Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies (Q28943315)

14 March 2017

title

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

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genome-wide association study

14 March 2017

main subject

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adult attention deficit hyperactivity disorder

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16

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Klaus-Peter Lesch

1

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Susanne Walitza

object named as

Susanne Walitza

15

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Andreas Warnke

12

object named as

Andreas Warnke

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14 March 2017

11

Christine Freitag

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3

Tobias J. Renner

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5

Christoph Röser

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Jasmin Romanos

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Monika Heine

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Jobst Meyer

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Helmut Schäfer

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Marcel Romanos

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Nina Timmesfeld

2

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Rebecca Halperin

4

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T. Trang Nguyen

6

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David W. Craig

7

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Dietrich A. Stephan

17

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Christian Jacob

18

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language of work or name

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1 November 2008

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Journal of Neural Transmission

14 March 2017

published in

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14 March 2017

volume

115

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issue

11

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14 March 2017

page(s)

1573–1585

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CSMD1 is a novel multiple domain complement-regulatory protein highly expressed in the central nervous system and epithelial tissues

14 March 2017

cites work

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https://api.crossref.org/works/10.1007%2FS00702-008-0119-3

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Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12.

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Applicability of DNA pools on 500 K SNP microarrays for cost-effective initial screens in genomewide association studies

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Identification of proteins associating with glycosylphosphatidylinositol- anchored T-cadherin on the surface of vascular endothelial cells: role for Grp78/BiP in T-cadherin-dependent cell survival

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Negative regulation of insulin-stimulated mitogen-activated protein kinase signaling by Grb10.

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Cortical abnormalities in children and adolescents with attention-deficit hyperactivity disorder

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Whole-genome analysis of sporadic amyotrophic lateral sclerosis

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Molecular genetics of attention-deficit/hyperactivity disorder

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Deletion in Catna2, encoding alpha N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

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Growth factor receptor-binding protein 10 (Grb10) as a partner of phosphatidylinositol 3-kinase in metabolic insulin action

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CNS gene encoding astrotactin, which supports neuronal migration along glial fibers

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Central nervous system neuronal migration

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Integrin-linked kinase is an essential mediator for T-cadherin-dependent signaling via Akt and GSK3beta in endothelial cells

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Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

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12 December 2020

Distinct roles for the two Rho GDP/GTP exchange factor domains of kalirin in regulation of neurite growth and neuronal morphology.

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Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

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

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Molecular genetics of nicotine dependence and abstinence: whole genome association using 520,000 SNPs

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[Neurobiology of attention-deficit hyperactivity disorder].

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Molecular genetics of successful smoking cessation: convergent genome-wide association study results

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A genome-wide association study in 574 schizophrenia trios using DNA pooling

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Grb10: more than a simple adaptor protein

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Identification of two new members of the CSMD gene family

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12 December 2020

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

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SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays

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Transcriptome analysis identifies pathways associated with enhanced maternal performance in QSi5 mice.

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12 December 2020

Lifetime prevalence and age-of-onset distributions of mental disorders in the World Health Organization's World Mental Health Survey Initiative

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12 December 2020

Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11.

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A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples

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Dendritic spine dynamics--a key role for kalirin-7.

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

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12 December 2020

Isoforms of kalirin, a neuronal Dbl family member, generated through use of different 5'- and 3'-ends along with an internal translational initiation site

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12 December 2020

Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies

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12 December 2020