Articles with public access mandates - A Jeremy WillseyLearn more
OverallNIHHHMICIHRMRCNIHRDFGWellcomeSwedish Research CouncilCZIVANHMRCGovernment of SpainNCNAutism Speaks Inc, USAAutism Science Foundation, USANSFDoDARCNSFCINSERMHRBNWOKnut and Alice Wallenberg FoundationKNAWDOEGatesGenome CanadaMTASFIEuropean CommissionRCNState of CalifoniaBMBFParkinson's Foundation, USA
Available somewhere: 68
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Health …
The contribution of de novo coding mutations to autism spectrum disorder
I Iossifov, BJ O’roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ...
Nature 515 (7526), 216-221, 2014
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch, MJ Raubeson, ...
Nature 485 (7397), 237-241, 2012
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
Mandates: US National Institutes of Health, Australian Research Council, National …
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
Mandates: US National Science Foundation, US National Institutes of Health, Autism …
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci
SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ...
Neuron 87 (6), 1215-1233, 2015
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
Mandates: US National Institutes of Health, Swedish Research Council, UK Medical …
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder
MJ Gandal, P Zhang, E Hadjimichael, RL Walker, C Chen, S Liu, H Won, ...
Science 362 (6420), eaat8127, 2018
Mandates: US National Institutes of Health, National Natural Science Foundation of China
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
AJ Willsey, SJ Sanders, M Li, S Dong, AT Tebbenkamp, RA Muhle, ...
Cell 155 (5), 997-1007, 2013
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Comprehensive functional genomic resource and integrative model for the human brain
D Wang, S Liu, J Warrell, H Won, X Shi, FCP Navarro, D Clarke, M Gu, ...
Science 362 (6420), eaat8464, 2018
Mandates: US National Institutes of Health
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
M Li, G Santpere, Y Imamura Kawasawa, OV Evgrafov, FO Gulden, ...
Science 362 (6420), eaat7615, 2018
Mandates: US National Institutes of Health, US Department of Veterans Affairs …
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature neuroscience 18 (2), 199-209, 2015
Mandates: US National Institutes of Health, National Institute for Health Research, UK
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 …
Common genetic variants, acting additively, are a major source of risk for autism
L Klei, SJ Sanders, MT Murtha, V Hus, JK Lowe, AJ Willsey, ...
Molecular autism 3, 1-13, 2012
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
J Cotney, RA Muhle, SJ Sanders, L Liu, AJ Willsey, W Niu, W Liu, L Klei, ...
Nature communications 6 (1), 6404, 2015
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia
Molecular autism 8, 1-17, 2017
Mandates: US Department of Energy, US National Institutes of Health, Howard Hughes …
The psychencode project
S Akbarian, C Liu, JA Knowles, FM Vaccarino, PJ Farnham, GE Crawford, ...
Nature neuroscience 18 (12), 1707-1712, 2015
Mandates: US National Institutes of Health, US Department of Veterans Affairs
Interrogating the genetic determinants of Tourette’s syndrome and other tic disorders through genome-wide association studies
D Yu, JH Sul, F Tsetsos, MS Nawaz, AY Huang, I Zelaya, C Illmann, ...
American Journal of Psychiatry 176 (3), 217-227, 2019
Mandates: US Department of Defense, US National Institutes of Health, German Research …
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
JY An, K Lin, L Zhu, DM Werling, S Dong, H Brand, HZ Wang, X Zhao, ...
Science 362 (6420), eaat6576, 2018
Mandates: US National Institutes of Health
Comparative flavivirus-host protein interaction mapping reveals mechanisms of dengue and Zika virus pathogenesis
PS Shah, N Link, GM Jang, PP Sharp, T Zhu, DL Swaney, JR Johnson, ...
Cell 175 (7), 1931-1945. e18, 2018
Mandates: US Department of Defense, US National Institutes of Health, Howard Hughes …
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