Articoli con mandati relativi all'accesso pubblico - Anthony P MonacoUlteriori informazioni
Disponibili pubblicamente: 59
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
Mandati: US National Institutes of Health, Australian Research Council, National …
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
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
Mandati: Genome Canada, German Research Foundation
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
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
A functional genetic link between distinct developmental language disorders
SC Vernes, DF Newbury, BS Abrahams, L Winchester, J Nicod, M Groszer, ...
New England Journal of Medicine 359 (22), 2337-2345, 2008
Mandati: US National Institutes of Health
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
Mandati: US National Institutes of Health, National Institute of Health and Medical …
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
Mandati: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
CS Leblond, C Nava, A Polge, J Gauthier, G Huguet, S Lumbroso, ...
PLoS genetics 10 (9), e1004580, 2014
Mandati: German Research Foundation, National Institute of Health and Medical …
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
Mandati: US National Institutes of Health, National Institute for Health Research, UK
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
Mandati: US Department of Energy, US National Institutes of Health, Howard Hughes …
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
Mandati: US National Institutes of Health, UK Medical Research Council, European …
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
C Francks, S Maegawa, J Laurén, BS Abrahams, A Velayos-Baeza, ...
Molecular psychiatry 12 (12), 1129-1139, 2007
Mandati: Swiss National Science Foundation
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
CS Leblond, J Heinrich, R Delorme, C Proepper, C Betancur, G Huguet, ...
PLoS genetics 8 (2), e1002521, 2012
Mandati: Canadian Institutes of Health Research, German Research Foundation, National …
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
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability
A Noor, A Whibley, CR Marshall, PJ Gianakopoulos, A Piton, AR Carson, ...
Science translational medicine 2 (49), 49ra68-49ra68, 2010
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder
R Maier, G Moser, GB Chen, S Ripke, D Absher, I Agartz, H Akil, F Amin, ...
The American Journal of Human Genetics 96 (2), 283-294, 2015
Mandati: US National Institutes of Health, Australian Research Council, National …
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
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
WM Brandler, AP Morris, DM Evans, TS Scerri, JP Kemp, NJ Timpson, ...
PLoS genetics 9 (9), e1003751, 2013
Mandati: UK Medical Research Council, Wellcome Trust
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia
AT Pagnamenta, E Bacchelli, MV de Jonge, G Mirza, TS Scerri, F Minopoli, ...
Biological psychiatry 68 (4), 320-328, 2010
Mandati: US National Institutes of Health, German Research Foundation
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
Mandati: US National Institutes of Health, German Research Foundation, Fondazione …
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