(Q41586761)

4 October 2017

New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder (English)

1 reference

adult attention deficit hyperactivity disorder

4 October 2017

0 references

1 reference

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

Josep Antoni Ramos-Quiroga

14 June 2020

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

Silvia Alemany

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

Marta Ribasés

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

Natalia Vilor-Tejedor

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

Mariona Bustamante

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

Cristina Sànchez-Mora

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

Rosa Bosch

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

author name string

Vanesa Richarte

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

Miguel Casas

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

Jordi Sunyer

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

publication date

14 July 2015

1 reference

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

4 October 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

volume

168

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

page(s)

459-470

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

Postnatal NMDA receptor ablation in corticolimbic interneurons confers schizophrenia-like phenotypes

14 June 2020

cites work

1 reference

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Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

21 January 2018

1 reference

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Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci

21 January 2018

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Genetic epidemiology of attention deficit hyperactivity disorder (ADHD index) in adults

21 January 2018

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Attention deficit hyperactivity disorder and substance use disorders

21 January 2018

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Rethinking environmental contributions to child and adolescent psychopathology: A meta-analysis of shared environmental influences

21 January 2018

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Neuroscience of attention-deficit/hyperactivity disorder: the search for endophenotypes

21 January 2018

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Attention-deficit/hyperactivity disorder, Tourette's syndrome, and restless legs syndrome: the iron hypothesis

21 January 2018

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Developmental twin study of attention problems: high heritabilities throughout development.

21 January 2018

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FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patients.

21 January 2018

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Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families.

21 January 2018

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Molecular genetics of attention-deficit/hyperactivity disorder

21 January 2018

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The genetics of attention deficit/hyperactivity disorder in adults, a review

21 January 2018

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SorCS2 regulates dopaminergic wiring and is processed into an apoptotic two-chain receptor in peripheral glia

21 January 2018

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Clinical assessment and diagnosis of adults with attention-deficit/hyperactivity disorder

21 January 2018

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The molecular genetic architecture of attention deficit hyperactivity disorder.

21 January 2018

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Genome-wide association study in German patients with attention deficit/hyperactivity disorder

21 January 2018

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Associations of sleep disturbance with ADHD: implications for treatment

21 January 2018

1 reference

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The prevalence and correlates of adult ADHD in the United States: results from the National Comorbidity Survey Replication

21 January 2018

1 reference

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Discovery and Replication of Gene Influences on Brain Structure Using LASSO Regression

21 January 2018

1 reference

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Increased echogenicity of the substantia nigra in children and adolescents with attention-deficit/hyperactivity disorder

21 January 2018

1 reference

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The IMAGE project: methodological issues for the molecular genetic analysis of ADHD.

21 January 2018

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The separation of ADHD inattention and hyperactivity-impulsivity symptoms: pathways from genetic effects to cognitive impairments and symptoms

21 January 2018

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Separation of cognitive impairments in attention-deficit/hyperactivity disorder into 2 familial factors

21 January 2018

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The impact of cyclothymic temperament in adult ADHD.

21 January 2018

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Genetic and environmental influences on adult attention deficit hyperactivity disorder symptoms: a large Swedish population-based study of twins

21 January 2018

1 reference

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Genetic variation in FGF20 modulates hippocampal biology

21 January 2018

1 reference

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Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

21 January 2018

1 reference

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Meta-analysis and imputation refines the association of 15q25 with smoking quantity

21 January 2018

1 reference

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A new multipoint method for genome-wide association studies by imputation of genotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

Family-based genome-wide association scan of attention-deficit/hyperactivity disorder

21 January 2018

1 reference

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A simple salting out procedure for extracting DNA from human nucleated cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

Genome-wide association scan of attention deficit hyperactivity disorder

21 January 2018

1 reference

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Case-control genome-wide association study of attention-deficit/hyperactivity disorder

21 January 2018

1 reference

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Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

Neto1 is a novel CUB-domain NMDA receptor-interacting protein required for synaptic plasticity and learning

21 January 2018

1 reference

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Synaptic scaffold evolution generated components of vertebrate cognitive complexity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

Normal attention orienting but abnormal stimulus alerting and conflict effect in combined subtype of ADHD.

21 January 2018

1 reference

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FGF-20, a novel neurotrophic factor, preferentially expressed in the substantia nigra pars compacta of rat brain

21 January 2018

1 reference

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Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

H¹-MR-spectroscopy of cerebellum in adult attention deficit/hyperactivity disorder

21 January 2018

1 reference

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The co-occurrence of autistic and ADHD dimensions in adults: an etiological study in 17,770 twins.

21 January 2018

1 reference

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

21 January 2018

1 reference

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APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study

21 January 2018

1 reference

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Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins

21 January 2018

1 reference

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Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)

21 January 2018

1 reference

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Structural abnormality of the substantia nigra in children with attention-deficit hyperactivity disorder

21 January 2018

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Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample

21 January 2018

1 reference

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The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans

21 January 2018

1 reference

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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

1 reference

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Exploring the genetic link between RLS and ADHD.

21 January 2018

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Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits

21 January 2018

1 reference

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Gray matter alterations in adults with attention-deficit/hyperactivity disorder identified by voxel based morphometry

21 January 2018

1 reference

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Prevalence and correlates of adult attention-deficit hyperactivity disorder: meta-analysis

21 January 2018

1 reference

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A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia

21 January 2018

1 reference

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A genetic risk factor for periodic limb movements in sleep

21 January 2018

1 reference

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Synaptic plasticity and dysconnection in schizophrenia

21 January 2018

1 reference

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Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

A novel gene encoding a putative transmembrane protein with two extracellular CUB domains and a low-density lipoprotein class A module: isolation of alternatively spliced isoforms in retina and brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32341

Preliminary study of the prevalence of restless legs syndrome in adults with attention deficit hyperactivity disorder.

21 January 2018

1 reference

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The amyloid precursor protein: beyond amyloid

21 January 2018

1 reference

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21 January 2018

Identifiers

DOI

10.1002/AJMG.B.32341

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26174813%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

1 reference