Articles with public access mandates - Joseph D Buxbaum - Genome CanadaLearn 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: 11
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
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
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
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
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
ET Lim, M Uddin, S De Rubeis, Y Chan, AS Kamumbu, X Zhang, ...
Nature neuroscience 20 (9), 1217-1224, 2017
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
GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis
Y Kajiwara, E Wang, M Wang, WC Sin, KJ Brennand, E Schadt, CC Naus, ...
Acta neuropathologica communications 6, 1-20, 2018
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
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
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