| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A potentiated startle study of uncertainty and contextual anxiety in adolescents diagnosed with autism spectrum disorder
|
Chamberlain, Paul D
|
|
2013
|
4 |
1 |
|
artikel
|
| 2 |
A review of the serotonin transporter and prenatal cortisol in the development of autism spectrum disorders
|
Rose’Meyer, Roselyn
|
|
2013
|
4 |
1 |
|
artikel
|
| 3 |
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
|
4 |
1 |
|
artikel
|
| 4 |
Autism in DSM-5: progress and challenges
|
Volkmar, Fred R
|
|
2013
|
4 |
1 |
|
artikel
|
| 5 |
Capping four years of growth of Molecular Autism: impact factor coming in 2014
|
Buxbaum, Joseph D
|
|
2013
|
4 |
1 |
|
artikel
|
| 6 |
Common variation contributes to the genetic architecture of social communication traits
|
St Pourcain, Beate
|
|
2013
|
4 |
1 |
|
artikel
|
| 7 |
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
|
4 |
1 |
|
artikel
|
| 8 |
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
|
4 |
1 |
|
artikel
|
| 9 |
Decreased tryptophan metabolism in patients with autism spectrum disorders
|
Boccuto, Luigi
|
|
2013
|
4 |
1 |
|
artikel
|
| 10 |
Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders
|
Chien, Wei-Hsien
|
|
2013
|
4 |
1 |
|
artikel
|
| 11 |
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
|
4 |
1 |
|
artikel
|
| 12 |
Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?
|
Amiet, Claire
|
|
2013
|
4 |
1 |
|
artikel
|
| 13 |
Do girls with anorexia nervosa have elevated autistic traits?
|
Baron-Cohen, Simon
|
|
2013
|
4 |
1 |
|
artikel
|
| 14 |
DSM-5 and autism spectrum disorders (ASDs): an opportunity for identifying ASD subtypes
|
Grzadzinski, Rebecca
|
|
2013
|
4 |
1 |
|
artikel
|
| 15 |
DSM-5: the debate continues
|
Buxbaum, Joseph D
|
|
2013
|
4 |
1 |
|
artikel
|
| 16 |
Enzymes in the glutamate-glutamine cycle in the anterior cingulate cortex in postmortem brain of subjects with autism
|
Shimmura, Chie
|
|
2013
|
4 |
1 |
|
artikel
|
| 17 |
Episodic memory retrieval for story characters in high-functioning autism
|
Komeda, Hidetsugu
|
|
2013
|
4 |
1 |
|
artikel
|
| 18 |
Evidence for differential alternative splicing in blood of young boys with autism spectrum disorders
|
Stamova, Boryana S
|
|
2013
|
4 |
1 |
|
artikel
|
| 19 |
Evidence of reactive oxygen species-mediated damage to mitochondrial DNA in children with typical autism
|
Napoli, Eleonora
|
|
2013
|
4 |
1 |
|
artikel
|
| 20 |
Exploring autistic traits in anorexia: a clinical study
|
Tchanturia, Kate
|
|
2013
|
4 |
1 |
|
artikel
|
| 21 |
Expression of non-protein-coding antisense RNAs in genomic regions related to autism spectrum disorders
|
Velmeshev, Dmitry
|
|
2013
|
4 |
1 |
|
artikel
|
| 22 |
Genetic background modulates phenotypes of serotonin transporter Ala56 knock-in mice
|
Kerr, Travis M
|
|
2013
|
4 |
1 |
|
artikel
|
| 23 |
Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism
|
Warrier, Varun
|
|
2013
|
4 |
1 |
|
artikel
|
| 24 |
Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder
|
Sarachana, Tewarit
|
|
2013
|
4 |
1 |
|
artikel
|
| 25 |
Identification of an age-dependent biomarker signature in children and adolescents with autism spectrum disorders
|
Ramsey, Jordan M
|
|
2013
|
4 |
1 |
|
artikel
|
| 26 |
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
|
4 |
1 |
|
artikel
|
| 27 |
Increased abundance of Sutterella spp. and Ruminococcus torques in feces of children with autism spectrum disorder
|
Wang, Lv
|
|
2013
|
4 |
1 |
|
artikel
|
| 28 |
Increased gene expression of FOXP1 in patients with autism spectrum disorders
|
Chien, Wei-Hsien
|
|
2013
|
4 |
1 |
|
artikel
|
| 29 |
Insulin-like growth factor-1 rescues synaptic and motor deficits in a mouse model of autism and developmental delay
|
Bozdagi, Ozlem
|
|
2013
|
4 |
1 |
|
artikel
|
| 30 |
Is metabotropic glutamate receptor 5 upregulated in prefrontal cortex in fragile X syndrome?
