Artigos com autorizações de acesso público - William Ted BrownSaiba mais
44 artigos disponíveis publicamente
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
Autorizações: Genome Canada, German Research Foundation
The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes
J Wegiel, I Kuchna, K Nowicki, H Imaki, J Wegiel, E Marchi, SY Ma, ...
Acta neuropathologica 119, 755-770, 2010
Autorizações: US National Institutes of Health, Autism Speaks Inc, USA
IL-6 is increased in the cerebellum of autistic brain and alters neural cell adhesion, migration and synaptic formation
H Wei, H Zou, AM Sheikh, M Malik, C Dobkin, WT Brown, X Li
Journal of neuroinflammation 8, 1-10, 2011
Autorizações: US National Institutes of Health
Autism spectrum disorder in fragile X syndrome: cooccurring conditions and current treatment
WE Kaufmann, SA Kidd, HF Andrews, DB Budimirovic, A Esler, ...
Pediatrics 139 (Supplement_3), S194-S206, 2017
Autorizações: US National Institutes of Health
Impact of farnesylation inhibitors on survival in Hutchinson-Gilford progeria syndrome
LB Gordon, J Massaro, RB D’Agostino Sr, SE Campbell, J Brazier, ...
Circulation 130 (1), 27-34, 2014
Autorizações: US National Institutes of Health
Brain region‐specific deficit in mitochondrial electron transport chain complexes in children with autism
A Chauhan, F Gu, MM Essa, J Wegiel, K Kaur, WT Brown, V Chauhan
Journal of neurochemistry 117 (2), 209-220, 2011
Autorizações: US National Institutes of Health, Autism Speaks Inc, USA
Epigenomic profiling reveals an association between persistence of DNA methylation and metabolic memory in the DCCT/EDIC type 1 diabetes cohort
Z Chen, F Miao, AD Paterson, JM Lachin, L Zhang, DE Schones, X Wu, ...
Proceedings of the National Academy of Sciences 113 (21), E3002-E3011, 2016
Autorizações: US National Institutes of Health, Juvenile Diabetes Research Foundation
Alterations in mitochondrial DNA copy number and the activities of electron transport chain complexes and pyruvate dehydrogenase in the frontal cortex from subjects with autism
F Gu, V Chauhan, K Kaur, WT Brown, G LaFauci, J Wegiel, A Chauhan
Translational psychiatry 3 (9), e299-e299, 2013
Autorizações: US National Institutes of Health
Stereological study of the neuronal number and volume of 38 brain subdivisions of subjects diagnosed with autism reveals significant alterations restricted to the striatum …
J Wegiel, M Flory, I Kuchna, K Nowicki, SY Ma, H Imaki, J Wegiel, ...
Acta neuropathologica communications 2, 1-18, 2014
Autorizações: US National Institutes of Health
Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers
SL Nolin, A Glicksman, N Ersalesi, C Dobkin, WT Brown, RU Cao, E Blatt, ...
Genetics in Medicine 17 (5), 358-364, 2015
Autorizações: US National Institutes of Health
Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles
SL Nolin, S Sah, A Glicksman, SL Sherman, E Allen, E Berry‐Kravis, ...
American Journal of Medical Genetics Part A 161 (4), 771-778, 2013
Autorizações: US National Institutes of Health
Fragile X targeted pharmacotherapy: lessons learned and future directions
CA Erickson, MH Davenport, TL Schaefer, LK Wink, EV Pedapati, ...
Journal of neurodevelopmental disorders 9, 1-14, 2017
Autorizações: US Department of Defense, US National Institutes of Health, Autism Speaks …
Autism spectrum disorder in children and adolescents with fragile X syndrome: within-syndrome differences and age-related changes
A McDuffie, L Abbeduto, P Lewis, S Kover, JS Kim, A Weber, WT Brown
American journal on intellectual and developmental disabilities 115 (4), 307-326, 2010
Autorizações: US National Institutes of Health
Mutations in the gene DNAJC5 cause autosomal dominant Kufs disease in a proportion of cases: study of the Parry family and 8 other families
M Velinov, N Dolzhanskaya, M Gonzalez, E Powell, I Konidari, W Hulme, ...
PloS one 7 (1), e29729, 2012
Autorizações: US National Institutes of Health
Effects of sampling context on spontaneous expressive language in males with fragile X syndrome or Down syndrome
ST Kover, A McDuffie, L Abbeduto, WT Brown
American Speech-Language-Hearing Association, 2012
Autorizações: US National Institutes of Health
Brain-region–specific alterations of the trajectories of neuronal volume growth throughout the lifespan in autism
J Wegiel, M Flory, I Kuchna, K Nowicki, SY Ma, H Imaki, J Wegiel, ...
Acta neuropathologica communications 2, 1-18, 2014
Autorizações: US National Institutes of Health
Autism severity is associated with child and maternal MAOA genotypes
IL Cohen, X Liu, MES Lewis, A Chudley, C Forster‐Gibson, M Gonzalez, ...
Clinical Genetics 79 (4), 355-362, 2011
Autorizações: Canadian Institutes of Health Research
Increased activities of Na+/K+-ATPase and Ca2+/Mg2+-ATPase in the frontal cortex and cerebellum of autistic individuals
L Ji, A Chauhan, WT Brown, V Chauhan
Life sciences 85 (23-26), 788-793, 2009
Autorizações: US National Institutes of Health, Autism Speaks Inc, USA
ASD comorbidity in fragile X syndrome: Symptom profile and predictors of symptom severity in adolescent and young adult males
L Abbeduto, AJ Thurman, A McDuffie, J Klusek, RT Feigles, W Ted Brown, ...
Journal of Autism and Developmental Disorders 49, 960-977, 2019
Autorizações: US National Institutes of Health
Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11. 2-q13 and idiopathic autism
J Wegiel, NC Schanen, EH Cook, M Sigman, WT Brown, I Kuchna, ...
Journal of Neuropathology & Experimental Neurology 71 (5), 382-397, 2012
Autorizações: US National Institutes of Health
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