Articles with public access mandates - Joseph D Buxbaum - US National Science FoundationLearn more
NoteFor this mandate, articles should be available from specific locations.
OverallNIHMRCWellcomeAutism Speaks Inc, USACIHRNIHRDFGEuropean CommissionGovernment of SpainINSERMVAHHMISwedish Research CouncilNHMRCGovernment of ItalyNWONSFGenome CanadaAutism Science Foundation, USADoDARCAlzheimers's UKFWOAcademy of FinlandSFIBBSRCZonMwRCNSNSFParkinson's UKBMBFHRBFCTNSERCTelethonCancer Research UKESRCKNAWNCNNSFCVersus Arthritis, UKDMTMotor Neurone Disease Association, UKJDRFFWFDSFMTADBTFormasFORTEMarianne and Marcus Wallenberg FoundationBHFDoris Duke Charitable FoundationANRState of CalifoniaFRQNTNMRCUK Research & InnovationRWJFAXA Research Fund, FranceHFSPFAPESPDOEGatesASPRAHAFRQSCASHelmholtzDFFDNATFBanking Foundation "la Caixa"Knut and Alice Wallenberg FoundationBank of Sweden Tercentenary FoundationA*StarAcademy of Medical Sciences, UKEPSRCNRFFondazione CariploChampalimaud FoundationMSFHRNKFIResearch Grants Council, Hong KongBrain Research, UKHealth Data Research, UKRoyal Society UKJSTBELSPOCZI
Not available based on mandate: 6
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
B Franke, JL Stein, S Ripke, V Anttila, DP Hibar, KJE Van Hulzen, ...
Nature neuroscience 19 (3), 420-431, 2016
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ...
Nature genetics 54 (9), 1320-1331, 2022
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, SD Rubeis, JY An, ...
BioRxiv, 484113, 2018
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, L Klei, ...
MedRxiv, 2021.12. 20.21267194, 2021
StandardRat: A multi-center consensus protocol to enhance functional connectivity specificity in the rat brain
J Grandjean, G Desrosiers-Gregoire, C Anckaerts, D Angeles-Valdez, ...
bioRxiv, 2022.04. 27.489658, 2022
Human TLR4 and noncanonical inflammasome differ in their ability to respond to distinct lipid A variants
J Alexander-Floyd, AR Bass, EM Harberts, D Grubaugh, JD Buxbaum, ...
bioRxiv, 2021.12. 16.472937, 2021
Available based on mandate: 5
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
A consensus protocol for functional connectivity analysis in the rat brain
J Grandjean, G Desrosiers-Gregoire, C Anckaerts, D Angeles-Valdez, ...
Nature neuroscience 26 (4), 673-681, 2023
Lipid A variants activate human TLR4 and the noncanonical inflammasome differently and require the core oligosaccharide for inflammasome activation
J Alexander-Floyd, AR Bass, EM Harberts, D Grubaugh, JD Buxbaum, ...
Infection and Immunity 90 (8), e00208-22, 2022
Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome
P Jain, T Miller-Fleming, A Topaloudi, D Yu, P Drineas, M Georgitsi, ...
Translational psychiatry 13 (1), 69, 2023
Genome-wide Association Study points to novel locus for Gilles de la Tourette Syndrome
F Tsetsos, A Topaloudi, P Jain, Z Yang, D Yu, P Kolovos, Z Tumer, ...
Biological psychiatry, 2023
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