(Q47982419)

7 February 2018

meta-analysis

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title

Lack of replication of previous autism spectrum disorder GWAS hits in European populations (English)

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7 February 2018

genome-wide association study

main subject

autism spectrum disorder

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autism

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6

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7 February 2018

Thomas Bourgeron

22

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7 February 2018

Bru Cormand

23

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7 February 2018

Claudio Toma

Claudio Toma

24

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Richard Delorme

Richard Delorme

19

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Francisco G Scholl

Francisco G Scholl

14

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Jan Buitelaar

7

Jan K Buitelaar

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7 February 2018

15

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7 February 2018

11

Christine M Freitag

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7 February 2018

Elena Bacchelli

3

Elena Bacchelli

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7 February 2018

Agatino Battaglia

17

Agatino Battaglia

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7 February 2018

Elena Maestrini

21

Elena Maestrini

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7 February 2018

Bàrbara Torrico

1

Bàrbara Torrico

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7 February 2018

Amaia Hervás

5

Amaia Hervás

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7 February 2018

Andreas G Chiocchetti

2

Andreas G Chiocchetti

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7 February 2018

author name string

Elisabetta Trabetti

4

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7 February 2018

Nanda Rommelse

8

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7 February 2018

Afsheen Yousaf

9

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7 February 2018

Eftichia Duketis

10

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7 February 2018

Rafaela Caballero-Andaluz

12

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7 February 2018

Amalia Martinez-Mir

13

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7 February 2018

ITAN

16

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7 February 2018

Giovanni Malerba

18

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7 February 2018

Marion Benabou

20

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7 February 2018

language of work or name

English

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publication date

15 July 2016

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7 February 2018

published in

Autism Research

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7 February 2018

volume

10

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7 February 2018

issue

2

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7 February 2018

page(s)

202-211

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7 February 2018

A genome-wide scan for common alleles affecting risk for autism

cites work

1 reference

From the genetic architecture to synaptic plasticity in autism spectrum disorder

21 January 2018

1 reference

Genetics in psychiatry: common variant association studies

21 January 2018

1 reference

Hotspots of large rare deletions in the human genome

21 January 2018

1 reference

Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample

21 January 2018

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Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population

21 January 2018

1 reference

Common body mass index-associated variants confer risk of extreme obesity

21 January 2018

1 reference

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

21 January 2018

1 reference

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder

21 January 2018

1 reference

Pervasive developmental disorders in preschool children: confirmation of high prevalence

21 January 2018

1 reference

An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk

21 January 2018

1 reference

Synaptic, transcriptional and chromatin genes disrupted in autism

21 January 2018

1 reference

Genetic architecture in autism spectrum disorder

21 January 2018

1 reference

Global prevalence of autism and other pervasive developmental disorders

21 January 2018

1 reference

Epidemiology of Pervasive Developmental Disorders

21 January 2018

1 reference

The genetics of autistic disorders and its clinical relevance: a review of the literature

21 January 2018

1 reference

minimac2: faster genotype imputation

21 January 2018

1 reference

Most genetic risk for autism resides with common variation

21 January 2018

1 reference

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

21 January 2018

1 reference

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

21 January 2018

1 reference

The contribution of de novo coding mutations to autism spectrum disorder

21 January 2018

1 reference

MACROD2 gene associated with autistic-like traits in a general population sample

21 January 2018

1 reference

Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10.

21 January 2018

1 reference

A noncoding RNA antisense to moesin at 5p14.1 in autism

21 January 2018

1 reference

Common genetic variants, acting additively, are a major source of risk for autism

21 January 2018

1 reference

Genome-wide association study identifies candidate genes for male fertility traits in humans

21 January 2018

1 reference

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

21 January 2018

1 reference

Excess of rare, inherited truncating mutations in autism

21 January 2018

1 reference

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

21 January 2018

1 reference

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

21 January 2018

1 reference

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 January 2018

1 reference

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

1 reference

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

21 January 2018

1 reference

Constitutional downregulation of SEMA5A expression in autism

21 January 2018

1 reference

Evaluating the evidence for transmission distortion in human pedigrees

21 January 2018

1 reference

A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability.

21 January 2018

1 reference

Patterns and rates of exonic de novo mutations in autism spectrum disorders

21 January 2018

1 reference

The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families.

21 January 2018

1 reference

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

21 January 2018

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PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

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Variants in several genomic regions associated with asperger disorder

21 January 2018

1 reference

Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder

21 January 2018

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

21 January 2018

1 reference

Genome-wide association study identifies five new schizophrenia loci

21 January 2018

1 reference

Biological insights from 108 schizophrenia-associated genetic loci

21 January 2018

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Two-marker association tests yield new disease associations for coronary artery disease and hypertension

21 January 2018

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Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population

21 January 2018

1 reference

Genetic architectures of psychiatric disorders: the emerging picture and its implications

21 January 2018

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Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC.

21 January 2018

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Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

21 January 2018

1 reference

Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability

21 January 2018

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The co-occurrence of autism spectrum disorder and attention-deficit/hyperactivity disorder symptoms in parents of children with ASD or ASD with ADHD.

21 January 2018

1 reference

Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders

21 January 2018

1 reference

Common genetic variants on 5p14.1 associate with autism spectrum disorders

21 January 2018

1 reference

A genome-wide linkage and association scan reveals novel loci for autism

21 January 2018

1 reference

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations

21 January 2018

1 reference

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

21 January 2018

1 reference

Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/AUR.1662

1 reference

7 February 2018

release_sl57msupcnbrfgfo5gzpmtde5q

Fatcat ID

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1 reference

7 February 2018