| 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
|
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