael E Coulter, Cristina M Dorobantu, Gerrald A Lodewijk, et al.
Annals of Neurology|March 6, 2014
SLC25A22 is a novel gene for migrating partial seizures in infancyAnnapurna Poduri, Erin L Heinzen, Vida Chitsazzadeh, et al.
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
The Journal of Experimental Medicine|April 18, 2024
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiencyMatthew B Johnson, Masato Ogishi, Clara Domingo-Vila, et al.
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