nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Abnormal lateralization of functional connectivity between language and default mode regions in autism
|
Nielsen, Jared A |
|
2014 |
|
1 |
|
artikel |
2 |
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region
|
McInnes, L Alison |
|
2010 |
|
1 |
|
artikel |
3 |
Altered glial marker expression in autistic post-mortem prefrontal cortex and cerebellum
|
Edmonson, Catherine |
|
2014 |
|
1 |
|
artikel |
4 |
A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism
|
Hussman, John P |
|
2011 |
|
1 |
|
artikel |
5 |
An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males
|
Chung, Ren-Hua |
|
2011 |
|
1 |
|
artikel |
6 |
A potentiated startle study of uncertainty and contextual anxiety in adolescents diagnosed with autism spectrum disorder
|
Chamberlain, Paul D |
|
2013 |
|
1 |
|
artikel |
7 |
A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders
|
Kim, Soo-Jeong |
|
2011 |
|
1 |
|
artikel |
8 |
A review of the evidence for the canonical Wnt pathway in autism spectrum disorders
|
Kalkman, Hans Otto |
|
2012 |
|
1 |
|
artikel |
9 |
A review of the serotonin transporter and prenatal cortisol in the development of autism spectrum disorders
|
Rose’Meyer, Roselyn |
|
2013 |
|
1 |
|
artikel |
10 |
Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk
|
Carayol, Jerome |
|
2010 |
|
1 |
|
artikel |
11 |
Association between the oxytocin receptor (OXTR) gene and mesolimbic responses to rewards
|
Damiano, Cara R |
|
2014 |
|
1 |
|
artikel |
12 |
Atypical brain lateralisation in the auditory cortex and language performance in 3- to 7-year-old children with high-functioning autism spectrum disorder: a child-customised magnetoencephalography (MEG) study
|
Yoshimura, Yuko |
|
2013 |
|
1 |
|
artikel |
13 |
Autism in DSM-5: progress and challenges
|
Volkmar, Fred R |
|
2013 |
|
1 |
|
artikel |
14 |
Autism risk assessment in siblings of affected children using sex-specific genetic scores
|
Carayol, Jerome |
|
2011 |
|
1 |
|
artikel |
15 |
Brain region-specific altered expression and association of mitochondria-related genes in autism
|
Anitha, Ayyappan |
|
2012 |
|
1 |
|
artikel |
16 |
Candidate gene study of HOXB1 in autism spectrum disorder
|
Muscarella, Lucia A |
|
2010 |
|
1 |
|
artikel |
17 |
Capping four years of growth of Molecular Autism: impact factor coming in 2014
|
Buxbaum, Joseph D |
|
2013 |
|
1 |
|
artikel |
18 |
Common genetic variants, acting additively, are a major source of risk for autism
|
Klei, Lambertus |
|
2012 |
|
1 |
|
artikel |
19 |
Common variation contributes to the genetic architecture of social communication traits
|
St Pourcain, Beate |
|
2013 |
|
1 |
|
artikel |
20 |
Comparing biobehavioral profiles across two social stress paradigms in children with and without autism spectrum disorders
|
Corbett, Blythe A |
|
2012 |
|
1 |
|
artikel |
21 |
Comparison of white matter integrity between autism spectrum disorder subjects and typically developing individuals: a meta-analysis of diffusion tensor imaging tractography studies
|
Aoki, Yuta |
|
2013 |
|
1 |
|
artikel |
22 |
Decitabine alters the expression of Mecp2 isoforms via dynamic DNA methylation at the Mecp2 regulatory elements in neural stem cells
|
Liyanage, Vichithra R B |
|
2013 |
|
1 |
|
artikel |
23 |
Decreased expression of axon-guidance receptors in the anterior cingulate cortex in autism
|
Suda, Shiro |
|
2011 |
|
1 |
|
artikel |
24 |
Decreased tryptophan metabolism in patients with autism spectrum disorders
|
Boccuto, Luigi |
|
2013 |
|
1 |
|
artikel |
25 |
Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders
|
Chien, Wei-Hsien |
|
2013 |
|
1 |
|
artikel |
26 |
Defining the broader, medium and narrow autism phenotype among parents using the Autism Spectrum Quotient (AQ)
|
Wheelwright, Sally |
|
2010 |
|
1 |
|
artikel |
27 |
Differential recruitment of coregulators to the RORA promoter adds another layer of complexity to gene (dys) regulation by sex hormones in autism
|
Sarachana, Tewarit |
|
2013 |
|
1 |
|
artikel |
28 |
Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?