|
Lohith, Talakad G
|
|
2013
|
4 |
1 |
|
artikel
|
| 31 |
Is synaesthesia more common in autism?
|
Baron-Cohen, Simon
|
|
2013
|
4 |
1 |
|
artikel
|
| 32 |
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder
|
Bahl, Samira
|
|
2013
|
4 |
1 |
|
artikel
|
| 33 |
MeCP2 modulates gene expression pathways in astrocytes
|
Yasui, Dag H
|
|
2013
|
4 |
1 |
|
artikel
|
| 34 |
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
|
4 |
1 |
|
artikel
|
| 35 |
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
|
4 |
1 |
|
artikel
|
| 36 |
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
|
4 |
1 |
|
artikel
|
| 37 |
Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndrome
|
Tordjman, Sylvie
|
|
2013
|
4 |
1 |
|
artikel
|
| 38 |
Prevalence of autism in mainland China, Hong Kong and Taiwan: a systematic review and meta-analysis
|
Sun, Xiang
|
|
2013
|
4 |
1 |
|
artikel
|
| 39 |
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency
|
Soorya, Latha
|
|
2013
|
4 |
1 |
|
artikel
|
| 40 |
RAADS-14 Screen: validity of a screening tool for autism spectrum disorder in an adult psychiatric population
|
Eriksson, Jonna M
|
|
2013
|
4 |
1 |
|
artikel
|
| 41 |
Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome
|
Campbell, Nicholas G
|
|
2013
|
4 |
1 |
|
artikel
|
| 42 |
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
|
4 |
1 |
|
artikel
|
| 43 |
Sex-biased gene expression in the developing brain: implications for autism spectrum disorders
|
Ziats, Mark N
|
|
2013
|
4 |
1 |
|
artikel
|
| 44 |
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
|
Abrahams, Brett S
|
|
2013
|
4 |
1 |
|
artikel
|
| 45 |
SHANK3 haploinsufficiency: a “common” but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders
|
Betancur, Catalina
|
|
2013
|
4 |
1 |
|
artikel
|
| 46 |
Spatial localisation in autism: evidence for differences in early cortical visual processing
|
Latham, Keziah
|
|
2013
|
4 |
1 |
|
artikel
|
| 47 |
Task-related functional connectivity in autism spectrum conditions: an EEG study using wavelet transform coherence
|
Catarino, Ana
|
|
2013
|
4 |
1 |
|
artikel
|
| 48 |
Test-retest reliability of the ‘Reading the Mind in the Eyes’ test: a one-year follow-up study
|
Fernández-Abascal, Enrique G
|
|
2013
|
4 |
1 |
|
artikel
|
| 49 |
Transcriptome profiling in engrailed-2 mutant mice reveals common molecular pathways associated with autism spectrum disorders
|
Sgadò, Paola
|
|
2013
|
4 |
1 |
|
artikel
|
| 50 |
Transcriptomic analysis of genetically defined autism candidate genes reveals common mechanisms of action
|
Lanz, Thomas A
|
|
2013
|
4 |
1 |
|
artikel
|
| 51 |
Whole-genome sequencing in an autism multiplex family
|
Shi, Lingling
|
|
2013
|
4 |
1 |
|
artikel
|
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