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Biological Psychiatry|March 30, 2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexiaAlistair T Pagnamenta, Elena Bacchelli, Maretha V de Jonge, et al.
Scientific Reports|November 23, 2021
Long-term sequelae are highly prevalent one year after hospitalization for severe COVID-19Mattia Bellan, Alessio Baricich, Filippo Patrucco, et al.
Nature Neuroscience|July 16, 2020
Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorderElaine T Lim, Mohammed Uddin, Silvia De Rubeis, et al.
American Journal of Human Genetics|August 8, 2020
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with PhenotypeMichael S Breen, Paras Garg, Lara Tang, et al.
Oncoimmunology|October 6, 2018
A point mutation in the Ncr1 signal peptide impairs the development of innate lymphoid cell subsetsFrancisca F Almeida, Sara Tognarelli, Antoine Marçais, et al.
Nature Neuroscience|July 18, 2017
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorderElaine T Lim, Mohammed Uddin, Silvia De Rubeis, et al.
Epilepsy & Behavior : E&B|September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part II: Experimental and translational approachesSebastian Bauer, Natascha van Alphen, Albert Becker, et al.
Epilepsy & Behavior : E&B|September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approachesFelix Rosenow, Natascha van Alphen, Albert Becker, et al.
The American Journal of Psychiatry|September 10, 2021
Interindividual Differences in Cortical Thickness and Their Genomic Underpinnings in Autism Spectrum DisorderChristine Ecker, Charlotte M Pretzsch, Anke Bletsch, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
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