Articles with public access mandates - Joseph D Buxbaum - German Research FoundationLearn more
NoteFor this mandate, articles should be available from specific locations.
OverallNIHMRCWellcomeAutism Speaks Inc, USACIHRNIHRDFGEuropean CommissionINSERMGovernment of SpainVAHHMISwedish Research CouncilNHMRCGovernment of ItalyNWOGenome CanadaNSFAutism Science Foundation, USADoDARCAlzheimers's UKFWOAcademy of FinlandSFIBBSRCZonMwRCNSNSFParkinson's UKBMBFHRBFCTNSERCTelethonCancer Research UKESRCKNAWNCNNSFCVersus Arthritis, UKDMTMotor Neurone Disease Association, UKJDRFFWFDSFDBTFormasFORTEMarianne and Marcus Wallenberg FoundationBHFDoris Duke Charitable FoundationANRState of CalifoniaFRQNTNMRCUK Research & InnovationRWJFAXA Research Fund, FranceHFSPFAPESPDOEGatesASPRAHAFRQSCASHelmholtzDFFDNATFBanking Foundation "la Caixa"MTAKnut 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
Available based on mandate: 27
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
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
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD
L Pavinato, A Delle Vedove, D Carli, M Ferrero, S Carestiato, JL Howe, ...
Brain 146 (2), 534-548, 2023
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
G Butler-Laporte, G Povysil, JA Kosmicki, ET Cirulli, T Drivas, S Furini, ...
PLoS genetics 18 (11), e1010367, 2022
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
Genome-wide Association Study identifies two novel loci for Gilles de la Tourette Syndrome
F Tsetsos, A Topaloudi, P Jain, Z Yang, D Yu, P Kolovos, Z Tumer, ...
medRxiv, 2021.12. 11.21267560, 2021
A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts
G Ni, J Zeng, JA Revez, Y Wang, Z Zheng, T Ge, R Restuadi, J Kiewa, ...
Biological psychiatry 90 (9), 611-620, 2021
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
Genetic risk for schizophrenia and autism, social impairment and developmental pathways to psychosis
E Velthorst, S Froudist-Walsh, E Stahl, D Ruderfer, I Ivanov, J Buxbaum, ...
Translational psychiatry 8 (1), 204, 2018
De novo sequence and copy number variants are strongly associated with Tourette disorder and implicate cell polarity in pathogenesis
S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ...
Cell reports 24 (13), 3441-3454. e12, 2018
Developmental social communication deficits in the Shank3 rat model of phelan‐mcdermid syndrome and autism spectrum disorder
EL Berg, NA Copping, JK Rivera, MC Pride, M Careaga, MD Bauman, ...
Autism Research 11 (4), 587-601, 2018
Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate …
E Di Gregorio, E Riberi, EF Belligni, E Biamino, M Spielmann, U Ala, ...
Clinical genetics 92 (4), 415-422, 2017
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
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics …
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
bioRxiv, 040493, 2016
Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID
DM Cochoy, A Kolevzon, Y Kajiwara, M Schoen, M Pascual-Lucas, ...
Molecular autism 6, 1-13, 2015
Most genetic risk for autism resides with common variation
T Gaugler, L Klei, SJ Sanders, CA Bodea, AP Goldberg, AB Lee, ...
Nature genetics 46 (8), 881-885, 2014
Characterization of SLITRK1 variation in obsessive-compulsive disorder
U Ozomaro, G Cai, Y Kajiwara, S Yoon, V Makarov, R Delorme, ...
PloS one 8 (8), e70376, 2013
Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model
JW Steele, ML Lachenmayer, S Ju, A Stock, J Liken, SH Kim, LM Delgado, ...
Molecular psychiatry 18 (8), 889-897, 2013
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis
DC Whitcomb, J LaRusch, AM Krasinskas, L Klei, JP Smith, RE Brand, ...
Nature genetics 44 (12), 1349-1354, 2012
Individual common variants exert weak effects on the risk for autism spectrum disorders
R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ...
Human molecular genetics 21 (21), 4781-4792, 2012
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