|
Amiet, Claire |
|
2013 |
|
1 |
|
artikel |
29 |
Do girls with anorexia nervosa have elevated autistic traits?
|
Baron-Cohen, Simon |
|
2013 |
|
1 |
|
artikel |
30 |
DSM-5 and autism spectrum disorders (ASDs): an opportunity for identifying ASD subtypes
|
Grzadzinski, Rebecca |
|
2013 |
|
1 |
|
artikel |
31 |
DSM-5: the debate continues
|
Buxbaum, Joseph D |
|
2013 |
|
1 |
|
artikel |
32 |
Dysregulation of fragile × mental retardation protein and metabotropic glutamate receptor 5 in superior frontal cortex of individuals with autism: a postmortem brain study
|
Fatemi, S Hossein |
|
2011 |
|
1 |
|
artikel |
33 |
Elevated cortisol during play is associated with age and social engagement in children with autism
|
Corbett, Blythe A |
|
2010 |
|
1 |
|
artikel |
34 |
Enzymes in the glutamate-glutamine cycle in the anterior cingulate cortex in postmortem brain of subjects with autism
|
Shimmura, Chie |
|
2013 |
|
1 |
|
artikel |
35 |
Episodic memory retrieval for story characters in high-functioning autism
|
Komeda, Hidetsugu |
|
2013 |
|
1 |
|
artikel |
36 |
Evidence for differential alternative splicing in blood of young boys with autism spectrum disorders
|
Stamova, Boryana S |
|
2013 |
|
1 |
|
artikel |
37 |
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci
|
Hedges, Dale J |
|
2012 |
|
1 |
|
artikel |
38 |
Evidence of reactive oxygen species-mediated damage to mitochondrial DNA in children with typical autism
|
Napoli, Eleonora |
|
2013 |
|
1 |
|
artikel |
39 |
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
|
Cukier, Holly N |
|
2014 |
|
1 |
|
artikel |
40 |
Exploring autistic traits in anorexia: a clinical study
|
Tchanturia, Kate |
|
2013 |
|
1 |
|
artikel |
41 |
Expression of non-protein-coding antisense RNAs in genomic regions related to autism spectrum disorders
|
Velmeshev, Dmitry |
|
2013 |
|
1 |
|
artikel |
42 |
Facial phenotypes in subgroups of prepubertal boys with autism spectrum disorders are correlated with clinical phenotypes
|
Aldridge, Kristina |
|
2011 |
|
1 |
|
artikel |
43 |
Failure to deactivate the default mode network indicates a possible endophenotype of autism
|
Spencer, Michael D |
|
2012 |
|
1 |
|
artikel |
44 |
Foetal testosterone and autistic traits in 18 to 24-month-old children
|
Auyeung, Bonnie |
|
2010 |
|
1 |
|
artikel |
45 |
Fragile X and autism: Intertwined at the molecular level leading to targeted treatments
|
Hagerman, Randi |
|
2010 |
|
1 |
|
artikel |
46 |
Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism
|
Tansey, Katherine E |
|
2011 |
|
1 |
|
artikel |
47 |
Further characterization of autoantibodies to GABAergic neurons in the central nervous system produced by a subset of children with autism
|
Wills, Sharifia |
|
2011 |
|
1 |
|
artikel |
48 |
Gene expression analysis in lymphoblasts derived from patients with autism spectrum disorder
|
Yasuda, Yuka |
|
2011 |
|
1 |
|
artikel |
49 |
Genetic background modulates phenotypes of serotonin transporter Ala56 knock-in mice
|
Kerr, Travis M |
|
2013 |
|
1 |
|
artikel |
50 |
Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism
|
Warrier, Varun |
|
2013 |
|
1 |
|
artikel |
51 |
Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder
|
Sarachana, Tewarit |
|
2013 |
|
1 |
|
artikel |
52 |
Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders
|
Cannon, Dale S |
|
2010 |
|
1 |
|
artikel |
53 |
Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees
|
Coon, Hilary |
|
2010 |
|
1 |
|
artikel |
54 |
Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
|
Bozdagi, Ozlem |
|
2010 |
|
1 |
|
artikel |
55 |
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters
|
Chaste, Pauline |
|
2012 |
|
1 |
|
artikel |
56 |
Histopathologic characterization of the BTBR mouse model of autistic-like behavior reveals selective changes in neurodevelopmental proteins and adult hippocampal neurogenesis
|
Stephenson, Diane T |
|
2011 |
|
1 |
|
artikel |
57 |
