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 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
Available based on mandate: 28
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
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
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
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
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
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 novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ...
Human genetics 131, 565-579, 2012
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility
E Maestrini, AT Pagnamenta, JA Lamb, E Bacchelli, NH Sykes, I Sousa, ...
Molecular psychiatry 15 (9), 954-968, 2010
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
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
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
Amyloid beta protein-induced zinc sequestration leads to synaptic loss via dysregulation of the ProSAP2/Shank3 scaffold
AM Grabrucker, MJ Schmeisser, PT Udvardi, M Arons, M Schoen, ...
Molecular neurodegeneration 6, 1-20, 2011
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
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
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders
RJL Anney, EM Kenny, C O'dushlaine, BL Yaspan, E Parkhomenka, ...
European journal of human genetics 19 (10), 1082-1089, 2011
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
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
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
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