Channel:  Simons Foundation Autism Research Initiative (SFARI)

bioRxiv posts many COVID19-related papers. A reminder: they have not been formally peer-reviewed and should not guide health-related behavior or be reported in the press as conclusive.

280 Articles

Excessive ERK-dependent synaptic clustering with enhanced motor learning in the MECP2 duplication syndrome mouse model of autism
Ash, R. T., Buffington, S. A., Park, J., Costa-Mattioli, M., Zoghbi, H. Y., Smirnakis, S. M.
10.1101/100875 — Posted: 2017-01-16
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
Weiner, D. J., Wigdor, E. M., Ripke, S., Walters, R. K., Kosmicki, J. A., Grove, J., Samocha, K. E., Goldstein, J., Okbay, A., Bybjerg-Gauholm, J., Werge, T., Hougaard, D. M., Taylor, J., Skuse, D., Devlin, B., Anney, R., Sanders, S., Bishop, S., Bo Mortensen, P., Borglum, A., Davey Smith, G., Daly, M. J., Robinson, E. B.
10.1101/089342 — Posted: 2016-11-23
Comprehensive Analysis of Two Shank3 and the Cacna1c Mouse Models of Autism Spectrum Disorder
Patricia A Kabitzke, Daniela Brunner, Dansha He, Pamela A Fazio, Kimberly Cox, Jane Sutphen, Lucinda Thiede, Emily Sabath, Taleen Hanania, Vadim Alexandrov, Randall Rasmusson, Will Spooren, Anirvan Ghosh, Pamela Feliciano, Barbara Biemans, Marta Benedetti, Alice Luo Clayton
10.1101/068866 — Posted: 2016-09-02
Exaggerated CpH Methylation in the Autism-Affected Brain
Shannon E Ellis, Simone Gupta, Anna Moes, Andrew B West, Dan E Arking
10.1101/069120 — Posted: 2016-08-15
A cell type-specific expression signature predicts haploinsufficient autism-susceptibility genes
Chaolin Zhang, Yufeng Shen
10.1101/058826 — Posted: 2016-06-14
CNView: a visualization and annotation tool for copy number variation from whole-genome sequencing
Ryan L Collins, Matthew R Stone, Harrison Brand, Joseph T Glessner, Michael E Talkowski
10.1101/049536 — Posted: 2016-04-20
Transcriptome Analysis of Cortical Tissue Reveals Shared Sets of Down-Regulated Genes in Autism and Schizophrenia
Shannon E Ellis, Rebecca Panitch, Andrew West, Dan E Arking
10.1101/029132 — Posted: 2016-02-18
Frequency and complexity of de novo structural mutation in autism
William M Brandler, Danny Antaki, Madhusudan Gujral, Amina Noor, Gabriel Rosanio, Timothy R Chapman, Daniel J Barrera, Guan Ning Lin, Dheeraj Malhotra, Amanda C Watts, Lawrence C Wong, Jasper A Estabillo, Therese E Gadomski, Oanh Hong, Karin V Fuentes Fajardo, Abhishek Bhandari, Renius Owen, Michael Baughn, Jeffrey Yuan, Terry Solomon, Alexandra G Moyzis, Stephan J Sanders, Gail E Reiner, Keith K Vaux, Charles M Strom, Kang Zhang, Alysson R Muotri, Natacha Akshoomoff, Suzanne M Leal, Karen Pierce, Eric Courchesne, Lilia M Iakoucheva, Christina Corsello, Jonathan Sebat
10.1101/030270 — Posted: 2015-10-30
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
Elise B Robinson, Beate St Pourcain, Verneri Anttila, Jack Kosmicki, Brendan Bulik-Sullivan, Jakob Grove, Julian Maller, Kaitlin E Samocha, Stephan Sanders, Stephan Ripke, Joanna Martin, Mads V Hollegaard, Thomas Werge, David M Hougaard, Benjamin M Neale, David Evans, David Skuse, Preben Bo Mortensen, Anders Borglum, Angelica Ronald, George Davey Smith, Mark J Daly
10.1101/027771 — Posted: 2015-09-29
Simple genetic models for autism spectrum disorder
Swagatam Mukhopadhyay, Michael Wigler, Dan Levy
10.1101/017301 — Posted: 2015-03-30

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