Identification of an age-dependent biomarker signature in children and adolescents with autism spectrum disorders
|
Ramsey, Jordan M |
|
2013 |
|
1 |
|
artikel |
58 |
Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder
|
Steinberg, Karyn Meltz |
|
2012 |
|
1 |
|
artikel |
59 |
Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder
|
Ramos, Paula S |
|
2012 |
|
1 |
|
artikel |
60 |
Impairment of fragile X mental retardation protein-metabotropic glutamate receptor 5 signaling and its downstream cognates ras-related C3 botulinum toxin substrate 1, amyloid beta A4 precursor protein, striatal-enriched protein tyrosine phosphatase, and homer 1, in autism: a postmortem study in cerebellar vermis and superior frontal cortex
|
Fatemi, S Hossein |
|
2013 |
|
1 |
|
artikel |
61 |
Increased abundance of Sutterella spp. and Ruminococcus torques in feces of children with autism spectrum disorder
|
Wang, Lv |
|
2013 |
|
1 |
|
artikel |
62 |
Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples
|
Scoles, Haley A |
|
2011 |
|
1 |
|
artikel |
63 |
Increased gene expression of FOXP1 in patients with autism spectrum disorders
|
Chien, Wei-Hsien |
|
2013 |
|
1 |
|
artikel |
64 |
Increased midgestational IFN-γ, IL-4 and IL-5 in women bearing a child with autism: A case-control study
|
Goines, Paula E |
|
2011 |
|
1 |
|
artikel |
65 |
Insulin-like growth factor-1 rescues synaptic and motor deficits in a mouse model of autism and developmental delay
|
Bozdagi, Ozlem |
|
2013 |
|
1 |
|
artikel |
66 |
Intranasal oxytocin versus placebo in the treatment of adults with autism spectrum disorders: a randomized controlled trial
|
Anagnostou, Evdokia |
|
2012 |
|
1 |
|
artikel |
67 |
Investigation of the serum levels of anterior pituitary hormones in male children with autism
|
Iwata, Keiko |
|
2011 |
|
1 |
|
artikel |
68 |
Is metabotropic glutamate receptor 5 upregulated in prefrontal cortex in fragile X syndrome?
|
Lohith, Talakad G |
|
2013 |
|
1 |
|
artikel |
69 |
Is synaesthesia more common in autism?
|
Baron-Cohen, Simon |
|
2013 |
|
1 |
|
artikel |
70 |
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder
|
Bahl, Samira |
|
2013 |
|
1 |
|
artikel |
71 |
Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci
|
Davis, Lea K |
|
2012 |
|
1 |
|
artikel |
72 |
MeCP2 modulates gene expression pathways in astrocytes
|
Yasui, Dag H |
|
2013 |
|
1 |
|
artikel |
73 |
Molecular Autism: accelerating and integrating research into neurodevelopmental conditions
|
Buxbaum, Joseph D |
|
2010 |
|
1 |
|
artikel |
74 |
Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome
|
Greco, Claudia M |
|
2011 |
|
1 |
|
artikel |
75 |
Non-synonymous single-nucleotide variations of the human oxytocin receptor gene and autism spectrum disorders: a case–control study in a Japanese population and functional analysis
|
Ma, Wen-Jie |
|
2013 |
|
1 |
|
artikel |
76 |
Optimizing the phenotyping of rodent ASD models: enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological, electrophysiological, neurological, and behavioral features
|
Buxbaum, Joseph D |
|
2012 |
|
1 |
|
artikel |
77 |
Paternal age increases the risk for autism in an Iranian population sample
|
Sasanfar, Roksana |
|
2010 |
|
1 |
|
artikel |
78 |
PCR and serology find no association between xenotropic murine leukemia virus-related virus (XMRV) and autism
|
Satterfield, Brent C |
|
2010 |
|
1 |
|
artikel |
79 |
Phosphorylated fragile X mental retardation protein at serine 499, is reduced in cerebellar vermis and superior frontal cortex of subjects with autism: implications for fragile X mental retardation protein-metabotropic glutamate receptor 5 signaling
|
Rustan, Øyvind G |
|
2013 |
|
1 |
|
artikel |
80 |
Platelets of mice heterozygous for neurobeachin, a candidate gene for autism spectrum disorder, display protein changes related to aberrant protein kinase A activity
|
Nuytens, Kim |
|
2013 |
|
1 |
|
artikel |
81 |
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry
|
Sousa, Inês |
|
2010 |
|
1 |
|
