Articles with public access mandates - Raphael BernierLearn more
Not available anywhere: 7
Review
Autism spectrum disorder, developmental and psychiatric features in 16p11. 2 duplication
LA Green Snyder, D D’Angelo, Q Chen, R Bernier, RP Goin-Kochel, ...
Journal of autism and developmental disorders 46, 2734-2748, 2016
Mandates: US National Institutes of Health
Review
Children with autism show altered autonomic adaptation to novel and familiar social partners
E Neuhaus, RA Bernier, TP Beauchaine
Autism Research 9 (5), 579-591, 2016
Mandates: Autism Speaks Inc, USA
Review
The role of mirror neuron dysfunction in autism
R Bernier, G Dawson
Mirror neuron systems: The role of mirroring processes in social cognition …, 2009
Mandates: US National Institutes of Health
Review
The Early Start Denver Model intervention and mu rhythm attenuation in autism spectrum disorders
B Aaronson, A Estes, SJ Rogers, G Dawson, R Bernier
Journal of autism and developmental disorders, 1-10, 2022
Mandates: US National Institutes of Health
Review
EEG and pupillary response in children with autism: Results from the ABC-CT feasibility study
A Naples, F Shic, A Levin, R Bernier, G Dawson, M Murias, S Jeste, ...
Annu. Meeting (INSAR), 2018
Mandates: US National Institutes of Health
Review
Unpacking The Autism Spectrum Disorder Profile of Children With De Novo Disruptive GRIN2B Variants: A Quantitative and Qualitative Analysis
CM Hudac, E Kurtz-Nelson, TM Rutter, JL Peterson, K Hoekzema, ...
Mandates: US National Institutes of Health
Review
Data Acquisition and Analysis Core ET Main Study Manual of Operations Version 4.8
F Shic, A Naples, E Barney, A Chang, B Li, T McAllister, M Kim, ...
Mandates: US National Science Foundation, US Department of Defense, US National …
Available somewhere: 172
Review
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
BJ O’Roak, L Vives, S Girirajan, E Karakoc, N Krumm, BP Coe, R Levy, ...
Nature 485 (7397), 246-250, 2012
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Review
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
JT Glessner, K Wang, G Cai, O Korvatska, CE Kim, S Wood, H Zhang, ...
Nature 459 (7246), 569-573, 2009
Mandates: US National Institutes of Health, Autism Speaks Inc, USA
Review
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
BJ O'Roak, P Deriziotis, C Lee, L Vives, JJ Schwartz, S Girirajan, ...
Nature genetics 43 (6), 585-589, 2011
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Review
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders
BJ O’Roak, L Vives, W Fu, JD Egertson, IB Stanaway, IG Phelps, G Carvill, ...
Science 338 (6114), 1619-1622, 2012
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Review
Common genetic variants on 5p14. 1 associate with autism spectrum disorders
K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ...
Nature 459 (7246), 528-533, 2009
Mandates: US National Institutes of Health, Autism Speaks Inc, USA
Review
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ...
The American Journal of Human Genetics 94 (5), 677-694, 2014
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
Disruptive CHD8 mutations define a subtype of autism early in development
R Bernier, C Golzio, B Xiong, HA Stessman, BP Coe, O Penn, ...
Cell 158 (2), 263-276, 2014
Mandates: US National Institutes of Health, Howard Hughes Medical Institute …
Review
A multisite study of the clinical diagnosis of different autism spectrum disorders
C Lord, E Petkova, V Hus, W Gan, F Lu, DM Martin, O Ousley, L Guy, ...
Archives of general psychiatry 69 (3), 306-313, 2012
Mandates: US National Institutes of Health
Review
Excess of rare, inherited truncating mutations in autism
N Krumm, TN Turner, C Baker, L Vives, K Mohajeri, K Witherspoon, ...
Nature genetics 47 (6), 582-588, 2015
Mandates: US National Institutes of Health
Review
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
HAF Stessman, BO Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, ...
Nature genetics 49 (4), 515-526, 2017
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, National …
Review
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
Mandates: US National Institutes of Health, UK Medical Research Council, European …
Review
SPARK: A US cohort of 50,000 families to accelerate autism research
P Feliciano, AM Daniels, LAG Snyder, A Beaumont, A Camba, A Esler, ...
Neuron 97 (3), 488-493, 2018
Mandates: US National Institutes of Health, Autism Speaks Inc, USA
Review
Relative burden of large CNVs on a range of neurodevelopmental phenotypes
S Girirajan, Z Brkanac, BP Coe, C Baker, L Vives, TH Vu, N Shafer, ...
PLoS genetics 7 (11), e1002334, 2011
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
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