artikel |
82 |
Prenatal versus postnatal sex steroid hormone effects on autistic traits in children at 18 to 24 months of age
|
Auyeung, Bonnie |
|
2012 |
|
1 |
|
artikel |
83 |
Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndrome
|
Tordjman, Sylvie |
|
2013 |
|
1 |
|
artikel |
84 |
Prevalence of autism in mainland China, Hong Kong and Taiwan: a systematic review and meta-analysis
|
Sun, Xiang |
|
2013 |
|
1 |
|
artikel |
85 |
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency
|
Soorya, Latha |
|
2013 |
|
1 |
|
artikel |
86 |
RAADS-14 Screen: validity of a screening tool for autism spectrum disorder in an adult psychiatric population
|
Eriksson, Jonna M |
|
2013 |
|
1 |
|
artikel |
87 |
Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome
|
Campbell, Nicholas G |
|
2013 |
|
1 |
|
artikel |
88 |
Reliability of self, parental, and researcher measurements of head circumference
|
Sullivan, Jillian C |
|
2014 |
|
1 |
|
artikel |
89 |
Review of neuroimaging in autism spectrum disorders: what have we learned and where we go from here
|
Anagnostou, Evdokia |
|
2011 |
|
1 |
|
artikel |
90 |
Self-referential and social cognition in a case of autism and agenesis of the corpus callosum
|
Lombardo, Michael V |
|
2012 |
|
1 |
|
artikel |
91 |
Serum levels of soluble platelet endothelial cell adhesion molecule-1 and vascular cell adhesion molecule-1 are decreased in subjects with autism spectrum disorder
|
Kameno, Yosuke |
|
2013 |
|
1 |
|
artikel |
92 |
Serum proteomic analysis identifies sex-specific differences in lipid metabolism and inflammation profiles in adults diagnosed with Asperger syndrome
|
Steeb, Hannah |
|
2014 |
|
1 |
|
artikel |
93 |
Sex-biased gene expression in the developing brain: implications for autism spectrum disorders
|
Ziats, Mark N |
|
2013 |
|
1 |
|
artikel |
94 |
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
|
Abrahams, Brett S |
|
2013 |
|
1 |
|
artikel |
95 |
SHANK3 haploinsufficiency: a “common” but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders
|
Betancur, Catalina |
|
2013 |
|
1 |
|
artikel |
96 |
Social and monetary reward processing in autism spectrum disorders
|
Delmonte, Sonja |
|
2012 |
|
1 |
|
artikel |
97 |
Spatial localisation in autism: evidence for differences in early cortical visual processing
|
Latham, Keziah |
|
2013 |
|
1 |
|
artikel |
98 |
Support for calcium channel gene defects in autism spectrum disorders
|
Lu, Ake Tzu-Hui |
|
2012 |
|
1 |
|
artikel |
99 |
Task-related functional connectivity in autism spectrum conditions: an EEG study using wavelet transform coherence
|
Catarino, Ana |
|
2013 |
|
1 |
|
artikel |
100 |
Test-retest reliability of the ‘Reading the Mind in the Eyes’ test: a one-year follow-up study
|
Fernández-Abascal, Enrique G |
|
2013 |
|
1 |
|
artikel |
101 |
The ongoing dissection of the genetic architecture of autistic spectrum disorder
|
Gillis, Rob F |
|
2011 |
|
1 |
|
artikel |
102 |
Transcriptome profiling in engrailed-2 mutant mice reveals common molecular pathways associated with autism spectrum disorders
|
Sgadò, Paola |
|
2013 |
|
1 |
|
artikel |
103 |
Transcriptomic analysis of genetically defined autism candidate genes reveals common mechanisms of action
|
Lanz, Thomas A |
|
2013 |
|
1 |
|
artikel |
104 |
Transient and steady-state auditory gamma-band responses in first-degree relatives of people with autism spectrum disorder
|
Rojas, Donald C |
|
2011 |
|
1 |
|
artikel |
105 |
Variation in the autism candidate gene GABRB3 modulates tactile sensitivity in typically developing children
|
Tavassoli, Teresa |
|
2012 |
|
1 |
|
artikel |
106 |
Variation in the human cannabinoid receptor CNR1 gene modulates gaze duration for happy faces
|
Chakrabarti, Bhismadev |
|
2011 |
|
1 |
|
artikel |
107 |
Vldlr overexpression causes hyperactivity in rats
|
Iwata, Keiko |
|
2012 |
|
1 |
|
artikel |
108 |
Whole-genome sequencing in an autism multiplex family
|
Shi, Lingling |
|
2013 |
|
1 |
|
artikel |